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HORMONAL CONTROL OF

CALCIUM METABOLISM

 Dr. M. Anbarasi, MD (Physiology)
HORMONES INVOLVED…
1,25 Dihydrocholecalciferol
Parathyroid hormone
Calcitonoin
Parathyroid hormone related protein
{ PTHrP}
Miscellaneous hormones :
   Glucocorticoids, Growth hormone,
Estrogen
CALCIUM & PHOSPHATE
    METABOLISM
NORMAL VALUES
Total body calcium – 1100 g {27.5 mol / L}
            99 % in bones

Plasma calcium : 9 – 11 mg / dL
              {5 m Eq / L or 2.5 mmol / L}
   Ionized calcium – 50 % {1.2 mmol / L}
   Protein bound – 41 % {1.0 mmol / L}
   Complexed with anions – 9 % {0.2 mmol / L}
FUNCTIONS OF CALCIUM

FREE IONIZED CALCIUM


        Blood coagulation
       Muscle contraction
  Transmission of nerve impulses
    Formation of skeleton ,etc.
EFFECTS OF ALTERED CALCIUM
           HYPOCALCEMIA

• Nerve and muscle cells becomes hyperexcitable.
    increased neuronal membrane
    permeability to Na + channels


  HYPOCALCEMIC TETANY – latent or manifest

    Calcium at 6 mg / dL --- TETANY
            at 4 mg / dL --- LETHAL
       Alkaline pH – tetany at higher values.
SIGNS OF MANIFEST TETANY
                           CARPOPEDAL SPAM
• Laryngeal stridor
• Convulsions
• Visceral features like
  intestinal spasm,
  bronchospasm and
  profuse sweating.



                              Obstetric hand /
LATENT TETANY
• CHVOSTEK’S SIGN

• TROUSSEAU’S SIGN
HYPERCALCEMIA
CALCIUM LEVEL > 12 mg / dL



 • Nervous system is depressed
 • Reflex activities are sluggish
 • Decreased QT interval
 • Lack of appetite
CALCIUM IN BONE
Two types

1. Readily exchangeable reservoir
      {500 mmol of Ca2+ is exchanged}
2. Stable calcium
      {7.5 mmol of Ca2+ is exchanged}
CALCIUM IN KIDNEYS
• 98 % - 99 % is reabsorbed

         60 % in PCT

        40 % in Ascending limb of LOH

               Distal tubule

            PARATHYROID HORMONE
CALCIUM IN GIT
• 30 – 80 % of ingested calcium is absorbed
• Actively transported out of the intestinal cells with
  the help of
       Ca 2+ dependent ATPase


             1,25 Vitamin D3

• Increased plasma calcium – decreased absorption
  from the gut
• Decreased by phosphates and oxalates and alkalis
• Increased by high protein diet
DIET
25mmol (1000 mg)                                           BONE

                                            RAPID
             ABSORPTION                     EXCHANGE     EXCHANGEABLE
     GIT                                                 100 mmol
                   15 mmol                    500 mmol
                               ECF
              SECRETION        35 mmol                     STABLE
                                          REABSORPTION     27,200 mmol
                   12.5 mmol
                                             7.5 mmol


              REABSORPTION
                 247.5
                 mmol GLOMERULAR
FECES                    FILTRATE
22.5mmol                  250 mmol


                               URINE
                               2.5 mmol
PHOSPHATE METABOLISM
NORMAL VALUES
• Total body phosphate – 500 to 800 g.
• 85 – 90 % in skeleton
• Plasma phosphate – 12 mg / dL
      2/3rd – organic
      1/3rd – inorganic {Pi}
                ex. PO43- , HPO42-, H2PO42-


FUNCTIONS
   ATPase , c AMP , 2-3, DPG
   Phosphorylation and Dephosphorylation
BONE:
   3 mg of PO4 enters and is again reabsorbed.


KIDNEYS:
   85 % - 90 % of filtered Pi is reabsorbed by
 Active Transport in PCT

                          Overflow mechanism

            PTH
GIT

• Absorbed in duodenum and small intestine
  by Active transport and passive diffusion.

• Absorption is linear to dietary intake.

