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Gentianella acuta-derived Gen-miR-5 regulates HDAC6 lactylation by targeting PFKP/YAP/p300 axis to attenuate cardiac hypertrophy
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作者 Hongyao Ge Jiahuan Sun +6 位作者 Zhenyu Du Weizhe Liu Cheng Dai Yu Zhang Yu Liu Gaoshan Yang Aiying Li 《Food Science and Human Wellness》 2026年第3期1260-1282,共23页
Impairment of cardiomyocyte mitochondrial function caused by pressure overload is a central event in the development of cardiac hypertrophy(CH).Gentianella acuta Hulten,widely consumed as an herbal tea alternative by ... Impairment of cardiomyocyte mitochondrial function caused by pressure overload is a central event in the development of cardiac hypertrophy(CH).Gentianella acuta Hulten,widely consumed as an herbal tea alternative by the Mongolian and Ewenki hunters,has demonstrated significant protective effects on cardiovascular.However,the bioactive components responsible for the medicinal efficacy of G.acuta,as well as the mechanisms underlying its anti-CH effects,remain incompletely understood.In the present study,we demonstrate that Gen-miR-5,isolated from G.acuta,effectively mitigates angiotensin Ⅱ induced CH.Mechanistically,Gen-miR-5 suppresses the sustained activation of Yes-associated protein(YAP) by downregulating platelet isoform phosphofructokinase,thereby disrupting the YAP/p300/histone deacetylase 6(HDAC6) interaction and subsequently reducing lactylation at the HDAC6 K901 site.Moreover,Gen-miR-5 curtails lactate accumulation in cardiomyocytes,further diminishing lactylation at this site.These processes collectively contribute to the alleviation of mitochondrial oxidative stress,the restoration of mitochondrial membrane potential,and the stabilization of mitochondrial dynamics,thus inhibiting myocardial hypertrophy.These findings highlight the therapeutic potential of miRNAs derived from G.acuta in treating cardiac remodeling diseases and clarify the molecular mechanisms of their cardioprotective effects. 展开更多
关键词 Gentianella acuta-derived miRNAs Cardiac hypertrophy Platelet isoform phosphofructokinase HDAC6 lactylation Mitochondrial homeostasis
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