Key result
Sodium hydrosulfide reduces myocardial damage, vascular spasm, and inflammation in rat alcoholic cardiomyopathy.
Why the study?
Alcoholic cardiomyopathy has a high prevalence and rapid complication development, but effective pharmacotherapy remains an open question, with hydrogen sulfide donors representing a prospective approach.
Does the hydrogen sulfide donor sodium hydrosulfide (NaHS) improve histological myocardial changes in rats with experimental alcoholic cardiomyopathy?
Does the hydrogen sulfide donor sodium hydrosulfide (NaHS) improve histological myocardial changes in rats with experimental alcoholic cardiomyopathy?
In a rat model of alcoholic cardiomyopathy, intraperitoneal administration of the hydrogen sulfide donor NaHS demonstrated cardioprotective effects by attenuating alcohol-induced microvascular and myocardial histological damage.
Answers are grounded in this paper and cite their sources.
Hypothesis-generating for hydrogen sulfide donors in cardiomyopathy; should not yet influence human practice.
Relevance. Alcoholic cardiomyopathy is an actual problem today, because it is characterized by high prevalence and rapid development of complications. The question of effective pharmacotherapy of alcoholic heart damage remains open. The use of hydrogen sulfide donors is prospective in this direction. Aim. To evaluate the influence of hydrogen sulfide donor on histological changes of rat myocardium during experimental alcoholic cardiomyopathy in rats. Methods. Experimental studies were conducted on 30 white non-linear male rats. According to the purpose of the study, all animals were divided into three groups (10 rats each): 1st group – control; 2nd group - animals that were simulated alcoholic cardiomyopathy by intragastric administration of 20% aqueous ethanol solution (at a dose of 8 g/kg/day) for 90 days; Group 3 - rats that, after the cessation of alcoholism, were injected with the donor H2S - NaHS in a dose of 3 mg/kg/day intraperitoneally for two weeks. Histological studies of fragments of the left ventricle were carried out on the basis of the Vinnytsia Regional Pathological and Anatomical Bureau according to the generally accepted method using an Olympus BX-41 light microscope (Olympus Europe GmbH, Japan). Results. Data from histological studies showed that alcoholic cardiomyopathy is accompanied by a number of changes in the vessels of the myocardial stroma and muscle fibers. Ischemia and spasm of blood vessels, partial detachment of the endothelial layer, signs of myocardial inflammation, as well as ischemia of muscle fibers, which is accompanied by myolysis, fragmentation, abrasion of transverse striations, areas of hypertrophy, are noted. Under the conditions of using the hydrogen sulfide donor NaHS, the expressiveness of the structural changes of the myocardium initiated by alcoholic cardiomyopathy decreases: the condition of the endothelial lining of the arterioles improves, the signs of vascular spasm, myocardial inflammation, and ischemia of muscle fibers decrease. Conclusion. The conducted histological studies confirmed the presence of donor hydrogen sulfide cardioprotective properties in experimental alcoholic cardiomyopathy.
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Matiash et al. (2025) studied Experimental alcoholic cardiomyopathy (n=30). Sodium hydrosulfide (NaHS, hydrogen sulfide donor) vs. Untreated alcoholic cardiomyopathy group (20% ethanol 8 g/kg/day for 90 days) and vehicle control group was evaluated on Histological changes of left ventricular myocardium (vascular stroma and muscle fibers). Sodium hydrosulfide (NaHS) at /kg/day for two weeks reduced myocardial histological damage, vascular spasm, inflammation, and muscle fiber ischemia in rats with alcoholic cardiomyopathy.
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