DIGESTION AND
ABSORPTION OF
NUTRITIONAL
CONSTITUENTS
Dr Ifat Ara Begum
Assistant Professor
Dept Of Biochemistry
Dhaka Medical College
Dhaka
DAY 1
Introduction to
digestion& absorption,
Local hormones of GIT,
Different digestive
juices
DIGESTION
 Digestion is the process of breakdown
of large/complex food molecules into
simple form, so that they can be
absorbed into the watery blood plasma
for subsequent utilization.
 It is often divided into two processes
based on how food is broken down:
mechanical and chemical digestion.
CONTD
 The term mechanical digestion refers to
the physical breakdown of large pieces
of food into smaller pieces which can
subsequently be accessed by digestive
enzymes.
 In chemical digestion, enzymes break
down food into the small molecules the
body can use.
CONTD
 The basic process involved in digestion :
hydrolysis.
 Enzymes involved: Hydrolases group of
enzyme
DIGESTIVE SYSTEM
 Digestive system is a 25 to 30 feet long
tube which includes organs that secret
digestive juices.
 It consists of alimentary canal/
gastrointestinal tract/ digestive tract
and the associated digestive
glands/organs.
 The digestive tract system comprise
of esophagus, mouth, stomach, small
intestine and large intestine or colon,
rectum and anus. 
FUNCTION OF DIGESTIVE
SYSTEM
 Ingestion
 Secretion of water, acid, buffer and
enzyme in to gastrointestinal
lumen
 Mixing and propulsion
 Digestion
 Absorption
 Excretion (Defecation)
ABSORPTION
 It is the process of transfer of
nutrients/ end product of digestion (as
well as the vitamins , minerals and
water ) from digestive system in to the
lymphatic / circulatory system for
eventual distribution to the body cells.
 Glucose and amino acids are absorbed
in to the circulatory system
 Fatty acids are absorbed in to the
lymphatic system
CONTD
 The nutrients in the lymph and blood
mix in the heart and are then sent to
the body cells via the circulatory
system
 Most absorption takes place in small
intestine
 Water, sodium and end product of
bacterial digestion are absorbed in the
large intestine
DIGESTIVE JUICES
 The digestive juices are the
secretions of the digestive tract that
break down food.
 They include saliva, gastric juice,
pancreatic juice, bile and intestinal
juice.
 The digestive juices are secreted by
different organs, vary widely in
chemical composition, and play
different roles in the digestive process.
CONTD
 Each juice is constantly produced by
the body in small amounts, but the
presence of food as it passes through
the digestive tract causes increased
production and secretion.
IMPORTANCE OF DIGESTIVE
JUICES
 Digestive juices are the most
important part of the whole digestive
process as in their absence the
digestion process cannot take place.
These are very vital for breaking down
of food so that the
essential nutrients are absorbed and
properly utilized by our body.
COMMON DIGESTIVE JUICES
Digestive
juice
Source Daily
secretion
(L/day)
pH Important
components
Saliva Salivary
glands
0.75-1.5 6.0-7.0 Mucus,
Salivary
amylase,
Lingual lipase
Gastric
juice
Gastric
glands
1.5 1.0-3.5 Mucus, HCl,
Pepsin,
Intrinsic
factor, Gastric
lipase
CONTD
Digestive
juice
Source Daily
secretio
n (L/day)
pH Important
components
Pancreat
-ic juice
Pancreas 0.8-1.2 8.0-8.3 Amylolytic enzyme (P.
amylase), Lipolytic
enzyme (P. lipase,
cholesterol esterase,
Phospholipase A2),
Colipase, HCO3 ion,
Nucleases, Proteolytic
enzyme (Trypsin,
Chymotrypsin,
Carboxypeptidase,
Elastase, Collagenase)
CONTD
Digestive
juice
Source Daily
secretion
(L/day)
pH Important
components
Bile Liver 0.5-1.0 7.8 Bile salts, Bile
pigments (e.g.
