Zipper J, Bruzzone M E, Angelo S, Muñoz V, Wheeler R G
Int J Fertil. 1982;27(4):242-5.
The contraceptive properties of two adrenergically active drugs, propranolol and reserpine, were measured in vivo and in vitro. Propranolol became effective as a spermicide for human sperm at a concentration of about 2 x 10(-3) M and for rat sperm at 2 x 10(-2) M. Reserpine was also more effective on human than rat sperm and about 20 times less effective than propranolol. Both propranolol and reserpine prevented implantation when instilled into the uteri of rats. The anti-implantation effect persisted for up to 5 days after instillation of propranolol. When freely breeding rats eventually became pregnant after daily vaginal instillation of propranolol, the number of uterine implantations decreased as the concentration of vaginally instilled propranolol increased. The implantations tended to be toward the fundal end of the uteri, away from the source of propranolol, thus indicating a topical rather than a systemic anti-implantation effect.
对两种具有肾上腺素能活性的药物——普萘洛尔和利血平的避孕特性进行了体内和体外测定。普萘洛尔在浓度约为2×10⁻³ M时对人类精子成为有效的杀精剂,在2×10⁻² M时对大鼠精子有效。利血平对人类精子也比对大鼠精子更有效,其效力约为普萘洛尔的20分之一。将普萘洛尔和利血平均注入大鼠子宫时,二者均能阻止着床。普萘洛尔注入后,抗着床作用可持续长达5天。当自由交配的大鼠在每天经阴道注入普萘洛尔后最终怀孕时,随着经阴道注入普萘洛尔浓度的增加,子宫着床数减少。着床倾向于子宫底部末端,远离普萘洛尔的来源,因此表明是局部而非全身的抗着床作用。