Endocrinology Flashcards

1
Q

What are the hormones secreted by anterior pituitary

A

FSH,LH, ACTH,TSH, PRL( prolactin), GH, Beta-endorphins and MSH

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2
Q

Out of all hormones produced by adenohypophysis which are basophils and which are acidophils

A

Basophils are : FSH,LH,ACTH, TSH

Acidophils are: PRL, GH

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3
Q

What are derivative of proopiomelanocortin

A

beta-endorphin, GH and MSH

Go Pro with BAM

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4
Q

What is the other name of anterior pituitary and what is it derived from

A

Adenohypophysis

Derived from oral ectoderm (Rathke pouch)

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5
Q

What is another name for posterior pituitary and what is it derived from

A

Neurohypophysis it is derived from neuroectoderm

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6
Q

Ft. Of posterior pituitary

A

Storage of vasopressin ( ADH) and oxytocin

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7
Q

Where are the hormones oxytocin and ADH produced

A

Hypothalamus (supraoptic and paraventricular nuclei)

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8
Q

How are the hormones produced in the hypothalamus moved to the posterior pituitary

A

By carrier proteins ( neurophysin)

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9
Q

Prolactin

A

Inhibited by: dopamine
Stimulated by : TRH

Inhibits: GnRH

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10
Q

Prolactin ft.

A

Causes lactation in breasts

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11
Q

GH

A

Released by anterior pituitary

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12
Q

How is it induced

A

By GHRH from hypothalamus

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13
Q

How is GHRH stimulated

A

By deep sleep, hypoglycemia and stress

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14
Q

Explain the pathway

A

GHRH stimulates GH from pituitary that activates IGF-1 in liver that stimulates bone and muscle growth and decrease glucose uptake and increase lipolysis

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15
Q

How is it inhibited

A

Negative feedback loop
GH inhibits GHRH

IGF-1 inhibits both GH and GHRH

Obesity, aging and glucose inhibits GHRH

Also by somatostatin and somatomedin

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16
Q

What happens in case of excess GH

A

Adults: Acromegaly

Children: gigantism

17
Q

ACTH

A

Produced by hypothalamus

Stored in posterior pituitary

18
Q

Ft. Of ACTH

A

Increase water permeability in DCT and covulated tubules by increasing expression of aquaporins

19
Q

What induces the release of ACTH

A

Increases serum osmolality and low blood volume

20
Q

What does ACTH do ?

A

Decreases osmolality and increase blood volume

21
Q

What happens in case of decreased ACTH

A

Diabetes insipidus ( central)

22
Q

What happens if tubules are resistant to ACTH

A

Diabetes insipidus ( nephrogenic)

23
Q

What is hypopituitarism ?

A

It is the absence of hormones released from pituitary gland

24
Q

Causes of hypopituitarism ?

A

Sheehan syndrome ( postpartum ischemia of the pituitary due to excessive bleeding )

Empty stella syndrome : absence of pituitary due to its atrophy or compression asc. with idiopathic intracranial hypertension

Pituitary apoplexy: hemorrhages of pituitary gland usually in presence of existing pituitary adenoma ( shows visual impairment) refer to first AID book for more info

25
Q

Symptoms of hypopituitarism

A

Depends on the hormones lost
dec. GH: impaired growth decreased muscle mass in adults and inc. LDL inc. risk of CVD

Dec. TSH: hypothyroidism

Dec. ADH : diabetes insipidus

Dec. LH And FSH and prolactin : amenorrhea, infertility, non-lactation, loss of secondary sexual characteristic

Dec. ACTH: adrenal insufficiency

Dec. MSH: decreased pigmentations in skin and hair

26
Q

How to diagnose hypopituitarism

A

MRI ( shows any lesions but might miss microadenomas)

And decrease in levels of hormones or their trophic hormones

27
Q

How to treat ( hypopituitarism)

A

Replacement therapy of hormones lost

28
Q

What is acromegaly

A

Acromegaly is a condition that occurs in adults due to increased GH release after the epiphyseal bone closure

29
Q

Findings of acromegaly?

A
Large tongue with deep furrows
Aging features 
Coarsening features 
Increased size of hands and feet
Cardiomyopathy 
Organomegally 
Frontal bossing 
Deep voice
30
Q

Metabolic features of Acromegaly ?

A

Insulin resistance ( DM) ( glucose intolerance)

Severe sweating ( hyperhidrosis)

Increased risk of colorectal polyp and cancer

31
Q

How to diagnose acromegaly ?

A

IGF-1 must be increased

Oral glucose tolerance test ( failure to suppress GH)

MRI ( showing any pituitary adenoma)

32
Q

Parasellar features ? Of acromegaly

A

Visual problems ( bitemporal hemisnopsia)

Headaches

HTN

Sleep apnea

33
Q

What is laron syndrome

A

Autosomal recessive syndrome ( defective GH receptors) characterized by: High GH low IGF-1

Features: short stature(dwarfism), small head circumference, prominent forehead and saddle nose, delayed skeletal maturation, small genitalia

34
Q

Syndrome of inappropriate ADH secretion:

A

Characterized by: volume expansion and hyponatremia

Continued excretion of sodium due to ANP AND BNP that will lead to normalization of ECF fluid and euvolemic Hyponatremia ( without edema)

Correct hyponatremia slowly not more than (0.5mEq/kg in 1 hr) to prevent osmotic demyelinization syndrome ( central pontine myelinolysis)

35
Q

Causes of SIADH ?

A

Neuronendocrine tumors : small cell lung carcinoma

CNS injury/ trauma

Pulmonary disease
Drugs: vincristine and cyclophosphamide