2017
DOI: 10.1016/j.metabol.2017.05.009
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Albiflorin ameliorates obesity by inducing thermogenic genes via AMPK and PI3K/AKT in vivo and in vitro

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Cited by 42 publications
(37 citation statements)
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“…Curcumin and astaxanthin can inhibit liver inflammation and fibrosis and decrease lipid and adipose tissue accumulation [30,31]. Albiflorin also significantly reduced the weights of liver and white adipose tissue [32]. In this study, we found that ginkgolide B administration was associated not only with weight loss and reduced epididymal adipose tissue weight but also with decreased fat accumulation and fat vacuoles in liver tissue of HFD-fed mice.…”
Section: Discussionsupporting
confidence: 49%
“…Curcumin and astaxanthin can inhibit liver inflammation and fibrosis and decrease lipid and adipose tissue accumulation [30,31]. Albiflorin also significantly reduced the weights of liver and white adipose tissue [32]. In this study, we found that ginkgolide B administration was associated not only with weight loss and reduced epididymal adipose tissue weight but also with decreased fat accumulation and fat vacuoles in liver tissue of HFD-fed mice.…”
Section: Discussionsupporting
confidence: 49%
“…Total RNA was extracted from BR, SR, or BR-SR mixture-treated cells using QIAzol lysis reagent (Qiagen Sciences Inc., Germantown, MD, USA) and GeneAll RiboEx Total RNA extraction kit (GeneAll Biotechnology, Seoul, Republic of Korea) as previously described [25]. mRNA evaluation was performed using a StepOnePlus Real-time RT-PCR System (Applied Biosystems, Foster City, CA, USA).…”
Section: Methodsmentioning
confidence: 99%
“…Determination of total protein concentration and western blot analysis were performed as described previously [25, 26]. …”
Section: Methodsmentioning
confidence: 99%
“…AMPK represents an attractive target for the treatment of NAFLD and diabetes, and its activity is modulated by various factors such as adiponectin, metformin, and an increase in intracellular AMP/ATP ratio [50,[53][54][55]. Metformin targets mitochondrial complex I to inhibit ATP synthesis [56,57], leading to an increase in AMP/ATP ratio and activation of AMPK [58,59].…”
Section: Fam3a and Hepatic Ampk Activationmentioning
confidence: 99%