Human excretion is the process of removing excess water, waste materail and harmful substances from human body.
Also excretion is the process of eliminationg waste products of metabolism and other non-useful materials.
It is an essintial process in all formes of life. It also eliminate waste products such as water, carbondioxide and nitrogenous wates formed during catabolism.
Fatty acid oxidation
Types of fatty acid oxidation
Overview of fatty acid oxidation
Beta-Oxidation of fatty acid
Steps in Beta-Oxidation of fatty acid
Stoichiometry of Beta oxidation
Reference
Fatty acid oxidation
Types of fatty acid oxidation
Overview of fatty acid oxidation
Beta-Oxidation of fatty acid
Steps in Beta-Oxidation of fatty acid
Stoichiometry of Beta oxidation
Reference
1 . EXCRETION
Waste product removal e.g. nitrogenous – uric acid (mammals urea , fish ammonia)
Kidneys – secrete uric acid (product of protein metabolism)
Gastro-intestinal tract secretions e.g. bile
No sweat glands
Salt glands (water birds)
Water loss – lungs
2. URINARY SYSTEM
• Major organs are the kidneys, the ureter and the cloaca.
• No urinary bladder in bird.
3 . ANATOMICAL STRUCTURE OF KIDNEY
Avian kidneys are paired fitted closely the bony depression on the dorsal wall of the pelvis . Each kidney is divided into three lobes.
4 .
5 . NEPHRON
Two kinds of nephrons.
1. Reptilian nephron
2. Mammalian nephron
• 6 .
• 7. DIFFERENCE BETWEEN AVIAN AND MAMMALIAN KIDNEY
8. RENAL PORTAL SYSTEM
Uric acid is formed in the liver as well as the kidneys of the birds from ammonia, which is the most toxic protein metabolic by product .
9. GLOMERULAR FILTRATION
Fluid pressure forces water and dissolved substances from glomerular blood to Bowman’s capsule .
Filtration averages 125 ml/min form two kidneys.
10 . TUBULAR REABSORPTION
Return of the useful substances from the filtrate to the blood capillaries or interstitial fluid.
11 . COUNTER CURRENT MECHANISM
This mechanism works in the loop of henle to increase water reabsorbed from the descending limb as a result of salt reabsorbed from the ascending limb .
12 . POST RENAL URINE MODIFICATION
After the presentation of urine to cloaca their might be retrograde flow or backward flow of urine into the colon.
In the colon reabsorption of excessive amount of water as well as sodium ion takes place.
13 . HORMONES RESPONSIBLE FOR URINE FORMATION
Arginine vasotocin ,Angiotensin ׀׀ ,Aldosterone ,ANP (arterial natriuretic peptide)
Aldosterone is responsible for the reabsorption of sodium and excretion of potassium in the filtrate.
There needs to be a balance between water ingested and water eliminated.
In order to maintain homeostatic levels of water, the body must undergo osmoregulation.
What is teaching methodology, Objectives, Parts of teaching methodologies, Types of Teaching methods, Lecture method, Basic feautres , Purpose of these methods, Advantages and Disadvantages, Limitation of teaching methods, Team teaching method, Steps of team teaching methods, Characterstics of teaching methods, TV or Video Presentations, Group discussion method, Kinds of team teaching, Discussion methods of learning, Seminar method, Advantages and Disadvntages of seminar method, Brainstorming, Advantages and Disadvantages of Brain storming, Project method, Strategy of Project based teaching strategy, Characterstics of Project method, Role of teacher, Merits and Demerits of Project method.
