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非酒精性脂肪性肝病中的新兴肝-肾相互作用。

Emerging Liver-Kidney Interactions in Nonalcoholic Fatty Liver Disease.

机构信息

Gradenigo Hospital, University of Turin, Turin, Italy.

Department of Medical Sciences, San Giovanni Battista Hospital, University of Turin, Turin, Italy.

出版信息

Trends Mol Med. 2015 Oct;21(10):645-662. doi: 10.1016/j.molmed.2015.08.005.

Abstract

Mounting evidence connects non-alcoholic fatty liver disease (NAFLD) to chronic kidney disease (CKD). We review emerging mechanistic links between NAFLD and CKD, including altered activation of angiotensin converting enzyme (ACE)-2, nutrient/energy sensors sirtuin-1 and AMP-activated kinase, as well as impaired antioxidant defense mediated by nuclear factor erythroid 2-related factor-2 (Nrf2). Dietary fructose excess may also contribute to NAFLD and CKD. NAFLD affects renal injury through lipoprotein dysmetabolism and altered secretion of the hepatokines fibroblast growth factor-21, fetuin-A, insulin-like growth factor-1, and syndecan-1. CKD may mutually aggravate NAFLD and associated metabolic disturbances through altered intestinal barrier function and microbiota composition, the accumulation of uremic toxic metabolites, and alterations in pre-receptor glucocorticoid metabolism. We conclude by discussing the implications of these findings for the treatment of NAFLD and CKD.

摘要

越来越多的证据表明非酒精性脂肪性肝病(NAFLD)与慢性肾脏病(CKD)有关。我们综述了 NAFLD 和 CKD 之间新出现的机制联系,包括血管紧张素转换酶(ACE)-2、营养/能量传感器 Sirtuin-1 和 AMP 激活的蛋白激酶的激活改变,以及核因子红细胞 2 相关因子-2(Nrf2)介导的抗氧化防御受损。饮食果糖过量也可能导致 NAFLD 和 CKD。NAFLD 通过脂蛋白代谢紊乱和肝分泌因子成纤维细胞生长因子-21、胎球蛋白-A、胰岛素样生长因子-1 和 syndecan-1 的改变影响肾脏损伤。CKD 可能通过改变肠道屏障功能和微生物群落组成、尿毒症毒性代谢物的积累以及前受体糖皮质激素代谢的改变,相互加重 NAFLD 和相关代谢紊乱。最后,我们讨论了这些发现对 NAFLD 和 CKD 治疗的意义。

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