1) Proteins in the diet are broken down into smaller peptides and individual amino acids through digestion by proteolytic enzymes in the stomach, pancreas, and intestines.
2) In the liver, amino acids are broken down through transamination and transdeamination reactions to produce ammonia, which is highly toxic.
3) Ammonia is detoxified in the liver through the urea cycle into urea, which is excreted in the urine. Deficiencies in urea cycle enzymes can cause a toxic buildup of ammonia in the blood.
The major dietary lipids are triacylglycerols, cholesterol, phospholipids, and free fatty acids. Lipids are insoluble in water and require digestion by lipases and emulsification by bile salts to be broken down into absorbable components. In the small intestine, pancreatic lipase breaks triacylglycerols into fatty acids and monoacylglycerols within mixed micelles. Bile salts also aid in emulsifying lipids into smaller particles. Digestion products are absorbed via micelle diffusion and resynthesized into triglycerides and phospholipids within intestinal cells before transport to the liver via the lymphatic system or blood.
The document summarizes the process of carbohydrate digestion in humans. It begins with mechanical digestion in the mouth through chewing. Chemical digestion then starts with salivary amylase breaking down some starch in the mouth. In the stomach, further mixing occurs and ptyalin continues breaking down starch, with around 30-40% being digested. The acidic stomach stops further digestion. In the small intestine, pancreatic amylase and intestinal enzymes hydrolyze starches and sugars into monosaccharides like glucose and fructose which are then absorbed into the bloodstream. Certain carbohydrates like cellulose are not digested but provide fiber.
There are three important ketone bodies - aceto-acetate, acetone, and β-hydroxybutyrate. Ketone body synthesis occurs in the liver from acetyl-CoA but their utilization occurs in other tissues like cardiac muscle and brain. Ketone bodies are produced during periods of fasting or starvation and act as an alternative fuel source. Increased ketone body production can lead to metabolic acidosis if the buffering system is overwhelmed by too many hydrogen ions being released.
Digestion and absorption of lipids ppt
what is lipid ppt
digestion of lipid ppt
phase of digestion and absorption ppt
phases of lipids ppt
digestion in mouth and stomach ppt
digestion in small intestine ppt
secretion of lipids ppt
enzyme involved in lipid digestion ppt
transportation phases of lipids ppt
principles of lipid digestion ppt
The document discusses protein digestion and absorption. Proteins are broken down into peptides and amino acids by digestive enzymes in the stomach and small intestine. Peptides and amino acids are then absorbed into the bloodstream. Most proteins must be fully broken down before absorption, though some intact proteins can be absorbed by infants or through abnormal routes in adults. The amino acids are used throughout the body for protein synthesis, energy production, and other purposes.
- Methionine and cysteine are sulfur-containing amino acids. Methionine is an essential amino acid while cysteine can be synthesized from methionine and serine.
- There are three major metabolic routes for methionine and cysteine: 1) methionine is used for transmethylation, 2) methionine is used for cysteine synthesis, and 3) cysteine is broken down to make specialized products.
- Deficiencies in enzymes involved in methionine and cysteine metabolism can cause inborn errors such as homocystinuria, cystathioninuria, and cystinosis.
1) Proteins in the diet are broken down into smaller peptides and individual amino acids through digestion by proteolytic enzymes in the stomach, pancreas, and intestines.
2) In the liver, amino acids are broken down through transamination and transdeamination reactions to produce ammonia, which is highly toxic.
3) Ammonia is detoxified in the liver through the urea cycle into urea, which is excreted in the urine. Deficiencies in urea cycle enzymes can cause a toxic buildup of ammonia in the blood.
The major dietary lipids are triacylglycerols, cholesterol, phospholipids, and free fatty acids. Lipids are insoluble in water and require digestion by lipases and emulsification by bile salts to be broken down into absorbable components. In the small intestine, pancreatic lipase breaks triacylglycerols into fatty acids and monoacylglycerols within mixed micelles. Bile salts also aid in emulsifying lipids into smaller particles. Digestion products are absorbed via micelle diffusion and resynthesized into triglycerides and phospholipids within intestinal cells before transport to the liver via the lymphatic system or blood.
The document summarizes the process of carbohydrate digestion in humans. It begins with mechanical digestion in the mouth through chewing. Chemical digestion then starts with salivary amylase breaking down some starch in the mouth. In the stomach, further mixing occurs and ptyalin continues breaking down starch, with around 30-40% being digested. The acidic stomach stops further digestion. In the small intestine, pancreatic amylase and intestinal enzymes hydrolyze starches and sugars into monosaccharides like glucose and fructose which are then absorbed into the bloodstream. Certain carbohydrates like cellulose are not digested but provide fiber.
There are three important ketone bodies - aceto-acetate, acetone, and β-hydroxybutyrate. Ketone body synthesis occurs in the liver from acetyl-CoA but their utilization occurs in other tissues like cardiac muscle and brain. Ketone bodies are produced during periods of fasting or starvation and act as an alternative fuel source. Increased ketone body production can lead to metabolic acidosis if the buffering system is overwhelmed by too many hydrogen ions being released.
Digestion and absorption of lipids ppt
what is lipid ppt
digestion of lipid ppt
phase of digestion and absorption ppt
phases of lipids ppt
digestion in mouth and stomach ppt
digestion in small intestine ppt
secretion of lipids ppt
enzyme involved in lipid digestion ppt
transportation phases of lipids ppt
principles of lipid digestion ppt
The document discusses protein digestion and absorption. Proteins are broken down into peptides and amino acids by digestive enzymes in the stomach and small intestine. Peptides and amino acids are then absorbed into the bloodstream. Most proteins must be fully broken down before absorption, though some intact proteins can be absorbed by infants or through abnormal routes in adults. The amino acids are used throughout the body for protein synthesis, energy production, and other purposes.
- Methionine and cysteine are sulfur-containing amino acids. Methionine is an essential amino acid while cysteine can be synthesized from methionine and serine.
- There are three major metabolic routes for methionine and cysteine: 1) methionine is used for transmethylation, 2) methionine is used for cysteine synthesis, and 3) cysteine is broken down to make specialized products.
- Deficiencies in enzymes involved in methionine and cysteine metabolism can cause inborn errors such as homocystinuria, cystathioninuria, and cystinosis.
This document summarizes the digestion and absorption of proteins in the human body. It discusses that proteins are obtained endogenously from digestive enzymes and cells, as well as exogenously from dietary intake. The stomach contains hydrochloric acid and pepsin to denature and break down proteins. The pancreas secretes trypsinogen, chymotrypsinogen, and other zymogens which are activated and further digest proteins into peptides and amino acids in the small intestine. Aminopeptidases and dipeptidases on intestinal cells complete the digestion. Amino acids are then absorbed via active transport systems involving sodium and ATP. Deficiencies or defects in these digestive processes can impair protein digestion.
Biochemistry ii protein (metabolism of amino acids) (new edition)abdulhussien aljebory
This document discusses the metabolism of amino acids. It begins with an introduction and overview of amino acid classification, definitions of terms like nitrogen balance and biological value, and the digestion and absorption of proteins. It then covers the metabolic fates of amino acids, including removal of ammonia via deamination, transamination, and transdeamination. The carbon skeletons of amino acids can be used for biosynthesis, the synthesis of non-protein nitrogen compounds, or energy production. Ammonia is further metabolized. Overall, the document provides a comprehensive overview of the key processes in amino acid metabolism.
Gluconeogenesis is the formation of glucose from non-carbohydrate precursors and occurs primarily in the liver and kidneys. Key substrates include lactate, glycerol, and glucogenic amino acids. The process is regulated by substrate availability and key enzymes such as pyruvate carboxylase and phosphoenolpyruvate carboxykinase. Gluconeogenesis is critical for maintaining blood glucose levels during periods of fasting or low carbohydrate intake.