INTRODUCTION OF COVID-19, ORIGIN OF COVID-19, STRUCTURE OF COVID-19, CAUSES OF CORON VIRUS, SYMPTOMS OF COVID-19, TYPICAL SYMPTOMS OF COVID-19, MODE OF TRANSMISSION, PEOPLE WHI ARE AT HIGHER RISK, WHY COVID-19 IS SAID T BE AS THE PANDEMIC BY WHO?, PREVENTION, WHAT TO DO, WHAT NOT TO DO, MYTHS AND FACTS OF COVID-19 SPREADING, SOME OTHER CONSEQUENCES OF COVID-19, MOST IMPORTANT POINTS OF COVID-19, COVID-19 VACCINES INTRODUCTION, TYPES OF VACCINES , COVAXIN, COVISHIELD, COVID VACCINE REGISTERATION, WHO CAN REGISTER, WHO SHOULDNT TAKE VACCINE SHOTS, STEP BY STEP GUIDE FOR REGISTERATION, COMPARISON BETWEEN COVAXIN AND COVISHIELD,
WHAT IS PHOTOSYNTHESIS?, IMPORTANCE OF PHOTOSYNTHESIS, STRUCTURAL FEATURE OF LEAF ADVANTAGE FOR PHOTOSYNTHESIS,LEAVES AND LEAF STRUCTURE,CHLOROPHYLL, TYPES OF REACTIONS, LIGHT REACTION AND DARK REACTION, CYCLIC AND NON-CYCLIC PHOTOPHOSPORYLATION, MECAHANISM OF ATP SYNTHESIS, SCHEMATIC PRESENTATION OF LIGHT REACTION, CRASSULACEAN ACID METABOLISM (CAM), C3 AND C4 PLANTS, FACTORS AFFECTING RATE OF PHOTOSYNTHESIS, INTERNAL FACTORS AND EXTERNAL FACTORS,
RECOMBINANT DNA GUIDELINES DEFINATION, RESEARCH ACTIVITIES AND ITS CATEGORIES,BIOSAFETY LEVELS, BSL-1, BSL-II, BSL-III, BSL-IV, WHAT IS BIOSAFETY GUIDELINES, AIM OF BIOSAFETY GUIDELINES, THE R-DNA BIOSAFETY GUIDELINES IN INDIA , COMMITTEES IMPANTED BY DBT, IBSC, ECGM, GEAC, CONTAINMENTS AND ITS TYPES, LEVELS OF CONTAINMENTS,PURPOSE OF THE CONTAINMENTS, ELEMENT OF CONTAINMENTS, IMPLEMENTATION OF BIOSAFETY GUIDELINES,MECHANISM OF IMPLEMENTATION, PHYSICAL CONTAINMENTS, BIOLOGICAL CONTAINMENTS, IMPLEMENTATION OF BIOSAFTEY GUIDELINES, RECOMBINANT DNA ADVISORY COMMITTEE, INSTITUTIONAL BIOSAFETY COMMITTEE,
Site directed mutgenesis, OLIGONUCLEOTIDE DIRECTED MUTAGENESIS Vipin Shukla
INTRODUCTION, HISTORY, MUTATION, DIRECTED MUTAGENESIS,BASIC MECHANISM OF SITE DIRECTED MUTAGENESIS,METHOD FOR SITE DIRECTED MUTATIONS,THE SINGLE PRIMER METHOD, CASETTEE MUTAGENESIS, PCR-SITED DIRECTED MUTAGENESIS, APPLICATION OF SITE DIRECTED MUTAGENESIS.
INTRODUCTION, DEFINATION OF ELECTROPHORESIS, ELECTROPHORESIS PRINCIPLE, TYPES OF ELECTROPHORESIS, FREE ELECTROPHORESIS, ZONE ELECTROPHORESIS,PAPER ELECTROPHORESIS, WORKING OF PAPER ELECTROPHORESIS, PROCEDURE FOR PAPER ELECTROPHORESIS, VISUALISATION, FACTORS AFFECTING SEPARATION OF MOLECULES, APPLICATIONS, working of paper electrophoresis ,procedure for paper electrophoresis ,visualisation ,factors affecting separation of molecules ,applications ,forensics ,dna fingerprinting ,molecular biology ,microbiology information about the organisms ,biochemistry mapping of cellular components ,paper electrophoresis is also used in study of sic ,hemoglobin abnormalities ,separation of blood clotting factors ,serum plasma proteins from blood sample ,used in separation and identification of alkaloids ,used for testing water samples ,toxicity of water ,drug industry to determine presence of illelgal drUGS
Introduction, Theme of the environment day, Role of teachers in environmental education, How the environment impact our health, How can we celebrate the day, Dangerous or Hazardous Waste, Seven Billion Dreams, Our planet consume with care, Examples such as Radioactivity wastes, Soil erosion
Reproductive system and its Classification Vipin Shukla
Human Reproductive system, Classificatio of Human reprodutive system, Parts and Functions male reproductive organs, Female Reproductive system, Parts and functions of female reproductive system,The Menstrual cycle, Assisted Reproductive Technology, Invitrofertilization, and its techniques, Most commonly used techniques, Les commonly used techniques, Transvaginal Oocytes Retrieval, Intra Cytoplasmic Injecection, (ICSI), Procedure of ICSI, Who are the patients required ICSI, Embryo Transfer, Zygote Intra Fallopain Transfer, Gametes Intrafallopian Transfer, Gift Technique, Surrogacy, Types of Surrogacy, Steps Involved in Surrogacy, Ither techniques,
Revised guideline for research in transgenic plants (Vipin Shukla
In 1998, BDT brought out seperate guidelines for carriying out research in transgenic planst called the Revised Guidelines for research guidelines in Transgenic Plants.