bilirubin),
Cholesterol ester,
PL (lecithin)
Succus
entericus
Small
intestinal
mucosa
1.0-2.0 7.5 Amylolytic enzyme
(maltase, sucrase,
lactase, α-limit
dextrinase),
Proteolytic enzyme
(aminopeptidase, di
and tri peptidases),
Enterokinase
(enteropeptidase)
CONTROL OF DIGESTIVE JUICE
SECRETION
 Nervous factor
 Hormonal factor (Gut hormones):
Liberated from GIT mucosa in
response to presence of food in gut
lumen. They signal the brain
(hypothalamus) to achieve
efficient nutrient digestion &
absorption (Gut-brain interaction)
LOCAL HORMONES OF GIT
Biologically active PPs that are
secreted by nerve and gland cells in the
mucosa , act in a paracrine fashion ,
also enters the circulation
2 family:
 Gastrin family: Includes gastrin & CCK
 Secretin family: Includes secretin, GIP,
VIP etc
Others: Neurotensin, Substance B,
Bombesin, GRP (gastrin releasing PP)
etc
CONTD
Local
hormone
Origin Stimulus
for
secretion
Target
tissue
Action
Gastrin G cell of
stomach
Products of
protein
digestion
Stomach  Stimulates
secretion of
gastric acid
(HCl) by the
parietal cells of
the stomach
 Aids in
gastric motility.
CCK I cells in
mucosal
epi of
small
intestine
and
secreted in
duodenum
Product of
protein
digestion,
fat and FA
Pancreas,
GB
 Stimulates
enzyme rich
pancreatic
secretion
 Release of bile
from GB
CONTD
Local
hormone
Origin Stimulus for
secretion
Target
tissue
Action
Secretin S cell of
duodenum
Acid chyme,
FA
Stomach,
Pancreas
Inhibits
secretion of
gastric acid
(HCl) by the
parietal cells of
the stomach
 Stimulate
bicarbonate
rich pancreatic
secretion
GIP K cells in
the mucosa
of
duodenum
& jejunum
Nutrients Stomach Decrease
stomach acid
secretion
 Induce insulin
secretion
CONTD
(GIP: Glucose-dependent
insulinotropic peptide)
Somatostatin: Secreted from D cells of
GIT . It is secreted when fat is
ingested and decreases gastrin and
gastric acid secretion
VIP: Secreted by N. endings in GIT
and increases pancreatic secretion &
decreases gastric secretion
SALIVA (SECRETION OF
SALIVARY GLAND)
CONTD
COMPOSITION OF SALIVA
 Mucus
 Salivary α amylase: Initiates starch
digestion
 Lingual lipase: Initiates fat
digestion
 Electrolyte solution (Na+, Cl-, K+,
HCO3-): moistens food
 Others: Lysozyme, Salivary
Peroxidase etc
FUNCTION OF SALIVA
 Digestive function: by salivary
amylase, Lingual lipase
 Mastication of food, bolus formation
& swallowing of food
 Moistens oral mucosa, helps in
speech
 Moistens dry food, cools hot food,
dilutes irritant substances
 A medium for dissolving foods to
stimulate the taste bud
 Control bacterial flora of oral cavity
CONTD
 Buffers oral cavity contents due to
high concentration of bicarbonate
ions
 Mineralization of new teeth &
repair of precarious enamel lesion
(as it is rich in calcium and
phosphate)
 Protects teeth by a protein coat on
teeth which contains antibacterial
compound. (Prevent dental caries)
MUCUS
Thick secretion containing water,
electrolytes and glycoproteins.
Adherence (to food& other particles to
get spread as thin film over the
surfaces)
Coating of gut wall and prevention of
actual contact of food with mucosa
Low resistance for slippage
Resistant to digestion by digestive
enzymes
CONTD
 Glycoproteins: buffer acid/alkali
 HCO3 ion: neutralizes acid
 Function:
 Lubrication of ingested food to favor
their slippage along GIT
 Protection of GIT from
mechanical/chemical injury)
GASTRIC JUICE
 Mixture of secretions of all the glands
present in stomach.
 It is mixed also with swallowed saliva
& refluxed duodenal contents.
