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茶碱诱导的小鼠伤害性行为反应:与脊髓 N-甲基-D-天冬氨酸受体可能的间接相互作用。

Theophylline-induced nociceptive behavioral response in mice: possible indirect interaction with spinal N-methyl-D-aspartate receptors.

作者信息

Nagaoka H, Sakurada S, Sakurada T, Takeda S, Nakagawa Y, Kisara K, Arai Y

机构信息

Department of Pharmacy, Yamagata University Hospital, Japan.

出版信息

Neurochem Int. 1993 Jan;22(1):69-74. doi: 10.1016/0197-0186(93)90070-l.

Abstract

Intrathecal administration of an adenosine receptor antagonist, theophylline, elicited nociceptive behavior such as licking, biting and scratching in mice. This behavioral response was dose-dependently reduced by simultaneous injection of an adenosine receptor agonist, 5'-N6-ethylcarboxamidoadenosine, or a selective N-methyl-D-aspartate (NMDA) receptor antagonist, D-2-amino-5-phosphonovalerate. This theophylline-induced behavior was not significantly reduced by the substance P (SP) analogue, the neurokinin receptor antagonist, [D-Arg1, D-Trp7.9, Leu11]SP (spantide). These results suggest the possibility that theophylline-induced nociceptive behavior may be mediated through interactions with both spinal adenosine- and NMDA receptors separately, or only through interaction(s) with adenosine receptors localized on the axon terminals of excitatory amino acid neurons. Present data have failed to reveal involvement of SP.

摘要

鞘内注射腺苷受体拮抗剂茶碱可引发小鼠出现舔舐、咬和抓挠等伤害感受行为。同时注射腺苷受体激动剂5'-N6-乙基羧基酰胺腺苷或选择性N-甲基-D-天冬氨酸(NMDA)受体拮抗剂D-2-氨基-5-磷酸戊酸,这种行为反应会呈剂量依赖性降低。P物质(SP)类似物、神经激肽受体拮抗剂[D-Arg1, D-Trp7.9, Leu11]SP(spantide)并未显著降低茶碱诱导的行为。这些结果表明,茶碱诱导的伤害感受行为可能分别通过与脊髓腺苷受体和NMDA受体相互作用来介导,或者仅通过与兴奋性氨基酸神经元轴突终末上的腺苷受体相互作用来介导。目前的数据未能揭示SP的参与情况。

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