Approaches of biotechnology in medicalVipin Shukla
Medical Biotechnology is defined as the branch of science that delas with the study of use of living cells in Research and pharmaceuticals and diagnostic products that help to treat and prevent human diseases.
Bio saftey in transgenics & its productsVipin Shukla
Transgenic plants are those plants were we insert an foreign gene in an host genome to modify its characters such as Stress tolerance, Virus resistant, Biotic and Abiotic Tolerance etc.
Polymerase Chin Reaction is a technique that takes specific sequences of DNA of small and amplifies it to be used for further testing.
it is also said to be as the Invitro Technique.We have seen an photocopy machine in an office, by which we can copy several pages. So, is the PCR machine in a molecular biology laboratory.
PCR is DNA raplication ina test tube.
Dr Kary Mullis developed PCR.
To amplify lot of double stranded DNA molecules with same size and sequence by enzymatic method and cycling condition.
Biosaftey means the needs to protect human and animal health along with the environment from the possible adverse effects of the products of modern biotechnology. Biosafety defines the containment conditions under which infectious agents can be safely manipulated. Biosafety word is used to reduce and eliminate the potential risk regulating from the modern biotechnology and its products.
HYBRIDOMA TECHNOLOGY IT IS DEFINED AS THE PROCESS WERE THERE IS A FUSION OF SPLLEN CELL AND MYELOMA CELLS IN THE PRESENCE OF POLYETHYLENE GLYCOL OR SENDAI VIRUS AND LEADS TO THE PRODUCTION OF MONOCLONL ANTIBODY.
COMPLEMENT SYSTEM IS DEFINED AS THE PART OF IMMUNE SYSTEM WHICH ENHANCES THE IMMUNITY OF AN INDIVIUAL. IT INCLUDES 30 SOLUBLE PROTEINS PRESENT IN PLASMA.
Complement system consists of a group of more then 30 proteins or soluble proteins which are present in the plasma. Basically it is a part of our immune system which enhance the abitlity of Antobody and the Phagocytic cells from the organisms body or also act in inflammation and form the MAC to kill the pathogens.
These are the complements protein or Glycoproteins or Specialized proteins.
Slide 1: Title Slide
Extrachromosomal Inheritance
Slide 2: Introduction to Extrachromosomal Inheritance
Definition: Extrachromosomal inheritance refers to the transmission of genetic material that is not found within the nucleus.
Key Components: Involves genes located in mitochondria, chloroplasts, and plasmids.
Slide 3: Mitochondrial Inheritance
Mitochondria: Organelles responsible for energy production.
Mitochondrial DNA (mtDNA): Circular DNA molecule found in mitochondria.
Inheritance Pattern: Maternally inherited, meaning it is passed from mothers to all their offspring.
Diseases: Examples include Leber’s hereditary optic neuropathy (LHON) and mitochondrial myopathy.
Slide 4: Chloroplast Inheritance
Chloroplasts: Organelles responsible for photosynthesis in plants.
Chloroplast DNA (cpDNA): Circular DNA molecule found in chloroplasts.
