Hypothalamic-Pit Relationship Flashcards

1
Q

Posterior Pituitary Gland

A

Collection of axons whose cell bodies are located int he hypothalamus.

Supraoptic nucleus (SON) and Paraventricular nucleus (PVN)

Secrete ADH (SON) and oxytocin (PVN)

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2
Q

Anterior Pituitary Gland

A

Collection of endocrine cells

Secrete: ACTH, TSH, FSH, LH, GH, Prolactin

Portal vessels connect it to hypothalamus

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3
Q

Hypothalamic-Hypophysial Portal Vessels

A
  • Hypothalamic hormones can be delivered to the anterior pituitary directly and in high concentrations
  • The hypothalamic hormones do not appear in the systemic circulation in high concetration
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4
Q

Endocrine Axes

A

Primary endocrine disorder= Peripheral endocrine gland

Secondary= pituitary gland

Tertiary= Hypothalamus

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5
Q

Corticotroph

A

Release ACTH

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6
Q

Thyrotroph

A

Release TSH

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7
Q

Gonadotroph

A

FSH and LH

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8
Q

Lactotroph

A

Prolactin

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9
Q

Acromegaly

A

Caused by prolonged, excessive secretion of GH in adult life

Excessive growth of soft tissue, cartilage, and bone in the face, hands, and feet

Develops gradually, may not recognize for many years

Sx-Hypertension, mental disturbance, cardiomegaly, organomegaly, hyperglycaemia, prominent lower jaw, increased heel pad and feet

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10
Q

Diagnosis of Acromegaly

A

GH stims somatomedin C (insulin like GF1) gene transcription and secretion by the liver

GH levels fluctuate throughout the day whereas IGF-1 levels remains constant

Inadequate suppression of serum GH after a glucose load confirms the dx

Increased IGF-1; failure to suppress serum GH following OGTT; pituitary mass seen on brain MRI

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11
Q

Acromegaly Tx

A

Work to lower GH serum levels or blocking the effects of GH
-Somatostatin analog, GH receptor antagonist

Surgery to remove pituitary gland

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12
Q

GH Pulsatory Manner

A

Secreted in pulses, each pulse corresponds to a pulse and bursts of hundreds of GH -secretory pulses by the somatotrophs

Integrated amount of GH secreted each day is higher during the pubertal growth than in younger children or in adults

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13
Q

GH Deficiency

A

Decrease secretion of GHRH (due to hypothalamic dysfunction), and decrease in GH secretion

Failure to gen somatomedins (the effect of GH that are mediated by somatomedins would be impaired)

GH or somatomedin resistance (deficiency of receptors)

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14
Q

GH Excess

A

Mostly due to a growth hormone-secreting pituitary adenoma

Consequences depend on development stage

Before puberty: Gigantism
After Puberty: increased periosteal bone growth, organ size, extremity size. Coarsening of facial features, insulin resistance, and glucose intolerance

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15
Q

GH Metablic functions

A

Diabetogenic effect-Increase in blood glucose concentration

  • Causes insulin resistance
  • Decrease glucose uptake and utilization by target tissues
  • Increased lipolysis in adipose tissue

Increased protein synthesis and organ growth

  • Increased AA uptake, stim syn of DNA and RNA
  • Effect mediated by somatomedins (IGF-1)

Increased linear growth

  • Stims syn of DNA and RNA
  • Increased metabilism in cartilage-forming cells and chondrocyte proliferation
  • Effect mediated by somatomedins (IGF-1)
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16
Q

Pituitary Adenomas

A

Occur spontaneously

Benign and slow growing

Functional tumors: adenomas that release an active hormone, usually an excessive amount
Clinically non-functional tumors release no active hormones

17
Q

Sheehan Syndrome

A

Postpartum hypopituitarism due to necrosis of pituitary gland

Px present with agalactorrhea and difficulties in lactation

Amenorrhea

Endocrine dysfunction also may be present

18
Q

Actions of ADH

A

Secretion triggers: increase plasma osmolarity, decrease blood pressure, decrease blood pressure, increased of angiotensin II, sympathetic stimulation, dehydration

Result: Increased blood pressure and volume

19
Q

Diabetes Insipidus

A

Lack of an effect of ADH on the renal collecting duct

Frequent urination

Large volume of dilute urine