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ENDOCRINE SYSTEM
DR.NILESH KATE.
M.D.
ASSOCIATE PROFESSOR,
DEPARTMENT OF PHYSIOLOGY,
OBJECTIVES
 Hormone : definition, classification.
 Hormones general consideration.
 Hormone receptors & mechanism of
action.
 Measurement of hormones.
HOMEOSTASIS & CONTROLS
 Successful
compensation
 Homeostasis
reestablished
 Failure to
compensate
 Pathophysiology
○ Illness
○ Death
Figure 1-5: Homeostasis
COMPARISON OF ENDOCRINE AND
NERVOUS SYSTEMS.
 NERVOUS SYSTEM
 “WIRED”
 CHEMICAL SIGNAL AT
TARGET CELL
 RAPID
 BRIEF DURATION
 CLOSE ANATOMICAL
PROXIMITY
 ENDOCRINE SYSTEM
 “WIRELESS”
 CHEMICAL SIGNAL IN
BLOOD.
 SLOW
 LONG DURATION
 SPECIFIC RECEPTORS
ENDOCRINE SYSTEM
 Hormaein-- Greek word means “to execute
or to arouse”.
Def:- Secretary product of ductless glands
which are released in catalytic amounts into
blood stream & transported to specific target
cells where they elicit physiologic,
morphologic & biochemical responses.
LOCATION OF DIFFERENT
ENDOCRINE GLANDS.
Long Distance Communication:
Endocrine Hormones
 Signal Chemicals
 Made in endocrine
cells
 Transported via
blood
 Receptors on target
cells
Figure 6-2a: Long distance cell-to-cell communication
TYPES OF HORMONES
 Functional
 ENDOCRINE HORMONES – Travel through the
blood to act at a site distant from the secreting cell
or gland
 PARACRINE HORMONES – Act on cells near the
secreting cell
 AUTOCRINE HORMONES – Act on the secreting
cell
 NEUROCRINE HORMONES – Secreted by neural
cells
○ neurotransmitters
○ neurohormones
Figure 6-2b, c: Long distance cell-to-cell communication
Paracrine and Autocrine
Hormones
 Local communication
 Signal chemicals
diffuse to target
 Example: Cytokines
 Autocrine–receptor on
same cell
 Paracrine–neighboring
cells
Figure 6-1c: Direct and local cell-to-cell communication
CHEMICAL CLASSIFICATION OF
HORMONES
Depending upon chemical nature
 Amines or amino acid derivatives:
 Proteins & Polypeptides:
 Steroid hormones
Depending upon mechanism of action.
 Group I hormones.
 Group II hormones. : A,B,C,D.
HORMONE : GENERAL
CONSIDERATION.
 Hormones chemistry, synthesis, storage &
release.
1 Amines / amino acid derivatives
2 Protein & polypeptide hormones.
3 Steroid hormones.
HORMONE TRANSPOT, PLASMA CONC,
HALF LIFE.
 Hormone transport.
 Unbound.
 Bound .
 Plasma concentrations.
 Peptide hormone 10 -12 mol/ L to 10-14 mol/L
 Epi / Nor Epi = 2× 10-10 to 13 × 10 -10
 Steroid & thyroid 10-9 mol/ L & 10-6 mol/ L.
 Half life.
 Peptide hormone – short
 Steroid, & thyroid – long.
FUNCTIONS OF HORMONES.
 Regulation of biochemical reactions
 Regulation of bodily process.
HORMONE DISPOSAL.
 Target cell uptake & intracellular degradation.
 Metabolic degradation / inactivation.
 Urinary / biliary secretions.
 Metabolic clearance rate (MCR):-
volume of plasma cleared per unit time.
REGULATION OF HORMONE
SECRETION.
 Feedback control
 Neural control.
 Chronotropic control
FEEDBACK SYSTEM.
Figure 6-26: Negative and positive feedback
Figure 7-14: Negative
feedback loops in the
hypothalamicanterior
pituitary pathway
NEGATIVE FEEDBACK REFLEXES : LONG , SHORT &
ULTRASHORT LOOP.
HORMONES RECEPTORS.
 Characteristics
 Specificity .
 Location .
○Internal
○External .
 Regulation of number.
○Down regulation
○Up regulation .
STRUCTURE OF RECEPTORS.
 Recognition domain.
 Coupling domain.
CLASSIFICATION OF RECEPTORS.