This document summarizes the digestion and absorption of carbohydrates. It discusses that carbohydrates are broken down into monosaccharides in the mouth by salivary amylase, pass undigested through the stomach, and are further broken down in the small intestine by pancreatic amylase and intestinal disaccharidases into absorbable monosaccharides like glucose, fructose and galactose. These monosaccharides are then absorbed into the bloodstream through active transport using sodium-glucose transporters or facilitated diffusion using glucose transporters. Lactose intolerance results if the enzyme lactase is deficient and lactose cannot be fully digested.
Carbohydrates are digested into monosaccharides like glucose, fructose, and galactose which are then absorbed in the small intestine. Glucose accounts for about 80% of absorbed monosaccharides and is actively transported into intestinal cells via sodium-glucose transporters, using the sodium gradient as an energy source. Galactose absorption is similar to glucose while fructose absorption occurs via facilitated diffusion without requiring sodium or energy. Absorption rates vary between sugars with galactose absorbing most rapidly, followed by glucose, then fructose and pentoses absorbing slowest. Health of the intestinal mucosa and various hormones can also impact carbohydrate absorption rates.
This document summarizes carbohydrate digestion in the human gastrointestinal tract. It describes how carbohydrates are broken down into smaller molecules by salivary and pancreatic amylases and intestinal disaccharidases and oligosaccharidases. The monosaccharides glucose, fructose and galactose that are produced are then absorbed into the bloodstream in the small intestine. Glucose absorption is an active process that utilizes sodium-glucose co-transporters, while fructose absorption occurs via facilitated diffusion. Factors that can influence carbohydrate absorption such as intestinal health, hormones and vitamins are also discussed.
Lipids are digested and absorbed in a multi-step process involving enzymes in the mouth, stomach, and small intestine. In the mouth, lingual lipase begins hydrolysis of triglycerides. In the stomach, gastric lipase continues this process. In the small intestine, pancreatic lipase works with bile salts to further digest triglycerides into fatty acids and monoglycerides. Bile salts emulsify lipids and facilitate absorption. Fatty acids and monoglycerides are absorbed into intestinal cells and re-esterified into triglycerides. These triglycerides are packaged into chylomicrons and enter the lymphatic system for transport.
1) The document discusses lipid metabolism, including the classification, digestion, and metabolism of various lipids like triglycerides, cholesterol, and phospholipids.
2) It provides details on the classification of fatty acids, the digestion of triglycerols in the small intestine, and the catabolism of triglycerols through beta-oxidation in the mitochondria to produce acetyl-CoA.
3) The synthesis of triglycerides is also summarized, including the monoacylglycerol and diacylglycerol pathways. Lipogenesis, the synthesis of fatty acids from acetyl-CoA, and the metabolism of cholesterol are also covered.
This document discusses protein metabolism. It covers:
1. Protein metabolism involves the synthesis and breakdown of proteins and amino acids. Catabolism of amino acids provides substrates for energy production and gluconeogenesis.
2. Proteins take on many forms in the body including enzymes, transporters, structural supports, and regulators. Protein turnover constantly synthesizes and degrades proteins.
3. Dietary proteins supply essential amino acids and are broken down into amino acids during digestion. Amino acids are absorbed and incorporated into tissues or oxidized to produce energy, ammonia, and ketone bodies.
Class 1 digestion and absorption of carbohydrateDhiraj Trivedi
Dr. Dhiraj J. Trivedi presenting Lecture on Carbohydrate metabolism for medical students.
Professor, SDM College of Medical Sciences, Dharwad, Karnataka, India
Lipids undergo a multi-step digestion and absorption process in the gastrointestinal tract. Dietary lipids are emulsified and broken down into smaller components like fatty acids and monoacylglycerols by lingual and gastric lipases in the stomach and pancreatic lipase in the small intestine. Bile salts produced by the liver play a key role in emulsification. The products of digestion are incorporated into micelles and absorbed by intestinal cells. Inside cells, fatty acids are reassembled into triglycerides and packaged into chylomicrons that enter the lymphatic system and bloodstream for transport to tissues. Defects in digestion, emulsification, or absorption can impair this process.
structure of proteins
definition of Digestion
sources of Proteins --> EXOGENEOUS SOURCES 50-100g/day and ENDOGENEOUS SOURCES 30-100g/day
Proteins DEGRADED BY --> HYDROLASES specifically PEPTIDASES(ENDOPEPTIDASES & EXOPEPTIDASES)
1. Gastric Digestion of Proteins
2. Pancreatic Digestion of Proteins
3. Digestion of Proteins by Small Intestine Enzymes
Absorption of Amino ACids by Na+Dependent, Na+ Independent, Meister Cycle or gama-glutamyl cycle
ketogenesis and utilisation of ketone bodies.pptxManoharKumar81
The document discusses ketone bodies, which are produced when fatty acids are broken down in excess. The three major ketone bodies are acetoacetate, acetone, and beta-hydroxybutyrate. Ketone bodies are an alternative energy source and are produced when glucose availability is limited, such as during starvation or uncontrolled diabetes. They are synthesized in the liver and can be used by tissues like the brain. Conditions that result in excessive ketone body production are called ketosis.
Lipids are digested and absorbed through a multi-step process. Dietary lipids are broken down by lingual and gastric lipases in the mouth and stomach. In the small intestine, pancreatic lipase works with bile salts to emulsify and further digest triglycerides into fatty acids and monoacylglycerols. These products form micelles that enable absorption by enterocytes. Within enterocytes, fatty acids and monoacylglycerols are re-esterified into triglycerides and combined with cholesterol to form chylomicrons, which transport the absorbed lipids into the lymphatic system and bloodstream. Chylomicrons are then broken down by lipoprotein lipase in capillary beds
Glycogenolysis is the breakdown of glycogen into glucose-1-phosphate. It occurs in three steps:
1) Phosphorolysis by glycogen phosphorylase cleaves α-1,4 glycosidic linkages, producing glucose-1-phosphate until four glucose residues remain.
2) A debranching enzyme removes these four residue branches through two activities, producing linear chains of glucose residues.
3) Phosphoglucomutase converts glucose-1-phosphate to glucose-6-phosphate, which can then enter glycolysis to produce energy or be released as free glucose from the liver. Glycogenolysis is regulated by allosteric effectors, hormones like glucagon and
Presentation on the mechanism of HCl production in the stomachMahtabUddinMojumder
The document presents information on the mechanism of HCl production in the stomach. It discusses the three phases of gastric secretion regulation and the two pathways of acid secretion - the cAMP dependent pathway and the Ca2+ dependent pathway. In both pathways, parietal cells in the stomach secrete acid through the action of histamine and stimulation of the H+/K+ ATPase pump. HCl production allows for protein digestion and creates an inhospitable environment for bacteria in the stomach. Common drugs for treating acid reflux include proton pump inhibitors which block acid secretion and H2 receptor blockers which prevent histamine from stimulating acid release.
Lect 6. (digestion and absorption in git)Ayub Abdi
The document discusses digestion and absorption in the gastrointestinal tract. It covers:
- How folds, villi, and microvilli in the small intestine increase the absorptive surface area by nearly 1000 times.
- The breakdown of carbohydrates, proteins, and fats through hydrolysis by enzymes in the mouth, stomach, and small intestine.
- How monosaccharides, amino acids, fatty acids, and glycerol are absorbed into the bloodstream through active transport mechanisms like sodium co-transport or passive diffusion using micelles.
- Water and electrolytes like sodium are also absorbed through diffusion or active transport processes.