Inheritance Pattern: Often maternally inherited in most plants, but can vary in some species.
Examples: Variegation in plants, where leaf color patterns are determined by chloroplast DNA.
Slide 5: Plasmid Inheritance
Plasmids: Small, circular DNA molecules found in bacteria and some eukaryotes.
Features: Can carry antibiotic resistance genes and can be transferred between cells through processes like conjugation.
Significance: Important in biotechnology for gene cloning and genetic engineering.
Slide 6: Mechanisms of Extrachromosomal Inheritance
Non-Mendelian Patterns: Do not follow Mendel’s laws of inheritance.
Cytoplasmic Segregation: During cell division, organelles like mitochondria and chloroplasts are randomly distributed to daughter cells.
Heteroplasmy: Presence of more than one type of organellar genome within a cell, leading to variation in expression.
Slide 7: Examples of Extrachromosomal Inheritance
Four O’clock Plant (Mirabilis jalapa): Shows variegated leaves due to different cpDNA in leaf cells.
Petite Mutants in Yeast: Result from mutations in mitochondrial DNA affecting respiration.
Slide 8: Importance of Extrachromosomal Inheritance
Evolution: Provides insight into the evolution of eukaryotic cells.
Medicine: Understanding mitochondrial inheritance helps in diagnosing and treating mitochondrial diseases.
Agriculture: Chloroplast inheritance can be used in plant breeding and genetic modification.
Slide 9: Recent Research and Advances
Gene Editing: Techniques like CRISPR-Cas9 are being used to edit mitochondrial and chloroplast DNA.
Therapies: Development of mitochondrial replacement therapy (MRT) for preventing mitochondrial diseases.
Slide 10: Conclusion
Summary: Extrachromosomal inheritance involves the transmission of genetic material outside the nucleus and plays a crucial role in genetics, medicine, and biotechnology.
Future Directions: Continued research and technological advancements hold promise for new treatments and applications.
Slide 11: Questions and Discussion
Invite Audience: Open the floor for any questions or further discussion on the topic.
This presentation explores a brief idea about the structural and functional attributes of nucleotides, the structure and function of genetic materials along with the impact of UV rays and pH upon them.
Salas, V. (2024) "John of St. Thomas (Poinsot) on the Science of Sacred Theol...Studia Poinsotiana
I Introduction
II Subalternation and Theology
III Theology and Dogmatic Declarations
IV The Mixed Principles of Theology
V Virtual Revelation: The Unity of Theology
VI Theology as a Natural Science
VII Theology’s Certitude
VIII Conclusion
Notes
Bibliography
All the contents are fully attributable to the author, Doctor Victor Salas. Should you wish to get this text republished, get in touch with the author or the editorial committee of the Studia Poinsotiana. Insofar as possible, we will be happy to broker your contact.
DERIVATION OF MODIFIED BERNOULLI EQUATION WITH VISCOUS EFFECTS AND TERMINAL V...Wasswaderrick3
In this book, we use conservation of energy techniques on a fluid element to derive the Modified Bernoulli equation of flow with viscous or friction effects. We derive the general equation of flow/ velocity and then from this we derive the Pouiselle flow equation, the transition flow equation and the turbulent flow equation. In the situations where there are no viscous effects , the equation reduces to the Bernoulli equation. From experimental results, we are able to include other terms in the Bernoulli equation. We also look at cases where pressure gradients exist. We use the Modified Bernoulli equation to derive equations of flow rate for pipes of different cross sectional areas connected together. We also extend our techniques of energy conservation to a sphere falling in a viscous medium under the effect of gravity. We demonstrate Stokes equation of terminal velocity and turbulent flow equation. We look at a way of calculating the time taken for a body to fall in a viscous medium. We also look at the general equation of terminal velocity.
