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Nicotine, smoking, podocytes, and diabetic nephropathy.
Jaimes, Edgar A; Zhou, Ming-Sheng; Siddiqui, Mohammed; Rezonzew, Gabriel; Tian, Runxia; Seshan, Surya V; Muwonge, Alecia N; Wong, Nicholas J; Azeloglu, Evren U; Fornoni, Alessia; Merscher, Sandra; Raij, Leopoldo.
Afiliação
  • Jaimes EA; Renal Service, Memorial Sloan Kettering Cancer Center, New York, New York.
  • Zhou MS; Department of Physiology, Shenyang Medical University, Shenyang, China.
  • Siddiqui M; Renal Division, University of Alabama at Birmingham, Birmingham, Alabama.
  • Rezonzew G; Renal Division, University of Alabama at Birmingham, Birmingham, Alabama.
  • Tian R; Nephrology Section, Miami Veterans Affairs Medical Center, Miami, Florida.
  • Seshan SV; Department of Pathology, Weill Cornell Medical College, New York, New York.
  • Muwonge AN; Division of Nephrology, Department of Medicine, Icahn Mount Sinai School of Medicine, New York, New York.
  • Wong NJ; Division of Nephrology, Department of Medicine, Icahn Mount Sinai School of Medicine, New York, New York.
  • Azeloglu EU; Division of Nephrology, Department of Medicine, Icahn Mount Sinai School of Medicine, New York, New York.
  • Fornoni A; Katz Family Division of Nephrology and Hypertension, University of Miami Miller School of Medicine, Miami, Florida.
  • Merscher S; Katz Family Division of Nephrology and Hypertension, University of Miami Miller School of Medicine, Miami, Florida.
  • Raij L; Katz Family Division of Nephrology and Hypertension, University of Miami Miller School of Medicine, Miami, Florida.
Am J Physiol Renal Physiol ; 320(3): F442-F453, 2021 03 01.
Article em En | MEDLINE | ID: mdl-33459165
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.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fumar / Nefropatias Diabéticas / Podócitos / Proteínas Quinases Ativadas por AMP / Nicotina Tipo de estudo: Prognostic_studies Limite: Animals / Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fumar / Nefropatias Diabéticas / Podócitos / Proteínas Quinases Ativadas por AMP / Nicotina Tipo de estudo: Prognostic_studies Limite: Animals / Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article