• All PO4 excreted in urine.
BONE PHYSIOLOGY
Made up of organic matrix and salts
        ORGANIC MATRIX

COLLAGEN FIBERS          GROUND
• 90 – 95 %                SUBSTANCES
• Type 1 collagen made   • Gelatinous substances
  up of triple helix     (ECF + proteoglycans)

                          Chondroitin sulphate
                            Hyaluranic acid
BONE SALTS
• Salts of calcium and phosphate.
         HYDROXYAPATITE
            Ca10(PO4)6. (OH)2
400 Å long
10 – 30 Å thick
100 Å wide
Ca / P ratio – 1.3 to 2.0
Other salts:
   Mg2+, Na+ , K+ ions conjugated to
  bone crystals.
STRUCTURE OF BONE
2 types of bones
Compact or Cortical bone – 80 %
•    surface to volume ratio is low
•    receive nutrients by canaliculi
Trabecular or Spongy bone – 20 %
•    made up of spicules or plates with high
  surface to volume ratio
•    receive nutrients from the ECF through
  Haversian canal
BONE GROWTH
Fetus to adults – ENCHONDRAL BONE
  FORMATION
Exception: clavicles, mandibles and certain
  skull bones.

   INTRAMEMBRANOUS BONE
        FORMATION
EPIHYSEAL PLATE – bone increases in length
Width is proportionate to growth and influenced by
 GH.

      EPIPHYSEAL CLOSURE

      Cartillage cells hypertropied

         Release VEGF

       Vascularization and ossification
BONE FORMATION &
         RESORPTION

• Bone formation by OSTEOBLASTS

• Bone resorption by OSTEOCLASTS
CELLS OF BONE

• OSTEOPROGENITOR CELLS

• OSTEOBLASTS

• OSTEOCYTES

• OSTEOCLASTS
OSTEOBLASTS
• Modified fibroblasts developed from
  mesenchymal cells
• Secrete collagen monomers and ground
  substances
• Finally forms an ‘OSTEOID’
• Calcium salts are deposited in the collagen
  fibers and forms hydroxyapatite crystals.
OSTEOCYTES
• Mature bone cells – imprisoned osteoblasts
  in the lacunae of osteon.
• Sends processes throughout bone matrix
• Maintains the metabolic activity of bone
• Opens the channels for distribution of
  nutrients
• Exchanges calcium between bone and ECF.
OSTEOCLASTS

• MEMBER OF MONOCYTE FAMILY
• Attach its ruffled border to bone via integrins in the
  “sealing zone”
• Proton pumps secrete acid and acidify the isolated area
• Proteolytic enzymes breaks down the organic matrix
• Eats away the bone in 3 wks - tunnel
• Osteoblasts are activated - forms a new Haversian
  canal.
CONTINUAL BONE FORMATION :
     strength
     shape for mechanical support
     replace old brittle bone.

BONE STRESS:
• Compressional load – bone in cast
• Shape of the bone
FRACTURE:

• Activates periosteal and intraosseous
  osteoblasts

• Stimulates osteoprogenitor cells.

• Formation of “ CALLUS ”
VITAMIN D 3
FORMATION OF VITAMIN D3
7 DEHYDROCHOLESTEROL

SUNLIGHT
           PREVITAMIN D3          VITAMIN D3
                                 CHOLECACIFEEROL

                 25 HYDROXYLASE            LIVER



                           25- HYDROXY CHOLECALCIFEROL


       24 α HYDROXYLASE                    1 α HYDROXYLASE

                           KIDNEY

     24, 25 DIHYDROXY
     CHOLECALCIFEROL                      1, 25 DIHYDROXY
                                           CHOLECALCIFEROL
MECHANISM OF ACTION
• 1,25 – dihydroxycholecalciferol is a steroid
  compound (secosteroid)
• Acts via the steroid receptor superfamily

• Exposes the DNA – binding domain and
  results in increased transcription of some
  mRNAs.
ACTIONS OF VITAMIN D3

1. Promotes intestinal calcium absorption
BY
  1. Formation of calcium binding protein
     (calbindin)
  2. Formation of calcium stimulated ATPase
  3. Formation of alkaline phosphatase
25-HYDROXYLASE
2. Promotes phosphate absorption by the
  intestines
• As a direct effect
• Calcium acts as a transport mediator for
    phosphate.