Deep Behavioral Phenotyping in Systems Neuroscience for Functional Atlasing a...Ana Luísa Pinho
Functional Magnetic Resonance Imaging (fMRI) provides means to characterize brain activations in response to behavior. However, cognitive neuroscience has been limited to group-level effects referring to the performance of specific tasks. To obtain the functional profile of elementary cognitive mechanisms, the combination of brain responses to many tasks is required. Yet, to date, both structural atlases and parcellation-based activations do not fully account for cognitive function and still present several limitations. Further, they do not adapt overall to individual characteristics. In this talk, I will give an account of deep-behavioral phenotyping strategies, namely data-driven methods in large task-fMRI datasets, to optimize functional brain-data collection and improve inference of effects-of-interest related to mental processes. Key to this approach is the employment of fast multi-functional paradigms rich on features that can be well parametrized and, consequently, facilitate the creation of psycho-physiological constructs to be modelled with imaging data. Particular emphasis will be given to music stimuli when studying high-order cognitive mechanisms, due to their ecological nature and quality to enable complex behavior compounded by discrete entities. I will also discuss how deep-behavioral phenotyping and individualized models applied to neuroimaging data can better account for the subject-specific organization of domain-general cognitive systems in the human brain. Finally, the accumulation of functional brain signatures brings the possibility to clarify relationships among tasks and create a univocal link between brain systems and mental functions through: (1) the development of ontologies proposing an organization of cognitive processes; and (2) brain-network taxonomies describing functional specialization. To this end, tools to improve commensurability in cognitive science are necessary, such as public repositories, ontology-based platforms and automated meta-analysis tools. I will thus discuss some brain-atlasing resources currently under development, and their applicability in cognitive as well as clinical neuroscience.
Seminar of U.V. Spectroscopy by SAMIR PANDASAMIR PANDA
Spectroscopy is a branch of science dealing the study of interaction of electromagnetic radiation with matter.
Ultraviolet-visible spectroscopy refers to absorption spectroscopy or reflect spectroscopy in the UV-VIS spectral region.
Ultraviolet-visible spectroscopy is an analytical method that can measure the amount of light received by the analyte.
What is greenhouse gasses and how many gasses are there to affect the Earth.moosaasad1975
What are greenhouse gasses how they affect the earth and its environment what is the future of the environment and earth how the weather and the climate effects.
(May 29th, 2024) Advancements in Intravital Microscopy- Insights for Preclini...Scintica Instrumentation
Intravital microscopy (IVM) is a powerful tool utilized to study cellular behavior over time and space in vivo. Much of our understanding of cell biology has been accomplished using various in vitro and ex vivo methods; however, these studies do not necessarily reflect the natural dynamics of biological processes. Unlike traditional cell culture or fixed tissue imaging, IVM allows for the ultra-fast high-resolution imaging of cellular processes over time and space and were studied in its natural environment. Real-time visualization of biological processes in the context of an intact organism helps maintain physiological relevance and provide insights into the progression of disease, response to treatments or developmental processes.
In this webinar we give an overview of advanced applications of the IVM system in preclinical research. IVIM technology is a provider of all-in-one intravital microscopy systems and solutions optimized for in vivo imaging of live animal models at sub-micron resolution. The system’s unique features and user-friendly software enables researchers to probe fast dynamic biological processes such as immune cell tracking, cell-cell interaction as well as vascularization and tumor metastasis with exceptional detail. This webinar will also give an overview of IVM being utilized in drug development, offering a view into the intricate interaction between drugs/nanoparticles and tissues in vivo and allows for the evaluation of therapeutic intervention in a variety of tissues and organs. This interdisciplinary collaboration continues to drive the advancements of novel therapeutic strategies.
3. Introduction:
Excretion is the process of elimination of unwanted
materials and waste products such as water, carbon
dioxide and nitrogenous wastes formed during
catabolism.
The chief excretory organs of vertebrates are the
Kidneys.
These are made up of millions of units, which are known
as the Uriniferous tubules or Nephrons or the renal
tubules.
4. Nitrogenous Waste Products in Vertebrates:
The metabolic waste products
which are excreted by the
animals my be grouped under
the following two heads:
Respiratory waste products.
Nitrogenous waste products.
5. Respiratory Waste Products:
The catabolic waste products of various types of food stuffs
are Co2 and water.
In lower animals Co2 is eliminated directly into the
environment through the general body surface.
In higher animals it is excreted with the expired air through
the lungs.
