Key result
N-acetyl cysteine significantly reduced cardiac cardiotrophin-1 expression (1.75 vs 2.75, p<0.001) and blunted metabolic and cardiovascular effects in a rat model of fructose-induced metabolic syndrome.
Why the study?
The study investigated the ability of N-acetyl cysteine to alleviate metabolic disorders and protect aortic and cardiac tissues via its influence on cardiotrophin-1 expression in fructose-induced metabolic syndrome.
Does N-acetyl cysteine improve metabolic and cardiovascular parameters in a rat model of fructose-induced metabolic syndrome?
Does N-acetyl cysteine improve metabolic and cardiovascular parameters in a rat model of fructose-induced metabolic syndrome?
Absolute Event Rate: 1.75% vs 2.75%
p-value: p=<0.001
N-acetyl cysteine protects against aortic and myocardial degeneration and fibrosis by down-regulating cardiotrophin-1 in a rat model of metabolic syndrome.
Hypothesis-generating for NAC in metabolic syndrome; human trials required before any clinical consideration.
In this study, we investigated the ability of N-acetyl cysteine (NAC) to alleviate the metabolic disorders in fructose-induced metabolic syndrome (MS) in male rats and to examine its protective effect on aortic and cardiac tissues via its influence on cardiotrophin-1 (CT-1) expression. NAC (20 mg/kg b.w./day) was administered to fructose induced MS animals for 12 weeks. Chronic fructose consumption (20% w/v) increased body weight gain, relative heart weight, systolic blood pressure (SBP), diastolic blood pressure (DBP), insulin resistance (IR), and associated with metabolic alterations. Histological and immunohistochemical examination revealed aortic stiffness and myocardial degeneration and fibrosis together with increased CT-1 expression. Treatment with NAC improved IR, SBP, DBP, and mitigated dyslipidaemia and oxidative stress. Additionally, NAC down-regulated CT-1 expression in the heart and aorta. These findings demonstrated the protective effect of NAC against aortic and myocardial degeneration and fibrosis through down-regulation of CT-1 in fructose induced MS animal model.
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Abdelhaffez et al. (2021) studied Fructose-induced metabolic syndrome (n=32). N-acetyl cysteine vs. Fructose (20% w/v) alone was evaluated on Cardiac cardiotrophin-1 (CT-1) expression score (p=<0.001). N-acetyl cysteine significantly reduced cardiac cardiotrophin-1 expression (1.75 vs 2.75, p<0.001) and blunted metabolic and cardiovascular effects in a rat model of fructose-induced metabolic syndrome.
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