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乳铁蛋白通过一氧化氮增强大鼠脊髓中阿片类药物介导的镇痛作用。

Lactoferrin enhances opioid-mediated analgesia via nitric oxide in the rat spinal cord.

作者信息

Hayashida Ken-ichiro, Takeuchi Takashi, Shimizu Hirohiko, Ando Kunio, Harada Etsumori

机构信息

Department of Veterinary Physiology, Faculty of Agriculture, Tottori University, Tottori 680-0945, Japan.

出版信息

Am J Physiol Regul Integr Comp Physiol. 2003 Aug;285(2):R306-12. doi: 10.1152/ajpregu.00760.2002. Epub 2003 Apr 17.

Abstract

Lactoferrin (LF) is a multifunctional protein that is found in milk, neutrophils, and other biological fluids, and its receptors have also been identified in the central nervous system. Recently, we found that bovine milk-derived LF (BLF) produced analgesia via a mu-opioid receptor-mediated response in the spinal cord. However, the precise mechanism of this analgesic effect remains unclear. In this study, spinally applied BLF produced analgesia that was reversed by coadministration with a nitric oxide (NO) synthase inhibitor, NG-nitro-l-arginine methyl ester, during phases 1 and 2 in the formalin test. Spinal coadministration of a mu-opioid receptor agonist, morphine, with a subeffective dose of BLF produced a much more highly potentiated analgesia than that produced by morphine alone during phases 1 and 2 in the formalin test. This potentiated analgesia by morphine with BLF was reversed by a mu-opioid receptor antagonist, d-Phe-Cys-Tyr-d-Trp-Orn-Thr-NH2, or by NG-nitro-l-arginine methyl ester. In the tail-flick test, continuous spinal infusion of morphine via an osmotic minipump over 6 days resulted in development of tolerance by day 4, but no tolerance of BLF was observed throughout the experiment. These results suggest that BLF acts as an enhancer of the spinal opioidergic system via an NO-mediated mechanism.

摘要

乳铁蛋白(LF)是一种多功能蛋白质,存在于牛奶、中性粒细胞及其他生物体液中,其受体也已在中枢神经系统中被鉴定出来。最近,我们发现源自牛乳的乳铁蛋白(BLF)通过脊髓中μ-阿片受体介导的反应产生镇痛作用。然而,这种镇痛作用的确切机制尚不清楚。在本研究中,在福尔马林试验的第1和第2阶段,脊髓给予BLF产生的镇痛作用可被与一氧化氮(NO)合酶抑制剂NG-硝基-L-精氨酸甲酯共同给药所逆转。在福尔马林试验的第1和第2阶段,脊髓共同给予μ-阿片受体激动剂吗啡和亚有效剂量的BLF产生的镇痛作用比单独给予吗啡更强。吗啡与BLF共同产生的这种增强的镇痛作用可被μ-阿片受体拮抗剂d-苯丙氨酸-半胱氨酸-酪氨酸-d-色氨酸-鸟氨酸-苏氨酸-NH2或NG-硝基-L-精氨酸甲酯逆转。在甩尾试验中,通过渗透微型泵连续6天脊髓输注吗啡,到第4天会产生耐受性,但在整个实验过程中未观察到BLF产生耐受性。这些结果表明,BLF通过NO介导的机制作为脊髓阿片能系统的增强剂。

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