Excess of water is eliminated in the form of urine and sweat.
6. Nitrogenous Waste Products:
The nitrogenous waste products are
derived from the deamination of the
excess of amino acid taken in with
the diet and also from the
breakdown of animal proteins and
nucleic acids.
Following are the specific
nitrogenous waste products excreted
by the animals:
7. Continued……
Ammonia:
It is formed by the deamination
of amino acids during protein
metabolism.
Ammonia is highly toxic and its
rapid elimination is essential.
Since it is highly soluble in
water & it is quickly eliminated
in surrounding water.
8. Urea:
It is less toxic than ammonia.
Most mammals, Fishes, Marine elasmobranches and
amphibians excrete their nitrogenous waste products in the
form of Urea.
Formation of urea enables elimination of both ammonia and
Co2.
Urea is formed of two molecules of ammonia and a molecule
of carbon dioxide.
10. Uric acid:
Insects, some snails, birds and reptiles with few
exceptions, excrete uric acid.
Uric acid is excreted in solid form.
Uric acid is insoluble in water.
It crystallizes out form the fluid urine and water is
reabsorbed, thereby allowing conservation of water.
11.
12. Amino-Acids:
In certain animals like molluscus and echinoderms, the excess
of amino acids is removed as such without undergoing any
change.
Other nitrogenous compounds:
Allantoin and allantoic acid are other nitrogenous excretory
products.
These are insoluble in water and are excreted during
embryonic development by amniotes with shelled eggs.
13. Continued……
There are some other nitrogenous waste products such
as Guanine and Adenine from nucleic acid breakdown
and creatine from the creatine of muscles that are
excreted along with other nitrogenous waste products in
the urine.
15. Mineral Ions:
Sodium, Potassium,
Calcium, magnesium
and Chloride are the
essential mineral ions
of the animals.
The excess of these
ions taken in with the
diet are excreted by
one means or the other.
16. Types of excretion:
Products' of catabolism are excreted from all animals by
diffusion.
The end products of oxidation of proteins, pyrimidines
and purines are nitrogen compounds chiefly ammonia.
But ammonia is a toxic substance and needs either to be
removed as soon as it is formed or to be converted to
some less toxic substance.
These substances are either “ Trimethylamine oxide,
urea or uric acid.
17. Continued…..
Therefore, the nitrogenous excretory substances in
animals are ammonia, Trimethylamine, urea and uric
acid.
Ammonia is very toxic and very much soluble in water.
Urea is less toxic and comparatively less soluble in
water.
Uric acid is less toxic than either ammonia or urea and is
almost insoluble in body fluids.
Thus, secretion of particular type of nitrogenous bases
depend upon its environment and mode of life.
18. Ammonotelic(Marine Invertebrates)
Most of the marine invertebrates excrete large
proportion of their nitrogen as Ammonia. such animals
are known as Ammonotelic.
Ammonia is highly soluble in water and its
concentration in the body fluids of marine invertebrates
varies from (o.4mg to 4.8 mg per 100ml).
Marine animals live in unlimited volume of water and
their body fluids are mostly isotonic or hypertonic to sea
water.
19. Continued…..
Therefore, ammonia which is soluble in water, readily
diffuses out to their body from higher to low
concentrations and never reaches a dangerous
concentration.
22. Ureotelic (Marine Fishes)
Marine fishes excrete urea not ammonia.
These are known as Ureotelic.
They cannot afford to excrete ammonia because of several
reasons.
In, marine cartilaginous fishes the body fluids are to be
maintained hypertonic to the sea water.
They retain (2 to 2.5 %) of urea in the blood and thus
maintained themselves hyper osmotic to their medium.
23.
24. Ammonotelic (Freshwater Animals)
Fresh water animals imbibe plenty of water and
moreover, being hypertonic to the surrounding water
these have the problem to get rid of excess of water.
Fresh water invertebrates as well as almost all
freshwater fishes are Ammonotelic.
25. Ornithine-Arginine Cycle or Ornithine Cycle:
During catabolism of proteins, amino acids, undergo
deamination and ammonia is liberated.
