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胍乙啶对大鼠颈上神经节小而强荧光细胞中多巴胺的影响。

Effect of guanethidine on dopamine in small intensely fluorescent cells of the superior cervical ganglion of the rat.

作者信息

Borghini N, Dalmaz Y, Peyrin L

机构信息

UA CNRS 1196, Laboratoire de Physiologie, Faculté de Médecine Lyon Grange-Blanche, France.

出版信息

J Auton Nerv Syst. 1991 Jan;32(1):13-9. doi: 10.1016/0165-1838(91)90230-z.

Abstract

To determine the portion of ganglionic dopamine stored in the small intensely fluorescent (SIF) cells of the superior cervical ganglion, rats were treated chronically with the neurotoxin guanethidine (50 mg/kg i.p. daily for 6, 13 or 18 days) which destroys noradrenergic neurons. The guanethidine effect was assessed in the ganglion using biochemistry of dopamine and norepinephrine and immunocytochemistry of tyrosine hydroxylase (TH) and dopamine beta-hydroxylase (DBH). After 18 days of treatment, the ganglionic norepinephrine content was reduced by 80%, but the dopamine content was reduced by only 20%. Morphologic analysis of ganglia stained to distinguish noradrenergic neurons (TH positive, DBH positive) and SIF cells (TH positive, DBH negative) indicated that guanethidine treatment reduced the number of noradrenergic neurons by 70%, dropping from 19413 +/- 1402 to 6515 +/- 1296 per ganglion, but increased the number of dopaminergic SIF cells by 80% from 578 +/- 150 to 1056 +/- 151 per ganglion. Based on these findings, it is concluded that a substantial portion of the dopamine in the rat superior cervical ganglion is located outside the noradrenergic neurons, i.e. in the SIF cells. Extrapolating the data obtained using guanethidine versus control rat leads to infer that although the proportion of SIF cells in the superior cervical ganglion is small (3 +/- 1% of the SIF and noradrenergic neurons combined), about 40% of the total ganglionic dopamine resides in SIF cells, with the remainder serving as precursor in noradrenergic neurons.

摘要

为了确定颈上神经节中小而密集荧光(SIF)细胞中储存的神经节多巴胺的比例,对大鼠长期给予神经毒素胍乙啶(每天腹腔注射50mg/kg,持续6、13或18天),该毒素会破坏去甲肾上腺素能神经元。使用多巴胺和去甲肾上腺素的生物化学以及酪氨酸羟化酶(TH)和多巴胺β-羟化酶(DBH)的免疫细胞化学方法评估胍乙啶对神经节的作用。治疗18天后,神经节中的去甲肾上腺素含量降低了80%,但多巴胺含量仅降低了20%。对神经节进行形态学分析,以区分去甲肾上腺素能神经元(TH阳性,DBH阳性)和SIF细胞(TH阳性,DBH阴性),结果表明胍乙啶治疗使去甲肾上腺素能神经元数量减少了70%,每个神经节从19413±1402个降至6515±1296个,但使多巴胺能SIF细胞数量增加了80%,从每个神经节578±150个增至1056±151个。基于这些发现,得出结论:大鼠颈上神经节中相当一部分多巴胺位于去甲肾上腺素能神经元之外,即在SIF细胞中。根据使用胍乙啶的大鼠与对照大鼠获得的数据推断,尽管颈上神经节中SIF细胞的比例很小(占SIF细胞和去甲肾上腺素能神经元总数的3±1%),但约40%的神经节总多巴胺存在于SIF细胞中,其余的则作为去甲肾上腺素能神经元的前体。

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