纹状体突触体中多巴胺和血清素合成的年龄相关性。

M. Messripour, A. Mesripour
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引用次数: 12

摘要

酪氨酸羟化酶和色氨酸羟化酶分别是生物合成多巴胺和血清素的关键限速酶。由于这两种酶在纹状体中都很活跃,且受年龄的影响,本研究探讨了衰老大鼠脑纹状体突触体中多巴胺和血清素合成的相互作用。采用断头法处死3、30月龄雄性Wistar大鼠,采用不连续Ficoll/蔗糖梯度法制备纹状体突触体。突触体在添加pargiline(单胺氧化酶抑制剂)的条件下孵育,用HPLC测定25 min合成的多巴胺或5 -羟色胺,电化学检测。在幼龄动物制备的突触体中,添加5 μ m血清素浓度(30%)可显著抑制多巴胺的合成,而将血清素浓度增加到50 μ m时,只会产生较小的额外抑制作用。老年大鼠突触体中多巴胺的合成明显低于幼鼠,血清素浓度达到50微米时对这些制剂的影响不大。在5 -羟色胺合成方面,外源性添加5 μ m多巴胺可抑制两种年龄大鼠突触体中5 -羟色胺的合成,其抑制率约为40%,而当多巴胺浓度较高(10-50 μ m)时,老年大鼠的抑制率明显高于幼鼠。由此得出结论,多巴胺和血清素的相互作用可能是显著的,在长期使用左旋多巴治疗帕金森病时应考虑到这一点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Age related interaction of dopamine and serotonin synthesis in striatal synaptosomes.
Tyrosine hydroxylase and tryptophan hydroxylase are key rate limiting enzymes in the biosynthesis of dopamine and serotonin, respectively. Since both enzymes are active in striatum, and affected by age, this study was undertaken to investigate interaction between dopamine and serotonin synthesis in brain striatal synaptosomes of aging rat. Male Wistar rats (3 and 30 month old) were killed by decapitation and brain striatal synaptosomes were prepared by discontinuous Ficoll/sucrose gradient technique. Synaptosomes were incubated in the presence of added pargiline (monoamineoxidase inhibitor), dopamine or serotonin synthesized during 25 min was measured by HPLC, employing electrochemical detection. Dopamine synthesis in synaptosomes prepared from young animals was markedly inhibited by addition of 5 microM serotonin concentrations (30%) and increasing serotonin concentrations up to 50 microM caused only a smaller additional inhibition. Dopamine synthesis in synaptosomes obtained from old rats was significantly lower than that of youg animals and addition of serotonin concentrations up to 50 microM had little effect on these preparations. In case of serotonin synthesis, exogenously added 5 microM dopamine inhibited serotonin synthesis in the synaptosomes of both ages by about 40%, whereas with higher concentration of dopamine (10-50 microM) the rate of inhibition was highly pronounced in old rats as compared to that of young animals. It is concluded that dopamine and serotonin interaction may be significant, and that these should be considered in long-term treatments of Parkinson's disease with L-DOPA.
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