Hurd W W, Gauvin J M, Dombrowski M P, Hayashi R H
Department of Obstetrics and Gynecology, University of Michigan Medical Center, Ann Arbor.
Am J Obstet Gynecol. 1993 Sep;169(3):644-9. doi: 10.1016/0002-9378(93)90637-x.
This study evaluated the in vitro effects of cocaine on the binding characteristics of alpha- and beta-adrenergic receptors from pregnant human myometrium.
By means of membrane fractions from myometrium obtained from 26 women at term undergoing cesarean section, equilibrium binding assays were performed with tritiated dihydroergocryptine for alpha-adrenergic receptors and iodine 125-cyanopindolol for beta-adrenergic receptors. Equilibrium competition curves were determined with and without cocaine. Results were compared by one-way analysis of variance.
Cocaine inhibited beta-adrenergic receptor binding (inhibition constant = 132 mumol/L) but had little effect on alpha-adrenergic receptor binding (inhibition constant = 1.63 mmol/L). Benzoylecgonine, a stable metabolite of cocaine, had no effect on binding to either receptor.
Cocaine selectively inhibits myometrial beta-adrenergic receptor binding. This may alter the contractile equilibrium of the pregnant uterus and could explain, in part, the association of cocaine abuse with premature delivery.
本研究评估了可卡因对妊娠子宫肌层α和β肾上腺素能受体结合特性的体外影响。
通过从26名足月行剖宫产的妇女的子宫肌层获取的膜部分,用氚标记的二氢麦角隐亭进行α肾上腺素能受体的平衡结合试验,用碘125-氰基吲哚洛尔进行β肾上腺素能受体的平衡结合试验。在有和没有可卡因的情况下测定平衡竞争曲线。结果通过单因素方差分析进行比较。
可卡因抑制β肾上腺素能受体结合(抑制常数=132μmol/L),但对α肾上腺素能受体结合影响很小(抑制常数=1.63mmol/L)。可卡因的稳定代谢产物苯甲酰爱康宁对两种受体的结合均无影响。
可卡因选择性抑制子宫肌层β肾上腺素能受体结合。这可能会改变妊娠子宫的收缩平衡,并可能部分解释可卡因滥用与早产之间的关联。