3. Decreases renal excretion of calcium &
  phosphate
• Increases reabsorption of Ca and PO4 by the
  renal tubules
4. Increases both bone resorption and bone
  mineralization

BONE RESORPTION – by stimulating PTH.
Calcitriol receptors are present in osteobasts
Receptor – calcitriol complex – stimulate osteoblasts
  --- activation & differentiation of osteoclasts.

BONE MINERALIZATION – by stimulation
 osteoblasts and alkaline phosphatase secretion
REGULATION OF SYNTHESIS
              PTH                      Ca


 25 –OH D3          1,25 (OH)2 D3   BONE
                                    &
                                    INTESTINES


24,25- (OH)2 D3                        PO4
RICKETS & OSTEOMALACIA
VITAMIN D deficiency in children and adults
   - defective bone mineralization and calcification
   - failure to deliver adequate Ca and PO4
FEATURES:
    Weakness and bowing of weight bearing bones,
  dental defects and hypocalcemia.
    Responsive to Vitamin D therapy.

VITAMIN D RESISTANT RICKETS:
   mutations in the gene coding for the enzyme
         1 α HYDROXYLASE
Rickety rosary
STRUCTURE
•   FOUR parathyroid
    glands located behind
    the thyroid gland

•   6 x 3 x 2 mm

•   Two types of cells
     1. Chief cells
     2. Oxyphil cells
CHEMISTRY

Pre pro PTH ( 115 aa)

Pro PTH ( 90 aa )

PTH ( 84 aa )



Normal plasma PTH
          10 -55 pg / mL
Half life – 10 mins
ACTIONS OF PTH
I.   Increases calcium and phosphate
     absorption from the bones
II. Decreases excretion of calcium by the
     kidneys
III. Increases the excretion of phosphate by
     the kidneys
IV. Increases intestinal absorption of calcium
     and phosphate.


     INCREASED PLASMA CALCIUM
I. Ca & PO4 absorption from the bone


      Two phases

1. Rapid phase – osteolysis by osteocytes

2. Slow phase – by osteoclasts
RAPID PHASE - OSTEOLYSIS

                              OCTEOCYTES
      OSTEOCYTIC MEMBRANE



            BONE FLUID



                            ECF
                                  BONE


ECF O.M B.FL   B
ECF    OSTEOCYTIC
                          BONE FLUID   BONE
             MEMBRANE
PTH




                                        Ca
        Ca                   Ca
                                        Ca

                                        Ca

                                        Ca

                                        Ca

                                        Ca

                                        Ca
SLOW PHASE
Done by OSTEOCLASTS…

  immediate activation of existing cells
  formation of new cells

    Excess bone resorption

   Stimulates osteoblastic activity
II. Excretion of calcium and phosphate...

 • Decreases excretion of calcium
          increases reabsorption in CD, DT
   and Ascending limb of LOH

 • Increases excretion of phosphate
      PHOSPHATURIC ACTION
           dimishes absorption in PCT
III. Absorption of Ca & PO4 in GIT…

  Enhances absorption of both calcium and
  phosphate by stimulating
  1,25 – dihydroxycholecalciferol.

 • cAMP mediated.
 • cAMP is in plenty in osteoblasts and
   osteocytes
MECHANISM OF ACTION

• Binds to PTH receptors – 3 types.

• REGULATION:
    stimulus : plasma calcium level.
• Produced by the parafollicular cells / C cells
  of thyroid gland.
• Remnants of ultimobrachial body.
STRUCTURE:
      Molecular weight – 3500 and has 32
  aminoacids.
   In brain “Calcitonin gene related
  polypeptide ( CGrP)” is formed.
• STIMULUS : Increased plasma calcium
  Others: β adrenergic agonists, dopamine and
  estrogen, GASTRIN, CCK, glucagon..

• ACTIONS:
   Decreases absorptive action of osteoclasts
   Deposits exchangeable Ca in bone salts
   Decreases the formation of osteoclasts

• CLINICAL USE:
   Used in the treatment of
      PAGET’S DISEASE.
DISORDERS OF PTH
• HYPOPARATHYROIDISM

• HYPERPARATHYROIDISM
    primary and secondary

• PSEUDOHYPOPARATHYROIDISM
HYPOPARATHYROIDISM
•   Body calcium level decreases
•   Osteoclasts are inactive
•   Sudden removal – signs of tetany appears
•   Responds to treatment with PTH or Vitamin D3

     PSEUDOHYPOPARATHYROIDISM

                PTH is normal
           Defect is in PTH receptors
       Not responsive to hormone therapy
PRIMARY
      HYPERPARATHYROIDISM
• Tumors – adenoma of parathyroid glands
• More common in women.
• Extreme osteolytic resorption - calcium and

        phosphate levels.

