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

dc.contributor.authorHabeichi, Nada J.
dc.contributor.authorMroueh, Ali
dc.contributor.authorKaplan, Abdullah
dc.contributor.authorGhali, Rana
dc.contributor.authorAl-Awassi, Hiam
dc.contributor.authorTannous, Cynthia
dc.contributor.authorHusari, Ahmad W.
dc.contributor.authorJurjus, Abdo R.
dc.contributor.authorAltara, Raffaele
dc.contributor.authorBooz, George Warren
dc.contributor.authorEl-Yazbi, Ahmed F.
dc.contributor.authorZouein, Fouad A.
dc.contributor.departmentPharmacology and Toxicology
dc.contributor.departmentInternal Medicine
dc.contributor.departmentAnatomy, Cell Biology, and Physiological Sciences
dc.contributor.facultyFaculty of Medicine (FM)
dc.contributor.institutionAmerican University of Beirut
dc.date.accessioned2025-01-24T11:39:43Z
dc.date.available2025-01-24T11:39:43Z
dc.date.issued2020
dc.description.abstractThe 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).
dc.identifier.doihttps://doi.org/10.1042/BSR20193229
dc.identifier.eid2-s2.0-85087096668
dc.identifier.pmid32519752
dc.identifier.urihttp://hdl.handle.net/10938/29331
dc.language.isoen
dc.publisherPortland Press Ltd
dc.relation.ispartofBioscience Reports
dc.sourceScopus
dc.subjectActins
dc.subjectAnimals
dc.subjectConnective tissue growth factor
dc.subjectCytokines
dc.subjectDisease models, animal
dc.subjectDna damage
dc.subjectFemale
dc.subjectKidney
dc.subjectKidney diseases
dc.subjectMale
dc.subjectMice, inbred c57bl
dc.subjectMyocardial infarction
dc.subjectNicotinamide phosphoribosyltransferase
dc.subjectPhosphotransferases (alcohol group acceptor)
dc.subjectPremenopause
dc.subjectReactive oxygen species
dc.subjectSex factors
dc.subjectSirtuin 1
dc.subjectSirtuin 3
dc.subjectSmoke
dc.subjectTobacco products
dc.subjectAlpha smooth muscle actin
dc.subjectNicotinamide riboside
dc.subjectNicotinamide riboside 1
dc.subjectReactive oxygen metabolite
dc.subjectUnclassified drug
dc.subjectActin
dc.subjectAlpha-smooth muscle actin, mouse
dc.subjectCcn2 protein, mouse
dc.subjectCytokine
dc.subjectNicotinamide phosphoribosyltransferase, mouse
dc.subjectNmrk1 protein, mouse
dc.subjectPhosphotransferase
dc.subjectSirt1 protein, mouse
dc.subjectSirt3 protein, mouse
dc.subjectAnimal experiment
dc.subjectAnimal model
dc.subjectAnimal tissue
dc.subjectArticle
dc.subjectC57bl 6 mouse
dc.subjectControlled study
dc.subjectDna fragmentation
dc.subjectGlomerulus
dc.subjectHeart ejection fraction
dc.subjectHeart hemodynamics
dc.subjectHeart infarction
dc.subjectHeart output
dc.subjectKidney fibrosis
dc.subjectKidney injury
dc.subjectKidney proximal tubule
dc.subjectLong term exposure
dc.subjectNonhuman
dc.subjectPassive smoking
dc.subjectRenal protection
dc.subjectSex difference
dc.subjectAnimal
dc.subjectC57bl mouse
dc.subjectComparative study
dc.subjectComplication
dc.subjectDisease model
dc.subjectGenetics
dc.subjectKidney disease
dc.subjectMetabolism
dc.subjectPathology
dc.subjectSex factor
dc.subjectTobacco
dc.titleSex-based differences in myocardial infarction-induced kidney damage following cigarette smoking exposure: More renal protection in premenopausal female mice
dc.typeArticle

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