Page 800 - Read Online
P. 800

Calabrò et al. Hepatoma Res 2020;6:69  I  http://dx.doi.org/10.20517/2394-5079.2020.63                                        Page 3 of 9






























































                                             Figure 2. Beneficial effects of coffee on the liver

               of focal adhesion kinase, inhibition of α-smooth muscle actin (α-sma), and up-regulation of the PPAR-α
               receptor (Peroxisome proliferator-activated receptor alpha) with action on fat deposits, as shown in
                                    [32]
               Figure 2 [30,31] . Quan et al.  showed that caffeine is able to reduce the gene expression of the transcription
               factors Sterol regulatory element-binding protein 1c and 2 (SREBP1c and SREBP2) in HepG2 cells which
               are involved in the synthesis of triglycerides and cholesterol in the liver. This down-regulation represents
               a particularly promising finding as it can facilitate the reduction ofhepatic lipid accumulation typically
               associated with NAFLD. In addition, caffeine also causes the reduction of 3-hydroxy 3-methylglutaryl CoA
               reductase and low density lipoprotein receptor in a dose dependent manner.

                                     [33]
               Furthermore, Helal et al.  conducted a study in animal models in order to demonstrate that the use
               of caffeine can improve liver damage induced by a high-fat diet (HFD). The rats were divided into
   795   796   797   798   799   800   801   802   803   804   805