2018
DOI: 10.1016/j.orcp.2017.02.002
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Phillyrin lowers body weight in obese mice via the modulation of PPAR<beta>/<delta>-ANGPTL 4 pathway

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Cited by 11 publications
(11 citation statements)
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“…The aqueous extract of Forsythiae Fructus reduced the serum gastrin content and promoted gastrointestinal movement, demonstrating an anti-vomiting effect in mice exposed to chemotherapy [ 9 ]. Phillyrin ( 60 ) was shown to exert a remarkable antiobesity effect in high glucose-induced lipid accumulation in HepG2 cells and 3T3-L1 adipocytes, as well as in obese mice [ 149 , 150 , 151 ]. The mechanism of action was possibly due to inducing the liver kinase B1 (LKB1) phosphorylation and activating AMP-activated protein kinase (AMPK), thus reducing expression of sterol regulatory element-binding protein-1c (SREBP-1c) and fatty acid synthase.…”
Section: Pharmacologymentioning
confidence: 99%
“…The aqueous extract of Forsythiae Fructus reduced the serum gastrin content and promoted gastrointestinal movement, demonstrating an anti-vomiting effect in mice exposed to chemotherapy [ 9 ]. Phillyrin ( 60 ) was shown to exert a remarkable antiobesity effect in high glucose-induced lipid accumulation in HepG2 cells and 3T3-L1 adipocytes, as well as in obese mice [ 149 , 150 , 151 ]. The mechanism of action was possibly due to inducing the liver kinase B1 (LKB1) phosphorylation and activating AMP-activated protein kinase (AMPK), thus reducing expression of sterol regulatory element-binding protein-1c (SREBP-1c) and fatty acid synthase.…”
Section: Pharmacologymentioning
confidence: 99%
“…Phillyrin, a major active component of Forsythia suspensa (Thunb. ), has various biological and pharmacological activities, including antiapoptotic, 22 antioxidative, 23 antiviral, 24,25 lipid reducing, 26 antiobesity 27 and anti-inflammatory activities. 28 However, no studies have addressed the effects and the underlying mechanisms of phillyrin in preventing and improving DN.…”
Section: Introductionmentioning
confidence: 99%
“…However, despite that there are many in vivo data supporting the anti-obese action of phillyrin, few studies in the literature have covered the underlying mechanisms. Xiao et al speculated that phillyrin functioned as an AMPK activator, increasing the expression of PPARβ/δ and ANGPTL4 to promote fat metabolism and weight loss in HFD mice [20]. In addition, by using molecular docking technology, phillyrin was identified as an inhibitor of phosphodiesterase 3B (PDE3B).…”
Section: Diabetic Nephropathy In Rats Induced By Hfd and Streptozotocinmentioning
confidence: 99%