TY - JOUR
T1 - Nicotine, smoking, podocytes, and diabetic nephropathy
AU - Jaimes, Edgar A.
AU - Zhou, Ming Sheng
AU - Siddiqui, Mohammed
AU - Rezonzew, Gabriel
AU - Tian, Runxia
AU - Seshan, Surya V.
AU - Muwonge, Alecia N.
AU - Wong, Nicholas J.
AU - Azeloglu, Evren U.
AU - Fornoni, Alessia
AU - Merscher, Sandra
AU - Raij, Leopoldo
N1 - Funding Information:
E.A.J. is the co-founder, shareholder, and chief medical officer of Goldilocks Therapeutics, Inc. A.F. is the Vice-President of L&F Health LLC and is a consultant for ZyVersa Therapeutics, Inc. A.F. is the founder of LipoNexT LLC. S.M. is a consultant for Kintai Therapeutics Inc. and holds equity interest in L&F Research. A.F. and S.M. are supported by Hoffman-La Roche and by Boehringer Ingelheim.
Funding Information:
This work was supported by the Miami Veterans Affairs Foundation for Research and Education (to L.R.) and by National Institutes of Health Grants RO1ES014948 and P30CA008748 (to E.A.J.); R01DK117599, R01DK104753, and R01CA227493 (to A.F. and S.M.); and U54DK083912, UM1DK100846, U01DK116101, and UL1TR000460 (to A.F.).
Publisher Copyright:
© 2021 American Physiological Society. All rights reserved.
PY - 2021
Y1 - 2021
N2 - 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.
AB - 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.
KW - Diabetes
KW - Nicotine
KW - Podocytes
KW - Reactive oxygen species
KW - Smoking
UR - http://www.scopus.com/inward/record.url?scp=85102965495&partnerID=8YFLogxK
U2 - 10.1152/AJPRENAL.00194.2020
DO - 10.1152/AJPRENAL.00194.2020
M3 - Article
C2 - 33459165
AN - SCOPUS:85102965495
SN - 1931-857X
VL - 320
SP - F442-F453
JO - American Journal of Physiology - Renal Physiology
JF - American Journal of Physiology - Renal Physiology
IS - 3
ER -