CONTD
 3 types of glands:
I. Cardiac glands: Present around cardiac
orifice of stomach, have mucous cells
(secret mucus)
II.Gastric/oxyntic glands: Have mucous
neck cells (secret mucus), peptic/chief
cells (secret pepsinogen) & parietal cells
(secret HCl & IF)
III.Pyloric glands: Present in antral part
of stomach , have mucous cells (secret
mucus) & G cells (secret gastrin)
CONSTITUENTS OF GASTRIC
JUICE
FUNCTION OF CHIEF
COMPONENTS OF GASTRIC JUICE
1. HCl:
 Denaturation of protein to facilitate its
digestion
 Converts pepsinogen to pepsin for chemical
digestion
 Provides optimal pH environment for pepsin
 Sterilizes upper GIT by destroying bacteria
 promotes the absorption of Fe2+
in small
intestine
CONTD
2. Pepsinogen (precursor of pepsin):
 Protein digestion (pepsin with HCl digest
protein up to peptone)
3. Mucus:
 Forms a protective barrier: mucus-bicarbonate
barrier
 Lubrication
4. Intrinsic factor of castle:
 Combines with vitamin B12 to make it
absorbable (ileum)
PRODUCTION
1. CO2 and Cl-
diffuse from
the blood into the
stomach cell.
2. Within cell, CO2 combines
with H2O in presence of
CA enzyme, to form
H2CO3.
3. H2CO3 dissociates into
HCO3-
and H+
.
4. H+
is secreted to gastric
lumen actively by proton
pump
5. HCO3-
is absorbed to
blood in exchange of Cl-
which subsequently
diffuse to gastric lumen
& combines with H+
to
form HCl.
CONTD
CONTROL OF GASTRIC ACID
SECRETION
By three mechanisms:
 Neurocrine (denoting an endocrine
influence on or by the nerves).
 Endocrine (gastrin)
 Paracrine (histamine) in contrast to
true endocrines these hormones are
not released into the bloodstream but
into the surrounding tissues and act
in the immediate vicinity, e.g.
intestinal mucosal hormones.
MUCUS- BICARBONATE BARRIER
 A protective barrier composed of unstirred
layer of mucus plus bicarbonate ion over the
mucosal surface of stomach & duodenum.
 Protects gastro-duodenal mucosa from acid-
peptic digestion & prevents ulceration
 Disruption of the barrier &/or excess HCl
secretion causes dev of PUD
CONTROL OF GASTRIC
HYDROCHLORIC ACID
SECRETION
Parietal cell is stimulated by
histamine, gastrin, Ach
Parietal cell is inhibited by PGE2,
somatostatin, VIP, GIP, CCK,
secretin
Proton pump is inhibited by
proton pump inhibitors (like
omeprazole)
PHASES OF GASTRIC
SECRETION
Phase Action
Cephalic phase
(accounts for 20% of
gastric secretion)
The sight, taste, smell or
thought of foods triggers
parasympathetic reflex (via
vagus nerve), gastric juice is
secreted in response
Gastric phase
(accounts for 70% of
gastric secretion)
Food in stomach chemically and
mechanically stimulates release
of gastrin, which in turn,
stimulates the secretion of
gastric juice. Reflex responses
(vagovagal reflex, local enteric
reflex) also stimulate gastric
juice secretion
CONTD
Phase Action
Intestinal phase Starts once acid chyme from
stomach goes to upper SI (esp.
duodenum). Intestinal cell release
intestinal gastrin, which
promotes gastric juice secretion
from stomach.
On the other hand, duodenal
activity, intestinal distension,
presence of breakdown products
of fat & protein initiate release of
VIP, GIP, somatostatin, & CCK
from SI, all of which inhibit
gastric secretion
ALKALI TIDE
 A condition, normally encountered
after eating a meal, where during the
production of HCl by parietal cells in
the stomach, the parietal cells secrete
bicarbonate ions across their
basolateral membranes and into the
blood, causing a temporary increase
in pH
 This is to maintain the plasma's
electrical balance, as the chloride
anions have been extracted
COMPOSITION
1. Enzymes
2. Trypsin inhibitor
ZYMOGENS/PROENZYME
 An inactive enzyme precursor
Requires a biochemical change (such
as a hydrolysis reaction revealing the
active site, or changing the
configuration to reveal the active site)
for it to become an active enzyme.
