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鞘内注射5-羟色胺对大鼠交感神经活动的兴奋和抑制作用。

Excitatory and inhibitory actions of intrathecally administered 5-hydroxytryptamine on sympathetic nerve activity in the rat.

作者信息

Yusof A P, Coote J H

机构信息

Department of Physiology, Medical School, University of Birmingham, U.K.

出版信息

J Auton Nerv Syst. 1988 Apr;22(3):229-36. doi: 10.1016/0165-1838(88)90111-7.

Abstract

In chloralose/urethane anaesthetised rats the effect of intrathecal (i.t.) administration of 5-hydroxytryptamine (5-HT) on activity in sympathetic nerves to the kidney was studied. Intrathecal 5-HT (20-100 micrograms, 10 microliter) increased activity in renal nerves (mean change for 50 micrograms dose 157% +/- 39). At higher doses of 5-HT the initial excitatory response was followed by inhibition 64% +/- 15. Intrathecally, alpha methyl 5-HT (10-400 micrograms) mimicked only the inhibitory action of 5-HT in a dose-dependent manner. These inhibitions were completely antagonised by i.t. ketanserin (25-100 micrograms). Intrathecal 2 methyl 5-HT (10-200 micrograms) had little effect on renal nerve activity. Intrathecal 5 carboxyamidotryptamine (10-200 micrograms) had a more powerful excitatory action on renal nerve activity than did 5-HT. Intrathecally, 8 OH-DPAT (10-200 micrograms) was without effect. Neither the inhibitory action of 5-HT or the excitatory action was affected by i.t. ICS 205 930 (1-10 micrograms) or MDL 72222 (200 micrograms). It was concluded that the actions of 5-HT were within the spinal cord and that the inhibitory effect on sympathetic activity is mediated via a 5-HT2-like receptor whilst the receptors involved in the excitatory action of 5-HT are not M- or 5-HT3-like but appear to be more like the 5-HT1 subtype.

摘要

在水合氯醛/乌拉坦麻醉的大鼠中,研究了鞘内注射5-羟色胺(5-HT)对肾交感神经活动的影响。鞘内注射5-HT(20-100微克,10微升)可增加肾神经活动(50微克剂量的平均变化为157%±39)。在较高剂量的5-HT作用下,最初的兴奋反应之后是抑制作用(64%±15)。鞘内注射α-甲基5-HT(10-400微克)仅以剂量依赖性方式模拟5-HT的抑制作用。这些抑制作用被鞘内注射酮色林(25-100微克)完全拮抗。鞘内注射2-甲基5-HT(10-200微克)对肾神经活动影响很小。鞘内注射5-羧基酰胺色胺(10-200微克)对肾神经活动的兴奋作用比5-HT更强。鞘内注射8-OH-DPAT(10-200微克)无作用。5-HT的抑制作用或兴奋作用均不受鞘内注射ICS 205 930(1-10微克)或MDL 72222(200微克)的影响。得出的结论是,5-HT的作用发生在脊髓内,对交感神经活动的抑制作用是通过5-HT2样受体介导的,而参与5-HT兴奋作用的受体不是M样或5-HT3样受体,似乎更类似于5-HT1亚型。

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