Nicotine, smoking, podocytes, and diabetic nephropathy Journal Article


Authors: Jaimes, E. A.; Zhou, M. S.; Siddiqui, M.; Rezonzew, G.; Tian, R.; Seshan, S. V.; Muwonge, A. N.; Wong, N. J.; Azeloglu, E. U.; Fornoni, A.; Merscher, S.; Raij, L.
Article Title: Nicotine, smoking, podocytes, and diabetic nephropathy
Abstract: 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.NEW & NOTEWORTHY 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.
Keywords: smoking; reactive oxygen species; nicotine; diabetes; podocytes
Journal Title: American Journal of Physiology - Renal Physiology
Volume: 320
Issue: 3
ISSN: 1931-857X
Publisher: American Physiological Society  
Date Published: 2021-03-01
Start Page: F442
End Page: F453
Language: English
DOI: 10.1152/ajprenal.00194.2020
PUBMED: 33459165
PROVIDER: scopus
PMCID: PMC7988804
DOI/URL:
Notes: Article -- Export Date: 1 April 2021 -- Source: Scopus
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  1. Edgar Alberto Jaimes
    80 Jaimes