The biochemical change usually
occurs in a lysosome where a specific
part of the precursor enzyme is
cleaved in order to activate it. 
CONTD
The pancreas secretes zymogens
partly to prevent the enzymes from
digesting proteins in the cells in
which they are synthesized.
Enzymes like pepsin are created in
the form of pepsinogen, an inactive
zymogen. Pepsinogen is activated
when chief cells release it into HCl
which partially activates it.
CONTD
Another partially activated
pepsinogen completes the activation
by removing the peptide turning the
pepsinogen into pepsin.
CONTD
Accidental activation of zymogens
can happen when the secretion duct
in the pancreas is blocked by a
gallstone resulting in
acute pancreatitis.
TYPE OF PANCREATIC
SECRETION
Hydroelactic secretion:
 Watery secretion
 Rich in HCO3-
 Poor in enzyme
Ecbolic secretion:
 Thick & viscid
 Rich in enzyme
 Poor in HCO3-
FUNCTION OF PANCREATIC
JUICE
1. Neutralization of acid chyme
emptied in to the duodenum from
stomach by the HCO3- content of
pancreatic juice to provide
optimum pH for activity of
pancreatic enzymes
2. Digestion of CHO, fat, NA &
cholesterol ester
BILE
COMPOSITION
Bile Salts:
 Na taurocholate
 K taurocholate
 Na glycocholate
 K glycocholate
Bile acid:
 Cholic acid
 Chenodeoxycholic acid
Bile pigment:
 Bilirubin
 Biliverdin
JUSTIFY BILE AS
DIGESTIVE JUICE
It activates pancreatic lipase
It helps in emulsification of fat
It forms micelle and helps in
absorption of fat
FUNCTION OF BILE
Bile salts of bile help in fat digestion
by emulsification of fat
Bile salts of bile help in the absorption
of the end products of digestion of fat
& other lipids
Bile serves as a mean for excretion of
some important waste products from
blood ( bile pigment/bilirubin,
cholesterol, drugs)

Introduction to digestion and absorption, local hormones of GIT, different digestive juices

  • 1.
    DIGESTION AND ABSORPTION OF NUTRITIONAL CONSTITUENTS DrIfat Ara Begum Assistant Professor Dept Of Biochemistry Dhaka Medical College Dhaka
  • 2.
    DAY 1 Introduction to digestion&absorption, Local hormones of GIT, Different digestive juices
  • 3.
    DIGESTION  Digestion is theprocess of breakdown of large/complex food molecules into simple form, so that they can be absorbed into the watery blood plasma for subsequent utilization.  It is often divided into two processes based on how food is broken down: mechanical and chemical digestion.
  • 4.
    CONTD  The term mechanicaldigestion refers to the physical breakdown of large pieces of food into smaller pieces which can subsequently be accessed by digestive enzymes.  In chemical digestion, enzymes break down food into the small molecules the body can use.
  • 6.
    CONTD  The basicprocess involved in digestion : hydrolysis.  Enzymes involved: Hydrolases group of enzyme
  • 7.
    DIGESTIVE SYSTEM  Digestivesystem is a 25 to 30 feet long tube which includes organs that secret digestive juices.  It consists of alimentary canal/ gastrointestinal tract/ digestive tract and the associated digestive glands/organs.  The digestive tract system comprise of esophagus, mouth, stomach, small intestine and large intestine or colon, rectum and anus. 
  • 10.
    FUNCTION OF DIGESTIVE SYSTEM Ingestion  Secretion of water, acid, buffer and enzyme in to gastrointestinal lumen  Mixing and propulsion  Digestion  Absorption  Excretion (Defecation)
  • 11.
    ABSORPTION  It isthe process of transfer of nutrients/ end product of digestion (as well as the vitamins , minerals and water ) from digestive system in to the lymphatic / circulatory system for eventual distribution to the body cells.  Glucose and amino acids are absorbed in to the circulatory system  Fatty acids are absorbed in to the lymphatic system
  • 12.
