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PANCREATIC HORMONES.

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Presentation on theme: "PANCREATIC HORMONES."— Presentation transcript:

1 PANCREATIC HORMONES

2 Learning Objectives Physiological anatomy of pancreas Insulin
Chemical nature Synthesis Mechanism of action Regulation of secretion Physiological effects

3 ACINI secrete digestive juices
Islets of Langerhans more in tail than body and head Alpha cells % Glucagon 2. Beta cells % Insulin, Amylin 3. Delta cells % somatostatin 4. PP cells Pancreatic Polypeptide

4 INSULIN Protein made up of two amino acid chains which are connected to each other by disulfide linkages Plasma half life of about 6 minutes Free insulin in plasma is destroyed by INSULINASE in liver, kidneys and muscles

5 FORMATION OF INSULIN BETA CELLS 1. Endoplasmic reticulum
Insulin Preprohormone cleaved to Proinsulin 2. Golgi Apparatus Proinsulin to insulin and peptide fragments

6 MECHANISM OF ACTION

7 With in seconds Increase uptake of glucose by the translocation of GLUT-4 in muscles and adipose tissues Permeable to K+, amino acids and phosphate

8 With in minutes Change the activity levels of many intracellular enzymes Hours to several days Translation Transcription

9 Learning Objectives Physiological effects of insulin
Glucagon (synthesis, chemical nature, regulation, physiological effects) Somatostatin (regulation & physiological effects)

10 Physiological effects of Insulin
On Carbohydrate metabolism Entry of glucose in cells of body (liver, muscle, adipose tissues) Utilization of glucose as energy source except brain Inhibition of gluconeogenesis Storage of glycogen Storage of fats

11 CARBOHYDRATE METABOLISM
INSULIN AND MUSCLES During resting state Slightly permeable to glucose and use free fatty acid for energy During heavy or moderate exercise Increase uptake of glucose in presence of low level of insulin because membrane becomes permeable (contraction) After meals High level of insulin causes increase uptake & use of glucose for energy and if muscles are not exercising excessive glucose is converted into glycogen.

12 INSULIN AND LIVER After Meal Increase uptake of glucose
Inactivation of glycogen phosphorylase (glycogen breakdown) Increased activity of glucokinase (phosphorylation of glucose) Increased activity of glycogen synthase Excess glucose to fatty acid---triglyceride—LDL---adipose tissue Between Meals Decrease blood glucose decreases insulin, all steps in reverse

13 INSULIN AND BRAIN Brain cells need glucose for energy and are permeable to glucose even in the absence of insulin Hypoglycemic shock When blood glucose level falls to 20 to 50 mg/100ml

14 Fat Metabolism Insulin acts as fat sparer
Synthesis of fats in liver (TG) Transport through VLDL Storage of TG in adipose tissues Anabolic effect of insulin on fat metabolism

15 FAT METABOLISM INSULIN AND LIVER
Excessive glucose is converted into fatty acid Fatty acid into triglycerides and then to LDL Insulin activates lipoprotein lipase (capillary wall of adipose tissue) which converts triglycerides to fatty acids essential for absorption in adipose tissue cells

16 ADIPOSE TISSUES After the Meal
Insulin inhibits hormone sensitive Lipase Increase glucose transport in adipose tissue and converted into glycerol phosphate which combines with fatty acids to form triglycerides Between the Meals Activation of hormone sensitive lipase Lack of insulin in liver Formation of phospholipids and cholesterol (atherosclerosis) Increase beta oxidation resulting formation of Ketone bodies and KETOSIS

17 PROTEIN METABOLISM ANABOLIC Uptake of amino acids Transcription
Translation Inhibits gluconeogenesis in liver Inhibits catabolism

18

19 MECHANISM OF INSULIN SECRETION

20

21 Switching between carbohydrate & fat metabolism
Insulin Glucagon Growth hormone & cortisol Epinephrine

22 GLUCAGON Secreted by alpha cells of the islets of Langerhans
Hyperglycemic hormone Glucagon is protein in nature Released in stressful & hypoglycemic conditions

23 Mechanism of action Through cAMP 2nd messenger system
Activation of glycogen phosphorylase Synthesis of glucose-1phosphate Release of glucose

24 EFFECT ON GLUCOSE METABOLISM
LIVER G-protein coupled receptors Glycogenolysis Gluconeogenesis

25 OTHER EFFECTS Activates adipose cell lipase Inhibits storage of triglycerides in liver Increases strength of heart Enhances bile secretion Inhibits gastric acid secretion