Cholesterol is synthesized in the body and obtained through diet. It has important functions but excess can promote atherosclerosis. Cholesterol synthesis occurs mainly in the liver and involves four stages. The rate-limiting enzyme HMG-CoA reductase is regulated by phosphorylation/dephosphorylation and repression/derepression. Cholesterol levels in cells are regulated by LDL receptor uptake and catabolism to bile acids. High LDL and triglycerides increase atherosclerosis risk while high HDL is protective. Risk factors like these are addressed through dietary and drug measures like statins that lower cholesterol synthesis.
This document summarizes ketone body metabolism. It describes that ketone bodies (acetone, acetoacetate, and beta-hydroxybutyrate) are produced in the liver from fatty acids during periods of low carbohydrate availability like starvation and untreated diabetes. The liver converts fatty acids into ketone bodies which can be used as fuel by other tissues. High glucagon and low insulin levels promote ketone body formation and their levels in the blood (ketonemia) and urine (ketonuria) increase if their production exceeds utilization, causing the metabolic condition of ketosis.
Metabolism is the sum of all chemical reactions in the body. Protein turnover involves the breakdown and synthesis of protein. The amino acid pool contains free amino acids distributed throughout extracellular fluid. Amino acids undergo intermediary metabolism through anabolism and catabolism, including transamination, deamination, and the urea cycle. Transamination is the transfer of amino groups between amino acids and keto acids without producing free ammonia. Deamination removes amino groups from amino acids, producing ammonia. Glutamate uniquely undergoes rapid oxidative deamination. The liver plays a key role in nitrogen metabolism by incorporating ammonia into urea or glutamine to prevent ammonia intoxication. Genetic disorders can result from inborn errors
The document discusses digestion and absorption of carbohydrates, proteins, and lipids. It explains that digestion breaks down macromolecules into smaller absorbable units using enzymes. Absorption then transports these digestion end products into the bloodstream. Carbohydrates are broken down into monosaccharides like glucose and galactose. Proteins become amino acids and peptides. Lipids are broken into fatty acids, glycerol, and other products through the action of bile and lipases.
This document provides an overview of the digestive system, including:
1) The roles and secretions of digestive juices and gastrointestinal hormones in breaking down food and stimulating digestion.
2) How carbohydrates, proteins, lipids, nucleic acids, and other nutrients are digested and absorbed in different parts of the GI tract through the actions of enzymes and transporters.
3) Common digestive issues like lactose intolerance, fat malabsorption, and protein digestion defects that can occur if there are problems with secretion or absorption along the GI tract.
This document summarizes the digestion and absorption of proteins in the human body. It discusses that proteins are obtained endogenously from digestive enzymes and cells, as well as exogenously from dietary intake. The stomach contains hydrochloric acid and pepsin to denature and break down proteins. The pancreas secretes trypsinogen, chymotrypsinogen, and other zymogens which are activated and further digest proteins into peptides and amino acids in the small intestine. Aminopeptidases and dipeptidases on intestinal cells complete the digestion. Amino acids are then absorbed via active transport systems involving sodium and ATP. Deficiencies or defects in these digestive processes can impair protein digestion.
Biochemistry ii protein (metabolism of amino acids) (new edition)abdulhussien aljebory
This document discusses the metabolism of amino acids. It begins with an introduction and overview of amino acid classification, definitions of terms like nitrogen balance and biological value, and the digestion and absorption of proteins. It then covers the metabolic fates of amino acids, including removal of ammonia via deamination, transamination, and transdeamination. The carbon skeletons of amino acids can be used for biosynthesis, the synthesis of non-protein nitrogen compounds, or energy production. Ammonia is further metabolized. Overall, the document provides a comprehensive overview of the key processes in amino acid metabolism.
Gluconeogenesis is the formation of glucose from non-carbohydrate precursors and occurs primarily in the liver and kidneys. Key substrates include lactate, glycerol, and glucogenic amino acids. The process is regulated by substrate availability and key enzymes such as pyruvate carboxylase and phosphoenolpyruvate carboxykinase. Gluconeogenesis is critical for maintaining blood glucose levels during periods of fasting or low carbohydrate intake.
This document summarizes the digestion and absorption of carbohydrates. It discusses that carbohydrates are broken down into monosaccharides in the mouth by salivary amylase, pass undigested through the stomach, and are further broken down in the small intestine by pancreatic amylase and intestinal disaccharidases into absorbable monosaccharides like glucose, fructose and galactose. These monosaccharides are then absorbed into the bloodstream through active transport using sodium-glucose transporters or facilitated diffusion using glucose transporters. Lactose intolerance results if the enzyme lactase is deficient and lactose cannot be fully digested.
Carbohydrates are digested into monosaccharides like glucose, fructose, and galactose which are then absorbed in the small intestine. Glucose accounts for about 80% of absorbed monosaccharides and is actively transported into intestinal cells via sodium-glucose transporters, using the sodium gradient as an energy source. Galactose absorption is similar to glucose while fructose absorption occurs via facilitated diffusion without requiring sodium or energy. Absorption rates vary between sugars with galactose absorbing most rapidly, followed by glucose, then fructose and pentoses absorbing slowest. Health of the intestinal mucosa and various hormones can also impact carbohydrate absorption rates.
This document summarizes carbohydrate digestion in the human gastrointestinal tract. It describes how carbohydrates are broken down into smaller molecules by salivary and pancreatic amylases and intestinal disaccharidases and oligosaccharidases. The monosaccharides glucose, fructose and galactose that are produced are then absorbed into the bloodstream in the small intestine. Glucose absorption is an active process that utilizes sodium-glucose co-transporters, while fructose absorption occurs via facilitated diffusion. Factors that can influence carbohydrate absorption such as intestinal health, hormones and vitamins are also discussed.
Lipids are digested and absorbed in a multi-step process involving enzymes in the mouth, stomach, and small intestine. In the mouth, lingual lipase begins hydrolysis of triglycerides. In the stomach, gastric lipase continues this process. In the small intestine, pancreatic lipase works with bile salts to further digest triglycerides into fatty acids and monoglycerides. Bile salts emulsify lipids and facilitate absorption. Fatty acids and monoglycerides are absorbed into intestinal cells and re-esterified into triglycerides. These triglycerides are packaged into chylomicrons and enter the lymphatic system for transport.
1) The document discusses lipid metabolism, including the classification, digestion, and metabolism of various lipids like triglycerides, cholesterol, and phospholipids.
2) It provides details on the classification of fatty acids, the digestion of triglycerols in the small intestine, and the catabolism of triglycerols through beta-oxidation in the mitochondria to produce acetyl-CoA.
3) The synthesis of triglycerides is also summarized, including the monoacylglycerol and diacylglycerol pathways. Lipogenesis, the synthesis of fatty acids from acetyl-CoA, and the metabolism of cholesterol are also covered.
This document discusses protein metabolism. It covers:
1. Protein metabolism involves the synthesis and breakdown of proteins and amino acids. Catabolism of amino acids provides substrates for energy production and gluconeogenesis.
2. Proteins take on many forms in the body including enzymes, transporters, structural supports, and regulators. Protein turnover constantly synthesizes and degrades proteins.
3. Dietary proteins supply essential amino acids and are broken down into amino acids during digestion. Amino acids are absorbed and incorporated into tissues or oxidized to produce energy, ammonia, and ketone bodies.
Class 1 digestion and absorption of carbohydrateDhiraj Trivedi
Dr. Dhiraj J. Trivedi presenting Lecture on Carbohydrate metabolism for medical students.