    CONTD  The nutrientsin the lymph and blood mix in the heart and are then sent to the body cells via the circulatory system  Most absorption takes place in small intestine  Water, sodium and end product of bacterial digestion are absorbed in the large intestine
  • 14.
    DIGESTIVE JUICES  Thedigestive juices are the secretions of the digestive tract that break down food.  They include saliva, gastric juice, pancreatic juice, bile and intestinal juice.  The digestive juices are secreted by different organs, vary widely in chemical composition, and play different roles in the digestive process.
  • 15.
    CONTD  Each juiceis constantly produced by the body in small amounts, but the presence of food as it passes through the digestive tract causes increased production and secretion.
  • 16.
    IMPORTANCE OF DIGESTIVE JUICES Digestive juices are the most important part of the whole digestive process as in their absence the digestion process cannot take place. These are very vital for breaking down of food so that the essential nutrients are absorbed and properly utilized by our body.
  • 17.
    COMMON DIGESTIVE JUICES Digestive juice SourceDaily secretion (L/day) pH Important components Saliva Salivary glands 0.75-1.5 6.0-7.0 Mucus, Salivary amylase, Lingual lipase Gastric juice Gastric glands 1.5 1.0-3.5 Mucus, HCl, Pepsin, Intrinsic factor, Gastric lipase
  • 18.
    CONTD Digestive juice Source Daily secretio n (L/day) pHImportant components Pancreat -ic juice Pancreas 0.8-1.2 8.0-8.3 Amylolytic enzyme (P. amylase), Lipolytic enzyme (P. lipase, cholesterol esterase, Phospholipase A2), Colipase, HCO3 ion, Nucleases, Proteolytic enzyme (Trypsin, Chymotrypsin, Carboxypeptidase, Elastase, Collagenase)
  • 19.
    CONTD Digestive juice Source Daily secretion (L/day) pH Important components BileLiver 0.5-1.0 7.8 Bile salts, Bile pigments (e.g. bilirubin), Cholesterol ester, PL (lecithin) Succus entericus Small intestinal mucosa 1.0-2.0 7.5 Amylolytic enzyme (maltase, sucrase, lactase, α-limit dextrinase), Proteolytic enzyme (aminopeptidase, di and tri peptidases), Enterokinase (enteropeptidase)
  • 20.
    CONTROL OF DIGESTIVEJUICE SECRETION  Nervous factor  Hormonal factor (Gut hormones): Liberated from GIT mucosa in response to presence of food in gut lumen. They signal the brain (hypothalamus) to achieve efficient nutrient digestion & absorption (Gut-brain interaction)
  • 21.
    LOCAL HORMONES OFGIT Biologically active PPs that are secreted by nerve and gland cells in the mucosa , act in a paracrine fashion , also enters the circulation 2 family:  Gastrin family: Includes gastrin & CCK  Secretin family: Includes secretin, GIP, VIP etc Others: Neurotensin, Substance B, Bombesin, GRP (gastrin releasing PP) etc
  • 23.
    CONTD Local hormone Origin Stimulus for secretion Target tissue Action Gastrin Gcell of stomach Products of protein digestion Stomach  Stimulates secretion of gastric acid (HCl) by the parietal cells of the stomach  Aids in gastric motility. CCK I cells in mucosal epi of small intestine and secreted in duodenum Product of protein digestion, fat and FA Pancreas, GB  Stimulates enzyme rich pancreatic secretion  Release of bile from GB
  • 24.
    CONTD Local hormone Origin Stimulus for secretion Target tissue Action SecretinS cell of duodenum Acid chyme, FA Stomach, Pancreas Inhibits secretion of gastric acid (HCl) by the parietal cells of the stomach  Stimulate bicarbonate rich pancreatic secretion GIP K cells in the mucosa of duodenum & jejunum Nutrients Stomach Decrease stomach acid secretion  Induce insulin secretion
  • 25.