26 REGULATION OF SECRETION

27 SOMATOSTATIN Paracrine hormone Secreted by delta cells
Depresses the secretion of insulin and glucagon Decrease the motility of stomach, duodenum and gall bladder Decreases Secretion and absorption in GIT

28 REGULATION INCREASE SECRETION Increase blood glucose
Increase amino acid Increase fatty acid Gastrointestinal hormones released in response to food intake

29 SUMMARY OF BLOOD GLUCOSE REGULATION (24 hrs.)
Fasting blood glucose is 80 to 90mg/100 ml Random blood glucose level is 120 to 140mg/100 ml So the normal blood glucose is maintained by Liver Insulin and glucagon Sympathetic nervous system (hypoglycemia) Growth hormone and Cortisol (prolonged hypoglycemia)

30 DIABETES MELLITUS Definition:
A syndrome of chronic hyper glycaemia due to altered metabolism of carbohydrates, lipids & proteins caused by a decrease or total lack of insulin or diminished effectiveness of circulating insulin (insulin resistance).

31 Clinical features: Greek word meaning large urine volume Polyuria Polydipsia Polyphagia Hyperglycemia Glycosuria Ketosis Acidosis coma

32 Classification OF DM Type I diabetes, Insulin dependent diabetes mellitus (IDDM), Juvenile diabetes mellitus Before age of 30 Type II diabetes, Non-Insulin dependent diabetes mellitus (NIDDM), Adult-onset diabetes After age of 40 Secondary diabetes

33 CAUSES Type 1 Viral infections Autoimmune disorder Injury
Hereditary tendency

34 Type 2 Metabolic syndrome or syndrome X Obesity Insulin resistance Fasting hyperglycemia Lipid abnormalities Hypertension

35

36 Secondary Diabetes Pancreatectomy Acute Pancreatitis
Chronic Pancreatitis Haemochromatosis Cushing's Disease Acromegaly

37 CLINCAL PRESENTATION Blood glucose level 300 to 1200mg/100ml
Glycosuria when blood glucose level rises to 180mg/100ml

38 Dehydration Severe cell dehydration due to osmotic pressure in ECF Osmotic diuresis Polyuria ECF dehydration Polydipsia

39 Complications of Diabetes
VASULAR DAMAGE High LDL, Atherosclerosis A. Microvascular damage Diabetic retinopathy Diabetic nephropathy B. Macrovascular damage Stroke Myocardial infarction Diabetic neuropathy Peripheral nerves Autonomic nervous system

40 Ulceration and Gangrene of limbs
diabetic neuropathy + vascular damage DIABETIC FOOT Protein metabolism Increased utilization and decreased storage Weight loss despite of eating large (Polyphagia) Asthenia (lack of energy)

41 Fat metabolism Excessive Ketone Bodies formation Leading to METABOLIC ACIDOSIS Rapid and deep respiration ( KUSSMAUL BREATHING) Kidneys try to compensate When pH falls below 7 leads to ACIDOTIC COMA

42

43 DIAGNOSIS Urinary glucose Fasting blood glucose level
Normal 80 to 90mg/100ml Blood insulin level Type 1 low or undetectable Type 2 high than normal Acetone breath Large amount of Acetoacetic acid is converted to Acetone which is volatile and vaporized in expired air

44 Glucose Tolerance Test

45 TREATMENT Nutritional Exercise Monitoring Pharmacologic Education

46 Type 2 Sulfonylureas (increase insulin release)
Oral hypoglycemic agents Sulfonylureas (increase insulin release) Thiazolidinediones (reduce insulin resistance) Biguanides or Metformin (reduced gluconeogensis) INSULIN

47 Insulin therapy TYPE 1 Prepared by recombinant DNA method
Rapid acting—Humalog. peak min and last from 2-4 hours Short acting—regular. peak in 2-3h and last for 4-6 hours. Intermediate insulins—NPH. peak 4-12 hours and last hours. Long acting—Humulin. peak h and lasts 20-30h. Prepared by recombinant DNA method

48 Combination insulins 70/30 (70% NPH and 30% regular)
Humolog 70/30 (Humolog and regular

49 HGB A1C Measures blood levels over 2-3 months
High levels of glucose will attach to hemoglobin

50

51 Insulinoma or Hyperinsulinism
Adenoma of islet of Langerhans Increase insulin level Severe hypoglycemia Hypoglycemic Shock or Insulin shock Immediate IV large quantities of glucose IV Glucagon


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