Professor, SDM College of Medical Sciences, Dharwad, Karnataka, India
Lipids undergo a multi-step digestion and absorption process in the gastrointestinal tract. Dietary lipids are emulsified and broken down into smaller components like fatty acids and monoacylglycerols by lingual and gastric lipases in the stomach and pancreatic lipase in the small intestine. Bile salts produced by the liver play a key role in emulsification. The products of digestion are incorporated into micelles and absorbed by intestinal cells. Inside cells, fatty acids are reassembled into triglycerides and packaged into chylomicrons that enter the lymphatic system and bloodstream for transport to tissues. Defects in digestion, emulsification, or absorption can impair this process.
structure of proteins
definition of Digestion
sources of Proteins --> EXOGENEOUS SOURCES 50-100g/day and ENDOGENEOUS SOURCES 30-100g/day
Proteins DEGRADED BY --> HYDROLASES specifically PEPTIDASES(ENDOPEPTIDASES & EXOPEPTIDASES)
1. Gastric Digestion of Proteins
2. Pancreatic Digestion of Proteins
3. Digestion of Proteins by Small Intestine Enzymes
Absorption of Amino ACids by Na+Dependent, Na+ Independent, Meister Cycle or gama-glutamyl cycle
ketogenesis and utilisation of ketone bodies.pptxManoharKumar81
The document discusses ketone bodies, which are produced when fatty acids are broken down in excess. The three major ketone bodies are acetoacetate, acetone, and beta-hydroxybutyrate. Ketone bodies are an alternative energy source and are produced when glucose availability is limited, such as during starvation or uncontrolled diabetes. They are synthesized in the liver and can be used by tissues like the brain. Conditions that result in excessive ketone body production are called ketosis.
Lipids are digested and absorbed through a multi-step process. Dietary lipids are broken down by lingual and gastric lipases in the mouth and stomach. In the small intestine, pancreatic lipase works with bile salts to emulsify and further digest triglycerides into fatty acids and monoacylglycerols. These products form micelles that enable absorption by enterocytes. Within enterocytes, fatty acids and monoacylglycerols are re-esterified into triglycerides and combined with cholesterol to form chylomicrons, which transport the absorbed lipids into the lymphatic system and bloodstream. Chylomicrons are then broken down by lipoprotein lipase in capillary beds
Glycogenolysis is the breakdown of glycogen into glucose-1-phosphate. It occurs in three steps:
1) Phosphorolysis by glycogen phosphorylase cleaves α-1,4 glycosidic linkages, producing glucose-1-phosphate until four glucose residues remain.
2) A debranching enzyme removes these four residue branches through two activities, producing linear chains of glucose residues.
3) Phosphoglucomutase converts glucose-1-phosphate to glucose-6-phosphate, which can then enter glycolysis to produce energy or be released as free glucose from the liver. Glycogenolysis is regulated by allosteric effectors, hormones like glucagon and
Presentation on the mechanism of HCl production in the stomachMahtabUddinMojumder
The document presents information on the mechanism of HCl production in the stomach. It discusses the three phases of gastric secretion regulation and the two pathways of acid secretion - the cAMP dependent pathway and the Ca2+ dependent pathway. In both pathways, parietal cells in the stomach secrete acid through the action of histamine and stimulation of the H+/K+ ATPase pump. HCl production allows for protein digestion and creates an inhospitable environment for bacteria in the stomach. Common drugs for treating acid reflux include proton pump inhibitors which block acid secretion and H2 receptor blockers which prevent histamine from stimulating acid release.
Lect 6. (digestion and absorption in git)Ayub Abdi
The document discusses digestion and absorption in the gastrointestinal tract. It covers:
- How folds, villi, and microvilli in the small intestine increase the absorptive surface area by nearly 1000 times.
- The breakdown of carbohydrates, proteins, and fats through hydrolysis by enzymes in the mouth, stomach, and small intestine.
- How monosaccharides, amino acids, fatty acids, and glycerol are absorbed into the bloodstream through active transport mechanisms like sodium co-transport or passive diffusion using micelles.
- Water and electrolytes like sodium are also absorbed through diffusion or active transport processes.
Cholesterol is synthesized in the body and obtained through diet. It has important functions but excess can promote atherosclerosis. Cholesterol synthesis occurs mainly in the liver and involves four stages. The rate-limiting enzyme HMG-CoA reductase is regulated by phosphorylation/dephosphorylation and repression/derepression. Cholesterol levels in cells are regulated by LDL receptor uptake and catabolism to bile acids. High LDL and triglycerides increase atherosclerosis risk while high HDL is protective. Risk factors like these are addressed through dietary and drug measures like statins that lower cholesterol synthesis.
This document summarizes ketone body metabolism. It describes that ketone bodies (acetone, acetoacetate, and beta-hydroxybutyrate) are produced in the liver from fatty acids during periods of low carbohydrate availability like starvation and untreated diabetes. The liver converts fatty acids into ketone bodies which can be used as fuel by other tissues. High glucagon and low insulin levels promote ketone body formation and their levels in the blood (ketonemia) and urine (ketonuria) increase if their production exceeds utilization, causing the metabolic condition of ketosis.
Metabolism is the sum of all chemical reactions in the body. Protein turnover involves the breakdown and synthesis of protein. The amino acid pool contains free amino acids distributed throughout extracellular fluid. Amino acids undergo intermediary metabolism through anabolism and catabolism, including transamination, deamination, and the urea cycle. Transamination is the transfer of amino groups between amino acids and keto acids without producing free ammonia. Deamination removes amino groups from amino acids, producing ammonia. Glutamate uniquely undergoes rapid oxidative deamination. The liver plays a key role in nitrogen metabolism by incorporating ammonia into urea or glutamine to prevent ammonia intoxication. Genetic disorders can result from inborn errors
The document discusses digestion and absorption of carbohydrates, proteins, and lipids. It explains that digestion breaks down macromolecules into smaller absorbable units using enzymes. Absorption then transports these digestion end products into the bloodstream. Carbohydrates are broken down into monosaccharides like glucose and galactose. Proteins become amino acids and peptides. Lipids are broken into fatty acids, glycerol, and other products through the action of bile and lipases.
This document provides an overview of the digestive system, including:
1) The roles and secretions of digestive juices and gastrointestinal hormones in breaking down food and stimulating digestion.
2) How carbohydrates, proteins, lipids, nucleic acids, and other nutrients are digested and absorbed in different parts of the GI tract through the actions of enzymes and transporters.
3) Common digestive issues like lactose intolerance, fat malabsorption, and protein digestion defects that can occur if there are problems with secretion or absorption along the GI tract.
Digestion and absorption review k&m chapter1Pave Medicine
The document discusses the digestive system and process of digestion and absorption. It describes how the digestive system breaks down food into smaller molecules through mechanical and chemical breakdown. Various organs secrete enzymes that break down carbohydrates, proteins, and fats. Nutrients are then absorbed through the small intestine into blood or lymph and transported to the liver and cells. Accessory organs like the pancreas, liver, and gallbladder aid digestion through secretion of enzymes and bile.
Digestion and absorption review k&m chapter1Pave Medicine
The document summarizes key aspects of digestion and absorption in the gastrointestinal (GI) tract. It describes how the digestive system breaks down food into smaller components through mechanical and enzymatic processes. Nutrients are then absorbed through the walls of the small intestine and transported to the liver and bloodstream. Accessory organs like the pancreas, liver, and gallbladder aid digestion by secreting enzymes and bile.
The document summarizes the key processes of digestion and absorption in the gastrointestinal tract. It discusses:
1) The three main stages of digestion - mechanical and chemical breakdown of food, secretion of enzymes and electrolytes to provide optimal conditions for digestion, and transport of nutrients into the bloodstream.
2) The major secretions at each stage - saliva, gastric juices, pancreatic and bile secretions, and secretions from the small intestine.
3) The enzymes and constituents involved in digesting carbohydrates, proteins, lipids, and their absorption mechanisms.
4) Some common digestive disorders that can result from enzyme deficiencies or malabsorption.
