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27 Cards in this Set

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31. If ketoconazole were a super-villin and had the opposite action (inhibition) of its super-hero counterpart, on what enzyme would it be acting on in the adrenal cortex?
a. Desmolase.
b. Ketoconazole inhibits Desmolase, while ACTH stimulates it.
c. Desmolase is responsible for the conversion of Cholesterol to pregnenolone.
32. Enzyme responsible for conversion of testosterone to estradiol?
a. Aromatase
33. Enzyme responsible for conversion of testosterone to DHT?
a. 5α-reductase.
34. What does AG II act on to produce aldosterone and via what enzyme?
a. Corticosterone via Aldosterone synthase.
35. What do all of the congenital adrenal enzyme deficiencies have in common (17α, 21, and 11β)?
a. All are characterized by enlargement of the adrenal glands due to ↑ in ACTH stimulation bc of ↓ levels of cortisol.
36. 17α-hydroxylase deficiency?
a. ↓ sex hormones
b. ↓ cortisol
c. ↑ aldosterone.
d. Sx: HTN, hypokalemia
37. 17α-hydroxylase deficiency in XY?
a. ↓ DHT -> pseudohermaphroditism (externally phenotypic female, no internal reproductive structures due to MIF).
38. 17α-hydroxylase deficiency in XX?
a. Externally phenotypic fm w/normal internal sex organs but lacking 2º sexual characteristics “sexual infantilism”.
39. What hormones are ↑ with 17α-hydroxylase deficiency?
a. Pregnenolone, progesterone, 11-deoxycorticosterone, aldosterone.
40. What hormones are ↓ w/17α-hydroxylase deficiency?
a. 17-hydroxypregnenolone
b. 17-hydroxyprogesterone
c. 11-deoxycortisol and cortisol
d. DHEA, androstenedione, and testosterone-bc these all come from 17 hydroxypregnenolone.
41. 21-hydroxylase deficiency (most common)?
a. ↓ cortisol (↑ ACTH)
b. ↓ Mineralcorticoids
c. ↑ sex hormones.
42. 21α-hydroxylase deficiency sx?
a. Masculinization
b. Female pseudohermaphroditism
c. HYPOtension, Hyperkalemia
d. ↑ plasma renin activity, and volume depletion
e. Salt wasting can lead to hypovolemic shock in the newborn.
43. What is ↑ in 21 hydroxylase deficiency?
a. Progesterone
b. Pregnenolone
c. 17-hydroxypregnenolone
d. 17-hydroxyprogesterone
e. DHEA, Androstenedione, testosterone
44. What is ↓ in 21-hydroxylase deficiency?
a. 11-deoxycorticosterone (from progesterone in mineral pw)
b. 11-deoxycortisol in cortisol pathway.
45. 11β-hydroxylase deficiency?
a. ↓ cortisol
b. ↓aldosterone and corticosterone
c. ↑ sex hormones
46. 11β-hydroxylase deficiency sx?
a. Masculinization
b. HTN (like aldosterone, 11-deoxycorticosterone is a mineralocorticoid and is secreted in excess).
47. 5 functions of cortisol?
1. Maintains blood pressure (permissive effect w/epinephrine- up-regulates α1 receptors on arterioles)
2. ↓ Bone formation
3. Anti-inflammatory
4. ↓ Immune function
5. ↑ Gluconeogenesis, lipolysis, proteolysis.
48. What is cortisol bound to in the blood?
a. Corticosteroid-binding globulin (CBG)
49. Source of PTH?
a. Chief cells of parathyroid.
50. 4 Functions of PTH?
a. ↑ bone resorption of calcium and phosphate
b. ↑ kidney reabsorption of calcium in DCT
c. ↓ Kidney reabsorption of phosphate
d. ↑ 1,25 (OH)2 (calcitriol) production by stimulating kidney 1α-hydroxylase.
51. What ↑ or ↓ PTH secretion?
a. ↓ Free serum Ca ↑ PTH
b. ↓ Free serum Mg ↓ PTH.
52. Common causes of ↓ Mg (↓’ing PTH) include:
1. Diarrhoea
2. Aminoglycosides
3. Diuretics
4. Alcohol abuse.
53. Effects of PTH on serum Ca and phosphate?
a. ↑’s Ca
b. ↓ (PO4)3-
c. ↑ urine (PO4)3-.
54. Effect of PTH on bone cells?
a. ↑ production of M-CSF and RANK-L in osteoblasts stimulating osteoclasts.
56. What cells secrete calcitonin?
a. Parafollicular cells (C cells) of thyroid.
57. Function of calcitonin?
a. ↓ bone resorption of calcium.
b. It opposes actions of PTH but is not important in normal calcium homeostasis.
58. What causes ↑ calcitonin secretion?
a. ↑ Serum Ca.