3. • Anterior Pituitary ectodermal in origin
• From Rathke’s Pouch
• Posterior Pituitary
• Neurohypophysis
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Pituitary development
4. Parts of Pituitary gland
• Anterior lobe or
ADENOHYPOPHYSIS
– Pars Distalis
– Pars intermedia
– Pars tuberalis
• Posterior lobe or
NEUROHYPOPHYSIS
– Pars Posterior
– Infundibular Stem
– Median Eminence
• Intermediate lobe or
PARS INTERMEDIA
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8. Blood Supply of Pituitary Gland
The Hypophyseal portal system
is a blood system of vessels in
the brain that connects the
hypothalamus with the anterior
pituitary.
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19. Common clinical pituitary disorders
Hypopituitarism
Abnormalities of Growth Hormone
Prolactin deficiency
Cushing’s syndrome
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20. Hypo
pituit
arism
Effects of Hypopituitarism
1. GH deficiency
2. Gonadotropin secretion
3. Thyrotropic hormone secretion
4. Adrenocorticotropin hormone
deficiency
5. Effect on water metabolism
6. Effect on insulin sensitivity
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21. Abnormalities of Growth Hormone secretion
Hyper-secretion
Gigantism
Acromegaly
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22. Gigantism
Hypersecretion of GH
BEFORE the closure of
epiphysis of long bones
Abnormal height
Large hands and feet
Coarse facial features
Bilateral Gynaecomastia
Loss of libido / impotence
Hyperglycemia >> deficiency
of insulin due to degeneration
of beta cells of pancreas
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23. PITUITARY TUMOR
Features
Headache
Visual field defects
Cranial nerve palsies
Enlargement of pituitary fossa
with destruction of CLINOID
process
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24. Acro
meg
aly
Excess of GH AFTER epiphyseal closure of
long bones; excess growth where cartilage
persists
Acromegalic face
Prognathism
Acral part abnormalities
Kyphosis
Excessive growth of internal organs
Cardiomegaly, hepatomegaly,
splenomegaly, renomegaly
Increased sympathetic activity
Sweating / hypertension
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26. Hyposecretion of GH
Deficiency of GH in Childhood
Dwarfism
Deficiency of GH in adulthood
Mild anemia
Reduction in muscle mass
Hypoglycemia
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27. Dwarfism
Endocrinal causes
GH Deficiency / Pituitary dwarf
Panhypopituitarism
Hypothyroid dwarf
Cushing’s syndrome
Non-Endocrinal causes
Familial dwarfism
Achondroplasia
Nutritional (malnutrition / Malabsorption)
Chromosomal abnormalities (Turner’s)
Psychological dwarfism (Kasper-Hauser’s Syndrome)
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28. GH related dwarfism
1. Pituitary dwarfism
2. African Pygmies
3. Laron dwarfism
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32. Negative feedback
i. Somatomedins
i. Somatomedin A, which is another name for
insulin-like growth factor 2
ii. Somatomedin B, which is derived from vitronectin
iii. Somatomedin C, which is another name for
insulin-like growth factor 1
ii. GH
iii. GHRH (ultra short loop)
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33. Other factors controlling GH secretion
• Thyroxine & cortisol stimulate GH
• Insulin represses GH gene expression
• Placental GH & placental lactogen decrease GH during
later part of pregnancy
• Obesity causes decreased response to GHRH
• Neurotransmitters – DA, NE, Ach, Serotonin, GABA,
Histamine increase GHRH & decrease somatostatin
• Oestradiol- increase GH
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35. GH
• Receptors present
on cell membrane
– liver & adipose tissue
• Mechanism of
action
• Insulin like growth
factors
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36. Act
ion
sof
GH
1. Growth promoting actions of GH
– Effect on cartilage – proliferation of chondrocytes
– Effect on bones – stimulates osteoblastic activity
2. Metabolic actions of GH
i. Effects on protein metabolism- anabolic
ii. Effects on fat metabolism - catabolic
iii. Effects on carbohydrate metabolism- increase
gluconeogenesis
iv. Effects on mineral metabolism- bone
mineralization
3. Effects on lactation – like prolactin03/09/2019 Jaideep J Rayapudi, Physiology PIMS 36