Effects of HAART drugs on endothelial dysfunction of pu*

HAART药物对pu*内皮功能障碍的影响

• 批准号: 7250204
• 负责人: Changyi Chen
• 金额: $ 35.56万
• 依托单位: BAYLOR COLLEGE OF MEDICINE
• 依托单位国家: 美国
• 财政年份: 2005
• 资助国家: 美国
• 起止时间: 2005-09-29 至 2010-06-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7250204
• 关键词: Anions; Antioxidants; Ascorbic Acid; Clinical; Complication; Data; Development; Drug effect disorder; Elevation; Endothelial Cells; Endothelin; Endothelium; Enzymes; Etiology; Family suidae; Frequencies; Functional disorder; Gene Expression; Gene Expression Regulation; Ginkgo biloba; Ginseng Preparation; Ginsenosides; Highly Active Antiretroviral Therapy; Human; In Vitro; Incidence; Injury; Lung; Molecular; Oxidative Stress; Oxides; Panax; Pathway interactions; Permeability; Pharmaceutical Preparations; Prevention strategy; Production; Prostaglandins; Pulmonary Hypertension; Pulmonary artery structure; Reactive Oxygen Species; Regulation; Reporting; Signal Transduction; Signal Transduction Pathway; Smooth Muscle Myocytes; Source; Structure; Superoxides; System; Testing; Vascular resistance; Vasodilation; Vasomotor; antiretroviral therapy; base; design; ginkgolide A; human NOS3 protein; multidisciplinary; pulmonary artery endothelial cell

DESCRIPTION (provided by applicant): The incidence of HIV-related pulmonary hypertension has been recognized in the last few years with increasing frequency. However, the etiology and underlying molecular mechanisms of this serious complication are unknown. Recent clinical reports indicate that highly active antiretroviral therapy (HAART) may increase the incidence of HIV-related pulmonary hypertension. Our preliminary data have demonstrated that some HAART drugs impaired endothelium-dependent vasorelaxation, reduced the expression of endothelial nitric oxide synthase (eNOS), and increased super oxide anion production in porcine pulmonary arteries in vitro. In addition, some HAART drugs increased endothelial permeability and oxidative stress, and decreased the expression of several junctional molecules inhuman pulmonary artery endothelial cells (HPAECs). Furthetntore, ginsenoside Rbl and ginkgolide A effectively blocked some HAART drug-induced endothelial dysfunction. Based on these studies, we have developed our central hypotheses that some HAART drugs may cause endothelial dysfunction and oxidative stress in pulmonary arteries through unique molecular pathways, and ginseng and ginkgo compounds may effectively block these detrimental effects of HAART drugs on pulmonary arteries. Thus, we propose a multidisciplinary study to test these central hypotheses. Four specific aims are proposed. Aim 1 is designed to determine the effect of HAART drugs on vasomotor activities and the eNOS system in porcine pulmonary arteries and human pulmonary artery endothelial cells. We will investigate the vasomotor activities, eNOS expression, signal transduction pathways, and prostaglandin and endothelin systems. Aim 2 is designed to determine the effect of HAART drugs on endothelial permeability, junction structures, and molecules in human pulmonary artery endothelial cells. We will investigate endothelial permeability, junction molecular expression, and regulation as well as signal transduction pathways. Aim 3 is designed to determine the effect of HAART drugs on the reactive oxygen species (ROS) system in porcine pulmonary arteries and human pulmonary artery endothelial cells. We will investigate the types and molecular sources of ROS production, the activities and gene expression of ROS-generating and internal antioxidant enzymes. Aim 4 is designed to determine the effect of ginseng and ginkgo compounds on HAART drug induced-endothelial dysfunction and oxidative stress in porcine pulmonary arteries and human pulmonary artery endothelial cells. We will study whether ginseng and ginkgo compounds can block some HAART drug-induced vasomotor dysfunction and permeability increase as well as oxidative stress and related gene expression and regulation. The differences of ginseng and ginkgo compounds will be compared with vitamins C and E in blocking HAART-induced endothelial dysfunction. This study will elucidate the molecular mechanisms of HAART drugs' action on pulmonary endothelial cells and provide valuable information for the development of effective strategies for the prevention and treatment of HIV-related pulmonary hypertension.

描述（由申请人提供）：HIV相关肺动脉高压的发病率在过去几年中已被认识到，其发生频率越来越高。然而，这种严重并发症的病因和潜在的分子机制尚不清楚。最近的临床报告表明，高效抗逆转录病毒治疗（HAART）可能会增加HIV相关肺动脉高压的发病率。我们的初步数据表明，一些HAART药物损害内皮依赖性血管舒张，减少内皮型一氧化氮合酶（eNOS）的表达，并增加超氧阴离子的生产在猪肺动脉在体外。此外，一些HAART药物增加内皮细胞通透性和氧化应激，并降低几种连接分子的表达人肺动脉内皮细胞（HPAECs）。此外，银杏内酯A和银杏内酯Rbl有效地阻断了一些HAART药物诱导的内皮功能障碍。基于这些研究，我们提出了我们的中心假设，即一些HAART药物可能通过独特的分子途径引起肺动脉内皮功能障碍和氧化应激，人参和银杏化合物可能有效地阻断HAART药物对肺动脉的这些不利影响。因此，我们提出了一个多学科的研究来测试这些中心的假设。提出了四个具体目标。 目的1研究HAART药物对猪肺动脉和人肺动脉内皮细胞血管活性和eNOS系统的影响。我们将探讨血管活性，eNOS表达，信号转导通路，前列腺素和内皮素系统。 目的2：研究HAART药物对人肺动脉内皮细胞通透性、连接结构和分子的影响。我们将研究内皮通透性，连接分子的表达和调控以及信号转导途径。 目的3研究HAART药物对猪肺动脉和人肺动脉内皮细胞活性氧系统的影响。我们将研究ROS产生的类型和分子来源，ROS生成酶和内部抗氧化酶的活性和基因表达。 目的4研究人参、银杏复方对HAART药物诱导的猪肺动脉和人肺动脉内皮细胞功能障碍和氧化应激的影响。我们将研究人参和银杏化合物是否可以阻断某些HAART药物引起的血管功能障碍和通透性增加以及氧化应激和相关基因的表达和调节。将比较人参和银杏化合物与维生素C和E在阻断HAART诱导的内皮功能障碍方面的差异。 本研究将阐明HAART药物对肺内皮细胞作用的分子机制，为制定有效的防治HIV相关肺动脉高压的策略提供有价值的信息。