Free ammonia is toxic to the body cells and need to be
eliminated from the body.
In vertebrates toxic ammonia is converted into nontoxic
urea by the liver cells.
The mechanism involved in the formation of urea
constitute “Ornithine – arginine cycle.
26. Continued….
The cyclic chain of chemical reactions involved in the
Ornithine-arginine cycle leading to the formation of urea
can be summarized as under:
An Important amino acid Ornithine occurs freely in the
liver cells. It forms the starting point in the chain of
Ornithine cycle.
Ornithine combines with (NH3 & CO2) and forms
citrulline and releases one molecule of water.
Citrulline combines with large quantities of (NH3) and
water to form arginine.
27. Continued……..
Arginine is catalyzed by enzyme arginase present in the
liver. This breaks arginine into Ornithine and urea, thus
completing the cycle.
The Ornithine once again combines with ammonia to
repeat the Ornithine cycle.
Thus arginase plays an important role.
Arginase is found in all the tissues in elasmobranches'
fishes and in liver cell of mammals.
28. Continued…..
Ornithine cycle was described by Krebs and Henseleit
(1932).
They demonstrated the action of arginase in urea
formation by using slices of rat liver.
29.
30. Significance of Ornithine Arginine Cycle:
Ammonia produced due to deamination of amino acids
is toxic to the body cells and less soluble in water.
In unicellular and simple multicellular organisms, living
in water immediately eliminate ammonia by simple
diffusion into the surrounding water.
But terrestrial animals having complex organization, can
neither afford to lose large amount of water, nor can
retain ammonia for long.
31. Continued……
Therefore, formation of urea as excretory product is a
device of retaining nitrogenous wastes in the body till
these are excreted out of the body.
Composition of water molecules:
In Ornithine-Arginine cycle three ATP
molecules are consumed:
32. Continued…..
In the formation of active Co2 = 1 ATP.
In the synthesis of carbamyl phosphate =1 ATP.
In the formation of Orginine-succinate = 1 ATP.
Total= 3 ATP,s are formed.
33. Formation of Urine:
Urine formation takes place in the kidneys. It involves
three process which are mentioned below:
Ultra filtration.
Tubular Re-absorption.
Tubular secretion.
34. Continued:….
Ultrafilteration of Glomerular Filtration:
Bowman's capsules act as ultra filters and lie in close
contact with Glomerulus.
As blood flows through Glomerular capillaries, water
and all the substances of plasma except blood cells and
plasma protein filter out of the blood into Bowman's
capsules.
35. Continued….
Filtration occurs rapidly because of the following
reasons:
Blood is separated from the cavity of Bowman's capsule
by two very thin membranes, the endothelial layer of the
blood capillaries and epithelial layer of Bowman's
capsule.
The capillary walls have numerous fine pores of about
(50-100nm) in diameter.
36. Continued…..
The epithelial cells of Bowman's capsule are specialized
and are called podocytes.
The fine or minor processes of podocytes reach up to the
basement membrane of Glomerular capillaries and
establish a very close contact.
Afferent arteriole is wider than the efferent arteriole.
Therefore, the amount of blood that enters the afferent
arteriole in a definite time is not fully drained out by
efferent arteriole.
37. Continued…..
This increases the hydrostatic pressure in the capillary
network of Glomerulus.
The effective filtration pressure (EFP) or pressure
gradient responsible for its filtration is the outcome of
the interaction of following pressures:
38. Continued…..
This increases the hydrostatic pressure in the capillary
network of Glomerulus.
The effective filtration pressure (EFP) or pressure
gradient responsible for its filtration is the outcome of
the interaction of following pressures:
A) The Glomerular hydrostatic pressure or the
capillary pressure is the main driving force that tends
to move out of the glomeruli.
It is exerted by blood while passing through Glomerulus.
39. Continued…..
The capsular hydrostatic pressure (renal interstitial
pressure+ renal intratubular pressure) about (20mmHg)
and blood colloidal osmotic pressure about (30mmHg)
exert force against capillary pressure.
Summary Filtration Pressure in Glomerulus:
1.) GHP (Glomerular Hydrostatic Pressure) ; 75mmHg.
