The document discusses the hormones that regulate digestive activity in the gastrointestinal tract. It describes that gastrointestinal hormones are peptides secreted by enteroendocrine cells located along the mucosa. These hormones support the function of the organs that release them and enter the circulatory system rather than the GI lumen. Some hormones exhibit potentiation, where a combined action is greater than the individual effects. Specific hormones discussed include gastrin, cholecystokinin, secretin, gastric inhibitory polypeptide, and motilin.
The classical GI hormones are secreted by epithelial cells lining the lumen of the stomach and small intestine. These hormone-secreting cells - endocrinocytes - are interspersed among a much larger number of epithelial cells that secrete their products (acid, mucus, etc.) into the lumen or take up nutrients from the lumen. GI hormones are secreted into blood, and hence circulate systemically, where they affect function of other parts of the digestive tube, liver, pancreas, brain and a variety of other targets.
Endocrine regulation : EEC secretes regulatory peptide or hormones that travel via blood stream to remote target organ. Ex gastrin, secretin
Paracrine regulation : regulatory peptide secreted by EEC acts on a nearby target cell by diffusion through interstitial space. Ex histamine, 5-HT
The classical GI hormones are secreted by epithelial cells lining the lumen of the stomach and small intestine. These hormone-secreting cells - endocrinocytes - are interspersed among a much larger number of epithelial cells that secrete their products (acid, mucus, etc.) into the lumen or take up nutrients from the lumen. GI hormones are secreted into blood, and hence circulate systemically, where they affect function of other parts of the digestive tube, liver, pancreas, brain and a variety of other targets.
Endocrine regulation : EEC secretes regulatory peptide or hormones that travel via blood stream to remote target organ. Ex gastrin, secretin
Paracrine regulation : regulatory peptide secreted by EEC acts on a nearby target cell by diffusion through interstitial space. Ex histamine, 5-HT
LOCATION: WALL OF GUT
NEURONS: 100 MILLIONS
GIT MOVEMENTS AND SECRETIONS
COMPOSED: TWO PLEXUSES
OUTER PLEXUS (MYENTERIC AND AUERBACH'S PLEXUS)
INNER PLEXUS (MEISSNER'S PLEXUS AND SUBMUCOSAL PLEXUS)
MYENTERIC PLEXUS
GI MOVEMENTS
SUBMUCOSAL PLEXUS
SECRETION AND LOCAL BLOOD FLOW
Gastrointestinal Hormones by Pandian M, Dept of Physiology DYPMCKOP, for MBBS...Pandian M
Classify GIT hormones
List the source and functions of different GI hormones
Explain the mechanism of action and regulation of secretion of different GI Hormones
Describe the role of GI hormones in regulation of GI functions
Explain the dysfunctions produced by alteration in secretion of GIT hormones
Intestines(movements and secretions of small and large intestines ) The Guyto...Maryam Fida
Intestines(movements and secretions of small and large intestines)
Distended Portion of small intestine with chyme stretching concentric contractions at intervals lasting a fraction of a minute These contraction causes “Segmentation” of the small intestine ---forms spaced segments new points every time chopping chyme 2-3 times/min mixing with intestinal secretions maximum frequencyof segmentation contraction depends on frequency of BER (Basic electrical rhythm) i.e. In duodenum and proximal jejunum is 12/min and in terminal ileum is 8-9/min.
