Cheng Peng, Zhang Fangfang, Yu Lechu, Lin Xiufei, He Luqing, Li Xiaokun, Lu Xuemian, Yan Xiaoqing, Tan Yi, Zhang Chi
The Chinese-American Research Institute for Diabetic Complications, Wenzhou Medical University, Wenzhou 325035, China; Ruian Center of the Chinese-American Research Institute for Diabetic Complications, The Third Affiliated Hospital, Wenzhou Medical University, Wenzhou 325200, China; School of Pharmaceutical Sciences, Wenzhou Medical University, Wenzhou 325035, China.
The Chinese-American Research Institute for Diabetic Complications, Wenzhou Medical University, Wenzhou 325035, China.
J Diabetes Res. 2016;2016:1540267. doi: 10.1155/2016/1540267. Epub 2016 May 9.
Cardiovascular disease (CVD) is one of the most severe diseases in clinics. Fibroblast growth factor 21 (FGF21) is regarded as an important metabolic regulator playing a therapeutic role in diabetes and its complications. The heart is a key target as well as a source of FGF21 which is involved in heart development and also induces beneficial effects in CVDs. Our review is to clarify the roles of FGF21 in CVDs. Strong evidence showed that the development of CVDs including atherosclerosis, coronary heart disease, myocardial ischemia, cardiac hypertrophy, and diabetic cardiomyopathy is associated with serum FGF21 levels increase which was regarded as a compensatory response to induced cardiac protection. Furthermore, administration of FGF21 suppressed the above CVDs. Mechanistic studies revealed that FGF21 induced cardiac protection likely by preventing cardiac lipotoxicity and the associated oxidative stress, inflammation, and apoptosis. Normally, FGF21 induced therapeutic effects against CVDs via activation of the above kinases-mediated pathways by directly binding to the FGF receptors of the heart in the presence of β-klotho. However, recently, growing evidence showed that FGF21 induced beneficial effects on peripheral organs through an indirect way mediated by adiponectin. Therefore whether adiponectin is also involved in FGF21-induced cardiac protection still needs further investigation.
心血管疾病(CVD)是临床上最严重的疾病之一。成纤维细胞生长因子21(FGF21)被视为一种重要的代谢调节因子,在糖尿病及其并发症中发挥治疗作用。心脏是FGF21的关键靶点和来源,FGF21参与心脏发育,并对心血管疾病产生有益影响。我们的综述旨在阐明FGF21在心血管疾病中的作用。有力证据表明,包括动脉粥样硬化、冠心病、心肌缺血、心脏肥大和糖尿病心肌病在内的心血管疾病的发展与血清FGF21水平升高有关,这被认为是诱导心脏保护的一种代偿反应。此外,给予FGF21可抑制上述心血管疾病。机制研究表明,FGF21可能通过预防心脏脂毒性以及相关的氧化应激、炎症和细胞凋亡来诱导心脏保护。正常情况下,FGF21在β-klotho存在时通过直接与心脏的FGF受体结合,激活上述激酶介导的途径,从而对心血管疾病产生治疗作用。然而,最近越来越多的证据表明,FGF21通过脂联素介导的间接方式对周围器官产生有益影响。因此,脂联素是否也参与FGF21诱导的心脏保护仍需进一步研究。