首页> 外文期刊>Journal of Lipid Research >Bile acid receptors as targets for the treatment of dyslipidemia and cardiovascular disease Thematic Review Series: New Lipid and Lipoprotein Targets for the Treatment of Cardiometabolic Diseases
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Bile acid receptors as targets for the treatment of dyslipidemia and cardiovascular disease Thematic Review Series: New Lipid and Lipoprotein Targets for the Treatment of Cardiometabolic Diseases

机译:胆汁酸受体作为治疗血脂异常和心血管疾病的靶标专题综述系列:治疗心血管代谢疾病的新脂质和脂蛋白靶标

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Dyslipidemia is an important risk factor for cardiovascular disease (CVD) and atherosclerosis. When dyslipidemia coincides with other metabolic disorders such as obesity, hypertension, and glucose intolerance, defined as the metabolic syndrome (MS), individuals present an elevated risk to develop type 2 diabetes (T2D) as well as CVD. Because the MS epidemic represents a growing public health problem worldwide, the development of therapies remains a major challenge. Alterations of bile acid pool regulation in T2D have revealed a link between bile acid and metabolic homeostasis. The bile acid receptors farnesoid X receptor (FXR) and TGR5 both regulate lipid, glucose, and energy metabolism, rendering them potential pharmacological targets for MS therapy. This review discusses the mechanisms of metabolic regulation by FXR and TGR5 and the utility relevance of natural and synthetic modulators of FXR and TGR5 activity, including bile acid sequestrants, in the treatment of the MS.
机译:血脂异常是心血管疾病(CVD)和动脉粥样硬化的重要危险因素。当血脂异常与其他代谢性疾病(例如肥胖症,高血压和葡萄糖耐量异常)同时发生时,被定义为代谢综合征(MS),个体患2型糖尿病(T2D)和CVD的风险就会升高。由于MS流行病在世界范围内代表着日益严重的公共卫生问题,因此疗法的开发仍然是一项重大挑战。 T2D中胆汁酸池调节的变化揭示了胆汁酸与代谢稳态之间的联系。胆汁酸受体法呢类X受体(FXR)和TGR5均调节脂质,葡萄糖和能量代谢,使其成为MS治疗的潜在药理靶标。这篇综述讨论了FXR和TGR5调节代谢的机制,以及FXR和TGR5活性的天然和合成调节剂(包括胆汁酸螯合剂)在MS治疗中的实用性。

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