PMID- 33489777 OWN - NLM STAT- PubMed-not-MEDLINE LR - 20231110 IS - 2214-7500 (Electronic) IS - 2214-7500 (Linking) VI - 8 DP - 2021 TI - Hepatoprotective, antioxidant and, anti-inflammatory potentials of gallic acid in carbon tetrachloride-induced hepatic damage in Wistar rats. PG - 177-185 LID - 10.1016/j.toxrep.2021.01.001 [doi] AB - Gallic acid (GA) is a known phenolic compound with anti-inflammatory, antioxidant, and anti-cancer activities. The objective of this research is to evaluate the preventive role of GA against carbon tetrachloride (CCl(4)) induced liver fibrosis. Thirty-five (35) male Wistar rats were used in this study and were equally distributed into five groups (7 rats each). All groups were acclimatized for a week, Group I (control) rats were administered distilled water only. Group II rats were induced with a single dose of CCl(4) (1.25 mL/kg in olive oil (1:1); IP) to cause hepatic damage, while Groups III, IV, and V, rats were intoxicated with CCl(4). After 24 h the rats in groups III, IV, and V were given 50 mg/kg of silymarin, 50 mg/kg of GA, and 100 mg/kg of GA daily for one week respectively. Rats were sacrificed and fasting blood was estimated for biochemical analysis while the liver was excised for molecular studies. Results from this study revealed that GA significantly decreases serum hepatic enzymes, down-regulate the expression of pro-inflammatory cytokines, interleukin 1 beta (IL-1B), interleukin 6 (IL-6), cyclooxygenase 2 (COX 2), and tumor necrosis factor-alpha (TNF alpha), and up-regulate antioxidant gene expression (superoxide dismutase and catalase). The use of gallic acid as natural antioxidants can be promising in ameliorating liver diseases. CI - (c) 2021 The Authors. Published by Elsevier B.V. FAU - Ojeaburu, S I AU - Ojeaburu SI AD - Department of Biochemistry, Faculty of Life Sciences, University of Benin, Benin City, Nigeria. FAU - Oriakhi, K AU - Oriakhi K AD - Department of Medical Biochemistry, School of Basic Medical Sciences, University of Benin, Benin City, Nigeria. LA - eng PT - Journal Article DEP - 20210108 PL - Ireland TA - Toxicol Rep JT - Toxicology reports JID - 101630272 PMC - PMC7806503 OTO - NOTNLM OT - ALB, albumin OT - ALP, alkaline phosphatase OT - ALT, alanine transaminase OT - ARE, antioxidant response element OT - AST, aspartate transaminase OT - Anti-inflammatory OT - Antioxidant OT - CAT, catalase OT - CCl4, carbon tetrachloride OT - COX2, cyclooxygenase 2 OT - Cytokines OT - DGA, dodecylgallate OT - GA, gallic acid OT - GAPDH, glyceraldehydes3-phosphate dehydrogenase OT - GGT, gamma-glutamyl transpeptidase OT - GSH, glutathione OT - Gallic acid OT - IL-1beta, interleukin 1beta OT - IL-6, interleukin 6 OT - Keap1, kelch-like ECH-associated protein 1 OT - Liver disease OT - MDA, maloniadehyde OT - NF-kappaB, nuclear factor kappa light chain enhancer of activated B cells OT - Nrf 2, nuclear factor erythroid- derived 2 like 2 genes OT - PBS, phosphate-buffered saline OT - RNA, ribonucleic acid OT - RT-PCR, reverse transcription-polymerase chain reaction OT - SOD, superoxide dismutase OT - SYBR, green fluorescent DNA Stain OT - TB, total bilirubin OT - TNF alpha, tumor necrosis factor-alpha OT - TP, total protein OT - cDNA, complementary deoxyribonucleic acid OT - iNOS, inducible nitric oxide synthase OT - qPCR, quantitative polymerase chain reaction COIS- The authors declare no conflict of interest EDAT- 2021/01/26 06:00 MHDA- 2021/01/26 06:01 PMCR- 2021/01/08 CRDT- 2021/01/25 05:43 PHST- 2020/10/01 00:00 [received] PHST- 2020/12/30 00:00 [revised] PHST- 2021/01/04 00:00 [accepted] PHST- 2021/01/25 05:43 [entrez] PHST- 2021/01/26 06:00 [pubmed] PHST- 2021/01/26 06:01 [medline] PHST- 2021/01/08 00:00 [pmc-release] AID - S2214-7500(21)00001-9 [pii] AID - 10.1016/j.toxrep.2021.01.001 [doi] PST - epublish SO - Toxicol Rep. 2021 Jan 8;8:177-185. doi: 10.1016/j.toxrep.2021.01.001. eCollection 2021.