    CONTD (GIP: Glucose-dependent insulinotropic peptide) Somatostatin:Secreted from D cells of GIT . It is secreted when fat is ingested and decreases gastrin and gastric acid secretion VIP: Secreted by N. endings in GIT and increases pancreatic secretion & decreases gastric secretion
  • 26.
  • 27.
  • 28.
    COMPOSITION OF SALIVA Mucus  Salivary α amylase: Initiates starch digestion  Lingual lipase: Initiates fat digestion  Electrolyte solution (Na+, Cl-, K+, HCO3-): moistens food  Others: Lysozyme, Salivary Peroxidase etc
  • 29.
    FUNCTION OF SALIVA Digestive function: by salivary amylase, Lingual lipase  Mastication of food, bolus formation & swallowing of food  Moistens oral mucosa, helps in speech  Moistens dry food, cools hot food, dilutes irritant substances  A medium for dissolving foods to stimulate the taste bud  Control bacterial flora of oral cavity
  • 30.
    CONTD  Buffers oralcavity contents due to high concentration of bicarbonate ions  Mineralization of new teeth & repair of precarious enamel lesion (as it is rich in calcium and phosphate)  Protects teeth by a protein coat on teeth which contains antibacterial compound. (Prevent dental caries)
  • 31.
    MUCUS Thick secretion containingwater, electrolytes and glycoproteins. Adherence (to food& other particles to get spread as thin film over the surfaces) Coating of gut wall and prevention of actual contact of food with mucosa Low resistance for slippage Resistant to digestion by digestive enzymes
  • 32.
    CONTD  Glycoproteins: bufferacid/alkali  HCO3 ion: neutralizes acid  Function:  Lubrication of ingested food to favor their slippage along GIT  Protection of GIT from mechanical/chemical injury)
  • 33.
    GASTRIC JUICE  Mixtureof secretions of all the glands present in stomach.  It is mixed also with swallowed saliva & refluxed duodenal contents.
  • 34.
    CONTD  3 typesof glands: I. Cardiac glands: Present around cardiac orifice of stomach, have mucous cells (secret mucus) II.Gastric/oxyntic glands: Have mucous neck cells (secret mucus), peptic/chief cells (secret pepsinogen) & parietal cells (secret HCl & IF) III.Pyloric glands: Present in antral part of stomach , have mucous cells (secret mucus) & G cells (secret gastrin)
  • 35.
  • 36.
    FUNCTION OF CHIEF COMPONENTSOF GASTRIC JUICE 1. HCl:  Denaturation of protein to facilitate its digestion  Converts pepsinogen to pepsin for chemical digestion  Provides optimal pH environment for pepsin  Sterilizes upper GIT by destroying bacteria  promotes the absorption of Fe2+ in small intestine
  • 37.
    CONTD 2. Pepsinogen (precursorof pepsin):  Protein digestion (pepsin with HCl digest protein up to peptone) 3. Mucus:  Forms a protective barrier: mucus-bicarbonate barrier  Lubrication 4. Intrinsic factor of castle:  Combines with vitamin B12 to make it absorbable (ileum)
  • 38.
    PRODUCTION 1. CO2 andCl- diffuse from the blood into the stomach cell. 2. Within cell, CO2 combines with H2O in presence of CA enzyme, to form H2CO3. 3. H2CO3 dissociates into HCO3- and H+ . 4. H+ is secreted to gastric lumen actively by proton pump 5. HCO3- is absorbed to blood in exchange of Cl- which subsequently diffuse to gastric lumen & combines with H+ to form HCl.
  • 39.
  • 40.
    CONTROL OF GASTRICACID SECRETION By three mechanisms:  Neurocrine (denoting an endocrine influence on or by the nerves).  Endocrine (gastrin)  Paracrine (histamine) in contrast to true endocrines these hormones are not released into the bloodstream but into the surrounding tissues and act in the immediate vicinity, e.g. intestinal mucosal hormones.
  • 41.
    MUCUS- BICARBONATE BARRIER A protective barrier composed of unstirred layer of mucus plus bicarbonate ion over the mucosal surface of stomach & duodenum.  Protects gastro-duodenal mucosa from acid- peptic digestion & prevents ulceration  Disruption of the barrier &/or excess HCl secretion causes dev of PUD
  • 42.
