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大麻素和吗啡对CD4(+)淋巴细胞及小胶质细胞培养物中HIV-1的表达有不同影响。

Cannabinoids and morphine differentially affect HIV-1 expression in CD4(+) lymphocyte and microglial cell cultures.

作者信息

Peterson P K, Gekker G, Hu S, Cabral G, Lokensgard J R

机构信息

Minneapolis Medical Research Foundation, 914 S. Eighth Street, Minneapolis, MN 55404, USA.

出版信息

J Neuroimmunol. 2004 Feb;147(1-2):123-6. doi: 10.1016/j.jneuroim.2003.10.026.

Abstract

The influence of substances of abuse on the progression of HIV-1 infection is controversial, and pharmacologic factors have been postulated as a potential explanation for conflicting data arising from epidemiological studies and animal models. In the present study, cell culture models of HIV-1 infection were used to test this hypothesis. The synthetic cannabinoid WIN 55,212-2 was found to potently inhibit HIV-1 expression in a concentration- and time-dependent manner in CD4(+) lymphocyte and microglial cell cultures. In sharp contrast, morphine either inhibited or stimulated viral expression, depending upon the time of drug exposure, and marked differences were observed between CD4(+) and microglial cells. Also, WIN 55,212-2 inhibited the stimulatory effect of morphine in HIV-1 infected CD4(+) cells. These in vitro findings support the notion that pharmacologic factors need to be considered in epidemiological studies and animal models that pertain to HIV-1 infection.

摘要

滥用物质对HIV-1感染进展的影响存在争议,药理学因素被认为是流行病学研究和动物模型中出现相互矛盾数据的一个潜在解释。在本研究中,HIV-1感染的细胞培养模型被用于检验这一假设。发现在CD4(+)淋巴细胞和小胶质细胞培养中,合成大麻素WIN 55,212-2以浓度和时间依赖性方式有效抑制HIV-1表达。与之形成鲜明对比的是,吗啡根据药物暴露时间不同,要么抑制要么刺激病毒表达,并且在CD4(+)细胞和小胶质细胞之间观察到显著差异。此外,WIN 55,212-2抑制吗啡对HIV-1感染的CD4(+)细胞的刺激作用。这些体外研究结果支持了这样一种观点,即在与HIV-1感染相关的流行病学研究和动物模型中需要考虑药理学因素。

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