Treatment of Tat neurotoxicity through the use of Gsk3-b inhibitors

使用 Gsk3-b 抑制剂治疗 Tat 神经毒性

• 批准号: 8151114
• 负责人: Fatah Kashanchi
• 金额: $ 18.26万
• 依托单位: GEORGE MASON UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2010
• 资助国家: 美国
• 起止时间: 2010-09-30 至 2013-06-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8151114
• 关键词: AIDS Dementia Complex; Address; Anti-HIV Therapy; Apoptosis; Biological Assay; Cell Death; Cell Line; Cells; Chemicals; Disease; Gene Expression; Generations; Genetic Transcription; Glycogen Synthase Kinase 3; Goals; HIV; HIV Envelope Protein gp120; HIV Infections; HIV-1; Highly Active Antiretroviral Therapy; Hippocampus (Brain); Impairment; In Vitro; Individual; Infection; Inflammatory; Inhibitory Concentration 50; Life; Mediator of activation protein; Microarray Analysis; Neurocognitive; Neurologic; Neuropathogenesis; Pharmaceutical Preparations; Phosphotransferases; Play; Preventive; Production; Rattus; Research; Screening procedure; Signal Transduction; System; Therapeutic; Toxic effect; base; cytokine; inhibitor/antagonist; macrophage; mild neurocognitive impairment; mouse model; nervous system disorder; neurotoxicity; novel; novel strategies; novel therapeutics; prevent; public health relevance; therapeutic target

DESCRIPTION (provided by applicant): The long-term goal of our research is to identify and/or develop novel therapeutics for the treatment of HAND. Here we proposed to study novel small chemical molecules that can inhibit GSK-3¿, which is known to have important implications in HAND. These studies may help to identify mechanisms that play key roles in HIV-1 infection and provide a new set of preventive and/or therapeutic targets. In our preliminary studies, we have identified the GSK-3 inhibitor BIO, as a Tat-dependent HIV-1 transcriptional inhibitor out of 4,000 compounds screened. We have verified its ability to inhibit HIV-1 transcription in an independent assay system, TZM-bl cells, with an IC50 of 40 nM and a new BIO derivative (BIOder) at 4 nM in primary Macrophages and 0.5 nM in U87MG cells when infected with HIV-1. MTT toxicity assay shows an inhibitory activity of more than 10 uM in either primary cells or cell line. In an in vitro GSK-3¿ kinase inhibition assay, we found that the drug has a very low IC50 of 0.03 nM. Finally we demonstrated that first generation BIO drug has neuroprotective effects on Tat induced cell death in rat mixed hippocampal cultures. Therefore BIO and its derivatives are unique compounds due to their dual mechanism of action with the ability to inhibit HIV-1 transcription as well as protect against Tat induced cell death. Based on these preliminary results we believe that BIO or its 2nd generation derivatives could be used as a therapeutic for HAND. The short term goal of our research is to determine if BIO is a potential HAND therapeutic. We hypothesize that BIO treatment is neuroprotective. The following specific aims address our hypothesis: Aim 1: Mechanism of BIO inhibition of HIV transcription. Aim 2: Effect of BIO on HIV induced neurotoxicity. PUBLIC HEALTH RELEVANCE: HIV infection can result in a number of neurological disorders including HIV-associated dementia, mild neurocognitive disorder, and asymptomatic neurocognitive impairment that are not prevented with HAART. Here we proposed to study novel small chemical molecules that can inhibit GSK-3b, which is known to have important implications in HAND, with the goal of abrogating Tat induced neuropathogenesis.

描述（由申请人提供）：我们研究的长期目标是鉴定和/或开发用于治疗HAND的新疗法。在这里，我们建议研究可以抑制GSK-3的新型小化学分子，这是已知的在HAND中具有重要意义。这些研究可能有助于确定在HIV-1感染中起关键作用的机制，并提供一套新的预防和/或治疗靶点。在我们的初步研究中，我们已经确定GSK-3抑制剂BIO是筛选的4，000种化合物中的Tat依赖性HIV-1转录抑制剂。我们已经在一个独立的试验系统中验证了它抑制HIV-1转录的能力，TZM-bl细胞，当感染HIV-1时，其IC 50为40 nM，新的BIO衍生物（BIOder）在原代Macrophage中为4 nM，在U87 MG细胞中为0.5 nM。MTT毒性测定显示在原代细胞或细胞系中超过10 μ M的抑制活性。在体外GSK-3 <$激酶抑制试验中，我们发现该药物的IC 50非常低，为0.03 nM。最后，我们证明了第一代BIO药物对大鼠混合海马培养物中达特诱导的细胞死亡具有神经保护作用。因此，BIO及其衍生物是独特的化合物，因为它们具有抑制HIV-1转录以及防止达特诱导的细胞死亡的双重作用机制。基于这些初步结果，我们认为BIO或其第二代衍生物可用作HAND的治疗剂。我们研究的短期目标是确定BIO是否是一种潜在的HAND治疗剂。我们假设BIO治疗具有神经保护作用。以下具体目标解决我们的假设：目标1：BIO抑制HIV转录的机制。目的2：BIO对HIV神经毒性的影响。 公共卫生相关性：HIV感染可导致许多神经系统疾病，包括HIV相关痴呆、轻度神经认知障碍和HAART无法预防的无症状神经认知障碍。在这里，我们提出了研究新的化学小分子，可以抑制GSK-3b，这是已知的有重要意义的手，与废除达特诱导的神经发病机制的目标。