PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 32193100-6 2020 Sirt1 activators resveratrol (RSV) and SRT1720 (SRT) ameliorated poly I:C-induced hepatic injury observed via histopathologic analysis and decreased aspartate aminotransferase (AST) and alanine aminotransferase (ALT) levels in the PBC murine model. Resveratrol 17-28 solute carrier family 17 (anion/sugar transporter), member 5 Mus musculus 177-180 32193100-6 2020 Sirt1 activators resveratrol (RSV) and SRT1720 (SRT) ameliorated poly I:C-induced hepatic injury observed via histopathologic analysis and decreased aspartate aminotransferase (AST) and alanine aminotransferase (ALT) levels in the PBC murine model. Resveratrol 17-28 solute carrier family 17 (anion/sugar transporter), member 5 Mus musculus 149-175 30619104-5 2018 Treatment with RES (100 mg/kg body weight) attenuated SEB-induced acute liver injury, as indicated by decreased AST levels and cellular infiltration in the liver. Resveratrol 15-18 solute carrier family 17 (anion/sugar transporter), member 5 Mus musculus 112-115 34180933-11 2021 Biochemical analysis showed that RSV significantly downregulated abnormal increases in serum levels of alanine aminotransferase (ALT), aspartate aminotransferase (AST), blood urea nitrogen (BUN) and creatinine (CRE) caused by long-term d-gal treatment, which effectively improved pathological damage, increased superoxide dismutase (SOD) activity and decreased the content of malondialdehyde (MDA) in the liver and kidneys. Resveratrol 33-36 solute carrier family 17 (anion/sugar transporter), member 5 Mus musculus 135-161 34180933-11 2021 Biochemical analysis showed that RSV significantly downregulated abnormal increases in serum levels of alanine aminotransferase (ALT), aspartate aminotransferase (AST), blood urea nitrogen (BUN) and creatinine (CRE) caused by long-term d-gal treatment, which effectively improved pathological damage, increased superoxide dismutase (SOD) activity and decreased the content of malondialdehyde (MDA) in the liver and kidneys. Resveratrol 33-36 solute carrier family 17 (anion/sugar transporter), member 5 Mus musculus 163-166 34508115-9 2021 In the group treated with AFB2 + 20 mg/kg resveratrol, ALT, AST, BUN and creatinine levels decreased significantly and GSH levels increased compared to only-AFB2 treated group. Resveratrol 42-53 solute carrier family 17 (anion/sugar transporter), member 5 Mus musculus 60-63 21086752-5 2010 Both resveratrol (5 mg kg(-1) day(-1)) and vitamin E (80 mg kg(-1) day(-1)) treatment significantly reduced AST, ALT, GST, IL-10, TNF-alpha, IFN-gamma, VEGF-A and TGF-beta1 activities and levels of TBARS and nitrite, and elevated albumin content, GSH level and activities of SOD, CAT, GR and GPx, compared to ethanol-treated group. Resveratrol 5-16 solute carrier family 17 (anion/sugar transporter), member 5 Mus musculus 108-111