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小鼠B16黑色素瘤细胞植入小鼠和大鼠脊髓后的抗伤害感受作用。

Antinociception following implantation of mouse B16 melanoma cells in mouse and rat spinal cord.

作者信息

Wu Hope H, Lester Bruce R, Sun Zhengqi, Wilcox George L

机构信息

Department of Pharmacology, University of Minnesota, Minneapolis, MN 55455 USA Department of Laboratory Medicine and Pathology, University of Minnesota, Minneapolis, MN 55455 USA Department of Graduate Program in Neuroscience, University of Minnesota, Minneapolis, MN 55455 USA.

出版信息

Pain. 1994 Feb;56(2):203-210. doi: 10.1016/0304-3959(94)90095-7.

Abstract

B16 F1C29 melanoma cells, which are thought to contain and release catecholamines, were implanted in mouse and rat spinal subarachnoid space. B16 F1C29 cell implants augmented the antinociceptive effect of morphine in tail-flick test, and this interaction was blocked by either the alpha 2-adrenergic antagonist idazoxan or the opioid antagonist naloxone. B16 F1C29 cell implants also augmented the antinociceptive effect of the catecholamine re-uptake blocker desipramine. Substance P-induced biting and scratching behaviors were inhibited in mice receiving B16 F1C29 cell implants, and this effect of B16 F1C29 cell implants was blocked by the alpha 2-adrenergic antagonist idazoxan. Mice receiving B16 F1C29 cell implants showed tolerance to intrathecal administration of the alpha 2-adrenergic agonist UK 14304. These results suggest that B16 cell implant-induced antinociception was mediated by catecholamines secreted from the cell implants and acting at spinal alpha 2-adrenergic receptors. Spinal implantation of catecholamine-releasing cells may provide an alternative approach for the therapy of chronic intractable pain and a useful model to study alpha 2-adrenergic receptor tolerance.

摘要

B16 F1C29黑色素瘤细胞被认为含有并释放儿茶酚胺,将其植入小鼠和大鼠的脊髓蛛网膜下腔。在甩尾试验中,B16 F1C29细胞植入增强了吗啡的镇痛作用,这种相互作用被α2-肾上腺素能拮抗剂咪唑克生或阿片类拮抗剂纳洛酮阻断。B16 F1C29细胞植入也增强了儿茶酚胺再摄取阻滞剂地昔帕明的镇痛作用。在接受B16 F1C29细胞植入的小鼠中,P物质诱导的咬和抓行为受到抑制,B16 F1C29细胞植入的这种作用被α2-肾上腺素能拮抗剂咪唑克生阻断。接受B16 F1C29细胞植入的小鼠对鞘内注射α2-肾上腺素能激动剂UK 14304表现出耐受性。这些结果表明,B16细胞植入诱导的镇痛是由细胞植入物分泌并作用于脊髓α2-肾上腺素能受体的儿茶酚胺介导的。植入释放儿茶酚胺的细胞可能为慢性顽固性疼痛的治疗提供一种替代方法,并为研究α2-肾上腺素能受体耐受性提供一个有用的模型。

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