Sex-based differences in myocardial infarction-induced kidney damage following cigarette smoking exposure: More renal protection in premenopausal female mice

Abstract

The impact of cigarette smoking (CS) on kidney homeostasis in the presence of myocardial infarction (MI) in both males and females remains poorly elucidated. C57BL6/J mice were exposed to 2 weeks of CS prior to MI induction followed by 1 week of CS exposure in order to investigate the impact of CS on kidney damage in the presence of MI. Cardiac hemodynamic analysis revealed a significant decrease in ejection fraction (EF) in CS-exposed MI male mice when compared with the relative female subjects, whereas cardiac output (CO) comparably decreased in CS-exposed MI mice of both sexes. Kidney structural alterations, including glomerular retraction, proximal convoluted tubule (PCT) cross-sectional area, and total renal fibrosis were more pronounced in CS-exposed MI male mice when compared with the relative female group. Although renal reactive oxygen species (ROS) generation and glomerular DNA fragmentation significantly increased to the same extent in CS-exposed MI mice of both sexes, alpha-smooth muscle actin (α-SMA) and connective tissue growth factor (CTGF) significantly increased in CS-exposed MI male mice, only. Metabolically, nicotinamide phosphoribosyltransferase (NAMPT) and nicotinamide riboside-1 (NMRK-1) substantially increased in CS-exposed MI female mice only, whereas sirtuin (SIRT)-1 and SIRT-3 substantially decreased in CS-exposed MI male mice compared with their relative female group. Additionally, renal NAD levels significantly decreased only in CS-exposed MI male mice. In conclusion, MI female mice exhibited pronounced renal protection following CS when compared with the relative male groups. © 2020 The Author(s). This is an open access article published by Portland Press Limited on behalf of the Biochemical Society and distributed under the Creative Commons Attribution License 4.0 (CC BY).

Description

Keywords

Actins, Animals, Connective tissue growth factor, Cytokines, Disease models, animal, Dna damage, Female, Kidney, Kidney diseases, Male, Mice, inbred c57bl, Myocardial infarction, Nicotinamide phosphoribosyltransferase, Phosphotransferases (alcohol group acceptor), Premenopause, Reactive oxygen species, Sex factors, Sirtuin 1, Sirtuin 3, Smoke, Tobacco products, Alpha smooth muscle actin, Nicotinamide riboside, Nicotinamide riboside 1, Reactive oxygen metabolite, Unclassified drug, Actin, Alpha-smooth muscle actin, mouse, Ccn2 protein, mouse, Cytokine, Nicotinamide phosphoribosyltransferase, mouse, Nmrk1 protein, mouse, Phosphotransferase, Sirt1 protein, mouse, Sirt3 protein, mouse, Animal experiment, Animal model, Animal tissue, Article, C57bl 6 mouse, Controlled study, Dna fragmentation, Glomerulus, Heart ejection fraction, Heart hemodynamics, Heart infarction, Heart output, Kidney fibrosis, Kidney injury, Kidney proximal tubule, Long term exposure, Nonhuman, Passive smoking, Renal protection, Sex difference, Animal, C57bl mouse, Comparative study, Complication, Disease model, Genetics, Kidney disease, Metabolism, Pathology, Sex factor, Tobacco

Citation

Endorsement

Review

Supplemented By

Referenced By