Bone :
Punched out cystic areas in the bone filled by osteoclasts
       – osteoclast tumors
           ‘ osteitis fibrosa cystica’
Serum Alkaline phosphatase is elevated.
Hypercalcemia:
         P. Calcium – 12 – 15 mg / dL

  CNS depression, muscle weakness, constipation,
  abdominal pain, peptic ulcer, lack of appetite etc…

Metastatic calcification:
 CaHPO4 crystals are deposited in renal tubules, lung
  alveoli, thyroid glands etc…

Renal stones:
  Calcium phosphate and also calcium oxalate stones
SECONDARY
   HYPERPARATHYROIDISM

• Increased levels of PTH is the result of
  compensatory mechanism to hypocalcemia

• Due to chronic renal disease or deficiency
  of Vitamin D 3
OSTEOPOROSIS
Diminished bone matrix due to poor
 oeteoblastic activity

Causes:
1. Lack of physical stress
2. Malnutrition
3. Postmenopausal lack of estrogen
4. Old age
5. Lack of Vitamin C
6. Cushing’s syndrome
OTHER HORMONES
PARATHYROID HORMONE RELATED PROTEIN
( PTHrP)
• Produced by different tissues of our body
• Binds to PTH receptors
• Marked effect on growth and development of cartilage in
   utero.
• Cartilage growth is stimulated by a protein called
             “Indian hedgehog”
• Other uses :
     Brain – prevents excitotoxic damage
     Placenta – transports calcium
• Defect in PTHrP – severe skeletal deformities.
GLUCOCORTICOIDS

Lowers plasma calcium by inhibiting
  osteoclasts.
Over Long periods – osteoporosis
Inhibit protein synthesis in osteoblasts,thereby
  synthesis of organic matrix
Inhibit absorption of Ca and Po4 from the gut
  and facilitate its excretion in the kidneys.
GROWTH HORMONE
  Increases intestinal absorption of Calcium
     “Positive calcium balance”
IGF – I
  Stimulates protein synthesis in bone.
THYROID HORMONE
  Hypercalcemia, Hypercalciuria and
  Osteoporosis.
ESTROGENS
  Prevents osteoporosis by inhibiting certain
  cytokines
INSULIN
  Increases bone formation

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Hormonal control of Calcium Metabolism

