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10.1016/j.cmet.2017.03.005 http://scihub22266oqcxt.onion/10.1016/j.cmet.2017.03.005 C5494834!5494834!28380381     free     free     free Warning: file_get_contents(https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&id=28380381&cmd=llinks): Failed to open stream: HTTP request failed! HTTP/1.1 429 Too Many Requests in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 215 Deprecated: Implicit conversion from float 233.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 233.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 233.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 233.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534       Cell+Metab 2017 ; 25 (4): 935-944.e4 Nephropedia Template TP {{tp|p=28380381|t=2017. FGF21 Regulates Metabolism Through Adipose-Dependent and -Independent Mechanisms |pdf=|usr=}}{{28380381}} gab.com Text FGF21 Regulates Metabolism Through Adipose-Dependent and -Independent Mechanisms JO: Cell Metab http://www.kidney.de/pget.php?&tw=1&pmid=28380381 #FOAvip FGF21 is an endocrine hormone that regulates energy homeostasis and insulin sensitivity. The mechanism of FGF21 action and the tissues responsible for these effects have been controversial, with both adipose tissues and the central nervous system being identified as the target site mediating FGF21-dependent increases in insulin sensitivity, energy expenditure, and weight loss. Here we show that while FGF21 signaling to adipose tissue is required for the acute insulin sensitizing effects of FGF21, FGF21 signaling to adipose tissue is not required for its chronic effects to increase energy expenditure and lower body weight. Also, in contrast to previous studies, we found that adiponectin is dispensable for the metabolic effects of FGF21 in increasing insulin sensitivity and energy expenditure. Instead, FGF21 acutely enhances insulin sensitivity through actions on brown adipose tissue. Our data reveal that the acute and chronic effects of FGF21 can be dissociated through adipose-dependent and -independent mechanisms. Twit Text FOAVip FGF21 Regulates Metabolism Through Adipose-Dependent and -Independent Mechanisms ????Cell Metab http://www.kidney.de/pget.php?&tw=1&pmid=28380381 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=28380381 #FOAvip English Wikipedia <ref>{{Cite pmid|28380381}}</ref> FGF21 Regulates Metabolism Through Adipose-Dependent and -Independent Mechanisms #MMPMID28380381 BonDurant LD; Ameka M; Naber MC; Markan KR; Idiga SO; Acevedo MR; Walsh SA; Ornitz DM; Potthoff MJ Cell Metab 2017[Apr]; 25 (4): 935-944.e4 PMID28380381show ga FGF21 is an endocrine hormone that regulates energy homeostasis and insulin sensitivity. The mechanism of FGF21 action and the tissues responsible for these effects have been controversial, with both adipose tissues and the central nervous system being identified as the target site mediating FGF21-dependent increases in insulin sensitivity, energy expenditure, and weight loss. Here we show that while FGF21 signaling to adipose tissue is required for the acute insulin sensitizing effects of FGF21, FGF21 signaling to adipose tissue is not required for its chronic effects to increase energy expenditure and lower body weight. Also, in contrast to previous studies, we found that adiponectin is dispensable for the metabolic effects of FGF21 in increasing insulin sensitivity and energy expenditure. Instead, FGF21 acutely enhances insulin sensitivity through actions on brown adipose tissue. Our data reveal that the acute and chronic effects of FGF21 can be dissociated through adipose-dependent and -independent mechanisms. äFGF21 Regulates Metabolism Through Adipose-Dependent and -Independent (epmc).pdf DeepDyve Pubget Overpricing