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机构地区:[1]中国科学院上海药物研究所
出 处:《生理学报》1995年第5期429-434,共6页Acta Physiologica Sinica
摘 要:应用HPLC-ECD测定DA更新率(DOPAC/DA),证明(-)SPD对黑质-纹状体、中脑-边缘系统、下丘脑-垂体DA神经系统的DA含量影响不明显,却显著增加DOPAC含量,并显著加强这些脑区的DA更新率,这可能是通过末梢的DA自身受体实现的。但(-)SPD既不显著影响中脑-前额叶和中脑-扣带回的DA含量,也不影响其中DOPAC含量,表明它不影响这些脑区DA更新率。这可能是由于皮层DA系统神经末梢缺乏DA自身受体的缘故。It has been shown before that DA antagonist (-) stepholidine[(-) SPD] changes the function of feedback regulation in the striatum. In order to compare the effect of the drug on other brain DA systems, the DA content and DOPAC level in brain areas or nuclei of rat were measured by HPLC--ECD. It was found that (-) SPD (10 mg/kg, ip) did not significantly affect the DA contents in the striatum, olfactory bulb, N. accumbens, substantia nigra, ventral tegmentum area, N. amygdala, hypothalamus, pituitary, piriform cortex, but did markedly increase the DOPAC levels in these brain areas or nuclei, and thus increase the DA turnover (DOPAC/DA). However, (-) SPD (10 mg/kg, ip) did not significantly affect either the DA contents or DOPAC levels in the pre frontal cortex and cingulate cortex, thus leaving the DA turnover in these areas unchanges. These results indicated that (-) SPD did affect the nigro-striatal, midbrainlimbic and hypothalamus-pituitary DA systems, but not the midbrain-cortex DA system. It is supposed that this difference may be due to the modulation by presynaptic DA autoreceptors in the major brain areas of DA nerve endings or neurosoma, but none in the cortex DA nerve endings.
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