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双孢蘑菇β-D-葡聚糖的抗伤害作用可能与蛋白激酶 C 抑制有关。

Antinociception of β-D-glucan from Pleurotus pulmonarius is possibly related to protein kinase C inhibition.

机构信息

Department of Pharmacology, Sector of Biological Sciences, Federal University of Paraná, Curitiba, PR, Brazil.

出版信息

Int J Biol Macromol. 2012 Apr 1;50(3):872-7. doi: 10.1016/j.ijbiomac.2011.10.023. Epub 2011 Nov 6.

Abstract

β-D-Glucan, a polysaccharide isolated from an edible mushroom Pleurotus pulmonarius (Fr.) Quel., presented antinociceptive activity in mice. This study evaluated the involvement of transient receptor potential (TRP) channels and protein kinase C (PKC) on antinociceptive effect of a (1→3),(1→6)-linked β-D-glucan (GL) in mice. Intraperitoneal administration of GL potently inhibited nociceptive responses induced by intraplantar injections of capsaicin, cinnamaldehyde, menthol, acidified saline and phorbol myristate acetate (PMA). Moreover, Western blot analysis revealed that GL treatment also prevented PMA-induced PKCɛ activation. Collectively, present results demonstrate that GL could constitute an attractive molecule of interest for the development of new analgesic drugs.

摘要

β-D-葡聚糖是一种从食用蘑菇杏鲍菇(Fr.) Quel. 中分离出来的多糖,具有抗伤害感受活性。本研究评估了瞬时受体电位(TRP)通道和蛋白激酶 C(PKC)在(1→3)、(1→6)-连接的 β-D-葡聚糖(GL)对小鼠抗伤害感受作用中的作用。腹腔内给予 GL 可有效抑制足底注射辣椒素、肉桂醛、薄荷醇、酸化盐水和十四烷酰佛波醇乙酸酯(PMA)引起的伤害感受反应。此外,Western blot 分析显示,GL 处理还可防止 PMA 诱导的 PKCɛ 激活。综上所述,本研究结果表明 GL 可能成为开发新型镇痛药的有吸引力的候选分子。

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