| Literature DB >> 30359962 |
Francesco Bifari1, Roberto Manfrini2, Michele Dei Cas3, Cesare Berra4, Matteo Siano2, Massimo Zuin5, Rita Paroni3, Franco Folli6.
Abstract
Accumulating experimental and clinical evidences over the last decade indicate that GLP-1 analogues have a series of central nervous system and peripheral target tissues actions which are able to significantly influence the liver metabolism. GLP-1 analogues pleiotropic effects proved to be efficacious in T2DM subjects not only reducing liver steatosis and ameliorating NAFLD and NASH, but also in lowering plasma glucose and liver inflammation, improving cardiac function and protecting from kidney dysfunction. While the experimental and clinical data are robust, the precise mechanisms of action potentially involved in these protective multi-target effects need further investigation. Here we present a systematic review of the most recent literature data on the multi-target effects of GLP-1 analogues on the liver, on adipose and muscular tissue and on the nervous system, all capable of influencing significant aspects of the fatty liver disease physiopathology. From this analysis, we can conclude that the multi-target beneficial action of the GLP-1 analogues could explain the positive effects observed in animal and human models on progression of NAFLD to NASH.Entities:
Keywords: GLP-1 analogues; Insulin resistance; Liver inflammation; Liver steatosis; Non-alcoholic fatty liver disease – NAFLD; Non-alcoholic steato-hepatitis NASH; Type 2 diabetes
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Year: 2018 PMID: 30359962 DOI: 10.1016/j.phrs.2018.09.025
Source DB: PubMed Journal: Pharmacol Res ISSN: 1043-6618 Impact factor: 7.658