  • 1. HORMONAL CONTROL OF CALCIUM METABOLISM Dr. M. Anbarasi, MD (Physiology)
  • 2. HORMONES INVOLVED… 1,25 Dihydrocholecalciferol Parathyroid hormone Calcitonoin Parathyroid hormone related protein { PTHrP} Miscellaneous hormones : Glucocorticoids, Growth hormone, Estrogen
  • 3. CALCIUM & PHOSPHATE METABOLISM
  • 4. NORMAL VALUES Total body calcium – 1100 g {27.5 mol / L} 99 % in bones Plasma calcium : 9 – 11 mg / dL {5 m Eq / L or 2.5 mmol / L} Ionized calcium – 50 % {1.2 mmol / L} Protein bound – 41 % {1.0 mmol / L} Complexed with anions – 9 % {0.2 mmol / L}
  • 5. FUNCTIONS OF CALCIUM FREE IONIZED CALCIUM Blood coagulation Muscle contraction Transmission of nerve impulses Formation of skeleton ,etc.
  • 6. EFFECTS OF ALTERED CALCIUM HYPOCALCEMIA • Nerve and muscle cells becomes hyperexcitable. increased neuronal membrane permeability to Na + channels HYPOCALCEMIC TETANY – latent or manifest Calcium at 6 mg / dL --- TETANY at 4 mg / dL --- LETHAL Alkaline pH – tetany at higher values.
  • 7. SIGNS OF MANIFEST TETANY CARPOPEDAL SPAM • Laryngeal stridor • Convulsions • Visceral features like intestinal spasm, bronchospasm and profuse sweating. Obstetric hand /
  • 8. LATENT TETANY • CHVOSTEK’S SIGN • TROUSSEAU’S SIGN
  • 9. HYPERCALCEMIA CALCIUM LEVEL > 12 mg / dL • Nervous system is depressed • Reflex activities are sluggish • Decreased QT interval • Lack of appetite
  • 10. CALCIUM IN BONE Two types 1. Readily exchangeable reservoir {500 mmol of Ca2+ is exchanged} 2. Stable calcium {7.5 mmol of Ca2+ is exchanged}
  • 11. CALCIUM IN KIDNEYS • 98 % - 99 % is reabsorbed 60 % in PCT 40 % in Ascending limb of LOH Distal tubule PARATHYROID HORMONE
  • 12. CALCIUM IN GIT • 30 – 80 % of ingested calcium is absorbed • Actively transported out of the intestinal cells with the help of Ca 2+ dependent ATPase 1,25 Vitamin D3 • Increased plasma calcium – decreased absorption from the gut • Decreased by phosphates and oxalates and alkalis • Increased by high protein diet
  • 13. DIET 25mmol (1000 mg) BONE RAPID ABSORPTION EXCHANGE EXCHANGEABLE GIT 100 mmol 15 mmol 500 mmol ECF SECRETION 35 mmol STABLE REABSORPTION 27,200 mmol 12.5 mmol 7.5 mmol REABSORPTION 247.5 mmol GLOMERULAR FECES FILTRATE 22.5mmol 250 mmol URINE 2.5 mmol
  • 15. NORMAL VALUES • Total body phosphate – 500 to 800 g. • 85 – 90 % in skeleton • Plasma phosphate – 12 mg / dL 2/3rd – organic 1/3rd – inorganic {Pi} ex. PO43- , HPO42-, H2PO42- FUNCTIONS ATPase , c AMP , 2-3, DPG Phosphorylation and Dephosphorylation
  • 16. BONE: 3 mg of PO4 enters and is again reabsorbed. KIDNEYS: 85 % - 90 % of filtered Pi is reabsorbed by Active Transport in PCT Overflow mechanism PTH
  • 17. GIT • Absorbed in duodenum and small intestine by Active transport and passive diffusion. • Absorption is linear to dietary intake. • All PO4 excreted in urine.
  • 19. Made up of organic matrix and salts ORGANIC MATRIX COLLAGEN FIBERS GROUND • 90 – 95 % SUBSTANCES • Type 1 collagen made • Gelatinous substances up of triple helix (ECF + proteoglycans) Chondroitin sulphate Hyaluranic acid
  • 20. BONE SALTS • Salts of calcium and phosphate. HYDROXYAPATITE Ca10(PO4)6. (OH)2 400 Å long 10 – 30 Å thick 100 Å wide Ca / P ratio – 1.3 to 2.0 Other salts: Mg2+, Na+ , K+ ions conjugated to bone crystals.
  • 21. STRUCTURE OF BONE 2 types of bones Compact or Cortical bone – 80 % • surface to volume ratio is low • receive nutrients by canaliculi Trabecular or Spongy bone – 20 % • made up of spicules or plates with high surface to volume ratio • receive nutrients from the ECF through Haversian canal
  • 22.
  • 23. BONE GROWTH Fetus to adults – ENCHONDRAL BONE FORMATION Exception: clavicles, mandibles and certain skull bones. INTRAMEMBRANOUS BONE FORMATION
  • 24.
  • 25. EPIHYSEAL PLATE – bone increases in length Width is proportionate to growth and influenced by GH. EPIPHYSEAL CLOSURE Cartillage cells hypertropied Release VEGF Vascularization and ossification
