Daval J L, Vert P
Brain Res. 1986 Jun;392(1-2):175-80. doi: 10.1016/0165-3806(86)90243-9.
Caffeine, theophylline or saline were injected daily into female rats during the gestation and lactation periods. Crude synaptosomal membranes were isolated from the brains of offsprings at various stages of development and their ability to specifically bind [3H]diazepam was tested. An other approach consisted of injecting [3H]diazepam into offsprings and cerebral specifically bound diazepam was measured. It was shown that methylxanthines were able to inhibit [3H]diazepam binding by reducing total number of binding sites in the brain of 5- and 15-day-old rats born from treated mothers, with a total recovery of control values at 25 days of age. Moreover, in vivo percentage of cerebral bound diazepam dramatically fell when rats were exposed to methylxanthines in utero and through the mother's milk. Since caffeine and theophylline displace diazepam binding not necessarily in a competitive manner, it is suggested that they could interfere with diazepam as adenosine antagonists.
在妊娠和哺乳期,每天给雌性大鼠注射咖啡因、茶碱或生理盐水。从处于不同发育阶段的后代大脑中分离出粗制突触体膜,并测试其特异性结合[3H]地西泮的能力。另一种方法是给后代注射[3H]地西泮,并测量大脑中特异性结合的地西泮。结果表明,甲基黄嘌呤能够通过减少来自接受治疗的母亲所生的5日龄和15日龄大鼠大脑中的结合位点总数来抑制[3H]地西泮的结合,在25日龄时结合位点总数完全恢复到对照值。此外,当大鼠在子宫内和通过母乳接触甲基黄嘌呤时,大脑中结合的地西泮的体内百分比显著下降。由于咖啡因和茶碱不一定以竞争性方式取代地西泮的结合,因此有人提出它们可能作为腺苷拮抗剂干扰地西泮的作用。