2) BCOP (Blood Colloidal Osmotic Pressure): 30mmHg
3) RIP (Renal Interstitial Pressure) : 10mmHg.
4) Renal Intratubular Pressure): 10mmHg.
40.
41. Continued…
Net Filtration Pressure =
75-(30+10+10 mmHg)
(75-50mmHg).
Therefore, the net filtration Pressure responsible for
filtration is about :
75-(20+30)= +25mmHg.
42. Tubular or Selective Reabsorption:
From, the Bowman's capsule, the Glomerular filtrate
courses through the tubule and passes into the collecting
duct.
During this course its composition osmotic pressure and
PH change due to Reabsorption of water and many
solutes from it in the tubules.
The process by which only useful substances are
reabsorbed from the Nephric filtrate in the blood
capillaries is called tubular or selective Reabsorption.
43. Continued….
This filtration is called Ultrafiltration.
As a result of Ultrafiltration almost all the substances
dissolved in plasma (Urea, Salts, Glucose, Creatine etc)
along with water except blood cells and colloids and
certain plasma and is called “ Nephric Filtrate or
Glomerular filtrate).
Glomerular filtration rate in a normal adult is
about(120ml per minute).
The average volume filtered from the plasma into
Bowman's capsule is about (190 liters per day).
44. Mechanism of tubular Reabsorption:
There are two mechanism for tubular Reabsorption:
Active reabsorption:
Substances like glucose and amino acids . Which are of
considerable importance to the body are reabsorbed
actively.
Active reabsorption is very rapid and continues even when
the concentration of the substance is far lower in the
glomerular filtrate than in the blood.
45. Passive reabsorption:
Some substances like Urea, ammonia , creatinine, ketone
bodies etc., are reabsorbed from the tubules slowly by
diffusion.
It continues so long as their concentration in the
glomerular filtrate exceeds their concentration in the
blood.
Thus these substances are never reabsorbed totally from
the urine.
Water is also reabsorbed by the passive process of
osmosis.
46.
47. Proximal Convoluted Tubule (PCT)
In the proximal convoluted tubule almost (100%) of glucose,
amino acids and vitamins C, about (70%) of (K+),nearly
(75%) of (Na+) and a large amount of (Ca2+) ions are
absorbed from the glomerular filtrate.
Chloride ion reabsorbed by diffusion from the PCT.
About (75%) of the water of the filtrate is also reabsorbed
here by osmosis during the reabsorption of the solutes.
48. Henle,s Loop:
About (5%) of water in the glomerular filtrate is
reabsorbed by osmosis from the descending limb of
Henle,s loop due to higher osmotic pressure of the
medullary extracellular fluid maintained by Vasa rectae.
The ascending limb is impermeable to water along its
entire length.
But it actively absorbs the remaining (25%) of the
filtered (K+) and some amounts of Cl- ions.
49. Continued….
So, the filtrate becomes dilute (hypotonic) than the
plasma as it follows through the ascending limb.
Distal Convoluted Tubules (DCT) and collecting duct:
The distal convoluted tubule, collecting tubule and
collecting duct actively reabsorb sodium from the filtrate
under the influence of the adrenal
hormone,aldestrone,which makes their walls permeable
to ions.
50. Continued…
These actively absorbs some (Na+) from the filtrate and
in exchange excrete some (K+) ions in the urine.
Some (Cl_) ions are also reabsorbed by diffusion.
51. Tubular Secretion:
This process is of considerable importance in marine
fishes and desert amphibians.
These animals lack Glomerulus and Bowman's capsule
in their nephrons.
So, these animals form urine by secreting solutes such as
Urea, Creatinine and minerals ions into their tubules.
52. Continued….
But, tubular secretion is of less importance in mammals.
Most of the (K+) eliminated in the mammalian urine is
secreted by the distal convoluted tubule and collecting
ducts in exchange of the reabsorbed (Na+).
The distal convoluted tubule and collecting tubule also
secrete uric acid and ammonia in the urine.
53. Continued….
The volume of urine formed is far less than the
volume of glomerular filtrate and its
composition is also quite different from that of
the glomerular filtrate.