 Receptor kinase
 Receptor linked kinase.
 G-protein coupled receptors.
 Ligand gated ion channels.
MECHANISM OF ACTION OF
HORMONES.
 Through change in membrane
permeability.
 Through effect on gene expression.
 Through second messengers.
 Through tyrosine kinase activation.
THROUGH CHANGE IN MEMBRANE
PERMEABILITY.
 Hormones bind with external receptors.
Conformational change in protein of
receptors.
Opening of Na, K, Ca channel.
Movement of ions.
THROUGH EFFECT ON GENE
EXPRESSION.
Figure 7-7: Steroid hormone action
THROUGH SECOND
MESSENGERS SYSTEM.
 Adenyl cyclase- cAMP system.
 Guanyl cyclase –cGMP system.
 Membrane phosplipase- phoapholipid
system.
 Calcium- calmodulin system.
ADENYLATE CYCLASE-CAMP (Sutherland
1961)
PHOSPHOLIPASE-C-CA2+ (CONTINUED)
CA2+- calmodulin system (CONTINUED)
THROUGH TYROSINE KINASE ACTIVATION.
MEASUREMENT OF
HORMONES.
 BIOASSAY.
 Injecting unknown sample of
plasma in experimental
animals & observing specific
biological effect.
 IMMUNOASSAY.(AG-AB
REACTION)
 RADIOIMMUNOASSAY
○ Mix
Unknown sample of plasma
containing hormone + purified
specific antibody + purified
hormone tagged with
radioactive isotopes.
 ELISA
○ Instead of specific antibody,
stained with suitable dye. &
intensity of colour measured by
spectrophotometer.
MEASUREMENT OF HORMONES.
 CYTOCHEMICAL ASSAY.
 Endocrine gland cut in
slices
 Incubate in ascorbate
enriched culture
medium
 Genesis of hormone
detected.
 DYNAMIC TESTS.
 Suppression type.
 Stimulation type.
ENDOCRINE REFLEX PATHWAYS:
OVERVIEW
Figure 7-9: Hormones may have multiple stimuli for their release
PATHOLOGIES: OVER OR UNDER
PRODUCTION
Figure 7-19: Negative feedback by exogenous cortisol
PATHOLOGIES: DUE TO RECEPTORS
Figure 7-20: Primary and secondary hypersecretion of cortisol
Thank you

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ENDOCRINE BASIC

  • 1. ENDOCRINE SYSTEM DR.NILESH KATE. M.D. ASSOCIATE PROFESSOR, DEPARTMENT OF PHYSIOLOGY,
  • 2. OBJECTIVES  Hormone : definition, classification.  Hormones general consideration.  Hormone receptors & mechanism of action.  Measurement of hormones.
  • 3. HOMEOSTASIS & CONTROLS  Successful compensation  Homeostasis reestablished  Failure to compensate  Pathophysiology ○ Illness ○ Death Figure 1-5: Homeostasis
  • 4. COMPARISON OF ENDOCRINE AND NERVOUS SYSTEMS.  NERVOUS SYSTEM  “WIRED”  CHEMICAL SIGNAL AT TARGET CELL  RAPID  BRIEF DURATION  CLOSE ANATOMICAL PROXIMITY  ENDOCRINE SYSTEM  “WIRELESS”  CHEMICAL SIGNAL IN BLOOD.  SLOW  LONG DURATION  SPECIFIC RECEPTORS
  • 5. ENDOCRINE SYSTEM  Hormaein-- Greek word means “to execute or to arouse”. Def:- Secretary product of ductless glands which are released in catalytic amounts into blood stream & transported to specific target cells where they elicit physiologic, morphologic & biochemical responses.
  • 7. Long Distance Communication: Endocrine Hormones  Signal Chemicals  Made in endocrine cells  Transported via blood  Receptors on target cells Figure 6-2a: Long distance cell-to-cell communication
  • 8. TYPES OF HORMONES  Functional  ENDOCRINE HORMONES – Travel through the blood to act at a site distant from the secreting cell or gland  PARACRINE HORMONES – Act on cells near the secreting cell  AUTOCRINE HORMONES – Act on the secreting cell  NEUROCRINE HORMONES – Secreted by neural cells ○ neurotransmitters ○ neurohormones
  • 9. Figure 6-2b, c: Long distance cell-to-cell communication
  • 10. Paracrine and Autocrine Hormones  Local communication  Signal chemicals diffuse to target  Example: Cytokines  Autocrine–receptor on same cell  Paracrine–neighboring cells Figure 6-1c: Direct and local cell-to-cell communication
  • 11. CHEMICAL CLASSIFICATION OF HORMONES Depending upon chemical nature  Amines or amino acid derivatives:  Proteins & Polypeptides:  Steroid hormones Depending upon mechanism of action.  Group I hormones.  Group II hormones. : A,B,C,D.