Atropine blocks the segmentation
law of gut
The peristaltic reflex +anal direction of movement of the peristalsis is called “LAW OF GUT”
LOCATION: WALL OF GUT
NEURONS: 100 MILLIONS
GIT MOVEMENTS AND SECRETIONS
COMPOSED: TWO PLEXUSES
OUTER PLEXUS (MYENTERIC AND AUERBACH'S PLEXUS)
INNER PLEXUS (MEISSNER'S PLEXUS AND SUBMUCOSAL PLEXUS)
MYENTERIC PLEXUS
GI MOVEMENTS
SUBMUCOSAL PLEXUS
SECRETION AND LOCAL BLOOD FLOW
Gastrointestinal Hormones by Pandian M, Dept of Physiology DYPMCKOP, for MBBS...Pandian M
Classify GIT hormones
List the source and functions of different GI hormones
Explain the mechanism of action and regulation of secretion of different GI Hormones
Describe the role of GI hormones in regulation of GI functions
Explain the dysfunctions produced by alteration in secretion of GIT hormones
Intestines(movements and secretions of small and large intestines ) The Guyto...Maryam Fida
Intestines(movements and secretions of small and large intestines)
Distended Portion of small intestine with chyme stretching concentric contractions at intervals lasting a fraction of a minute These contraction causes “Segmentation” of the small intestine ---forms spaced segments new points every time chopping chyme 2-3 times/min mixing with intestinal secretions maximum frequencyof segmentation contraction depends on frequency of BER (Basic electrical rhythm) i.e. In duodenum and proximal jejunum is 12/min and in terminal ileum is 8-9/min.
Atropine blocks the segmentation
law of gut
The peristaltic reflex +anal direction of movement of the peristalsis is called “LAW OF GUT”
The digestive system is made up of the gastrointestinal tract—also called the GI tract or digestive tract—and the liver, pancreas, and gallbladder. The GI tract is a series of hollow organs joined in a long, twisting tube from the mouth to the anus.
Lung Cancer: Artificial Intelligence, Synergetics, Complex System Analysis, S...Oleg Kshivets
RESULTS: Overall life span (LS) was 2252.1±1742.5 days and cumulative 5-year survival (5YS) reached 73.2%, 10 years – 64.8%, 20 years – 42.5%. 513 LCP lived more than 5 years (LS=3124.6±1525.6 days), 148 LCP – more than 10 years (LS=5054.4±1504.1 days).199 LCP died because of LC (LS=562.7±374.5 days). 5YS of LCP after bi/lobectomies was significantly superior in comparison with LCP after pneumonectomies (78.1% vs.63.7%, P=0.00001 by log-rank test). AT significantly improved 5YS (66.3% vs. 34.8%) (P=0.00000 by log-rank test) only for LCP with N1-2. Cox modeling displayed that 5YS of LCP significantly depended on: phase transition (PT) early-invasive LC in terms of synergetics, PT N0—N12, cell ratio factors (ratio between cancer cells- CC and blood cells subpopulations), G1-3, histology, glucose, AT, blood cell circuit, prothrombin index, heparin tolerance, recalcification time (P=0.000-0.038). Neural networks, genetic algorithm selection and bootstrap simulation revealed relationships between 5YS and PT early-invasive LC (rank=1), PT N0—N12 (rank=2), thrombocytes/CC (3), erythrocytes/CC (4), eosinophils/CC (5), healthy cells/CC (6), lymphocytes/CC (7), segmented neutrophils/CC (8), stick neutrophils/CC (9), monocytes/CC (10); leucocytes/CC (11). Correct prediction of 5YS was 100% by neural networks computing (area under ROC curve=1.0; error=0.0).
CONCLUSIONS: 5YS of LCP after radical procedures significantly depended on: 1) PT early-invasive cancer; 2) PT N0--N12; 3) cell ratio factors; 4) blood cell circuit; 5) biochemical factors; 6) hemostasis system; 7) AT; 8) LC characteristics; 9) LC cell dynamics; 10) surgery type: lobectomy/pneumonectomy; 11) anthropometric data. Optimal diagnosis and treatment strategies for LC are: 1) screening and early detection of LC; 2) availability of experienced thoracic surgeons because of complexity of radical procedures; 3) aggressive en block surgery and adequate lymph node dissection for completeness; 4) precise prediction; 5) adjuvant chemoimmunoradiotherapy for LCP with unfavorable prognosis.
