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Mechanism of
Hormone
Action
Mechanism of Hormone
Action
 Each hormone exerts a characteristic
 effects on the target organ by acting on
 the cells of the organ
    But same chemical category of hormone
     have similar mechanisms of action
      Involves
      a.   Location of cellular receptor proteins
      b.   Events occurring in the target cells after
           the hormone has combined w/ its
           receptor protein
Mechanism of Hormone
Action
 Hormones   are delivered by blood to
 every cell in the body
    But! Only target cells are able to respond to
     these hormones.
      Target cells must have specific receptor
       proteins that is SPECIFIC
 Hormonesbind with a high affinity and
 low capacity
Location of Hormone’s
Receptor Protein
   Depends on the chemical nature of hormone
       Lipid-soluble hormone receptor are located
        within the target cells
           Because they can pass through cell membrane
            and enter target cell
       Water-soluble hormone receptor are located
        outside the target cells
         Because they can’t pass through cell
          membrane
         Therefore they need the activation of 2nd
          messengers within the cell for hormone action
Lipid-soluble Hormone Action
  Hormones includes thyroid and steroid
  hormones + nitric acid
 Attached to plasma carrier proteins then
 dissociate to pass thru lipid component of
 plasma membrane to enter cell where
 the receptor proteins are located
Lipid-soluble Hormone Action
 Receptorare called “nuclear hormone
 receptors”
    Because they func. w/in the nucleus to
     activate genetic transcription (production
     of mRNA)
    Thus func. as transcription factors
    Has two regions or domains
       a.   ligand-binding domain/hormone-binding
            domain
       b.   DNA-binding domain
Nuclear Hormone Receptors
   With two families:
        a. Steroid family
       b.    Thyroid Hormone family – includes
             receptors for active form of Vit. D
             and for retinoic acid that play
             important roles in the regulation of
             cell function and organ physiology

           Receptors for unknown hormone
            ligands are called “orphan receptors”
Mechanism of Steroid
Hormone Action
1.       Hormone-receptor binding(in cytoplasm)
2.       Translocation to nucleus
3.       DNA-binding domain binds to specific
         hormone-response element of DNA
     •     Hormone response element of DNA have
           two half-sites, each 6 nucleotide bases
           long, separated by 3-nucleotide spacer
           segment.
Mechanism of Steroid
Hormone Action
 Onesteroid receptor binds to one half-site
 and another to the other half-site
    Thus called “dimerization”
    “Monodimer” due to same receptor unit
     binds to the DNA hormone-response
     element
Ligand-binding
Dimerization of receptors       domain

