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Chloroquine-induced scratching is mediated by NO/cGMP pathway in mice

机译:氯喹诱导的scratch抓是通过NO / cGMP途径介导的

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Chloroquine (CQ), a 4-aminoquinoline drug, has long been used in the treatment and prevention of malaria. However its side effect generalized pruritus contributes to treatment failures, and consequently results in the development of chloroquine resistant strains of Plasmodium falciparum. It was proposed that the administration of CQ correlated with increase in nitric oxide (NO) production. Nitric oxide is involved in some pruritic disorders such as atopic dermatitis, psoriasis and scratching behavior evoked by pruritogens like substance P. Therefore, the aim of this study was to investigate the involvement of NO/cGMP pathway in CQ-induced scratching in mice. Scratching behaviors were recorded by a camera after intradermal (ID) injection of CQ in the shaved rostral back of the mice. The results obtained show that CQelicited scratching in a dose-dependent manner with a peak effective dose of 400 mu g/site. Injection of non-specific NOS inhibitor, N-nitro-L-arginine methyl ester or neuronal NOS selective inhibitor and 7-nitroindazole, reduced CQ-induced scratching significantly. On the other hand, administration of aminoguanidine as inducible NOS inhibitor has no inhibitory effect on this behavior. Also, injection of L-arginine as a precursor of NO significantly increased this response. Conversely, accumulation of cGMP by sildenafil as a selective phosphodiesterase type 5 inhibitor, potentiated the scratching behavior by al This study therefore shows that CQ-induced scratching behavior is mediated by the NO/cGMP pathway. (C) 2015 Elsevier Inc. All rights reserved.
机译:氯喹(CQ)是一种4-氨基喹啉药物,长期以来一直用于治疗和预防疟疾。然而,其普遍性瘙痒的副作用导致治疗失败,并因此导致恶性疟原虫的氯喹抗药性菌株的发展。有人提出CQ的管理与一氧化氮(NO)产量的增加有关。一氧化氮与某些瘙痒性疾病有关,例如特应性皮炎(如P物质)引起的特应性皮炎,牛皮癣和抓挠行为。因此,本研究的目的是研究NO / cGMP途径与CQ诱导的小鼠抓挠有关。皮内(ID)注射CQ在小鼠剃毛的鼻背后,用相机记录其抓痒行为。获得的结果表明,CQ以剂量依赖的方式引起刮擦,峰值有效剂量为400μg /位。注射非特异性NOS抑制剂,N-硝基-L-精氨酸甲酯或神经元NOS选择性抑制剂和7-硝基吲唑,可显着降低CQ诱导的抓挠。另一方面,给予氨基胍作为可诱导的NOS抑制剂对此行为没有抑制作用。而且,注射L-精氨酸作为NO的前体显着增加了该反应。相反,西地那非作为选择性5型磷酸二酯酶抑制剂对cGMP的蓄积增强了所有动物的抓挠行为。因此,这项研究表明CQ诱导的抓挠行为是由NO / cGMP途径介导的。 (C)2015 Elsevier Inc.保留所有权利。

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