脂肪肝
医学
胰岛素抵抗
肾脏疾病
串扰
急性肾损伤
肝损伤
肾
酒精性肝病
氧化应激
生物信息学
肝病
疾病
内科学
生物
胰岛素
肝硬化
物理
光学
作者
Nisha Sharma,Anannya Sircar,Hans‐Joachim Anders,Anil Bhanudas Gaikwad
标识
DOI:10.1080/13813455.2020.1745851
摘要
Liver and kidney are vital organs that maintain homeostasis and injury to either of them triggers pathogenic pathways affecting the other. For example, non-alcoholic fatty liver disease (NAFLD) promotes the progression of chronic kidney disease (CKD), vice versa acute kidney injury (AKI) endorses the induction and progression of liver dysfunction. Progress in clinical and basic research suggest a role of excessive fructose intake, insulin resistance, inflammatory cytokines production, activation of the renin–angiotensin system, redox imbalance, and their impact on epigenetic regulation of gene expression in this context. Recent developments in experimental and clinical research have identified several biochemical and molecular pathways for AKI-liver interaction, including altered liver enzymes profile, metabolic acidosis, oxidative stress, activation of inflammatory and regulated cell death pathways. This review focuses on the current preclinical and clinical findings on kidney–liver crosstalk in NAFLD-CKD and AKI-liver dysfunction settings and highlights potential molecular mechanisms and therapeutic targets.
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