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      SCOPUS SCIE

      Betulinic acid inhibits high-fat diet-induced obesity and improves energy balance by activating AMPK

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      https://www.riss.kr/link?id=A107699483

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      <P><B>Abstract</B></P> <P><B>Background and aim</B></P> <P>Metabolic syndromes are prevalent worldwide and result in various complications including obesity, cardiovascular disease and type II dia...

      <P><B>Abstract</B></P> <P><B>Background and aim</B></P> <P>Metabolic syndromes are prevalent worldwide and result in various complications including obesity, cardiovascular disease and type II diabetes. Betulinic acid (BA) is a naturally occurring triterpenoid that has anti-inflammatory properties. We hypothesized that treatment with BA may result in decreased body weight gain, adiposity and hepatic steatosis in a diet-induced mouse model of obesity.</P> <P><B>Methods and results</B></P> <P>Mice fed a high-fat diet and treated with BA showed less weight gain and tissue adiposity without any change in calorie intake. Gene expression profiling of mouse tissues and cell lines revealed that BA treatment increased expression of lipid oxidative genes and decreased that of lipogenesis-related genes. This modulation was mediated by increased AMP-activated protein kinase (AMPK) phosphorylation, which facilitates energy expenditure, lipid oxidation and thermogenic capacity and exerts protective effects against obesity and nonalcoholic fatty liver disease. Overall, BA markedly inhibited the development of obesity and nonalcoholic fatty liver disease in mice fed a high-fat diet, and AMPK activation in various tissues and enhanced thermogenesis are two possible mechanisms underlying the antiobesity and antisteatogenic effects of BA.</P> <P><B>Conclusions</B></P> <P>The current findings suggest that treatment with BA is a potential dietary strategy for preventing obesity and nonalcoholic fatty liver disease.</P> <P><B>Highlights</B></P> <P> <UL> <LI> Betulinic acid (BA) decreased body weight gain, adiposity and hepatic steatosis in a diet-induced obese mouse model. </LI> <LI> BA treatment increased expression of lipid oxidative genes and decreased mRNA expression related to lipogenesis. </LI> <LI> BA treatment enhanced activation of AMPK, which facilitates energy expenditure, lipid oxidation and thermogenesis. </LI> <LI> BA intake may be a potential dietary strategy for preventing obesity and nonalcoholic fatty liver disease. </LI> </UL> </P>

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