2018
DOI: 10.1016/j.clnu.2017.05.028
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Genistein supplementation improves insulin resistance and inflammatory state in non-alcoholic fatty liver patients: A randomized, controlled trial

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Cited by 84 publications
(82 citation statements)
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“…Consistent with the findings in ESRRA null mice, ESRRA inverse agonists, compound 29 (C29) and compound 50 (C50), also show obesity resistance in DIO mouse models [94][95][96]. Recent studies on the ESRRA activator, genistein, have shown beneficial effects in preclinical dietary NAFLD models, as well as in a randomized, controlled clinical trial on NAFLD patients [97][98][99][100][101]. Genistein increases AMPK activity, lipid catabolism, and mitochondrial activity, while reducing de novo lipogenesis.…”
Section: Esrra As a Target For Nafldsupporting
confidence: 64%
“…Consistent with the findings in ESRRA null mice, ESRRA inverse agonists, compound 29 (C29) and compound 50 (C50), also show obesity resistance in DIO mouse models [94][95][96]. Recent studies on the ESRRA activator, genistein, have shown beneficial effects in preclinical dietary NAFLD models, as well as in a randomized, controlled clinical trial on NAFLD patients [97][98][99][100][101]. Genistein increases AMPK activity, lipid catabolism, and mitochondrial activity, while reducing de novo lipogenesis.…”
Section: Esrra As a Target For Nafldsupporting
confidence: 64%
“…Despite no inhibition of hepatic steatosis, genistein can attenuate steatohepatitis induced in methionine‐choline‐deficient (MCD) diet‐fed mice by alleviating AMPK inactivation and suppressing inflammation . In a recently conducted trial, oral supplementation with genistein could reduce insulin resistance, oxidative, and inflammatory indices along with improvement in fat metabolism in patients with NAFLD . Anthocyanins belong to a class of plant flavonoids rich‐contained in the berries of bilberry and black currant.…”
Section: Nafld Therapeutics From a Mitochondria‐centric Perspectivementioning
confidence: 99%
“…13,14 Subsequently, emerging clinical trials and animal experiments verified the benefits of genistein on glucose intolerance, insulin sensitivity and lipid profile disorders. 15,16 It has been indicated that the potential mechanisms deciphering the protective effects of genistein against metabolic disorders included directly enhancing the proliferation of β-cells, inhibiting apoptosis, promoting insulin secretion, epigenetic modifications, regulating the cAMP/PKA signaling pathway, and modulating the gut microbiota. 12,17 However, studies exploring the effects and mechanism of perinatal genistein consumption on transgenerational metabolic health are lacking.…”
Section: Introductionmentioning
confidence: 99%