Molecular and cellular mechanisms of cigarette smoke-induced myocardial injury: prevention by vitamin C.

Cardiovascular disease (CVD) remains one of the major killers in modern society. One strong risk factor of CVD is cigarette smoking that causes myocardial injury and leads to the genesis of pathological cardiovascular events. However, the exact toxic component(s) of cigarette smoke (CS) and its mole...

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Main Authors: Archita Das, Neekkan Dey, Arunava Ghosh, Shovanendu Das, Dhruba J Chattopadhyay, Indu B Chatterjee
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2012-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3435405?pdf=render
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spelling doaj-343554d7b0d84524aeaa2c59e53e1e502020-11-25T00:47:14ZengPublic Library of Science (PLoS)PLoS ONE1932-62032012-01-0179e4415110.1371/journal.pone.0044151Molecular and cellular mechanisms of cigarette smoke-induced myocardial injury: prevention by vitamin C.Archita DasNeekkan DeyArunava GhoshShovanendu DasDhruba J ChattopadhyayIndu B ChatterjeeCardiovascular disease (CVD) remains one of the major killers in modern society. One strong risk factor of CVD is cigarette smoking that causes myocardial injury and leads to the genesis of pathological cardiovascular events. However, the exact toxic component(s) of cigarette smoke (CS) and its molecular and cellular mechanisms for causing myocardial injury leading to heart damage and its prevention are largely unknown.Using a guinea pig model, here we show that chronic exposure to CS produces myocardial injury that is prevented by vitamin C. Male guinea pigs were fed either vitamin C-deficient (0.5 mg/day) or vitamin C-sufficient (15 mg/day) diet and subjected to CS exposure from 5 Kentucky Research cigarettes (3R4F)/day (6 days/week) in a smoke chamber up to 8 weeks. Pair-fed sham controls were subjected to air exposure instead of CS exposure under similar conditions. Myocardial injury was produced in CS-exposed marginal vitamin C-deficient guinea pigs as evidenced by release of cardiac Troponin-T and I in the serum, oxidative stress, inflammation, apoptosis, thrombosis and collagen deposition in the myocardium. Treatment of rat cardiomyocyte cells (H9c2) in vitro and guinea pigs in vivo with p-benzoquinone (p-BQ) in amounts derived from CS revealed that p-BQ was a major factor responsible for CS-induced myocardial damage. A moderately large dose of vitamin C (15 mg/day) prevented CS/p-BQ-induced myocardial injury. Population based studies indicated that plasma vitamin C levels of smokers without disease were significantly lower (p = 0,0000) than that of non-smokers. Vitamin C levels of CS-related cardiovascular patients were further lower (p = 0.0000) than that of smokers without disease.The results indicate that dietary supplementation of vitamin C may be a novel and simple therapy for the prevention of pathological cardiovascular events in habitual smokers.http://europepmc.org/articles/PMC3435405?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Archita Das
Neekkan Dey
Arunava Ghosh
Shovanendu Das
Dhruba J Chattopadhyay
Indu B Chatterjee
spellingShingle Archita Das
Neekkan Dey
Arunava Ghosh
Shovanendu Das
Dhruba J Chattopadhyay
Indu B Chatterjee
Molecular and cellular mechanisms of cigarette smoke-induced myocardial injury: prevention by vitamin C.
PLoS ONE
author_facet Archita Das
Neekkan Dey
Arunava Ghosh
Shovanendu Das
Dhruba J Chattopadhyay
Indu B Chatterjee
author_sort Archita Das
title Molecular and cellular mechanisms of cigarette smoke-induced myocardial injury: prevention by vitamin C.
title_short Molecular and cellular mechanisms of cigarette smoke-induced myocardial injury: prevention by vitamin C.
title_full Molecular and cellular mechanisms of cigarette smoke-induced myocardial injury: prevention by vitamin C.
title_fullStr Molecular and cellular mechanisms of cigarette smoke-induced myocardial injury: prevention by vitamin C.
title_full_unstemmed Molecular and cellular mechanisms of cigarette smoke-induced myocardial injury: prevention by vitamin C.
title_sort molecular and cellular mechanisms of cigarette smoke-induced myocardial injury: prevention by vitamin c.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2012-01-01
description Cardiovascular disease (CVD) remains one of the major killers in modern society. One strong risk factor of CVD is cigarette smoking that causes myocardial injury and leads to the genesis of pathological cardiovascular events. However, the exact toxic component(s) of cigarette smoke (CS) and its molecular and cellular mechanisms for causing myocardial injury leading to heart damage and its prevention are largely unknown.Using a guinea pig model, here we show that chronic exposure to CS produces myocardial injury that is prevented by vitamin C. Male guinea pigs were fed either vitamin C-deficient (0.5 mg/day) or vitamin C-sufficient (15 mg/day) diet and subjected to CS exposure from 5 Kentucky Research cigarettes (3R4F)/day (6 days/week) in a smoke chamber up to 8 weeks. Pair-fed sham controls were subjected to air exposure instead of CS exposure under similar conditions. Myocardial injury was produced in CS-exposed marginal vitamin C-deficient guinea pigs as evidenced by release of cardiac Troponin-T and I in the serum, oxidative stress, inflammation, apoptosis, thrombosis and collagen deposition in the myocardium. Treatment of rat cardiomyocyte cells (H9c2) in vitro and guinea pigs in vivo with p-benzoquinone (p-BQ) in amounts derived from CS revealed that p-BQ was a major factor responsible for CS-induced myocardial damage. A moderately large dose of vitamin C (15 mg/day) prevented CS/p-BQ-induced myocardial injury. Population based studies indicated that plasma vitamin C levels of smokers without disease were significantly lower (p = 0,0000) than that of non-smokers. Vitamin C levels of CS-related cardiovascular patients were further lower (p = 0.0000) than that of smokers without disease.The results indicate that dietary supplementation of vitamin C may be a novel and simple therapy for the prevention of pathological cardiovascular events in habitual smokers.
url http://europepmc.org/articles/PMC3435405?pdf=render
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