  • 12. HORMONE : GENERAL CONSIDERATION.  Hormones chemistry, synthesis, storage & release. 1 Amines / amino acid derivatives 2 Protein & polypeptide hormones. 3 Steroid hormones.
  • 13. HORMONE TRANSPOT, PLASMA CONC, HALF LIFE.  Hormone transport.  Unbound.  Bound .  Plasma concentrations.  Peptide hormone 10 -12 mol/ L to 10-14 mol/L  Epi / Nor Epi = 2× 10-10 to 13 × 10 -10  Steroid & thyroid 10-9 mol/ L & 10-6 mol/ L.  Half life.  Peptide hormone – short  Steroid, & thyroid – long.
  • 14. FUNCTIONS OF HORMONES.  Regulation of biochemical reactions  Regulation of bodily process.
  • 15. HORMONE DISPOSAL.  Target cell uptake & intracellular degradation.  Metabolic degradation / inactivation.  Urinary / biliary secretions.  Metabolic clearance rate (MCR):- volume of plasma cleared per unit time.
  • 16. REGULATION OF HORMONE SECRETION.  Feedback control  Neural control.  Chronotropic control
  • 17. FEEDBACK SYSTEM. Figure 6-26: Negative and positive feedback
  • 18. Figure 7-14: Negative feedback loops in the hypothalamicanterior pituitary pathway NEGATIVE FEEDBACK REFLEXES : LONG , SHORT & ULTRASHORT LOOP.
  • 19. HORMONES RECEPTORS.  Characteristics  Specificity .  Location . ○Internal ○External .  Regulation of number. ○Down regulation ○Up regulation .
  • 20. STRUCTURE OF RECEPTORS.  Recognition domain.  Coupling domain.
  • 21. CLASSIFICATION OF RECEPTORS.  Receptor kinase  Receptor linked kinase.  G-protein coupled receptors.  Ligand gated ion channels.
  • 22. MECHANISM OF ACTION OF HORMONES.  Through change in membrane permeability.  Through effect on gene expression.  Through second messengers.  Through tyrosine kinase activation.
  • 23. THROUGH CHANGE IN MEMBRANE PERMEABILITY.  Hormones bind with external receptors. Conformational change in protein of receptors. Opening of Na, K, Ca channel. Movement of ions.
  • 24. THROUGH EFFECT ON GENE EXPRESSION. Figure 7-7: Steroid hormone action
  • 25. THROUGH SECOND MESSENGERS SYSTEM.  Adenyl cyclase- cAMP system.  Guanyl cyclase –cGMP system.  Membrane phosplipase- phoapholipid system.  Calcium- calmodulin system.
  • 28. CA2+- calmodulin system (CONTINUED)
  • 29. THROUGH TYROSINE KINASE ACTIVATION.
  • 30. MEASUREMENT OF HORMONES.  BIOASSAY.  Injecting unknown sample of plasma in experimental animals & observing specific biological effect.  IMMUNOASSAY.(AG-AB REACTION)  RADIOIMMUNOASSAY ○ Mix Unknown sample of plasma containing hormone + purified specific antibody + purified hormone tagged with radioactive isotopes.  ELISA ○ Instead of specific antibody, stained with suitable dye. & intensity of colour measured by spectrophotometer.
  • 31. MEASUREMENT OF HORMONES.  CYTOCHEMICAL ASSAY.  Endocrine gland cut in slices  Incubate in ascorbate enriched culture medium  Genesis of hormone detected.  DYNAMIC TESTS.  Suppression type.  Stimulation type.
  • 32. ENDOCRINE REFLEX PATHWAYS: OVERVIEW Figure 7-9: Hormones may have multiple stimuli for their release
  • 33. PATHOLOGIES: OVER OR UNDER PRODUCTION Figure 7-19: Negative feedback by exogenous cortisol
  • 34. PATHOLOGIES: DUE TO RECEPTORS Figure 7-20: Primary and secondary hypersecretion of cortisol