01d: GH and Growth Flashcards

1
Q

T/F: GH is the single most important hormone required for post-natal growth.

A

True

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2
Q

T/F: Attainment of adult size is absolutely dependent on GH.

A

True

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3
Q

GH exerts its effect through mediation by the following chemical messengers: Star the most important

A
  1. IGF-I*
  2. IGF-II
  3. Somatomedin C
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4
Q

In general, plasma concentrations of (X) reflect availability of (Y) hormone and/or the rate of growth.

A
X = IGF-I
Y = GH
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5
Q

Children whose growth is slower than average have lower concentrations of (X). Administration of (Y) can restore growth to nearly normal.

A

X = Y = IGF-I

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6
Q

IGF is which type of receptor?

A

Tyr kinase

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7
Q

T/F: IGF-I stimulates cell growth in cartilage and many other tissues.

A

False - cell proliferation in those tissues

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8
Q

T/F: IGF-I primarily exerts its effects locally (autocrine/paracrine) and has only minor role in circulation.

A

True

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9
Q

GH acts directly on (X) to promote IGF-I production. (Y) is the main source of IGF-I in blood.

A
X = liver and peripheral tissues
Y = liver
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10
Q

T/F: Both IGF-I and II are present in blood at relatively high concentrations until adult life (after puberty).

A

False - high throughout life

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11
Q

T/F: IGF-I and II circulate in blood, bound to IGF binding proteins.

A

True

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12
Q

GH is secreted (tonically/episodically), with the largest secretion normally associated with (X). List some other factors that induce its secretion.

A

Episodically (bursts);
X = early hours of sleep

Stress, X, fasting, low glucose

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13
Q

Changes in GH secretion with age primarily reflects changes in (frequency/magnitude) of pulses.

A

Magnitude

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14
Q

T/F: In the absence of GHRH, GH secretion completely ceases.

A

True

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15
Q

Plasma IGF-(I/II) plays important role in (stimulating/inhibiting) GH secretion by (stimulating/inhibiting) (X).

A

I;
Inhibiting;
Inhibiting;
X = GHRH effect on pituitary

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16
Q

(X) growth is stunted in children suffering from unremediated hypothyroidism. This is primarily due to (increase/decrease) in (Y) synthesis.

A

X = linear;
Decrease;
Y = GH

17
Q

T/F: During fetal growth, it’s actually thyroid hormones, not GH, that serves as growth-promoting hormone.

A

False - Insulin!

18
Q

The (X) organ cell mass is especially important in embryo/fetus, since it produces the growth-promoting hormone during fetal life. This cell mass is determined by locally produced (Y).

A
X = pancreatic (insulin)
Y = IGF-II (predominant IGF in embryo/fetus tissue)
19
Q

T/F: Insulin concentrations are not as important/effective in maintaining normal growth postnatally.

A

False - optimal concentrations still required to maintain normal growth

20
Q

T/F: Unlike IGF-I and II, Insulin doesn’t require plasma-binding protein.

A

True

21
Q

When it comes to adolescent growth spurt, (X) hormones are responsible. Specifically, they promote which two key changes?

A

X = gonadal sex steroids (primarily estrogens)

  1. Linear growth
  2. Closure of epiphyses
22
Q

T/F: Hypogonadal individuals tend to have stunted growth and shorter limbs.

A

False - opposite (tall with long arms/legs)

23
Q

T/F: During growth spurt, there isn’t normally a significant change in plasma IGF-I and GH concentrations.

A

False! Spike in both (responsible for increase in height)

24
Q

Observations have shown that (estrogens/androgens) are responsible for pubertal growth. This is because (M/F) children lacking (X) don’t experience this growth.

A

Estrogens;
Both M and F
X = aromatase enzyme

25
Q

The short stature of Pygmies is caused by (high/low) levels of (X), specifically during which stage of (pre/post)-natal life?

A

Low (genetic inability to produce);
X = IGF-I
Puberty (GH and IGF-I levels normal before that)

26
Q

(X), although required for synthesis of GH, will decrease GH secretion in excess.

A

X = glucocorticoids

27
Q

Mid-parental height is calculated in which way? How does that number change depending on if child is M/F?

A

Average of father and mother height;

Add 2.5 in for M and subtract for F

28
Q

Mid-parental and Target Height: Limits of (X) SD above/below target height are displayed.

A

X = 2

29
Q

(X) is a phenomenon when child’s growth curve deviates from normal family pattern, but eventually catches up with cohort (late puberty).

A

X = constitutional delay

30
Q

GH hypersecretion, caused by (X) tumor, will cause (Y) if arises before puberty.

A
X = pituitary;
Y = gigantism (due to bone lengthening)
31
Q

GH hypersecretion, caused by (X) tumor, will cause (Y) if arises after puberty.

A
X = pituitary
Y = acromegaly (disfiguring bone thickening; bones can't grow anymore, so expand)
32
Q

GH excess can be treated with analog to (X).

A

X = somatostatin