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产前接触可卡因会导致外侧缰核出现神经退行性变的迹象。

Prenatal cocaine produces signs of neurodegeneration in the lateral habenula.

作者信息

Murphy C A, Ghazi L, Kokabi A, Ellison G

机构信息

Department of Biology, Franklin and Marshall College, Lancaster, PA 17604, USA.

出版信息

Brain Res. 1999 Dec 18;851(1-2):175-82. doi: 10.1016/s0006-8993(99)02181-2.

DOI:10.1016/s0006-8993(99)02181-2
PMID:10642841
Abstract

The lateral habenula is a nucleus in the dorsal thalamus that innervates midbrain dopaminergic and serotonergic nuclei via projections through its major efferent pathway, the fasciculus retroflexus (FR). It was previously demonstrated that cocaine administered continuously to adult rats over several days produces neurodegeneration in the lateral habenula and FR. Because exposure to cocaine during pregnancy reportedly can cause neurobehavioral deficits, we examined whether rat fetuses exposed to continuous cocaine during the last week of gestation would similarly demonstrate selective neurodegeneration in the lateral habenula. On day 17 of gestation, dams were implanted with two silicone pellets, each containing either vehicle or one of 2 doses of cocaine (80 mg or 55 mg per pellet). Degenerating neurons containing silver deposits were counted in lateral habenula and in the striatum. Cocaine-exposed pups had significantly more silver-stained cells in the lateral habenula than vehicle-treated pups, but similar numbers of silver-stained cells were present in the striatum of all three groups. When similarly treated vehicle- and cocaine-exposed animals were tested behaviorally at 60 days of age, they did not differ on measures of open field activity, open arm avoidance on the elevated plus-maze or conditioned place preference for cocaine, although a linear trend analysis indicated some hyperactivity of the cocaine-pretreated pups during the place preference test. These results indicate that continuous cocaine exposure has selective neurotoxic effects on the habenula of the developing fetus similar to cocaine's effects in the adult.

摘要

外侧缰核是背侧丘脑的一个核团,它通过其主要传出通路——后屈束(FR)发出投射,支配中脑的多巴胺能和5-羟色胺能核团。先前的研究表明,成年大鼠连续数天给予可卡因会导致外侧缰核和后屈束发生神经退行性变。据报道,孕期接触可卡因会导致神经行为缺陷,因此我们研究了在妊娠最后一周持续接触可卡因的大鼠胎儿是否也会在外侧缰核出现选择性神经退行性变。在妊娠第17天,给孕鼠植入两个硅胶丸,每个硅胶丸要么含赋形剂,要么含两种剂量可卡因中的一种(每个硅胶丸含80毫克或55毫克可卡因)。对外侧缰核和纹状体中含有银沉积物的退化神经元进行计数。接触可卡因的幼崽外侧缰核中银染细胞明显多于接受赋形剂处理的幼崽,但三组幼崽纹状体中的银染细胞数量相似。当对接受类似处理的接触赋形剂和可卡因的动物在60日龄时进行行为测试时,它们在旷场活动、高架十字迷宫中对开放臂的回避或对可卡因的条件性位置偏爱测量方面没有差异,尽管线性趋势分析表明,在位置偏爱测试期间,经可卡因预处理的幼崽有一些多动现象。这些结果表明,持续接触可卡因对发育中胎儿的缰核有选择性神经毒性作用,类似于可卡因对成年动物的作用。

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