    CONTROL OF GASTRIC HYDROCHLORICACID SECRETION Parietal cell is stimulated by histamine, gastrin, Ach Parietal cell is inhibited by PGE2, somatostatin, VIP, GIP, CCK, secretin Proton pump is inhibited by proton pump inhibitors (like omeprazole)
  • 43.
    PHASES OF GASTRIC SECRETION PhaseAction Cephalic phase (accounts for 20% of gastric secretion) The sight, taste, smell or thought of foods triggers parasympathetic reflex (via vagus nerve), gastric juice is secreted in response Gastric phase (accounts for 70% of gastric secretion) Food in stomach chemically and mechanically stimulates release of gastrin, which in turn, stimulates the secretion of gastric juice. Reflex responses (vagovagal reflex, local enteric reflex) also stimulate gastric juice secretion
  • 44.
    CONTD Phase Action Intestinal phaseStarts once acid chyme from stomach goes to upper SI (esp. duodenum). Intestinal cell release intestinal gastrin, which promotes gastric juice secretion from stomach. On the other hand, duodenal activity, intestinal distension, presence of breakdown products of fat & protein initiate release of VIP, GIP, somatostatin, & CCK from SI, all of which inhibit gastric secretion
  • 46.
    ALKALI TIDE  Acondition, normally encountered after eating a meal, where during the production of HCl by parietal cells in the stomach, the parietal cells secrete bicarbonate ions across their basolateral membranes and into the blood, causing a temporary increase in pH  This is to maintain the plasma's electrical balance, as the chloride anions have been extracted
  • 48.
  • 49.
    ZYMOGENS/PROENZYME  An inactive enzyme precursor Requiresa biochemical change (such as a hydrolysis reaction revealing the active site, or changing the configuration to reveal the active site) for it to become an active enzyme. The biochemical change usually occurs in a lysosome where a specific part of the precursor enzyme is cleaved in order to activate it. 
  • 50.
    CONTD The pancreas secretes zymogens partly toprevent the enzymes from digesting proteins in the cells in which they are synthesized. Enzymes like pepsin are created in the form of pepsinogen, an inactive zymogen. Pepsinogen is activated when chief cells release it into HCl which partially activates it.
  • 51.
    CONTD Another partially activated pepsinogencompletes the activation by removing the peptide turning the pepsinogen into pepsin.
  • 54.
    CONTD Accidental activation ofzymogens can happen when the secretion duct in the pancreas is blocked by a gallstone resulting in acute pancreatitis.
  • 55.
    TYPE OF PANCREATIC SECRETION Hydroelacticsecretion:  Watery secretion  Rich in HCO3-  Poor in enzyme Ecbolic secretion:  Thick & viscid  Rich in enzyme  Poor in HCO3-
  • 56.
    FUNCTION OF PANCREATIC JUICE 1.Neutralization of acid chyme emptied in to the duodenum from stomach by the HCO3- content of pancreatic juice to provide optimum pH for activity of pancreatic enzymes 2. Digestion of CHO, fat, NA & cholesterol ester
  • 57.
  • 58.
    COMPOSITION Bile Salts:  Nataurocholate  K taurocholate  Na glycocholate  K glycocholate Bile acid:  Cholic acid  Chenodeoxycholic acid Bile pigment:  Bilirubin  Biliverdin
  • 59.
    JUSTIFY BILE AS DIGESTIVEJUICE It activates pancreatic lipase It helps in emulsification of fat It forms micelle and helps in absorption of fat
  • 60.
    FUNCTION OF BILE Bilesalts of bile help in fat digestion by emulsification of fat Bile salts of bile help in the absorption of the end products of digestion of fat & other lipids Bile serves as a mean for excretion of some important waste products from blood ( bile pigment/bilirubin, cholesterol, drugs)

Editor's Notes

  • #39 Insert Process Fig. 24.12 with verbiage. Insert Animation: Hydrochloric Acid Production by Parietal Cells in the Gastric.exe