The digestive system has two major parts: the gastrointestinal tract and accessory organs. The gastrointestinal tract includes the mouth, esophagus, stomach, small intestine and large intestine. Accessory organs include the teeth, tongue, liver, gallbladder and pancreas. Food is ingested, mechanically and chemically digested, absorbed in the small intestine, and waste is excreted. Digestion involves enzymes from the mouth, stomach, pancreas, and small intestine breaking down food into smaller molecules that can be absorbed and used by the body. Hormones like gastrin and secretin regulate digestive processes.
DIGESTION & ABSORPTION OF BIOMOLECULES by Dr. Santhosh Kumar N.docxDr. Santhosh Kumar. N
The document summarizes the digestion and absorption of carbohydrates, proteins, and lipids in the human digestive system. It describes how:
Carbohydrates are broken down into monosaccharides like glucose through the actions of salivary and pancreatic amylases and intestinal disaccharidases. Proteins are broken into amino acids through digestion by stomach acid and pancreatic proteases like trypsin and chymotrypsin. Lipids are emulsified by bile and broken into fatty acids and glycerol by lingual and pancreatic lipases. The resulting simple molecules are then absorbed into the bloodstream through active transport mechanisms.
The document provides an overview of the digestive system, including its main components and functions. It discusses the roles and structures of the mouth, esophagus, stomach, small intestine, large intestine, liver, gallbladder and pancreas. Key points covered include the breakdown of carbohydrates, proteins and fats by digestive enzymes, and the absorption of nutrients into the bloodstream. The digestive tract protects itself through secretions, peristalsis and layers of tissue.
This document provides an overview of the physiology of the gastrointestinal system. It begins with an introduction and then covers the functions and contents of various parts of the GI tract, including the mouth, stomach, small intestine, large intestine, liver, gallbladder and pancreas. Specific topics discussed include the role of saliva, gastric juice, pancreatic juice, and bile in digestion and absorption of nutrients. The functions of digestive enzymes and how carbohydrates, proteins and fats are broken down are also explained.
This document provides an overview of the physiology of the gastrointestinal system. It begins with an introduction and then covers the functions and contents of various parts of the GI tract, including the mouth, stomach, small intestine, large intestine, liver, gallbladder and pancreas. Specific topics discussed include the role of saliva, gastric juice, pancreatic juice, and bile in digestion and absorption of nutrients. The functions of digestive enzymes and how carbohydrates, proteins and fats are broken down are also explained.
The document summarizes the digestion and absorption of carbohydrates, lipids, and proteins in the human body. It describes how carbohydrates are broken down by salivary and pancreatic amylases into monosaccharides like glucose and fructose in the mouth, stomach, and small intestine. It outlines the roles of bile salts and pancreatic lipase in emulsifying and breaking down triglycerides into fatty acids and monoglycerides for absorption. Finally, it discusses protein digestion by pepsin in the stomach and pancreatic proteases like trypsin in the small intestine, reducing proteins to dipeptides and amino acids that are absorbed.
The document discusses lipid digestion and absorption. It begins by describing the sources and roles of lipids in the body. Lipid digestion is initiated in the mouth by lingual lipase and continued in the stomach. In the small intestine, pancreatic lipase works with bile salts to break down triglycerides into fatty acids and monoacylglycerols. Bile salts emulsify lipids and facilitate fat absorption. Absorbed lipids are resynthesized into triglycerides and cholesterol esters within enterocytes then packaged into chylomicrons for transport to lymph and circulation. Any defects in this process can lead to lipid malabsorption disorders.
The document summarizes digestion and absorption in non-ruminants. It describes how carbohydrates are broken down into monosaccharides in the small intestine through enzymes like amylase and absorbed into the bloodstream. Proteins are broken into oligopeptides and amino acids by stomach and pancreatic enzymes and absorbed across the intestinal wall. Lipids are emulsified and broken into fatty acids and glycerol by pancreatic lipase in the small intestine and absorbed via chylomicrons. Vitamins and minerals are also absorbed in the small intestine through various mechanisms.
Lipids are digested and absorbed through a multi-step process. They are emulsified in the small intestine by bile salts to increase surface area for pancreatic lipase. Pancreatic lipase breaks triglycerides into fatty acids and monoglycerols. These products and other lipids form micelles which transport the lipids across the intestinal wall. Inside cells, lipids reassemble into triglycerides and combine with proteins to form chylomicrons, which transport the absorbed lipids into the lymphatic system and bloodstream.
The document discusses lipid digestion and absorption. It begins by defining lipids and describing the organs involved in digestion. It then discusses the different types of lipases secreted in the oral cavity, stomach, and pancreas to break down lipids. The role of bile salts in emulsifying lipids in the small intestine is also covered. Finally, it summarizes how lipids are further digested by pancreatic lipases in the duodenum, absorbed via micelles, and transported to the liver within chylomicrons.
The document summarizes lipid digestion and absorption. Dietary lipids are broken down into fatty acids and glycerol by lingual lipase in the mouth, gastric lipase in the stomach, and pancreatic lipase in the small intestine. Bile salts produced by the liver emulsify lipids and aid the action of pancreatic lipase. Fatty acids and monoglycerides are absorbed into intestinal cells and reassembled into triglycerides. These triglycerides along with cholesterol and vitamins are packaged into chylomicrons and enter the lymphatic system before reaching circulation. Deficiencies in lingual, gastric, or pancreatic lipases can impair digestion while problems with bile salt production or chylomicron
The document summarizes the key stages and processes of digestion. It describes the functions of the main parts of the digestive system including the mouth, stomach, small intestine, liver, gallbladder and pancreas. It explains the mechanical and chemical breakdown of food as well as the roles of enzymes and hormones in digesting carbohydrates, proteins and fats. Absorption and motility in the small intestine is also summarized.
The digestive system breaks down food and absorbs nutrients and water. It has two major parts - the gastrointestinal tract and accessory organs like the liver and pancreas. Food moves through the mouth, esophagus, stomach, and small and large intestines while digestive enzymes break it down. The small intestine absorbs most nutrients before waste is eliminated in the large intestine and rectum. Accessory organs like the liver, gallbladder and pancreas produce bile and enzymes to further break down food into absorbable components.
The digestive system breaks down food into nutrients that can be absorbed and used by the body. It consists of the gastrointestinal tract and accessory organs. The gastrointestinal tract includes the mouth, esophagus, stomach, small intestine, and large intestine. Accessory organs that contribute to digestion include the teeth, tongue, salivary glands, liver, gallbladder and pancreas. Each organ has a unique role in the multi-step digestive process which includes ingestion, digestion, absorption and elimination.
The document summarizes lipid digestion and absorption. It describes how lipids are broken down in the mouth, stomach and small intestine by lingual, gastric and pancreatic lipases. Bile salts emulsify lipids into micelles in the small intestine to aid digestion by pancreatic lipase. This breaks triglycerides down into fatty acids and glycerol. Fatty acids and monoglycerides are absorbed via micelles in the small intestine. The liver plays a key role in recycling bile salts through enterohepatic circulation to aid continuous fat digestion and absorption.
The document discusses the flow of genetic information from DNA to mRNA to protein. It describes how the template strand of DNA is read to produce mRNA. A transcription unit includes promoter signals for transcription initiation, elongation and termination. RNA polymerase binds to the promoter and synthesizes mRNA in the 5' to 3' direction on the template strand from 3' to 5'. The primary transcript undergoes post-transcriptional modifications like capping, polyadenylation and splicing before becoming a mature mRNA.
Photometry broadly deals with the study of light absorption by molecules in solution. It is one of the most common analytical techniques used in clinical biochemistry laboratories to measure the intensity of a light beam. Most clinical chemistry reactions involve linking a chemical or enzymatic reaction to the development of a colored product, the intensity of which is then measured photometrically. The amount of light transmitted through a colored solution decreases exponentially with increases in the concentration and thickness of the colored substance, as governed by Beer's and Lambert's laws. Common photometers include colorimeters, which measure visible light, and spectrophotometers, which can measure ultraviolet and visible light.