Prix Galien International 2024 Forum ProgramLevi Shapiro
June 20, 2024, Prix Galien International and Jerusalem Ethics Forum in ROME. Detailed agenda including panels:
- ADVANCES IN CARDIOLOGY: A NEW PARADIGM IS COMING
- WOMEN’S HEALTH: FERTILITY PRESERVATION
- WHAT’S NEW IN THE TREATMENT OF INFECTIOUS,
ONCOLOGICAL AND INFLAMMATORY SKIN DISEASES?
- ARTIFICIAL INTELLIGENCE AND ETHICS
- GENE THERAPY
- BEYOND BORDERS: GLOBAL INITIATIVES FOR DEMOCRATIZING LIFE SCIENCE TECHNOLOGIES AND PROMOTING ACCESS TO HEALTHCARE
- ETHICAL CHALLENGES IN LIFE SCIENCES
- Prix Galien International Awards Ceremony
Explore natural remedies for syphilis treatment in Singapore. Discover alternative therapies, herbal remedies, and lifestyle changes that may complement conventional treatments. Learn about holistic approaches to managing syphilis symptoms and supporting overall health.
Flu Vaccine Alert in Bangalore Karnatakaaddon Scans
As flu season approaches, health officials in Bangalore, Karnataka, are urging residents to get their flu vaccinations. The seasonal flu, while common, can lead to severe health complications, particularly for vulnerable populations such as young children, the elderly, and those with underlying health conditions.
Dr. Vidisha Kumari, a leading epidemiologist in Bangalore, emphasizes the importance of getting vaccinated. "The flu vaccine is our best defense against the influenza virus. It not only protects individuals but also helps prevent the spread of the virus in our communities," he says.
This year, the flu season is expected to coincide with a potential increase in other respiratory illnesses. The Karnataka Health Department has launched an awareness campaign highlighting the significance of flu vaccinations. They have set up multiple vaccination centers across Bangalore, making it convenient for residents to receive their shots.
To encourage widespread vaccination, the government is also collaborating with local schools, workplaces, and community centers to facilitate vaccination drives. Special attention is being given to ensuring that the vaccine is accessible to all, including marginalized communities who may have limited access to healthcare.
Residents are reminded that the flu vaccine is safe and effective. Common side effects are mild and may include soreness at the injection site, mild fever, or muscle aches. These side effects are generally short-lived and far less severe than the flu itself.
Healthcare providers are also stressing the importance of continuing COVID-19 precautions. Wearing masks, practicing good hand hygiene, and maintaining social distancing are still crucial, especially in crowded places.
Protect yourself and your loved ones by getting vaccinated. Together, we can help keep Bangalore healthy and safe this flu season. For more information on vaccination centers and schedules, residents can visit the Karnataka Health Department’s official website or follow their social media pages.
Stay informed, stay safe, and get your flu shot today!
New Directions in Targeted Therapeutic Approaches for Older Adults With Mantl...i3 Health
i3 Health is pleased to make the speaker slides from this activity available for use as a non-accredited self-study or teaching resource.
This slide deck presented by Dr. Kami Maddocks, Professor-Clinical in the Division of Hematology and
Associate Division Director for Ambulatory Operations
The Ohio State University Comprehensive Cancer Center, will provide insight into new directions in targeted therapeutic approaches for older adults with mantle cell lymphoma.
STATEMENT OF NEED
Mantle cell lymphoma (MCL) is a rare, aggressive B-cell non-Hodgkin lymphoma (NHL) accounting for 5% to 7% of all lymphomas. Its prognosis ranges from indolent disease that does not require treatment for years to very aggressive disease, which is associated with poor survival (Silkenstedt et al, 2021). Typically, MCL is diagnosed at advanced stage and in older patients who cannot tolerate intensive therapy (NCCN, 2022). Although recent advances have slightly increased remission rates, recurrence and relapse remain very common, leading to a median overall survival between 3 and 6 years (LLS, 2021). Though there are several effective options, progress is still needed towards establishing an accepted frontline approach for MCL (Castellino et al, 2022). Treatment selection and management of MCL are complicated by the heterogeneity of prognosis, advanced age and comorbidities of patients, and lack of an established standard approach for treatment, making it vital that clinicians be familiar with the latest research and advances in this area. In this activity chaired by Michael Wang, MD, Professor in the Department of Lymphoma & Myeloma at MD Anderson Cancer Center, expert faculty will discuss prognostic factors informing treatment, the promising results of recent trials in new therapeutic approaches, and the implications of treatment resistance in therapeutic selection for MCL.
