Renal Service, Memorial Sloan Kettering Cancer Center, New York, New York.
Department of Physiology, Shenyang Medical University, Shenyang, China.
Am J Physiol Renal Physiol. 2021 Mar 1;320(3):F442-F453. doi: 10.1152/ajprenal.00194.2020. Epub 2021 Jan 18.
Diabetic nephropathy (DN) is the leading cause of end-stage kidney disease. Besides glycemic and blood pressure control, environmental factors such as cigarette smoking (CS) adversely affect the progression of DN. The effects of CS on DN progression have been attributed to combustion-generated molecules without consideration to the role of nicotine (NIC), responsible for the addictive properties of both CS and electronic cigarettes (ECs). Podocytes are essential to preserve the structure and function of the glomerular filtration barrier, and strong evidence indicates that early podocyte loss promotes DN progression. We performed experiments in human podocytes and in a mouse model of diabetes that develops nephropathy resembling human DN. We determined that NIC binding to podocytes in concentrations achieved with CS and ECs activated NADPH oxidase, which sets in motion a dysfunctional molecular network integrated by cyclooxygenase 2, known to induce podocyte injury; downregulation of AMP-activated protein kinase, important for maintaining cellular energy stores and antioxidation; and upregulation of CD36, which increased lipid uptake and promoted apoptosis. In diabetic mice, NIC increased proteinuria, a recognized marker of chronic kidney disease progression, accompanied by reduced glomerular podocyte synaptopodin, a crucial stabilizer of the podocyte cytoskeleton, and increased fibronectin expression. This novel study critically implicates NIC itself as a contributor to DN progression in CS and EC users. In this study, we demonstrate that nicotine increases the production of reactive oxygen species, increases cyclooxygenase-2 expression, and upregulates Cd36 while inducing downregulation of AMP-activated protein kinase. In vivo nicotine increases proteinuria and fibronectin expression in diabetic mice. This study demonstrates that effects of nicotine on podocytes are responsible, at least in part, for the deleterious effects of smoking in the progression of chronic kidney disease, including diabetic nephropathy.
糖尿病肾病(DN)是终末期肾病的主要原因。除了血糖和血压控制外,环境因素如吸烟(CS)也会对 DN 的进展产生不利影响。CS 对 DN 进展的影响归因于燃烧产生的分子,而没有考虑到尼古丁(NIC)的作用,NIC 是 CS 和电子烟(EC)成瘾性的原因。足细胞对于维持肾小球滤过屏障的结构和功能至关重要,有强有力的证据表明早期足细胞丢失会促进 DN 的进展。我们在人足细胞和一种发展为类似于人类 DN 的肾病的糖尿病小鼠模型中进行了实验。我们确定,在 CS 和 EC 达到的浓度下,NIC 与足细胞结合会激活 NADPH 氧化酶,从而启动一个功能失调的分子网络,该网络由已知会诱导足细胞损伤的环氧化酶 2 整合;下调 AMP 激活的蛋白激酶,该激酶对维持细胞能量储存和抗氧化作用很重要;上调 CD36,这会增加脂质摄取并促进细胞凋亡。在糖尿病小鼠中,NIC 增加蛋白尿,这是慢性肾脏病进展的公认标志物,同时肾小球足细胞突触蛋白减少,这是足细胞细胞骨架的重要稳定剂,纤连蛋白表达增加。这项新的研究严重表明,NIC 本身就是 CS 和 EC 用户中 DN 进展的一个因素。在这项研究中,我们证明尼古丁增加活性氧的产生,增加环氧化酶-2 的表达,并上调 Cd36,同时诱导 AMP 激活的蛋白激酶下调。体内尼古丁增加糖尿病小鼠的蛋白尿和纤连蛋白表达。这项研究表明,尼古丁对足细胞的影响至少部分是导致吸烟在慢性肾脏病进展中产生有害影响的原因,包括糖尿病肾病。