   Steroid                  DNA-binding
  hormone                     domain

       Half-sites


                                DNA


              Genetic transcription
  Hormone-response element                   RNA
Mechanism of Thyroid
Hormone Action
 Major  hormone secreted is thyroxine or
  tetraiodothyrinine(T4)
 Small amount of triiodothyronine (T3)
    Travels through blood and attached to
     carrier proteins primarily “thyroxine-binding
     globulin” or TBG which has higher affinity to
     T4 than T3
Mechanism of Thyroid
Hormone Action
   Approximately 99.96% of thyroxine in the
    blood is attached to carrier proteins in the
    plasma
        •    The rest are free
   Only thyroxine and T3 can enter target cells
   Protein bound thyroxine serves as reservoir of
    the hormone in the blood
   Once free thyroxine enter cytoplasm, it is
    enzymatically converted to T3
    •       T3 is the one active in cytoplasm
Mechanism of Thyroid
Hormone Action
 Inactive   receptor proteins for T3 are
  located in the nucleus
 Incapable of binding to DNA and
  stimulate transcription unless bind with T3
 T3 enters cell from plasma or may be
  produced in the cell by converting T4
 Needs a binding protein to enter nucleus
Mechanism of Thyroid
Hormone Action
 Difference   to steriod:
    Binds with non-specific binding protein in
     the cytoplasm
     nuclear receptor is heterodimer(diff.
     receptor proteins attached to the half-sites)
Water-soluble Hormone Action
   Includes catecholamines (epi and
    norepinephrine), polypeptides and
    glycoproteins
   Cannot pass through lipid barrier of target cell
   Some may enter through “pinocytosis” but
    mostly acts on the outer surface of the target
    cell and therefore can be mediated by other
    molecules
   Uses 2nd messenger to exert their effects
Second-messenger Systems
A.   Adenylate Cyclase-Cyclic AMP (cAMP)
     Second Messenger System
B.   Phospholipase C-Ca2+ Second-
     Messenger System
C.   Tyrosine Kinase Second-Messenger
     System
Adenylate Cyclase-Cyclic
AMP
(cAMP) Second Messenger
System
 For  activation of adenylate cyclase
 First known and understood “second
  messenger”
 Responsible for b-adrenergic effects of
  epi and norepinephrine
Cyclic Adenosine
Monophosphate
 Hormone(water-soluble)     binds to receptor
  protein results to dissociation of subunit
  from the G-protein
 G-protein subunits moves thru membrane
  to bind and activates adenylate cyclase
  as catalyst
     ATP     cAMP + Ppi
 Intracellular   concentration of this
  increases
Cyclic Adenosine
Monophosphate
 Activates     protein kinase
      Inactivated form:
        Catalytic   subunit and inhibitory subunit
      Becomes active once cAMP binds to
       inhibitory and dissociate from catalytic
       subunit
 insummary, the hormone causes an
  increase in protein kinase enzyme activity
  within its target cells
Cyclic Adenosine
Monophosphate
 Activeprotein kinase catalyzes
  phosphorylation of diff. proteins in the cell
  causing some enzymes to be activated
  and others to be inactivated
 cAMP must be rapidly inactivated by
  phosphosdiesterase to function effectively
Phospholipase C-Ca2+
Second Messenger System
   Ca pumps in the plasma membrane and
    endoplasmic          reticulum      keeps     Ca
    concentration very low in the cytoplasm
   The steep concentration gradient for Ca that
    results allows various stimuli to evoke a rapid
    diffusion of Ca into the cytoplasm that serves
    as a signal in diff. control systems
   The entry of the Ca thru voltage-regulated Ca
    channels in the plasma membrane serves as
    a signal for the release of neurotransmitters
Phospholipase C-Ca2+
Second Messenger System
 When  epinephrine stimulates target
  organ, it must first bind to andrenergic
  receptor proteins in the membrane
 2 types of adrenergic receptors:
  a.   Alpha
  b.   Beta
          Alpha adrenergic receptors by
           epinephrine activates the target cell via
           the Ca second-messenger system
Phospholipase C-Ca2+
Second Messenger System
 G-proteinintermediate enables binding of
 epinephrine to alpha-adrenergic receptor
 and the binding activates phospholipase
 C
 •   Substrate is split by an active enzyme into
     inositol triphosphate (IP3) and
     diacylglycerol (DAG) that both acts as
     second messengers but IP3 is better
     understood
Phospholipase C-Ca2+
Second Messenger System
 IP3leaves the plasma membrane and
 diffuses thru the cytoplasm to the
 endoplasmic reticulum
  •   Membrane of ER has receptor for IP3 so the
      message of hormone is carried by IP3 from
      cytoplasm to ER
       Thebinding of IP3 to receptor causes specific
        Ca channels to open.
Phospholipase C-Ca2+
Second Messenger System
 Results  to rapid and transient rise of
  cytoplasmic Ca concentration
 Ca that enters the cytoplasm binds to a
  protein called “calmodulin”
 Activated    calmodulin then activates
  other specific protein kinase enzymes that
  modify actions of other enzymes in the
  cell
Tyrosine Kinase
Second-Messenger System
 Insulin promotes glucose and amino acid
  transport and stimulates glycogen, fat
  and protein synthesis
 Primary target organs are liver, skeletal
  muscles and adipose tissue
 Insulin’s mechanism of action is same with
  growth factors’
Insulin Mechanism of Action
   “Tyrosine kinase” is the enzyme that serves as
    receptor protein for insulin and GF
       Specifically adds phosphate groups to amino
        acid tyrosine with in the protein
       With two units(dimer) when binds to insulin
        forming active tyrosine kinase enzyme
       Each unit have ligand-binding site and an
        enzymatic site
         Ligand binding site-outside site that binds with
          insulin
         Enzymatic site-part that spans the plasma
          membrane
Insulin Mechanism of Action
 Enzymatic    site activates only after binding
  of insulin to ligand-binding site and causes
  dimerization of the receptor
 One unit then phosphorylates the other
  - “autophosphorylation”
 Signaling molecules are proteins
  phosphorylated by the activated tyrosine
  kinase receptor
     Activates second messenger systems
Insulin Mechanism of Action
 The complex reactions enables the insulin
 to regulate the metabolism of its target
 cells.
    Example:
 •     binding of insulin to its receptor indirectly
     causes the activation of “glycogen
     synthetase”
           Enzyme in liver and skeletal muscles that
            catalyzes the production of glycogen