Target Audience
Hematology/oncology fellows, attending faculty, and other health care professionals involved in the treatment of patients with mantle cell lymphoma (MCL).
Learning Objectives
1.) Identify clinical and biological prognostic factors that can guide treatment decision making for older adults with MCL
2.) Evaluate emerging data on targeted therapeutic approaches for treatment-naive and relapsed/refractory MCL and their applicability to older adults
3.) Assess mechanisms of resistance to targeted therapies for MCL and their implications for treatment selection
Pulmonary Thromboembolism - etilogy, types, medical- Surgical and nursing man...VarunMahajani
Disruption of blood supply to lung alveoli due to blockage of one or more pulmonary blood vessels is called as Pulmonary thromboembolism. In this presentation we will discuss its causes, types and its management in depth.
MANAGEMENT OF ATRIOVENTRICULAR CONDUCTION BLOCK.pdfJim Jacob Roy
Cardiac conduction defects can occur due to various causes.
Atrioventricular conduction blocks ( AV blocks ) are classified into 3 types.
This document describes the acute management of AV block.
The prostate is an exocrine gland of the male mammalian reproductive system
It is a walnut-sized gland that forms part of the male reproductive system and is located in front of the rectum and just below the urinary bladder
Function is to store and secrete a clear, slightly alkaline fluid that constitutes 10-30% of the volume of the seminal fluid that along with the spermatozoa, constitutes semen
A healthy human prostate measures (4cm-vertical, by 3cm-horizontal, 2cm ant-post ).
It surrounds the urethra just below the urinary bladder. It has anterior, median, posterior and two lateral lobes
It’s work is regulated by androgens which are responsible for male sex characteristics
Generalised disease of the prostate due to hormonal derangement which leads to non malignant enlargement of the gland (increase in the number of epithelial cells and stromal tissue)to cause compression of the urethra leading to symptoms (LUTS
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Anti ulcer drugs and their Advance pharmacology ||
Anti-ulcer drugs are medications used to prevent and treat ulcers in the stomach and upper part of the small intestine (duodenal ulcers). These ulcers are often caused by an imbalance between stomach acid and the mucosal lining, which protects the stomach lining.
||Scope: Overview of various classes of anti-ulcer drugs, their mechanisms of action, indications, side effects, and clinical considerations.
Ethanol (CH3CH2OH), or beverage alcohol, is a two-carbon alcohol
that is rapidly distributed in the body and brain. Ethanol alters many
neurochemical systems and has rewarding and addictive properties. It
is the oldest recreational drug and likely contributes to more morbidity,
mortality, and public health costs than all illicit drugs combined. The
5th edition of the Diagnostic and Statistical Manual of Mental Disorders
(DSM-5) integrates alcohol abuse and alcohol dependence into a single
disorder called alcohol use disorder (AUD), with mild, moderate,
and severe subclassifications (American Psychiatric Association, 2013).
In the DSM-5, all types of substance abuse and dependence have been
combined into a single substance use disorder (SUD) on a continuum
from mild to severe. A diagnosis of AUD requires that at least two of
the 11 DSM-5 behaviors be present within a 12-month period (mild
AUD: 2–3 criteria; moderate AUD: 4–5 criteria; severe AUD: 6–11 criteria).
