Cigarette smoking causes epigenetic changes associated with cardiorenal fibrosis

Author:

Drummond Christopher A.1ORCID,Crotty Alexander Laura E.2ORCID,Haller Steven T.1,Fan Xiaoming1,Xie Jeffrey X.1,Kennedy David J.1,Liu Jiang3,Yan Yanling3,Hernandez Dawn-Alita4,Mathew Denzil P.2,Cooper Christopher J.1,Shapiro Joseph I.3,Tian Jiang1

Affiliation:

1. College of Medicine and Life Sciences, Department of Medicine, Division of Cardiovascular Medicine and Center for Hypertension and Personalized Medicine, University of Toledo, Toledo, Ohio;

2. Pulmonary Critical Care Section, Veterans Affairs San Diego Healthcare System and Division of Pulmonary, Critical Care and Sleep Medicine, University of California San Diego Health Sciences, San Diego, California; and

3. Joan C. Edwards School of Medicine, Marshall University, Huntington, West Virginia

4. Division of Pulmonary Medicine (Critical Care and Sleep Medicine), University of Toledo, Toledo, Ohio;

Abstract

Clinical studies indicate that smoking combustible cigarettes promotes progression of renal and cardiac injury, leading to functional decline in the setting of chronic kidney disease (CKD). However, basic studies using in vivo small animal models that mimic clinical pathology of CKD are lacking. To address this issue, we evaluated renal and cardiac injury progression and functional changes induced by 4 wk of daily combustible cigarette smoke exposure in the 5/6th partial nephrectomy (PNx) CKD model. Molecular evaluations revealed that cigarette smoke significantly ( P < 0.05) decreased renal and cardiac expression of the antifibrotic microRNA miR-29b-3 and increased expression of molecular fibrosis markers. In terms of cardiac and renal organ structure and function, exposure to cigarette smoke led to significantly increased systolic blood pressure, cardiac hypertrophy, cardiac and renal fibrosis, and decreased renal function. These data indicate that decreased expression of miR-29b-3p is a novel mechanism wherein cigarette smoke promotes accelerated cardiac and renal tissue injury in CKD. (155 words)

Funder

HHS | NIH | National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)

HHS | NIH | National Heart, Lung, and Blood Institute (NHBLI)

American Heart Association (AHA)

U.S. Department of Veterans Affairs (VA)

Publisher

American Physiological Society

Subject

Genetics,Physiology

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