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吗啡和去甲肾上腺素在脊髓水平诱导的镇痛作用是由腺苷介导的。

Morphine and norepinephrine-induced antinociception at the spinal level is mediated by adenosine.

作者信息

Yang S W, Zhang Z H, Chen J Y, Xie Y F, Qiao J T, Dafny N

机构信息

Department of Neurobiology, Shanxi Medical College, Taiyuan, P.R. China.

出版信息

Neuroreport. 1994 Jul 21;5(12):1441-4. doi: 10.1097/00001756-199407000-00009.

Abstract

The purpose of this study was to examine whether adenosine or serotonin is involved in mediation of the antinociception produced by norepinephrine at the spinal cord level. Aminophylline, an adenosine receptor antagonist and naloxone given intrathecally (i.t.) were used to test the antinociception produced by i.t. norepinephrine, serotonin, morphine or the adenosine receptor agonist 5'-N-ethylcarboxamidoadenosine (NECA) by using the tail-flick assay in rats. It was observed that (1) aminophylline blocked the antinociception produced by norepinephrine, but exhibited no effect on the antinociception produced by serotonin, (2) aminophylline blocked the antinociception produced by morphine similarly to naloxone, (3) aminophylline blocked the antinociception produced by NECA and (4) naloxone failed to block the antinociception produced by NECA and serotonin. The results suggest that adenosine is involved in mediation of the norepinephrine-produced antinociception at the spinal level and that norepinephrine and adenosine may act in a sequential manner in norepinephrine-induced antinociception.

摘要

本研究的目的是检验腺苷或5-羟色胺是否参与去甲肾上腺素在脊髓水平产生的镇痛作用的介导过程。通过在大鼠身上采用甩尾试验,使用鞘内注射(i.t.)的腺苷受体拮抗剂氨茶碱和纳洛酮,来测试鞘内注射去甲肾上腺素、5-羟色胺、吗啡或腺苷受体激动剂5'-N-乙基羧酰胺腺苷(NECA)所产生的镇痛作用。观察到:(1)氨茶碱阻断了去甲肾上腺素产生的镇痛作用,但对5-羟色胺产生的镇痛作用无影响;(2)氨茶碱与纳洛酮类似,阻断了吗啡产生的镇痛作用;(3)氨茶碱阻断了NECA产生的镇痛作用;(4)纳洛酮未能阻断NECA和5-羟色胺产生的镇痛作用。结果表明,腺苷参与了去甲肾上腺素在脊髓水平产生的镇痛作用的介导过程,并且去甲肾上腺素和腺苷在去甲肾上腺素诱导的镇痛作用中可能按顺序发挥作用。

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