{"title":"服用可卡因可保护肠道粘膜屏障,降低血浆中 TNF-α 的水平。","authors":"Xiaoyu Fu, Chuanxiu Bian, Anna Kruyer, Zejun Zhou, Zhenwu Luo, Azizul Haque, Amanda Wagner, Ren Lang, Sylvia Fitting, Catrina Robinson, Aimee McRae-Clark, Davide Amato, Wei Jiang","doi":"10.2174/2211556011666220818091709","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Cocaine affects not only the central nervous system, but also systemic immunity. The role of cocaine in gut mucosal integrity is not fully understood.</p><p><strong>Methods: </strong>Here we evaluated the effect of cocaine use on gut endothelial permeability and system inflammation in rats that self-administered cocaine or saline and in humans using immunohistochemistry, qPCR, ELISA, and Transepithelial/transendothelial electrical resistance (TEER).</p><p><strong>Results: </strong>Cocaine administration maintained intact and undisturbed intestinal mucosal structures, increased tight junction claudin 1 and 2 mRNA expression, and decreased plasma TNF-α levels, compared to the control group, at the end of study in rats. Further, cocaine treatment decreased gut endothelial permeability in a dose-dependent manner in human epithelial Caco-2 cells <i>in vitro</i>. Consistently, chronic cocaine users exhibited decreased plasma levels of TNF-α compared with non-drug users <i>in vivo</i>. However, plasma IL-6 levels were similar between cocaine use and control groups both in humans and rats <i>in vivo</i>.</p><p><strong>Conclusions: </strong>Our results from both human and rat studies <i>in vivo</i> and <i>in vitro</i> suggest that cocaine use may exert a protective effect on the integrity of gut mucosa and suppresses plasma TNF-α levels. This study may provide information on some beneficial effects of cocaine use on gut endothelial cells integrity and systemic inflammation.</p>","PeriodicalId":10751,"journal":{"name":"Current Psychopharmacology","volume":"11 2","pages":"1-8"},"PeriodicalIF":0.0000,"publicationDate":"2022-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9974179/pdf/nihms-1832033.pdf","citationCount":"0","resultStr":"{\"title\":\"Cocaine administration protects gut mucosa barrier and reduces plasma level of TNF-α.\",\"authors\":\"Xiaoyu Fu, Chuanxiu Bian, Anna Kruyer, Zejun Zhou, Zhenwu Luo, Azizul Haque, Amanda Wagner, Ren Lang, Sylvia Fitting, Catrina Robinson, Aimee McRae-Clark, Davide Amato, Wei Jiang\",\"doi\":\"10.2174/2211556011666220818091709\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>Cocaine affects not only the central nervous system, but also systemic immunity. The role of cocaine in gut mucosal integrity is not fully understood.</p><p><strong>Methods: </strong>Here we evaluated the effect of cocaine use on gut endothelial permeability and system inflammation in rats that self-administered cocaine or saline and in humans using immunohistochemistry, qPCR, ELISA, and Transepithelial/transendothelial electrical resistance (TEER).</p><p><strong>Results: </strong>Cocaine administration maintained intact and undisturbed intestinal mucosal structures, increased tight junction claudin 1 and 2 mRNA expression, and decreased plasma TNF-α levels, compared to the control group, at the end of study in rats. Further, cocaine treatment decreased gut endothelial permeability in a dose-dependent manner in human epithelial Caco-2 cells <i>in vitro</i>. Consistently, chronic cocaine users exhibited decreased plasma levels of TNF-α compared with non-drug users <i>in vivo</i>. However, plasma IL-6 levels were similar between cocaine use and control groups both in humans and rats <i>in vivo</i>.</p><p><strong>Conclusions: </strong>Our results from both human and rat studies <i>in vivo</i> and <i>in vitro</i> suggest that cocaine use may exert a protective effect on the integrity of gut mucosa and suppresses plasma TNF-α levels. This study may provide information on some beneficial effects of cocaine use on gut endothelial cells integrity and systemic inflammation.</p>\",\"PeriodicalId\":10751,\"journal\":{\"name\":\"Current Psychopharmacology\",\"volume\":\"11 2\",\"pages\":\"1-8\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2022-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9974179/pdf/nihms-1832033.pdf\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Current Psychopharmacology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.2174/2211556011666220818091709\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2022/9/12 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current Psychopharmacology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.2174/2211556011666220818091709","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2022/9/12 0:00:00","PubModel":"Epub","JCR":"","JCRName":"","Score":null,"Total":0}
Cocaine administration protects gut mucosa barrier and reduces plasma level of TNF-α.
Background: Cocaine affects not only the central nervous system, but also systemic immunity. The role of cocaine in gut mucosal integrity is not fully understood.
Methods: Here we evaluated the effect of cocaine use on gut endothelial permeability and system inflammation in rats that self-administered cocaine or saline and in humans using immunohistochemistry, qPCR, ELISA, and Transepithelial/transendothelial electrical resistance (TEER).
Results: Cocaine administration maintained intact and undisturbed intestinal mucosal structures, increased tight junction claudin 1 and 2 mRNA expression, and decreased plasma TNF-α levels, compared to the control group, at the end of study in rats. Further, cocaine treatment decreased gut endothelial permeability in a dose-dependent manner in human epithelial Caco-2 cells in vitro. Consistently, chronic cocaine users exhibited decreased plasma levels of TNF-α compared with non-drug users in vivo. However, plasma IL-6 levels were similar between cocaine use and control groups both in humans and rats in vivo.
Conclusions: Our results from both human and rat studies in vivo and in vitro suggest that cocaine use may exert a protective effect on the integrity of gut mucosa and suppresses plasma TNF-α levels. This study may provide information on some beneficial effects of cocaine use on gut endothelial cells integrity and systemic inflammation.