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小鼠和人类孕期的苯巴比妥。

Phenobarbital during pregnancy in mouse and man.

作者信息

Middaugh L D

出版信息

Neurotoxicology. 1986 Summer;7(2):287-301.

PMID:3785754
Abstract

Phenobarbital appears to produce similar behavioral effects on mice and humans with excitation at low and sedation or depression at higher doses. If plasma concentrations of phenobarbital reflect levels in other tissue, then brain concentrations producing excitation (near 10 micrograms/g) and depression (near 20 micrograms/g) are not substantially different for the two species. The doses needed to produce these levels are much higher in mice than man. Plasma concentrations of phenobarbital decline during pregnancy in humans. Whether this decline is accompanied by increased seizure frequency has not been confirmed empirically and whether pregnancy influences the frequency of seizures at all is controversial. The reduction in phenobarbital levels in plasma or serum during pregnancy has been confirmed in rodents. Two of these studies however reported no difference brain concentrations of the drug during pregnancy. One study indicated increased potency of the drug, however this was not confirmed by the other two reports. The effects of phenobarbital on the progression of pregnancy and on offspring is not well defined in humans partly because the disease and the treatment effects are confounded. There are a few studies however which suggest that the effects might be drug specific. Animal studies in this area differ substantially from humans in design making any comparison tentative. The effects of the drug on pregnancy and neonates in rodents depends on the method of administering the drug and dose. Drug administration via the diet can provide high blood levels in the dams and causes lowered birthweight as well as several anatomical and hormonal abnormalities in offspring. This procedure, however, also severely reduced food intake and weight gains during pregnancy which might confound drug effects with nutritional deficiency. The drug can be injected in doses which produce plasma levels well within the therapeutic range for humans. Under these conditions the drug is less detrimental to the progression of pregnancy, however, the higher doses can increase neonatal mortality and reduce body weight of surviving offspring. Although mortality and body weight are not adversely effected by lower doses, changes are still apparent in the behavior as well as several biochemical parameters. Fostering studies on animals suggest that the effects of maternal injections of phenobarbital on offspring are due to the IN UTERO exposure rather than postnatal maternal factors and that effects produced by fostering itself may be confounded with the drug effects.

摘要

苯巴比妥对小鼠和人类似乎产生相似的行为效应,低剂量时引起兴奋,高剂量时导致镇静或抑制。如果苯巴比妥的血浆浓度反映其他组织中的水平,那么产生兴奋(接近10微克/克)和抑制(接近20微克/克)的脑浓度在这两个物种中并无实质性差异。在小鼠中产生这些水平所需的剂量比人类高得多。人类怀孕期间苯巴比妥的血浆浓度会下降。这种下降是否伴随着癫痫发作频率增加尚未得到实证证实,而且怀孕是否根本影响癫痫发作频率也存在争议。在啮齿动物中已证实怀孕期间血浆或血清中苯巴比妥水平会降低。然而,其中两项研究报告称怀孕期间该药物的脑浓度没有差异。一项研究表明该药物的效力增加,但其他两项报告未证实这一点。苯巴比妥对人类妊娠进展和后代的影响尚未明确界定,部分原因是疾病和治疗效果相互混淆。然而,有一些研究表明这些影响可能具有药物特异性。该领域的动物研究在设计上与人类有很大不同,因此任何比较都只是初步的。该药物对啮齿动物妊娠和新生儿的影响取决于给药方法和剂量。通过饮食给药可使母鼠血液中药物水平升高,并导致出生体重降低以及后代出现一些解剖学和激素异常。然而,此方法也会在怀孕期间严重减少食物摄入量和体重增加,这可能会将药物作用与营养缺乏混淆。可以注射能产生远在人类治疗范围内的血浆水平的剂量。在这些情况下,该药物对妊娠进展的危害较小,然而,较高剂量会增加新生儿死亡率并降低存活后代的体重。尽管较低剂量不会对死亡率和体重产生不利影响,但行为以及一些生化参数仍有明显变化。对动物的寄养研究表明,母体注射苯巴比妥对后代的影响是由于子宫内接触,而非产后母体因素,而且寄养本身产生的影响可能与药物作用混淆。

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