The four main behavioral effects of AUD are impaired control over
drinking, negative social consequences, risky use, and altered physiological
effects (tolerance, withdrawal). This chapter presents an overview
of the prevalence and harmful consequences of AUD in the U.S.,
the systemic nature of the disease, neurocircuitry and stages of AUD,
comorbidities, fetal alcohol spectrum disorders, genetic risk factors, and
pharmacotherapies for AUD.
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
1. Hormone regulate digestive activity Characteristics of GI hormone GI hormones are peptides Individual enteroendocrine cells in the mucosa secrete GI hormone. GI hormone released from single cell located along the mucosa GI hormone support the function of the organ that releases them GI hormones enter the circulatory system, not the lumen of GI tract Some GI hormones exhibit potentiation. Potentiation occurs when a combined action of two hormones is greater than the sum of their individual effect
3. Gastrin G cells in the pyloric antrum of the stomach secrete gastrin. Gastrin stimulate hydrochloric acid (HCL) secretion in the stomach
4. CCK I cells in the duodenum and jejunum secret CCK CCK causes the gallbladder to contract moving bile to the small intestine It causes the exocrine pancreas to secret digestive enzymes into small intestine CCK stimulate growth of the exocrine pancreas and mucosa of gallbladder
5. Secretin S cells in the duodenum secret hormone secretin Secretin causes both the liver and the exocrine pancreas to secrete bicarbonate into small intestine Secretin inhibits gastric acid secretion
6. GIP Cells in the duodenum and proximal jejunum secrete secret GIP In the presence of glucose, GIP stimulate the secretion of insulin by endocrine pancreas
7. Motilin Cells in the duodenum and jejunum secrete motilin about every 90 minutes during postabsorptive period Motilin moves the contents of the small intestine toward the terminal ileum
9. Fluid Secretion of GI Tract IN Absorbed Eliminated 800gm food ingested 750 gm 50 gm 2 L fluid ingested 1.5 L salivary 2 L gastric juice 8.85 L 0.15 L 1.5 L pancreatic fluid 0.5 L bile 1.5 L small intestine
10. Salivary Glands Salivary glands produce saliva Paired parotid, submandibular and sublingual glands are called extrinsic glands because they are lie outside the oral cavity There are smaller intrinsic salivary glands within the oral mucosa
11. Salivary Glands Saliva delivered through ducts to the mouth its function: Protection Saliva dilute, buffers, cleanses and help prevent destruction of teeth Produces lysozyme and IgA that capable of destroying certain bacteria Lubrication Mucus eases passage of foods Digestion Amylase digest carbohydrates
12. Nerves control of salivation Its mediated by the nervous system Both parasympathetic and sympathetic branch of ANS stimulate salivation
13. The parasympathetic is the primary controller of salivation Parasympathetic initiates and maintains salivation Stimulation of parasympathetic produces large amount of watery saliva containing enzyme Nerves control of salivation
14. Stimulation of salivation Thought, smell and taste of food stimulate the salivary center in the medulla to increase parasympathetic activity and salivation Acidic substances and chewing food are powerful stimuli of salivation Inhibition of salivation Fear, fatigue and sleep inhibits salivation Nerves control of salivation
15. Esophagus Secretion Mucus is the only secretion produced by the esophagus. Its function: Lubrication which facilitate passage of bolus along its length
16. Gastric Secretion The gastric mucosal epithelium is made entirely of secretary cells includes exocrine, endocrine and paracrine cells Exocrine secrete products into the stomach lumen includes: Mucus: Secreted throughout the stomach Pepsinogen: Secreted throughout the stomach HCL and intrinsic factor: Secreted from the same cell in the fundus and the body of the stomach
17. Enteroendocrine cells secrete gastrin and paracrine cells secrete histamine Gastrin Secreted in pyloric region of the stomach. Histamine secreted in the fundus and the body of the stomach. Gastric Secretion
18. Stomach Secretion Gastric mucosa has gastric pits in the folds. Cells that line the folds deeper in the mucosa, are gastric glands. Insert fig. 18.7