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PRESENTED BY:- SHAILESH PRADHAN
J.K. COLLEGE OF PHARMACY (BILASPUR
CHHATTISGARH)
INTRODUCTION:-
 Insulin is an anbolic hormone secreted by the endocrine
pancreas.
 ENDOCRINE PANCREAS:-Endocrine pancreas are secreted
three type hormones –
 A) INSULIN-
 Secreted from Beta cells of pancreas due to high blood
glucose level.
 Increase glucose up take in to tissue.
 Convert-glucose to glycogen.
 B)GLUCAGON-
 Secreted from alpha cells of pancreas due to low blood
glucose level.
 It is a hyperglycemic facilitator.
 Convert-glycogen to glucose.
 C) SOMATOSTATIN-
 Secreted from gama cells of pancreas.
 It is a universal inhibitor of secretory cells.
 GLUCOSE HOMEOSTASIS-
 NORMAL GLUCOSE CONTROL-
 1) Post absorptive period-
 Normal individual low basal level of circulating insulin
maintain through constant beta cell secretion by
suppression lipolysis , proteolysis and glycogenolysis.
 2)After ingesting meal-
 Brust of insulin secretion is response to elevated to
glucose and amino acid level.
 3)When glucose level return to basal levels-
 Insulin return to its basal level.
INSULIN
 Insulin was discovered in 1921 by Banting.
 It was 1st obtain in crystalline form in 1926 and
chemical structure was fully worked out in 1956 by
Sanger.
 Insulin are two chain polypeptide having 51 amino
acid.
 A chain-21 amino acid
 B chain- 30 amino acid
 MO. WT. of insulin- 5734 g/mol
BIO SYNTHESIS OF INSULIN
 Rough endoplasmic reticulum preproinsulin
 Golgi apparatus prohormone convertase proinsulin
 Secretory granules insulin + c- pepetide
SECRETION OF INSULIN
 Intracellular transport of glucose is mediated by
GLUT-2 an insulin independent glucose transporter in
Beta cells.
 Glucose undergoes oxidative metabolism yiEld ATP.
 ATP inhibit K+ channel receptor on Beta cell surface
 This receptor leads to membrane depolarization.
 Influx of Ca++ ion and release stored insulin .
CLASSIFICATION OF INSULIN
INSULIN
RAPID ACTING SHORT ACTING INTERMADIATE
ANALOGOUS
ACTING
-Insulin lispro -Regular soluble -
Glargine
-Insulin aspart insulin -Insulin zinc susp. -Ins.
Determir
-Insulin glulisine
MOA OF INSULIN
ACTION OF INSULIN IN VARIOUS
TISSUE
 1)IN LIVER-
 Decrease glucose production.
 Increase glycogenesis.
 Increase TG synthesis.
 Increase protein synthesis.
 2)IN MUSCLES-
 Increase glucose transport.
 Increase glycolysis.
 Increase glycogen deposition.
 Increase protein synthesis.
 3)IN ADEPOSE
 Increase glucose transport.
 Increase lipogenesis.
 PHARMACOKINETIC OF INSULIN-
 Inj. SC
 Metabolized by kidney and liver.
 Elimination t1/2 is 5-10 min.
 Highly bond with tissue receptor.
 ADR OF INSULIN-
 Hypoglycemia.
 Allergic reactions.
 Insulin registance.
 Weight gain.
 DRUG INTRACTION-
 Beta adrenergic drug.
 Furosemide,solbutamol,oral contraceptive(increase
blood sugar and decrease effect of insulin)
THANK YOU….

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Insulin ppt

  • 1. PRESENTED BY:- SHAILESH PRADHAN J.K. COLLEGE OF PHARMACY (BILASPUR CHHATTISGARH)
  • 2. INTRODUCTION:-  Insulin is an anbolic hormone secreted by the endocrine pancreas.  ENDOCRINE PANCREAS:-Endocrine pancreas are secreted three type hormones –  A) INSULIN-  Secreted from Beta cells of pancreas due to high blood glucose level.  Increase glucose up take in to tissue.  Convert-glucose to glycogen.  B)GLUCAGON-  Secreted from alpha cells of pancreas due to low blood glucose level.  It is a hyperglycemic facilitator.  Convert-glycogen to glucose.
  • 3.  C) SOMATOSTATIN-  Secreted from gama cells of pancreas.  It is a universal inhibitor of secretory cells.  GLUCOSE HOMEOSTASIS-
  • 4.  NORMAL GLUCOSE CONTROL-  1) Post absorptive period-  Normal individual low basal level of circulating insulin maintain through constant beta cell secretion by suppression lipolysis , proteolysis and glycogenolysis.  2)After ingesting meal-  Brust of insulin secretion is response to elevated to glucose and amino acid level.  3)When glucose level return to basal levels-  Insulin return to its basal level.
  • 5. INSULIN  Insulin was discovered in 1921 by Banting.  It was 1st obtain in crystalline form in 1926 and chemical structure was fully worked out in 1956 by Sanger.  Insulin are two chain polypeptide having 51 amino acid.  A chain-21 amino acid  B chain- 30 amino acid  MO. WT. of insulin- 5734 g/mol
  • 6. BIO SYNTHESIS OF INSULIN  Rough endoplasmic reticulum preproinsulin  Golgi apparatus prohormone convertase proinsulin  Secretory granules insulin + c- pepetide
  • 7. SECRETION OF INSULIN  Intracellular transport of glucose is mediated by GLUT-2 an insulin independent glucose transporter in Beta cells.  Glucose undergoes oxidative metabolism yiEld ATP.  ATP inhibit K+ channel receptor on Beta cell surface  This receptor leads to membrane depolarization.  Influx of Ca++ ion and release stored insulin .
  • 8.
  • 9. CLASSIFICATION OF INSULIN INSULIN RAPID ACTING SHORT ACTING INTERMADIATE ANALOGOUS ACTING -Insulin lispro -Regular soluble - Glargine -Insulin aspart insulin -Insulin zinc susp. -Ins. Determir -Insulin glulisine
  • 11. ACTION OF INSULIN IN VARIOUS TISSUE  1)IN LIVER-  Decrease glucose production.  Increase glycogenesis.  Increase TG synthesis.  Increase protein synthesis.  2)IN MUSCLES-  Increase glucose transport.  Increase glycolysis.
  • 12.  Increase glycogen deposition.  Increase protein synthesis.  3)IN ADEPOSE  Increase glucose transport.  Increase lipogenesis.  PHARMACOKINETIC OF INSULIN-  Inj. SC  Metabolized by kidney and liver.  Elimination t1/2 is 5-10 min.  Highly bond with tissue receptor.
  • 13.  ADR OF INSULIN-  Hypoglycemia.  Allergic reactions.  Insulin registance.  Weight gain.  DRUG INTRACTION-  Beta adrenergic drug.  Furosemide,solbutamol,oral contraceptive(increase blood sugar and decrease effect of insulin)