首页> 外文期刊>Atherosclerosis >Peroxisome proliferator-activated receptor-alpha (PPARalpha): at the crossroads of obesity, diabetes and cardiovascular disease.
【24h】

Peroxisome proliferator-activated receptor-alpha (PPARalpha): at the crossroads of obesity, diabetes and cardiovascular disease.

机译:过氧化物酶体增殖物激活受体-α(PPARalpha):在肥胖,糖尿病和心血管疾病的十字路口。

获取原文
获取原文并翻译 | 示例
获取外文期刊封面目录资料

摘要

Cardiovascular disease is the leading cause of morbidity and mortality world-wide. The burden of disease is also increasing as a result of the global epidemics of diabetes and obesity. Peroxisome proliferator-activated receptor alpha (PPARalpha), a member of this nuclear receptor family, has emerged as an important player in this scenario, with evidence supporting a central co-ordinated role in the regulation of fatty acid oxidation, lipid and lipoprotein metabolism and inflammatory and vascular responses, all of which would be predicted to reduce atherosclerotic risk. Additionally, the Fenofibrate Intervention and Event Lowering in Diabetes (FIELD) study has indicated the possibility of preventive effects in diabetes-related microvascular complications, although the mechanisms of these effects warrant further study. The multimodal pharmacological profile of PPARalpha has prompted development of selective PPAR modulators (SPPARMs) to maximise therapeutic potential. It is anticipated that PPARalpha will continue to have important clinical application in addressing the major challenge of cardiometabolic risk associated with type 2 diabetes, obesity and metabolic syndrome.
机译:心血管疾病是全世界发病率和死亡率的主要原因。由于糖尿病和肥胖症的全球流行,疾病的负担也在增加。过氧化物酶体增殖物激活受体α(PPARalpha),是该核受体家族的成员,在这种情况下已成为重要参与者,证据支持在脂肪酸氧化,脂质和脂蛋白代谢和炎症和血管反应,所有这些都可降低动脉粥样硬化的风险。此外,非诺贝特干预和降低糖尿病事件(FIELD)的研究表明了预防糖尿病相关微血管并发症的可能性,尽管这些作用的机制值得进一步研究。 PPARalpha的多峰药理学特征促进了选择性PPAR调节剂(SPPARM)的开发,以最大化治疗潜力。预期PPARalpha在应对与2型糖尿病,肥胖症和代谢综合征相关的心脏代谢风险的重大挑战方面将继续具有重要的临床应用。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号