首页> 外文期刊>The Journal of Pharmacology and Experimental Therapeutics: Official Publication of the American Society for Pharmacology and Experimental Therapeutics >Gerder-Dependent Enhanced Adult Neurotoxic Response to Methamphetamine following Fetal Exposure to the Drug
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Gerder-Dependent Enhanced Adult Neurotoxic Response to Methamphetamine following Fetal Exposure to the Drug

机译:胎儿暴露于毒品后对甲基苯丙胺的Gerder依赖性增强的成人神经毒性反应

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摘要

Methamphetamine use by females of child-bearing age has become a major public health concern in terms of the long-term risk to the exposed fetus. We examined the possibility of en- hanced adult neurotoxic potential of the drug in offspring that had been exposed to methamphetamine in utero during ges- tational days 7 to 18. While basal levels of monoamines were not affected by prenatal exposure to methamphetamine, we observed an enhanced neurotoxicity in adult male offspring following drug challenge with effects localized primarily to the dopaminergic nigrostriatal projection. This was evidenced by greater methamphetamine-induced reductions of dopaminer- gic markers in the striatum [dopamine (DA), dihydroxyphenyla- cetic acid, homovanillic acid (HVA), and 3-methoxytyramine (3-Mnl and ventral brainstem (DA) of prenatal methamphet-amine-treated males compared with saline-treated animals. Some effects of prenatal methamphetamine exposure were observed in female offspring, but these were limited to striatal levels of 3-MT and HVA. Differential gender sensitivity to the neurotoxic effect of methamphetamine was shown to be cor- related with hyperthermic response. Hyperthermic effects, however, do not account for the increased susceptibility of prenatal methamphetamine-treated males to drug-induced stri- atal DA neurotoxicity since methamphetamine challenge did not evoke a significantly greater hyperthermic response in these animals compared with prenatal saline-treated males. The findings raise the concern that male methamphetamine abusers may be at risk for an enhanced neurotoxic risk if they were exposed to the drug in utero.
机译:就暴露于胎儿的长期风险而言,育龄妇女使用甲基苯丙胺已成为主要的公共卫生问题。我们检查了在妊娠第7至18天暴露于子宫内甲基苯丙胺的后代中该药物增强的成年神经毒性潜力的可能性。尽管产前暴露于甲基苯丙胺对单胺的基本水平没有影响,但我们观察到药物攻击后增强成年雄性后代的神经毒性,其作用主要局限于多巴胺能黑质纹状体投射。甲基苯丙胺引起的纹状体中多巴胺能标记物的减少[多巴胺(DA),二羟苯基乙酸,高香草酸(HVA)和3-甲氧基酪胺(3-Mnl和腹侧脑干(DA)]证明了这一点。甲基苯丙胺处理的雄性与生理盐水处理的动物相比,雌性后代观察到了产前甲基苯丙胺暴露的一些影响,但仅限于纹状体水平的3-MT和HVA,显示出对甲基苯丙胺神经毒性作用的性别敏感性差异然而,高温影响并不能说明产前经甲基苯丙胺治疗的雄性对药物诱导的纹状体DA神经毒性的敏感性增加,因为甲基苯丙胺攻击并未引起这些动物明显更高的高温反应与产前生理盐水处理过的男性相比,这一发现引起了人们的担忧,即甲基苯丙胺滥用者可能会患上如果他们在子宫内接触该药物,可增加神经毒性风险。

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