Medical Pharmacology Chapter 32: Hypothalamic and Pituitary Hormones
Levels:
Physiologic levels:cause milk ejection in lactating women
Pharmacological doses:
Induce uterine contraction/maintain labor
9-amino acid peptide
IV administration for labor stimulation
Nasal spray: postpartum lactation induction
Catabolism: renal and hepatic
Half-life: (circulating) 5 min.
Influences ionic currents in myometrial smooth muscle : uterine contraction
Uterine sensitivity to oxytocin: increases in pregnancy
Inhibition of oxytocin-induced myometrial uterine contraction:
Magnesium sulfate
β-adrenergic receptor agonists
Inhalation anesthetics
Promotes myoepithelial cell contraction (surrounding mammary alveolar) : milk ejection
Normal lactation requires oxytocin
Diagnostic Applications: oxytocin
Therapeutic Uses: oxytocin
Labor induction
Promoting dysfunctional labor
When early vaginal delivery is required
Rh factor concerns, maternal diabetes, preeclampsia
Uterine inertia
Incomplete abortion
Control of postpartum uterine bleeding
Enhance impaired milk ejection (nasal Route of Administration)
Serious toxicity: rare
Reported adverse reactions include: hypertensive reactions, uterine rupture, water intoxication, fetal death, afibrinogenemia
Fetal distress, abnormal fetal presentations, factors predisposing to uterine rupture
Peptide hormone
Released by posterior pituitary in reaction to:
Rising plasma tonicity
Decreasing blood pressure
Antidiuretic properties
Vasopressor properties
Vasopressin deficiency: diabetes insipidus
Structure: vasopressin
Nonapeptide
Routes of administration:
IV, intramuscular, intranasal
Half-life: 20 minutes
Renal and hepatic catabolism
Minimal vasopressin excreted unchanged in the urine
Receptor types
V1-- vascular smooth muscle (vasoconstriction)
V2 -- renal tubule cells: antidiuresis
Mechanism:
(1) increased water permeability
(2) increased collecting tubule water resorption
Extrarenal V2 receptors--promote coagulation factor VIIIc and von Willebrand factor release.
Desmopressin acetate (DDAVP, 1-desamino-8-D-arginine vasopressin)
Synthetic vasopressin derivative
Long-acting
Limited V1 receptor activity
Significant antidiuretic/vasopressor ratio compared to vasopressin (4000: 1)
Vasopressin and desmopressin: alternative treatment for pituitary diabetes insipidus
Nocturnal enuresis (desmopressin at bedtime) -- mechanism: reduced night urine production
IV vasopressin: may be effective in managing esophageal variceal bleeding and colonic diverticular leading
Vasopressin (not desmopressin): vasoconstriction -- cause issues in patients with coronary vascular disease
Unusual side effects include: agitation, allergic reactions, abdominal cramping, headache, nausea
Primary Reference: Fitzgerald, P.A. and Klonoff, D.C. Hypothalamic and Pituitary Hormones, in Basic and Clinical Pharmacology, (Katzung, B. G., ed) Appleton-Lange, 1998, pp 603-618.
Primary Reference: Biller, Beverly M. K. and Daniels, Gilbert, H. Neuroendocrine Regulation and Diseases of the Anterior Pituitary and Hypothalamus, In Harrison's Principles of Internal Medicine 14th edition, (Isselbacher, K.J., Braunwald, E., Wilson, J.D., Martin, J.B., Fauci, A.S. and Kasper, D.L., eds) McGraw-Hill, Inc (Health Professions Division), 1998, pp 1972-1998
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