Intrauterine diazepam exposure: effects on physical and neurobehavioral development in the rat.

C L Ryan, B A Pappas
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Abstract

Primiparous timed-pregnant Wistar dams were administered a single daily SC injection of diazepam (1.0 or 5.0 mg/kg) or vehicle, over gestation days 14-20. The offspring were assessed on a number of developmental parameters. Pups exposed to the lower dose exhibited a decrease in birth weight and a delay in hair growth. Although these parameters were apparently not affected in the higher dose group, a significant dose-dependent decrease in pup viability was observed, both at birth and at one week of age. No differences were manifested for incisor eruption, pinna uncurling, eye opening, righting, geotaxis, acoustic startle, swimming, or forward locomotion. Rotarod performance was affected in the prenatal DZP animals and body weight at 60 days of age was depressed in the males of the 1.0 mg/kg group. The high dose of diazepam produced an increased susceptibility to minor metrazol-induced seizures in a kindling paradigm, but these altered seizure thresholds were not evidenced in an acute metrazol dose-response study. The NE and DA contents of hypothalamus, brainstem, hippocampus, and cortex of adult brains were assessed in each group. DA was not altered in any brain region while a single significant effect on NE was found. In the 1.0 mg/kg exposed rats only males, but not females, showed higher brainstem levels than controls. These results indicate that in the rat, prenatal exposure to clinically relevant doses of diazepam causes both fetal toxicity and long-term neurobehavioral alterations.

子宫内地西泮暴露:对大鼠身体和神经行为发育的影响。
在妊娠14-20天内,首次怀孕的Wistar母鼠每天注射一次地西泮(1.0或5.0 mg/kg)或对照物。对后代进行了一些发育参数的评估。暴露于较低剂量的幼崽表现出出生体重下降和毛发生长延迟。虽然这些参数在高剂量组中明显没有受到影响,但在出生时和1周龄时,观察到幼犬生存能力的显著剂量依赖性下降。门牙出牙、耳廓开卷、睁眼、翻正、地向性、声惊、游泳或向前运动无差异。1.0 mg/kg DZP组影响了产前DZP动物的轮轮生产性能,抑制了60日龄雄性的体重。在点火实验中,高剂量地西泮增加了对美曲唑引起的轻微癫痫发作的易感性,但在急性美曲唑剂量-反应研究中,这些改变的癫痫发作阈值并未得到证实。测定各组成人大脑下丘脑、脑干、海马和皮层的NE和DA含量。DA在任何脑区都没有改变,而NE则有单一的显著影响。暴露在1.0 mg/kg的大鼠中,只有雄性而不是雌性的脑干水平高于对照组。这些结果表明,在大鼠中,产前暴露于临床相关剂量的地西泮会导致胎儿毒性和长期神经行为改变。
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