This document discusses diabetes mellitus and hypoglycemia. It defines hypoglycemia as low blood glucose levels and describes its symptoms. It identifies the main causes of hypoglycemia as insulin-induced, postprandial, fasting, and neonatal. It also discusses the body's counterregulatory systems to combat hypoglycemia. The document further describes the different types of diabetes, their signs and symptoms, classifications, metabolic effects, and long-term complications. It provides details on glucose tolerance tests and glycated hemoglobin for diagnosing diabetes.
Liver function tests (LFTs) assess the health of the liver by measuring certain proteins and enzymes. LFTs can help diagnose liver disease, monitor treatment, and assess prognosis. They test the liver's metabolic, secretory, excretory, storage, detoxifying, and synthetic functions. Specific tests include bilirubin to assess conjugation/excretion, albumin and prothrombin time to evaluate synthesis, and AST/ALT to detect cellular damage. Elevations in certain enzymes or proteins indicate conditions like hepatitis, cirrhosis, or blockages of the bile ducts. LFTs are important for understanding liver function and identifying underlying liver issues.
Renal function tests are important for detecting and assessing kidney disease but not for determining the cause. Tests include urine analysis and serum markers like creatinine and urea. Glomerular filtration rate is estimated using clearance tests. Tubular function is tested via water deprivation and acidification. Proteinuria over 150mg/day is abnormal, with glomerular proteinuria seen in glomerulopathies and tubular proteinuria in tubular diseases. Microalbuminuria predicts early renal damage in diabetes and is detected via urine albumin-creatinine ratio. Abnormal urine constituents provide clues to underlying diseases.
The document discusses thyroid function tests and thyroid hormones. It describes:
1. The anatomy of the thyroid gland and its histology. Thyroid hormones include T4 and T3, which bind to transport proteins in the blood and act through the hypothalamic-pituitary-thyroid axis.
2. The tests used to evaluate thyroid function, including TSH, T4, and T3 levels, and tests to determine the cause of dysfunction like thyroid antibodies. Signs and symptoms of hyperthyroidism and hypothyroidism are also outlined.
3. The hormone changes associated with different thyroid conditions - primary and secondary hyperthyroidism and hypothyroidism. TSH,
The citric acid cycle, also known as the Krebs cycle or tricarboxylic acid cycle, is a series of chemical reactions in the mitochondria that breaks down food for energy production. It is the final common pathway for the oxidation of carbohydrates, lipids, and proteins. The cycle produces carbon dioxide and reduces coenzymes that are later used to form ATP through electron transport. Vitamins like thiamine, riboflavin, niacin, and pantothenic acid play key roles as cofactors in the reactions of the citric acid cycle. Each turn of the cycle generates three NADH molecules, one FADH2 molecule, and one ATP through substrate-level phosphorylation.
Dr. Farhana Atia's document discusses lipid metabolism, including:
1. Fatty acids are stored as triglycerides and are mobilized from triglycerides to meet energy needs through oxidation.
2. Fatty acid oxidation involves activation of fatty acids to fatty acyl-CoA, transport into mitochondria via carnitine shuttle, and beta-oxidation within mitochondria to generate acetyl-CoA.
3. Beta-oxidation is a cyclic process that removes two carbon acetyl-CoA units from the fatty acyl-CoA with each turn, generating reduced electron carriers FADH2 and NADH utilized in the electron transport chain.
Ketone bodies are produced in the liver from fatty acid breakdown during periods of low carbohydrate availability. They serve as an alternate fuel source for tissues like the brain. The liver exports ketone bodies to extrahepatic tissues for energy production via beta-oxidation in the mitochondria. Conditions of starvation, low-carbohydrate diets, or uncontrolled diabetes can cause ketosis - elevated levels of ketone bodies in the blood and urine to be used as fuel when glucose is limited.
This document discusses cholesterol, including that it is a major sterol in animal tissues, is both obtained through diet and synthesized in the body, and serves various structural and metabolic functions. It describes cholesterol biosynthesis occurring primarily in the liver, intestine, and other tissues, requiring acetyl-CoA, ATP, and NADPH. The rate-limiting enzyme HMG-CoA reductase is regulated by feedback and hormones. Factors like genetics, diet, lifestyle, and drugs can affect serum cholesterol levels. Disorders like familial hypercholesterolemia involve inherited defects in lipid metabolism and LDL receptors, elevating LDL and total cholesterol and increasing atherosclerosis risk.
This document discusses the metabolism of lipoproteins in the human body. It describes the four major classes of lipids that are present in lipoproteins and transported in the blood plasma. The four major types of lipoproteins are described along with their composition and roles in lipid transport. Chylomicrons transport lipids from the intestine to tissues, VLDL transports lipids from the liver, LDL transports cholesterol to tissues, and HDL transports cholesterol from tissues back to the liver. The roles of apolipoproteins are outlined. The document then summarizes the metabolism and fate of each type of lipoprotein, including reverse cholesterol transport by HDL. Finally, it describes classifications of abnormal lipoprotein patterns called dyslipoproteinemias
This document summarizes carbohydrate metabolism pathways. It discusses glycolysis, which breaks down glucose to pyruvate or lactate with ATP production in the cytoplasm. Pyruvate is further oxidized to acetyl-CoA in mitochondria to enter the TCA cycle. Glycolysis is regulated by hormones like insulin and glucagon. It provides energy and carbon skeletons for various biosynthetic pathways. The document also explains aerobic versus anaerobic glycolysis and the fate of pyruvate under different conditions.
Gluconeogenesis is the formation of glucose from non-carbohydrate precursors like lactate, glycerol, and certain amino acids. It is important for maintaining blood glucose levels during periods of fasting or low carbohydrate intake to supply glucose to the brain and red blood cells. The key steps of gluconeogenesis occur in the liver and kidneys and involve the reversal of three irreversible reactions in glycolysis through different enzymes. Gluconeogenesis is regulated by hormones like glucagon and substrates availability to control blood glucose levels.
Metabolism refers to all chemical reactions that occur in living cells and are catalyzed by enzymes. These reactions allow cells to release energy from food, build macromolecules, and respond to hormones and vitamins. There are three main types of metabolic pathways: anabolic pathways that build complex molecules, catabolic pathways that break down molecules to release energy, and amphibolic pathways that can be either anabolic or catabolic. A key molecule in metabolism is ATP, which acts as an energy carrier as it is able to donate its high-energy phosphate during reactions. The process of oxidative phosphorylation in the mitochondrial respiratory chain uses redox reactions to generate a proton gradient that drives the synthesis of ATP from ADP and phosphate.
The document summarizes the pentose phosphate pathway (PPP), an alternative glucose metabolism pathway that generates reducing power in the form of NADPH and pentoses for nucleotide synthesis. The PPP occurs in the cytoplasm of most tissues and has two phases: an oxidative phase that irreversibly generates NADPH and a non-oxidative phase that reversibly produces pentoses. A key importance is providing NADPH for fatty acid synthesis and antioxidant defenses. Deficiencies in the PPP can cause hemolytic anemia due to oxidative damage from hydrogen peroxide accumulation.
Glycogen is the major storage carbohydrate in animals and is stored primarily in the liver and skeletal muscle. Glycogenesis is the process of glycogen synthesis from glucose, which takes place in the cytoplasm of liver and muscle cells. Glycogenolysis is the breakdown of glycogen into glucose-1-phosphate, and is regulated by hormones like glucagon and insulin to control blood glucose levels. Deficiencies in enzymes involved in glycogen metabolism can cause glycogen storage diseases.