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Endo 2 kevin

  • 2. Mechanism of Hormone Action  Each hormone exerts a characteristic effects on the target organ by acting on the cells of the organ  But same chemical category of hormone have similar mechanisms of action  Involves a. Location of cellular receptor proteins b. Events occurring in the target cells after the hormone has combined w/ its receptor protein
  • 3. Mechanism of Hormone Action  Hormones are delivered by blood to every cell in the body  But! Only target cells are able to respond to these hormones.  Target cells must have specific receptor proteins that is SPECIFIC  Hormonesbind with a high affinity and low capacity
  • 4. Location of Hormone’s Receptor Protein  Depends on the chemical nature of hormone  Lipid-soluble hormone receptor are located within the target cells  Because they can pass through cell membrane and enter target cell  Water-soluble hormone receptor are located outside the target cells  Because they can’t pass through cell membrane  Therefore they need the activation of 2nd messengers within the cell for hormone action
  • 5. Lipid-soluble Hormone Action Hormones includes thyroid and steroid hormones + nitric acid  Attached to plasma carrier proteins then dissociate to pass thru lipid component of plasma membrane to enter cell where the receptor proteins are located
  • 6. Lipid-soluble Hormone Action  Receptorare called “nuclear hormone receptors”  Because they func. w/in the nucleus to activate genetic transcription (production of mRNA)  Thus func. as transcription factors  Has two regions or domains a. ligand-binding domain/hormone-binding domain b. DNA-binding domain
  • 7. Nuclear Hormone Receptors  With two families: a. Steroid family b. Thyroid Hormone family – includes receptors for active form of Vit. D and for retinoic acid that play important roles in the regulation of cell function and organ physiology  Receptors for unknown hormone ligands are called “orphan receptors”
  • 8. Mechanism of Steroid Hormone Action 1. Hormone-receptor binding(in cytoplasm) 2. Translocation to nucleus 3. DNA-binding domain binds to specific hormone-response element of DNA • Hormone response element of DNA have two half-sites, each 6 nucleotide bases long, separated by 3-nucleotide spacer segment.
  • 9. Mechanism of Steroid Hormone Action  Onesteroid receptor binds to one half-site and another to the other half-site  Thus called “dimerization”  “Monodimer” due to same receptor unit binds to the DNA hormone-response element
  • 10. Ligand-binding Dimerization of receptors domain Steroid DNA-binding hormone domain Half-sites DNA Genetic transcription Hormone-response element RNA
  • 11.
  • 12. Mechanism of Thyroid Hormone Action  Major hormone secreted is thyroxine or tetraiodothyrinine(T4)  Small amount of triiodothyronine (T3)  Travels through blood and attached to carrier proteins primarily “thyroxine-binding globulin” or TBG which has higher affinity to T4 than T3
  • 13. Mechanism of Thyroid Hormone Action  Approximately 99.96% of thyroxine in the blood is attached to carrier proteins in the plasma • The rest are free  Only thyroxine and T3 can enter target cells  Protein bound thyroxine serves as reservoir of the hormone in the blood  Once free thyroxine enter cytoplasm, it is enzymatically converted to T3 • T3 is the one active in cytoplasm
  • 14. Mechanism of Thyroid Hormone Action  Inactive receptor proteins for T3 are located in the nucleus  Incapable of binding to DNA and stimulate transcription unless bind with T3  T3 enters cell from plasma or may be produced in the cell by converting T4  Needs a binding protein to enter nucleus
  • 15. Mechanism of Thyroid Hormone Action  Difference to steriod:  Binds with non-specific binding protein in the cytoplasm  nuclear receptor is heterodimer(diff. receptor proteins attached to the half-sites)
  • 16.
  • 17.
  • 18. Water-soluble Hormone Action  Includes catecholamines (epi and norepinephrine), polypeptides and glycoproteins  Cannot pass through lipid barrier of target cell  Some may enter through “pinocytosis” but mostly acts on the outer surface of the target cell and therefore can be mediated by other molecules  Uses 2nd messenger to exert their effects
  • 19. Second-messenger Systems A. Adenylate Cyclase-Cyclic AMP (cAMP) Second Messenger System B. Phospholipase C-Ca2+ Second- Messenger System C. Tyrosine Kinase Second-Messenger System