  • 26. BONE FORMATION & RESORPTION • Bone formation by OSTEOBLASTS • Bone resorption by OSTEOCLASTS
  • 27. CELLS OF BONE • OSTEOPROGENITOR CELLS • OSTEOBLASTS • OSTEOCYTES • OSTEOCLASTS
  • 28.
  • 29. OSTEOBLASTS • Modified fibroblasts developed from mesenchymal cells • Secrete collagen monomers and ground substances • Finally forms an ‘OSTEOID’ • Calcium salts are deposited in the collagen fibers and forms hydroxyapatite crystals.
  • 30. OSTEOCYTES • Mature bone cells – imprisoned osteoblasts in the lacunae of osteon. • Sends processes throughout bone matrix • Maintains the metabolic activity of bone • Opens the channels for distribution of nutrients • Exchanges calcium between bone and ECF.
  • 31. OSTEOCLASTS • MEMBER OF MONOCYTE FAMILY • Attach its ruffled border to bone via integrins in the “sealing zone” • Proton pumps secrete acid and acidify the isolated area • Proteolytic enzymes breaks down the organic matrix • Eats away the bone in 3 wks - tunnel • Osteoblasts are activated - forms a new Haversian canal.
  • 32.
  • 33.
  • 34. CONTINUAL BONE FORMATION : strength shape for mechanical support replace old brittle bone. BONE STRESS: • Compressional load – bone in cast • Shape of the bone
  • 35. FRACTURE: • Activates periosteal and intraosseous osteoblasts • Stimulates osteoprogenitor cells. • Formation of “ CALLUS ”
  • 38. 7 DEHYDROCHOLESTEROL SUNLIGHT PREVITAMIN D3 VITAMIN D3 CHOLECACIFEEROL 25 HYDROXYLASE LIVER 25- HYDROXY CHOLECALCIFEROL 24 α HYDROXYLASE 1 α HYDROXYLASE KIDNEY 24, 25 DIHYDROXY CHOLECALCIFEROL 1, 25 DIHYDROXY CHOLECALCIFEROL
  • 39. MECHANISM OF ACTION • 1,25 – dihydroxycholecalciferol is a steroid compound (secosteroid) • Acts via the steroid receptor superfamily • Exposes the DNA – binding domain and results in increased transcription of some mRNAs.
  • 40. ACTIONS OF VITAMIN D3 1. Promotes intestinal calcium absorption BY 1. Formation of calcium binding protein (calbindin) 2. Formation of calcium stimulated ATPase 3. Formation of alkaline phosphatase
  • 42.
  • 43. 2. Promotes phosphate absorption by the intestines • As a direct effect • Calcium acts as a transport mediator for phosphate. 3. Decreases renal excretion of calcium & phosphate • Increases reabsorption of Ca and PO4 by the renal tubules
  • 44. 4. Increases both bone resorption and bone mineralization BONE RESORPTION – by stimulating PTH. Calcitriol receptors are present in osteobasts Receptor – calcitriol complex – stimulate osteoblasts --- activation & differentiation of osteoclasts. BONE MINERALIZATION – by stimulation osteoblasts and alkaline phosphatase secretion
  • 45. REGULATION OF SYNTHESIS PTH Ca 25 –OH D3 1,25 (OH)2 D3 BONE & INTESTINES 24,25- (OH)2 D3 PO4
  • 46. RICKETS & OSTEOMALACIA VITAMIN D deficiency in children and adults - defective bone mineralization and calcification - failure to deliver adequate Ca and PO4 FEATURES: Weakness and bowing of weight bearing bones, dental defects and hypocalcemia. Responsive to Vitamin D therapy. VITAMIN D RESISTANT RICKETS: mutations in the gene coding for the enzyme 1 α HYDROXYLASE
  • 48.
  • 49. STRUCTURE • FOUR parathyroid glands located behind the thyroid gland • 6 x 3 x 2 mm • Two types of cells 1. Chief cells 2. Oxyphil cells
  • 50. CHEMISTRY Pre pro PTH ( 115 aa) Pro PTH ( 90 aa ) PTH ( 84 aa ) Normal plasma PTH 10 -55 pg / mL Half life – 10 mins
  • 51. ACTIONS OF PTH I. Increases calcium and phosphate absorption from the bones II. Decreases excretion of calcium by the kidneys III. Increases the excretion of phosphate by the kidneys IV. Increases intestinal absorption of calcium and phosphate. INCREASED PLASMA CALCIUM
  • 52. I. Ca & PO4 absorption from the bone Two phases 1. Rapid phase – osteolysis by osteocytes 2. Slow phase – by osteoclasts
