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硫酸镁通过激活 L-精氨酸/一氧化氮/环鸟苷酸途径诱导小鼠外周镇痛。

Magnesium sulphate activates the L-arginine/NO/cGMP pathway to induce peripheral antinociception in mice.

机构信息

Department of Pharmacology, Institute of Biological Sciences, Federal University of Minas Gerais (UFMG), Av. Antônio Carlos, 6627, 31.270-100, Belo Horizonte, Brazil

出版信息

Magnes Res. 2022 Jan 1;35(1):1-10. doi: 10.1684/mrh.2022.0495.

Abstract

In the present study, we investigated whether magnesium sulphate activates the L-arginine/NO/cGMP pathway and elicits peripheral antinociception. The male Swiss mice paw pressure test was performed with hyperalgesia induced by intraplantar injection of prostaglandin E2. All drugs were administered locally into the right hind paw of animals. Magnesium sulphate (20, 40, 80 and 160 μg/paw) induced an antinociceptive effect. The dose of 80 μg/paw elicited a local antinociceptive effect that was antagonized by the non-selective NOS inhibitor, L-NOArg, and by the selective neuronal NOS inhibitor, L-NPA. The inhibitors, L-NIO and L-NIL, selectively inhibited endothelial and inducible NOS, respectively, but were ineffective regarding peripheral magnesium sulphate injection. The soluble guanylyl cyclase inhibitor, ODQ, blocked the action of magnesium sulphate, and the cGMP-phosphodiesterase inhibitor, zaprinast, enhanced the antinociceptive effects of intermediate dose of magnesium sulphate. Our results suggest that magnesium sulphate stimulates the NO/cGMP pathway via neuronal NO synthase to induce peripheral antinociceptive effects.

摘要

在本研究中,我们研究了硫酸镁是否通过激活 L-精氨酸/NO/cGMP 途径来产生外周镇痛作用。采用前列腺素 E2 足底注射诱导的雄性瑞士小鼠足底压痛试验来进行研究。所有药物均局部注射到动物的右后足底。硫酸镁(20、40、80 和 160μg/足底)可诱导镇痛作用。80μg/足底的剂量可产生局部镇痛作用,该作用可被非选择性 NOS 抑制剂 L-NOArg 和选择性神经元 NOS 抑制剂 L-NPA 拮抗。抑制剂 L-NIO 和 L-NIL 分别选择性地抑制内皮型和诱导型 NOS,但对硫酸镁的外周注射无效。可溶性鸟苷酸环化酶抑制剂 ODQ 阻断了硫酸镁的作用,而 cGMP 磷酸二酯酶抑制剂扎普司特增强了硫酸镁中间剂量的镇痛作用。我们的结果表明,硫酸镁通过神经元型一氧化氮合酶刺激 NO/cGMP 途径来诱导外周镇痛作用。

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