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乳铁蛋白通过一氧化氮增强大鼠外周阿片类药物介导的抗伤害感受作用。

Lactoferrin enhances peripheral opioid-mediated antinociception via nitric oxide in rats.

作者信息

Hayashida Ken-ichiro, Takeuchi Takashi, Harada Etsumori

机构信息

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

出版信息

Eur J Pharmacol. 2004 Jan 26;484(2-3):175-81. doi: 10.1016/j.ejphar.2003.11.007.

Abstract

Lactoferrin (LF) is a multifunctional protein found in various biological fluids. However, the peripheral action of lactoferrin remains unknown. In this study, peripherally applied bovine lactoferrin showed antinociceptive effect that was reversed by a mu-opioid receptor antagonist, D-Phe-Cys-Tyr-D-Trp-Orn-Thr-NH(2) (CTOP), or by a nitric oxide synthase (NOS) inhibitor, N(G)-nitro-L-arginine methyl ester (L-NAME), but not by an inactive enantiomer of L-NAME, N(G)-nitro-D-arginine methyl ester (D-NAME), during phase 1 and phase 2 in the rat formalin test. Peripheral coadministration of a micro-opioid receptor agonist, morphine, with subeffective dose of bovine lactoferrin produced a potentiated antinociceptive effect compared to that of morphine alone during both phases in the formalin test. This potentiated antinociception by morphine with bovine lactoferrin was reversed by CTOP or by L-NAME. These results suggest that bovine lactoferrin exerts an antinociceptive activity via potentiation of the peripheral micro-opioidergic system, and that nitric oxide (NO) is involved in this potentiation.

摘要

乳铁蛋白(LF)是一种存在于多种生物体液中的多功能蛋白质。然而,乳铁蛋白的外周作用尚不清楚。在本研究中,在大鼠福尔马林试验的第1阶段和第2阶段,外周应用牛乳铁蛋白显示出抗伤害感受作用,该作用可被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-酰胺(CTOP)或一氧化氮合酶(NOS)抑制剂N-硝基-L-精氨酸甲酯(L-NAME)逆转,但不能被L-NAME的无活性对映体N-硝基-D-精氨酸甲酯(D-NAME)逆转。在福尔马林试验的两个阶段中,与单独使用吗啡相比,微阿片受体激动剂吗啡与亚有效剂量的牛乳铁蛋白外周联合给药产生了增强的抗伤害感受作用。吗啡与牛乳铁蛋白联合使用所产生的这种增强的抗伤害感受作用可被CTOP或L-NAME逆转。这些结果表明,牛乳铁蛋白通过增强外周微阿片能系统发挥抗伤害感受活性,并且一氧化氮(NO)参与了这种增强作用。

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