| Titre : |
Cigarette smoking and atherosclerotic cardiovascular disease |
| Type de document : |
document électronique |
| Auteurs : |
Mari Ishida, Auteur ; Chiemi Sakai, Auteur ; Takafumi Ishida, Auteur ; Yusuke Kobayashi, Auteur |
| Editeur : |
Tokyo [Japan] : Japan atherosclerosis society |
| Année de publication : |
2024 |
| Collection : |
Journal of atherosclerosis and thrombosis |
| Importance : |
12 p. |
| Présentation : |
ill. |
| Langues : |
Anglais (eng) |
| Catégories : |
[TABAC] tabagisme:pathologie:pathologie cardio-vasculaire:athérosclérose
[TABAC] tabagisme:tabagisme actif
|
| Index. décimale : |
TA 3.2.2.5 Pathologies cardiovasculaires |
| Résumé : |
The detrimental effects of cigarette smoking on cardiovascular health, particularly atherosclerosis and thrombosis, are well established, and more detailed mechanisms continue to emerge. As the fundamentalpathophysiology of the adverse effects of smoking, endothelial dysfunction, inflammation, and thrombosis are considered to be particularly important. Cigarette smoke induces endothelial dysfunction, leading to impaired vascular dilation and hemostasis regulation. Factors contributing to endothelial dysfunction include reduced bioavailability of nitric oxide, increased levels of superoxide anion, and endothelin release. Chronic inflammation
of the vascular wall is a central pathogenesis of smoking-induced atherosclerosis. Smoking systemically elevates inflammatory markers and induces the expression of adhesion molecules and cytokines in various tissues. Pattern recognition receptors and damage-associated molecular patterns play crucial roles in the mechanism underlying smoking-induced inflammation. Smoking-induced DNA damage and activation of innate immunity, such as the NLRP3 inflammasome, cyclic GMP–AMP synthase (cGAS)-stimulator of interferon genes (STING) pathway, and Toll-like receptor 9, are shown to amplify inflammatory cytokine expression. Cigarette smoke-induced
oxidative stress and inflammation influence platelet adhesion, aggregation, and coagulation via adhesion molecule upregulation. Furthermore, it affects the coagulation cascade and fibrinolysis balance, causing thrombus formation. Matrix metalloproteinases contribute to plaque vulnerability and atherothrombotic events. The impact of smoking on inflammatory cells and adhesion molecules further intensifies the risk of atherothrombosis.Collectively, exposure to cigarette smoke exerts profound effects on endothelial function, inflammation, and thrombosis, contributing to the development and progression of atherosclerosis and atherothrombotic
cardiovascular diseases. Understanding these intricate mechanisms highlights the urgent need for smoking cessation to protect cardiovascular health. This comprehensive review investigates the multifaceted mechanisms through which smoking contributes to these life-threatening conditions.
|
| En ligne : |
https://doi.org/10.5551%2Fjat.RV22015 |
| Format de la ressource électronique : |
Article en ligne |
| Permalink : |
https://biblio.fares.be/opac_css/index.php?lvl=notice_display&id=10183 |
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