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体外实验表明,[3H]多巴胺可被大鼠黑质中的非多巴胺能神经末梢摄取并释放。

Evidence that [3H]dopamine is taken up and released from nondopaminergic nerve terminals in the rat substantia nigra in vitro.

作者信息

Kelly E, Jenner P, Marsden C D

出版信息

J Neurochem. 1985 Jul;45(1):137-44. doi: 10.1111/j.1471-4159.1985.tb05485.x.

Abstract

Potassium chloride (25 mM) and (+)-amphetamine (100 microM) both stimulated the release of radioactivity from slices of substantia nigra preincubated with [3H]3,4-dihydroxyphenylethylamine [( 3H]dopamine). Potassium chloride (25 mM) released radioactivity from slices of both zona compacta and zona reticulata. Prior 6-hydroxydopamine (6-OHDA) lesions of one nigrostriatal pathway did not reduce the spontaneous release of radioactivity, or the potassium chloride- or amphetamine-induced release of radioactivity from slices of nigra ipsilateral to the lesion after preincubation with [3H]dopamine. The accumulation of radioactivity following incubation of nigral slices from 6-OHDA-lesioned animals with [3H]dopamine was increased when compared to uptake into slices from intact tissue. In synaptosomal preparations of striatum, nomifensine but not desipramine or fluoxetine inhibited [3H]dopamine uptake. In contrast, nomifensine, desipramine, and fluoxetine all inhibited [3H]dopamine uptake in nigral synaptosomal preparations. Following 6-OHDA lesions of one nigrostriatal pathway the uptake of [3H]dopamine into nigral synaptosomal preparations was unchanged but uptake into striatal preparations was substantially decreased. In contrast, bilateral electrolesions of the dorsal and medial raphe nuclei reduced [3H]dopamine uptake into nigral preparations but not into striatal synaptosomes. The uptake of [3H]5-hydroxytryptamine ([3H]5-HT) into synaptosomal preparations of substantia nigra was abolished by fluoxetine and reduced by desipramine, but was unaffected by nomifensine. In contrast, fluoxetine, desipramine, and nomifensine all inhibited [3H]5-HT uptake into striatal synaptosomal preparations. Following 6-OHDA lesions of one nigro-striatal pathway the uptake of [3H]5-HT into nigral synaptosomal preparations was unchanged but uptake into striatal preparations was reduced.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

氯化钾(25毫摩尔)和(+)-苯丙胺(100微摩尔)均能刺激预先用[3H]3,4-二羟基苯乙胺([3H]多巴胺)预孵育的黑质切片释放放射性。氯化钾(25毫摩尔)能从致密带和网状带的切片中释放放射性。一条黑质纹状体通路预先进行6-羟基多巴胺(6-OHDA)损伤,并不会降低放射性的自发释放,也不会降低在用[3H]多巴胺预孵育后,损伤同侧黑质切片中由氯化钾或苯丙胺诱导的放射性释放。与完整组织切片的摄取相比,6-OHDA损伤动物的黑质切片与[3H]多巴胺孵育后的放射性积累增加。在纹状体的突触体制剂中,诺米芬辛可抑制[3H]多巴胺摄取,而地昔帕明或氟西汀则无此作用。相反,诺米芬辛、地昔帕明和氟西汀均能抑制黑质突触体制剂中的[3H]多巴胺摄取。一条黑质纹状体通路经6-OHDA损伤后,黑质突触体制剂中[3H]多巴胺的摄取未改变,但纹状体制剂中的摄取则大幅降低。相反,背侧和内侧中缝核的双侧电损伤会降低黑质制剂中[3H]多巴胺的摄取,但不会降低纹状体突触体中的摄取。氟西汀可消除[3H]5-羟色胺([3H]5-HT)在黑质突触体制剂中的摄取,地昔帕明可使其减少,但诺米芬辛对其无影响。相反,氟西汀、地昔帕明和诺米芬辛均能抑制[3H]5-HT在纹状体突触体制剂中的摄取。一条黑质纹状体通路经6-OHDA损伤后,黑质突触体制剂中[3H]5-HT的摄取未改变,但纹状体制剂中的摄取减少。(摘要截短至250字)

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