  • 20. Adenylate Cyclase-Cyclic AMP (cAMP) Second Messenger System  For activation of adenylate cyclase  First known and understood “second messenger”  Responsible for b-adrenergic effects of epi and norepinephrine
  • 21. Cyclic Adenosine Monophosphate  Hormone(water-soluble) binds to receptor protein results to dissociation of subunit from the G-protein  G-protein subunits moves thru membrane to bind and activates adenylate cyclase as catalyst  ATP cAMP + Ppi  Intracellular concentration of this increases
  • 22. Cyclic Adenosine Monophosphate  Activates protein kinase  Inactivated form:  Catalytic subunit and inhibitory subunit  Becomes active once cAMP binds to inhibitory and dissociate from catalytic subunit  insummary, the hormone causes an increase in protein kinase enzyme activity within its target cells
  • 23. Cyclic Adenosine Monophosphate  Activeprotein kinase catalyzes phosphorylation of diff. proteins in the cell causing some enzymes to be activated and others to be inactivated  cAMP must be rapidly inactivated by phosphosdiesterase to function effectively
  • 24.
  • 25. Phospholipase C-Ca2+ Second Messenger System  Ca pumps in the plasma membrane and endoplasmic reticulum keeps Ca concentration very low in the cytoplasm  The steep concentration gradient for Ca that results allows various stimuli to evoke a rapid diffusion of Ca into the cytoplasm that serves as a signal in diff. control systems  The entry of the Ca thru voltage-regulated Ca channels in the plasma membrane serves as a signal for the release of neurotransmitters
  • 26. Phospholipase C-Ca2+ Second Messenger System  When epinephrine stimulates target organ, it must first bind to andrenergic receptor proteins in the membrane  2 types of adrenergic receptors: a. Alpha b. Beta  Alpha adrenergic receptors by epinephrine activates the target cell via the Ca second-messenger system
  • 27. Phospholipase C-Ca2+ Second Messenger System  G-proteinintermediate enables binding of epinephrine to alpha-adrenergic receptor and the binding activates phospholipase C • Substrate is split by an active enzyme into inositol triphosphate (IP3) and diacylglycerol (DAG) that both acts as second messengers but IP3 is better understood
  • 28. Phospholipase C-Ca2+ Second Messenger System  IP3leaves the plasma membrane and diffuses thru the cytoplasm to the endoplasmic reticulum • Membrane of ER has receptor for IP3 so the message of hormone is carried by IP3 from cytoplasm to ER  Thebinding of IP3 to receptor causes specific Ca channels to open.
  • 29.
  • 30. Phospholipase C-Ca2+ Second Messenger System  Results to rapid and transient rise of cytoplasmic Ca concentration  Ca that enters the cytoplasm binds to a protein called “calmodulin”  Activated calmodulin then activates other specific protein kinase enzymes that modify actions of other enzymes in the cell
  • 31. Tyrosine Kinase Second-Messenger System  Insulin promotes glucose and amino acid transport and stimulates glycogen, fat and protein synthesis  Primary target organs are liver, skeletal muscles and adipose tissue  Insulin’s mechanism of action is same with growth factors’
  • 32. Insulin Mechanism of Action  “Tyrosine kinase” is the enzyme that serves as receptor protein for insulin and GF  Specifically adds phosphate groups to amino acid tyrosine with in the protein  With two units(dimer) when binds to insulin forming active tyrosine kinase enzyme  Each unit have ligand-binding site and an enzymatic site  Ligand binding site-outside site that binds with insulin  Enzymatic site-part that spans the plasma membrane
  • 33. Insulin Mechanism of Action  Enzymatic site activates only after binding of insulin to ligand-binding site and causes dimerization of the receptor  One unit then phosphorylates the other - “autophosphorylation”  Signaling molecules are proteins phosphorylated by the activated tyrosine kinase receptor  Activates second messenger systems
  • 34. Insulin Mechanism of Action  The complex reactions enables the insulin to regulate the metabolism of its target cells.  Example: • binding of insulin to its receptor indirectly causes the activation of “glycogen synthetase”  Enzyme in liver and skeletal muscles that catalyzes the production of glycogen

Editor's Notes

  1. RNA