Major Electrolytes & Their Homeostasis Part-2Farhana Atia
Major electrolytes such as sodium, potassium, calcium, magnesium, chloride, bicarbonate, and phosphate are distributed differently between the extracellular fluid (ECF) and intracellular fluid (ICF) compartments. Calcium homeostasis is tightly regulated by parathyroid hormone (PTH), vitamin D, and calcitonin which act to increase or decrease calcium resorption in bones and reabsorption in kidneys. Hypocalcemia and hypercalcemia can result from disorders of the parathyroid glands or kidneys. Similarly, phosphate levels are regulated by PTH, vitamin D, and calcitonin to affect bone levels, and disorders can cause hypo- or hyperphosphatemia. Magnesium is also regulated and
NVBDCP.pptx Nation vector borne disease control programSapna Thakur
NVBDCP was launched in 2003-2004 . Vector-Borne Disease: Disease that results from an infection transmitted to humans and other animals by blood-feeding arthropods, such as mosquitoes, ticks, and fleas. Examples of vector-borne diseases include Dengue fever, West Nile Virus, Lyme disease, and malaria.
Rasamanikya is a excellent preparation in the field of Rasashastra, it is used in various Kushtha Roga, Shwasa, Vicharchika, Bhagandara, Vatarakta, and Phiranga Roga. In this article Preparation& Comparative analytical profile for both Formulationon i.e Rasamanikya prepared by Kushmanda swarasa & Churnodhaka Shodita Haratala. The study aims to provide insights into the comparative efficacy and analytical aspects of these formulations for enhanced therapeutic outcomes.
Title: Sense of Taste
Presenter: Dr. Faiza, Assistant Professor of Physiology
Qualifications:
MBBS (Best Graduate, AIMC Lahore)
FCPS Physiology
ICMT, CHPE, DHPE (STMU)
MPH (GC University, Faisalabad)
MBA (Virtual University of Pakistan)
Learning Objectives:
Describe the structure and function of taste buds.
Describe the relationship between the taste threshold and taste index of common substances.
Explain the chemical basis and signal transduction of taste perception for each type of primary taste sensation.
Recognize different abnormalities of taste perception and their causes.
Key Topics:
Significance of Taste Sensation:
Differentiation between pleasant and harmful food
Influence on behavior
Selection of food based on metabolic needs
Receptors of Taste:
Taste buds on the tongue
Influence of sense of smell, texture of food, and pain stimulation (e.g., by pepper)
Primary and Secondary Taste Sensations:
Primary taste sensations: Sweet, Sour, Salty, Bitter, Umami
Chemical basis and signal transduction mechanisms for each taste
Taste Threshold and Index:
Taste threshold values for Sweet (sucrose), Salty (NaCl), Sour (HCl), and Bitter (Quinine)
Taste index relationship: Inversely proportional to taste threshold
Taste Blindness:
Inability to taste certain substances, particularly thiourea compounds
Example: Phenylthiocarbamide
Structure and Function of Taste Buds:
Composition: Epithelial cells, Sustentacular/Supporting cells, Taste cells, Basal cells
Features: Taste pores, Taste hairs/microvilli, and Taste nerve fibers
Location of Taste Buds:
Found in papillae of the tongue (Fungiform, Circumvallate, Foliate)
Also present on the palate, tonsillar pillars, epiglottis, and proximal esophagus
Mechanism of Taste Stimulation:
Interaction of taste substances with receptors on microvilli
Signal transduction pathways for Umami, Sweet, Bitter, Sour, and Salty tastes
Taste Sensitivity and Adaptation:
Decrease in sensitivity with age
Rapid adaptation of taste sensation
Role of Saliva in Taste:
Dissolution of tastants to reach receptors
Washing away the stimulus
Taste Preferences and Aversions:
Mechanisms behind taste preference and aversion
Influence of receptors and neural pathways
Impact of Sensory Nerve Damage:
Degeneration of taste buds if the sensory nerve fiber is cut
Abnormalities of Taste Detection:
Conditions: Ageusia, Hypogeusia, Dysgeusia (parageusia)
Causes: Nerve damage, neurological disorders, infections, poor oral hygiene, adverse drug effects, deficiencies, aging, tobacco use, altered neurotransmitter levels
Neurotransmitters and Taste Threshold:
Effects of serotonin (5-HT) and norepinephrine (NE) on taste sensitivity
Supertasters:
25% of the population with heightened sensitivity to taste, especially bitterness
Increased number of fungiform papillae
Title: Sense of Smell
Presenter: Dr. Faiza, Assistant Professor of Physiology
Qualifications:
MBBS (Best Graduate, AIMC Lahore)
FCPS Physiology
ICMT, CHPE, DHPE (STMU)
MPH (GC University, Faisalabad)
MBA (Virtual University of Pakistan)
Learning Objectives:
Describe the primary categories of smells and the concept of odor blindness.
Explain the structure and location of the olfactory membrane and mucosa, including the types and roles of cells involved in olfaction.
Describe the pathway and mechanisms of olfactory signal transmission from the olfactory receptors to the brain.
Illustrate the biochemical cascade triggered by odorant binding to olfactory receptors, including the role of G-proteins and second messengers in generating an action potential.
Identify different types of olfactory disorders such as anosmia, hyposmia, hyperosmia, and dysosmia, including their potential causes.
Key Topics:
Olfactory Genes:
3% of the human genome accounts for olfactory genes.
400 genes for odorant receptors.
Olfactory Membrane:
Located in the superior part of the nasal cavity.
Medially: Folds downward along the superior septum.
Laterally: Folds over the superior turbinate and upper surface of the middle turbinate.
Total surface area: 5-10 square centimeters.
Olfactory Mucosa:
Olfactory Cells: Bipolar nerve cells derived from the CNS (100 million), with 4-25 olfactory cilia per cell.
Sustentacular Cells: Produce mucus and maintain ionic and molecular environment.
Basal Cells: Replace worn-out olfactory cells with an average lifespan of 1-2 months.
Bowman’s Gland: Secretes mucus.
Stimulation of Olfactory Cells:
Odorant dissolves in mucus and attaches to receptors on olfactory cilia.
Involves a cascade effect through G-proteins and second messengers, leading to depolarization and action potential generation in the olfactory nerve.
Quality of a Good Odorant:
Small (3-20 Carbon atoms), volatile, water-soluble, and lipid-soluble.
Facilitated by odorant-binding proteins in mucus.
Membrane Potential and Action Potential:
Resting membrane potential: -55mV.
Action potential frequency in the olfactory nerve increases with odorant strength.
Adaptation Towards the Sense of Smell:
Rapid adaptation within the first second, with further slow adaptation.
Psychological adaptation greater than receptor adaptation, involving feedback inhibition from the central nervous system.
Primary Sensations of Smell:
Camphoraceous, Musky, Floral, Pepperminty, Ethereal, Pungent, Putrid.
Odor Detection Threshold:
Examples: Hydrogen sulfide (0.0005 ppm), Methyl-mercaptan (0.002 ppm).
Some toxic substances are odorless at lethal concentrations.
Characteristics of Smell:
Odor blindness for single substances due to lack of appropriate receptor protein.
Behavioral and emotional influences of smell.
Transmission of Olfactory Signals:
From olfactory cells to glomeruli in the olfactory bulb, involving lateral inhibition.
Primitive, less old, and new olfactory systems with different path
Basavarajeeyam is an important text for ayurvedic physician belonging to andhra pradehs. It is a popular compendium in various parts of our country as well as in andhra pradesh. The content of the text was presented in sanskrit and telugu language (Bilingual). One of the most famous book in ayurvedic pharmaceutics and therapeutics. This book contains 25 chapters called as prakaranas. Many rasaoushadis were explained, pioneer of dhatu druti, nadi pareeksha, mutra pareeksha etc. Belongs to the period of 15-16 century. New diseases like upadamsha, phiranga rogas are explained.
