STD/AIDS Research Center, Department of Infectious Diseases, Beijing You An Hospital, Capital Medical University, Beijing 100069, China.
Brain Res. 2012 Jan 11;1431:13-22. doi: 10.1016/j.brainres.2011.10.053. Epub 2011 Nov 6.
Although combined antiretroviral therapy has significantly improved the prognosis of HIV-1 infected patients and decreased the incidence of HIV-1 associated dementia, the cumulative prevalence of this disease, in particular, mild or asymptomatic neurocognitive impairment, has not decreased. Thus, in addition to active antiretroviral therapy, the search for an effective neuroprotective approach is very important. Sigma-1 receptors are widely distributed in the central nervous system. Sigma-1 receptor agonists are robustly neuroprotective in many neuropathy and neurotoxicity in vivo and in vitro studies. This study aims to investigate possible neuroprotective effects of sigma-1 receptor agonist, 4-phenyl-1-(4-phenylbutyl) piperidine (PPBP) against HIV-1 protein gp120. Primary cortical neuronal cultures were exposed to gp120 in different concentrations; to investigate neuroprotective effects of sigma-1 receptor agonist, cells were pre-treated with PPBP (10μM) in the presence or absence of pre-incubated sigma-1 receptor antagonist rimcazole (5μM). Cell apoptosis was confirmed with calcein/PI uptake test, lactate dehydrogenase (LDH) leakage assay or TUNEL assay and neurite degeneration was evaluated with morphometry via MAP-2 stained immunofluorescence. The mRNA and protein levels of apoptosis associated bax and bcl-2 were determined with real-time qPCR and Western blot. The results showed that gp120 could induce neuronal apoptosis and neurite degeneration in a concentration dependent manner and PPBP could attenuate the neurotoxicity of gp120. Simultaneously, gp120 could induce low expression of bcl-2 and bax, but only low expression of bcl-2 could be reversed by PPBP. The present data suggest that PPBP, at least, in part protects the neuron against gp120 by regulating bcl-2 expression.
虽然联合抗逆转录病毒疗法显著改善了 HIV-1 感染患者的预后,并降低了 HIV-1 相关痴呆的发生率,但这种疾病的累积患病率,特别是轻度或无症状的神经认知障碍,并没有降低。因此,除了积极的抗逆转录病毒治疗外,寻找有效的神经保护方法非常重要。西格玛-1 受体广泛分布于中枢神经系统。西格玛-1 受体激动剂在许多神经病和神经毒性的体内和体外研究中具有很强的神经保护作用。本研究旨在探讨西格玛-1 受体激动剂 4-苯基-1-(4-苯基丁基)哌啶(PPBP)对 HIV-1 蛋白 gp120 的可能神经保护作用。原代皮质神经元培养物暴露于不同浓度的 gp120 中;为了研究西格玛-1 受体激动剂的神经保护作用,细胞先用 PPBP(10μM)预处理,存在或不存在预先孵育的西格玛-1 受体拮抗剂 Rimcazole(5μM)。用 calcein/PI 摄取试验、乳酸脱氢酶(LDH)渗漏试验或 TUNEL 试验证实细胞凋亡,用 MAP-2 染色免疫荧光通过形态计量学评估神经突退化。用实时 qPCR 和 Western blot 测定凋亡相关 bax 和 bcl-2 的 mRNA 和蛋白水平。结果表明,gp120 可诱导神经元凋亡和神经突退化呈浓度依赖性,PPBP 可减轻 gp120 的神经毒性。同时,gp120 可诱导 bcl-2 和 bax 的低表达,但只有 bcl-2 的低表达可被 PPBP 逆转。本数据表明,PPBP 至少部分通过调节 bcl-2 表达来保护神经元免受 gp120 的侵害。