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氯胺酮类似物甲氧基氯胺酮诱导大鼠膀胱炎症和功能障碍。

Ketamine Analog Methoxetamine Induced Inflammation and Dysfunction of Bladder in Rats.

作者信息

Wang Qiang, Wu Qinghui, Wang Junpeng, Chen Yang, Zhang Guihao, Chen Jiawei, Zhao Jie, Wu Peng

机构信息

Department of Urology, Nanfang Hospital, Southern Medical University, Guangzhou 510515, China.

School of Pharmaceutical Sciences, Southern Medical University, Guangzhou 510515, China.

出版信息

Int J Mol Sci. 2017 Jan 18;18(1):117. doi: 10.3390/ijms18010117.

Abstract

The novel synthetic psychoactive ketamine analog methoxetamine is reportedly being used for recreational purposes. As ketamine use can result in urinary dysfunction, we conducted the present study to investigate how methoxetamine affects the bladder. A cystometry investigation showed that female Sprague-Dawley rats experienced increased micturition frequency bladder dysfunction after receiving a daily intraperitoneal injection of 30 mg/kg methoxetamine or ketamine for periods of 4 or 12 weeks. Histologic examinations of rat bladder tissue revealed damaged urothelium barriers, as well as evidence of inflammatory cell infiltration and matrix deposition. The drug-treated rats showed significantly upregulated levels of pro-inflammatory cytokines such as IL-1β, IL-6, CCL-2, CXCL-1, CXCL-10, NGF, and COX-2. In addition, interstitial fibrosis was confirmed by increased levels of collagen I, collagen III, fibronectin and TGF-β. Besides direct toxic effect on human urothelial cells, methoxetaminealso induced the upregulation related cytokines. Our results indicate that long term methoxetamine treatment can induce bladder dysfunction and inflammation in rats. Methoxetamine was confirmed to produce direct toxic and pro-inflammatory effects on human urothelial cells. Methoxetamine-associated bladder impairment may be similar to ketamine-induced cystitis.

摘要

据报道,新型合成精神活性物质氯胺酮类似物甲氧基乙胺正被用于娱乐目的。由于氯胺酮的使用会导致排尿功能障碍,我们开展了本研究以探究甲氧基乙胺如何影响膀胱。膀胱内压测量研究表明,雌性斯普拉格-道利大鼠在每天腹腔注射30mg/kg甲氧基乙胺或氯胺酮,持续4周或12周后,出现排尿频率增加的膀胱功能障碍。对大鼠膀胱组织的组织学检查显示尿路上皮屏障受损,以及炎症细胞浸润和基质沉积的证据。经药物处理的大鼠显示促炎细胞因子如IL-1β、IL-6、CCL-2、CXCL-1、CXCL-10、NGF和COX-2的水平显著上调。此外,通过I型胶原、III型胶原、纤连蛋白和TGF-β水平的升高证实了间质纤维化。除了对人尿路上皮细胞有直接毒性作用外,甲氧基乙胺还诱导相关细胞因子上调。我们的结果表明,长期给予甲氧基乙胺可诱导大鼠膀胱功能障碍和炎症。已证实甲氧基乙胺对人尿路上皮细胞产生直接毒性和促炎作用。与甲氧基乙胺相关的膀胱损伤可能与氯胺酮诱发的膀胱炎相似。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4096/5297751/f35b39be8e8d/ijms-18-00117-g001.jpg

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