Here is the updated list of Top Best Ayurvedic medicine for Gas and Indigestion and those are Gas-O-Go Syp for Dyspepsia | Lavizyme Syrup for Acidity | Yumzyme Hepatoprotective Capsules etc
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Integrating Ayurveda into Parkinson’s Management: A Holistic ApproachAyurveda ForAll
Explore the benefits of combining Ayurveda with conventional Parkinson's treatments. Learn how a holistic approach can manage symptoms, enhance well-being, and balance body energies. Discover the steps to safely integrate Ayurvedic practices into your Parkinson’s care plan, including expert guidance on diet, herbal remedies, and lifestyle modifications.
micro teaching on communication m.sc nursing.pdfAnurag Sharma
Microteaching is a unique model of practice teaching. It is a viable instrument for the. desired change in the teaching behavior or the behavior potential which, in specified types of real. classroom situations, tends to facilitate the achievement of specified types of objectives.
2. Learning objectives
Define digestion & absorption
Enumerate digestive juices, their composition & functions
Enumerate local hormones of GIT, their source & functions
State the names & sources of digestive enzymes & their
location
Process of digestion & absorption of carbohydrate
Process of digestion & absorption of protein
Process of digestion & absorption of lipids (TAG, phospholipids,
cholesterol esters)
3. Digestion
It is defined as a physiological
process by which complex
food particles are broken
down into simple forms which
can be absorbed from the gut
for utilization by the body.
4. Absorption
A process by which end
product of digestion pass
through the intestinal
epithelium to enter into
blood or lymph
5. Digestive juices
Mainly secreted from the glands of the digestive tract
Help in the digestion of food
They are-
Saliva- 1000 ml/day
Gastric juice- 1500 ml/day
Pancreatic juice- 1000 ml/day
Succus entericus- 1800 ml/day
Bile- 1000ml/day
14. Local Hormones of GIT
Biologically active polypeptide
Secreted by nerve cells & gland cells in the mucosa
Act in paracrine fashion
But also enter the circulation
15. Types
According to structural & functional similarity
Others
Gastrin Family Secretin Family
Gastrin
Cholecystokinin
Secretin
Glucagon
Glicentin
VIP- Vasoactive Inhibitory Polypeptide
GIP- Gastric Inhibitory Polypeptide
Motilin
Neurotensin
Substance P
Gastrin releasing PP
Bombesin
Somatostatin
Guanylin
Enkephalin
Villikinin
16. Gastrin
Source Site of action Actions
G cell of
gastric
mucosa
• Stomach
• Lower esophageal
sphincter
• Small intestine
• Gall bladder
• Stimulate gastric acid &
pepsin secretion
• Stimulate growth of
mucosa of stomach, small
& large intestine
• Increase gastric motility
17. Cholecystokinin- Pancreozymin (CCK-PZ)
Source Site of action Actions
I cell of
mucosa of
duodenum
& jejunum
• Gall bladder Stimulates
• Pancreatic enzyme secretion
• Pancreatic HCO₃⁻ secretion
• Gall bladder contraction
• Growth of exocrine pancreas
Inhibit
• Gastric emptying
• Gastric motility
18. Secretin
Source Site of action Actions
S cell of
mucosa of
duodenum
• Pancreatic
duct cell
Stimulates
• Pepsin secretion
• Pancreatic HCO₃⁻ secretion
• Biliary HCO₃⁻ secretion
• Growth of exocrine pancreas
Inhibit
• Gastric acid secretion
• Effect of gastrin on growth of
gastric mucosa
19. GIP- Gastric inhibitory polypeptide
(43 amino acids)
Source Site of action Actions
S cell of
mucosa of
duodenum
• Stimulate Insulin secretion
• Inhibit gastric acid secretion
• Decrease gastric motility
23. Carbohydrates in diet
Polysaccharide
• Starch
• Glycogen
Disaccharide
• Lactose
• Maltose
• Sucrose
Monosaccharide
• Glucose
• Fructose
In GIT, all complex
carbohydrates are
converted to simpler
monosaccharide
24.
25. Digestion in mouth
Salivary α-amylase
Location: mouth
Hydrolyses α-1→ 4 glycosidic linkages
Ptyalin action stops in the stomach (pH falls to 3.0)
Food present in shorter duration, so
Incomplete digestion
26. There is no enzyme to break the glycosidic bonds in
gastric juice.
However, HCl present in the stomach causes
hydrolysis of sucrose to fructose and glucose.
Sucrose Fructose + Glucose
Digestion in the Stomach
HCl
27. Digestion in Duodenum
Food bolus reaches the
duodenum
Meets the pancreatic juice
Pancreatic juice contains
carbohydrate splitting
enzyme,
Pancreatic amylase
similar to salivary amylase.
Main digestion takes place
in the small intestine by
pancreatic amylase
Disaccharidases present in
the brush border epithelium
of intestinal mucosal cell
Maltase
Sucrase-Isomaltase
Lactase
Digestion in Small Intestine
28. Pancreatic amylase
An α- Amylase
Optimum pH=7.1
It hydrolyses α-1→ 4
glycosidic linkages
Note: Pancreatic amylase,
an isoenzyme of salivary
amylase, differs only in the
optimum pH of action.
Starch/Glycogen
Maltose/ Isomaltose
+
Dextrins and
oligosaccharides
Amylase
30. Lactose intolerance
Inability to digest lactose due to the deficiency of Lactase
enzyme.
Presents as abdominal cramps, distensions, diarrhea,
constipation, flatulence upon ingestion of milk or dairy
products
Undigested lactose in intestine is converted to CO2, H2, 2 &
3 carbon compounds [by bacteria]
CO2 & H2 causes distensions and flatulence
Lactose + 2C + 3C are osmotically active
Cause osmotic diarrhea or constipation because of
undigested bulk
32. Emulsification
Emulsification is a prerequisite for digestion of lipids
The lipids are dispersed into
smaller droplets
surface tension is reduced
surface area of droplets is ↑
This process is favoured by:
1. Bile salts (detergent action)
2. Peristalsis (mechanical mixing)
3. Phospholipids
33. End products of lipid digestion
TAG Monoacylglycerol + 2FFA
Cholesterol ester Cholesterol + FA
Phospholipid Lysophospholipid + FA
Pancreatic lipase
Cholesterol esterase
Phospholipase A2
34. Lipid absorption
1. Short & medium chain FA (<10 carbons) directly enter
the portal circulation liver (albumin bound form)
2. LCFA (>12 carbons) are absorbed to the lymph
Portal
blood
35. Micelle Formation
The products of digestion are incorporated into molecular
aggregates to form micelle
They are spherical particles with a hydrophilic exterior &
hydrophobic interior core
Bile salts help to form micelle
Essential for the absorption of fat-soluble vitamins
Aligned at the microvillus surface of the mucosa
Fatty acids, 2-MAG and other digested products passively
diffuse into the mucosal cell
36. Chylomicrons
Inside the intestinal mucosal cell, the long chain fatty acids are re-
esterified to form triglycerides
They are surrounded by a thin layer of apolipoproteins (A1 and B-
48) & phospholipids. These particles are chylomicrons
Released into lymphatic vessels by exocytosis
Enter into thoracic duct systemic circulation peripheral
tissues (muscle, adipose tissue) liver
38. Physiologically important lipases
Lipase Site of action Preferred substrate Product(s)
Lingual / acid stable
lipase
Mouth, stomach TAG with medium chain
FA
FFA+DAG
Pancreatic lipase +
co-lipase
Small intestine TAG with long chain FA FFA+2-MAG
Intestinal lipase Small intestine TAG with medium chain
FA
FFA + glycerol
Phospholipase A2 Small intestine Phospholipids FFA +
Lysolecithin
Lipoprotein lipase Capillary wall TAG in CM or VLDL FFA+ glycerol
Hormone sensitive
lipase
Adipose cell TAG stored in adipose cells FFA+ glycerol