  • 53. RAPID PHASE - OSTEOLYSIS OCTEOCYTES OSTEOCYTIC MEMBRANE BONE FLUID ECF BONE ECF O.M B.FL B
  • 54. ECF OSTEOCYTIC BONE FLUID BONE MEMBRANE PTH Ca Ca Ca Ca Ca Ca Ca Ca Ca
  • 55. SLOW PHASE Done by OSTEOCLASTS… immediate activation of existing cells formation of new cells Excess bone resorption Stimulates osteoblastic activity
  • 56. II. Excretion of calcium and phosphate... • Decreases excretion of calcium increases reabsorption in CD, DT and Ascending limb of LOH • Increases excretion of phosphate PHOSPHATURIC ACTION dimishes absorption in PCT
  • 57. III. Absorption of Ca & PO4 in GIT… Enhances absorption of both calcium and phosphate by stimulating 1,25 – dihydroxycholecalciferol. • cAMP mediated. • cAMP is in plenty in osteoblasts and osteocytes
  • 58. MECHANISM OF ACTION • Binds to PTH receptors – 3 types. • REGULATION: stimulus : plasma calcium level.
  • 59. • Produced by the parafollicular cells / C cells of thyroid gland. • Remnants of ultimobrachial body. STRUCTURE: Molecular weight – 3500 and has 32 aminoacids. In brain “Calcitonin gene related polypeptide ( CGrP)” is formed.
  • 60. • STIMULUS : Increased plasma calcium Others: β adrenergic agonists, dopamine and estrogen, GASTRIN, CCK, glucagon.. • ACTIONS: Decreases absorptive action of osteoclasts Deposits exchangeable Ca in bone salts Decreases the formation of osteoclasts • CLINICAL USE: Used in the treatment of PAGET’S DISEASE.
  • 61. DISORDERS OF PTH • HYPOPARATHYROIDISM • HYPERPARATHYROIDISM primary and secondary • PSEUDOHYPOPARATHYROIDISM
  • 62. HYPOPARATHYROIDISM • Body calcium level decreases • Osteoclasts are inactive • Sudden removal – signs of tetany appears • Responds to treatment with PTH or Vitamin D3 PSEUDOHYPOPARATHYROIDISM PTH is normal Defect is in PTH receptors Not responsive to hormone therapy
  • 63. PRIMARY HYPERPARATHYROIDISM • Tumors – adenoma of parathyroid glands • More common in women. • Extreme osteolytic resorption - calcium and phosphate levels. Bone : Punched out cystic areas in the bone filled by osteoclasts – osteoclast tumors ‘ osteitis fibrosa cystica’ Serum Alkaline phosphatase is elevated.
  • 64. Hypercalcemia: P. Calcium – 12 – 15 mg / dL CNS depression, muscle weakness, constipation, abdominal pain, peptic ulcer, lack of appetite etc… Metastatic calcification: CaHPO4 crystals are deposited in renal tubules, lung alveoli, thyroid glands etc… Renal stones: Calcium phosphate and also calcium oxalate stones
  • 65. SECONDARY HYPERPARATHYROIDISM • Increased levels of PTH is the result of compensatory mechanism to hypocalcemia • Due to chronic renal disease or deficiency of Vitamin D 3
  • 66. OSTEOPOROSIS Diminished bone matrix due to poor oeteoblastic activity Causes: 1. Lack of physical stress 2. Malnutrition 3. Postmenopausal lack of estrogen 4. Old age 5. Lack of Vitamin C 6. Cushing’s syndrome
  • 67. OTHER HORMONES PARATHYROID HORMONE RELATED PROTEIN ( PTHrP) • Produced by different tissues of our body • Binds to PTH receptors • Marked effect on growth and development of cartilage in utero. • Cartilage growth is stimulated by a protein called “Indian hedgehog” • Other uses : Brain – prevents excitotoxic damage Placenta – transports calcium • Defect in PTHrP – severe skeletal deformities.
  • 68. GLUCOCORTICOIDS Lowers plasma calcium by inhibiting osteoclasts. Over Long periods – osteoporosis Inhibit protein synthesis in osteoblasts,thereby synthesis of organic matrix Inhibit absorption of Ca and Po4 from the gut and facilitate its excretion in the kidneys.
  • 69. GROWTH HORMONE Increases intestinal absorption of Calcium “Positive calcium balance” IGF – I Stimulates protein synthesis in bone. THYROID HORMONE Hypercalcemia, Hypercalciuria and Osteoporosis. ESTROGENS Prevents osteoporosis by inhibiting certain cytokines INSULIN Increases bone formation