Pharmacology of Gonadal Hormones 1 Flashcards

Describe why and how gonadotropin releasing hormone and/or analogs are used diagnostically and for stimulatory and inhibitory effects.

1
Q

Describe the process of regulation for androgen secretion in males.

A

See image.

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2
Q

Describe the structure, secretion pattern, and mechanism of action for GnRH in males.

A
  • Structure - decapeptide
  • Secretion
    • from hypothalamic nucleus
    • pulsatile
    • 1 pulse/120 min in male
  • Mechanism and actions
    • GnRH acts through G protein coupled membrane receptors on gonadotropes
    • causes secretion of FSH and LH
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3
Q

What causes GnRH receptor desensitization?

A
  • Continuous GnRH secretion
  • Receptors are also desensitized by long-acting “superagonists” that are resistant to degradation
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4
Q

List the common GnRH analogs.

A
  • Gonadorelin
  • Leuprolide
  • Cetrorelix
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5
Q

Describe the mechanism and pharmacokinetics of gonadorelin.

A
  • Function
    • synthetic GnRH
  • Pharmacokinetics
    • sc or iv administration
    • well absorbed, short half-life
    • administered by pump in a pulsatile manner for sustained stimulatory effect
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6
Q

What are the uses of gonadorelin?

A
  • diagnostic
    • distinguish whether pituitary unresponsiveness is due to hypothalamic or pituitary failure
    • LH is measured after injection
    • positive response indicates deficiency is hypothalamic, but a long term GnRH deficiency can impair responsiveness
  • replacement
    • treatment of hypothalamic hypogonadotropic hypogonadism
    • administered by pump
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7
Q

What is leuprolide and what are its pharmacokinetics?

A
  • GnRH superagonist
    • desensitizes GnRH receptors at the pituitary
    • leads to decreased gonadotropins and androgen
  • Pharmacokinetics
    • adminstered sc or im
    • depot forms for monthly or longer intervals
    • intranasal agents create a lower bioavailability
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8
Q

What are the uses of leuprolide?

A
  • Precocious puberty
    • suppress gonadotropins and arrest premature exual maturation
  • Metastatic prostate cancer
    • same uses and effects as true antagonists such as cetrorelix/ganirelix
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9
Q

What is cetrorelix and what are its pharmacokinetics?

A
  • True GnRH receptor antagonists
    • ganirelix is another drug in this category
    • decreases gonadotropins, decreasing androgen
  • Pharmacokinetics
    • administered sc or im once daily
    • good bioavailability
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10
Q

What are the uses of cetrorelix?

A
  • Metastatic prostate cancer
    • used interchangeably with leuprolide
    • lowers PSA, reduces effects of skeletal metastases and ureteral obstruction
      • prolongs survival
    • duration of response is generally 14-20 months
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11
Q

What are the adverse effects of GnRH superagonists and antagoinsts?

A
  • Erectile dysfunction
  • Antagonists can lead to hypersensitivity reactions
  • Superagonists have elicited a syndrome of:
    • headache
    • neurologic symptoms
    • pituitary dysfunction
    • thought to be a result of infarction of a pituitary adenoma
  • Superagonists produce an initial “flare”
    • results in bone pain and urethral obstruction
    • may require anti-androgen treatment
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12
Q

Describe the process of female gonadal hromone secretion.

A

See image.

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13
Q

Describe the secretion pattern of GnRH in females.

A
  • Rate is more rapid than the male
    • one pulse per 60-90 min
  • Rate is slower in luteal phase than in the follicular phase of the cycle
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14
Q

What are the uses of Gonadorelin and leuprolide in females?

A
  • Gonadorelin
    • used to induce ovulation in the treatment of infertility
  • Leuprolide
    • suppression of endometriosis and uterine fibroids
    • palliation of breast carcinoma
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15
Q

What are side effects of GnRH superagonists specific to the female?

A
  • Vaginal dryness
  • Vaginal atrophy
  • Bone loss (male and female)
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