Evans B K, Burnstock G
J Reprod Fertil. 1979 Jul;56(2):715-24. doi: 10.1530/jrf.0.0560715.
Adult virgin female rats were injected daily with low doses (5 or 10 mg/kg) or a high dose (30 mg/kg) of guanethidine for 12 or 18 weeks respectively. 'Short' and 'long' noradrenergic neurones were unaffected by low doeses. This contrasts markedly to earlier findings in male rats in which long-term damage of 'short' noradrenergic neurones occurred, and indicates a basic difference between 'short' noradrenergic neurones in male and female rats. Widespread degeneration of both types of neurones followed treatment with high doses and little reinnervation was observed 8 weeks after cessation of treatment. Fertility, pregnancy and litter size were apparently unaffected. Some teratogenic effects were observed in the offspring of female rats treated with guanethidine (10 or 25 mg/kg/day) before and throughout pregnancy. However, these effects had largely disappeared by the time the offspring were 10 weeks old. Since noradrenergic neurones of newborn rats are particularly sensitive to damage by guanethidine it would appear that either very little guanethidine crosses the placental barrier or that noradrenergic neurones are not susceptible during prenatal development to the cytotoxic effects of guanethidine.
成年未交配的雌性大鼠分别每天注射低剂量(5或10毫克/千克)或高剂量(30毫克/千克)的胍乙啶,持续12周或18周。低剂量对“短”和“长”去甲肾上腺素能神经元没有影响。这与早期在雄性大鼠中的发现形成显著对比,在雄性大鼠中,“短”去甲肾上腺素能神经元会发生长期损伤,这表明雄性和雌性大鼠的“短”去甲肾上腺素能神经元之间存在根本差异。高剂量治疗后,两种类型的神经元都出现广泛退化,治疗停止8周后几乎没有观察到再支配现象。生育力、妊娠和产仔数显然未受影响。在用胍乙啶(10或25毫克/千克/天)在妊娠前及整个妊娠期处理的雌性大鼠的后代中观察到了一些致畸作用。然而,这些作用在后代10周大时已基本消失。由于新生大鼠的去甲肾上腺素能神经元对胍乙啶的损伤特别敏感,因此似乎要么只有极少的胍乙啶能穿过胎盘屏障,要么去甲肾上腺素能神经元在产前发育期间对胍乙啶的细胞毒性作用不敏感。