PMID- 35861275 OWN - NLM STAT- MEDLINE DCOM- 20220722 LR - 20220727 IS - 1743-2928 (Electronic) IS - 1351-0002 (Print) IS - 1351-0002 (Linking) VI - 27 IP - 1 DP - 2022 Dec TI - Beneficial role of naringin against methotrexate-induced injury to rat testes: biochemical and ultrastructural analyses. PG - 158-166 LID - 10.1080/13510002.2022.2101832 [doi] AB - BACKGROUND: Methotrexate (MTX) is a commonly used chemotherapeutic drug that has adverse toxic effects on germ cells. Naringin (NG) is a natural flavanone glycoside, with different phytotherapeutic applications, and its possible protective effects against MTX-induced testicular tissue damage were investigated in this study. METHODS: Low and high doses of NG (40 and 80 mg/kg/day) were given for 10 days by intraperitoneal (i.p.) injection and MTX (20 mg/kg i.p.) was given at the 4th day of the experiment, with or without NG in rats. RESULTS: The obtained results showed that exposure to MTX increased malondialdehyde (MDA) levels and nitric oxide (NO) production compared with the control. In the meantime, MTX depleted catalse (CAT), superoxide dismutase (SOD), glutathione reductase (GR), glutathione peroxidase (GPx), and reduced glutathione (GSH) in the testicular tissue. Further, serum testosterone levels were significantly decreased in the MTX group. NG significantly counteracted the aforementioned effects of MTX; however, NG80 was more effective in restoring SOD, GR, MDA and NO. Interestingly, NG80 achieved a better improvement in the ultrastructural pattern of the testicular cells in MTX-exposed rats. CONCLUSION: These results indicated, for the first time, that NG could be a potential candidate therapy against MTX-reprotoxic impacts. FAU - Elsawy, Hany AU - Elsawy H AUID- ORCID: 0000-0001-8250-4023 AD - Department of Chemistry, College of Science, King Faisal University, Al-Ahsa, Saudi Arabia. AD - Department of Chemistry, Faculty of Science, Tanta University, Tanta, Egypt. FAU - Alzahrani, Abdullah M AU - Alzahrani AM AD - Department of Biological Sciences, College of Science, King Faisal University, Al-Ahsa, Saudi Arabia. FAU - Alfwuaires, Manal AU - Alfwuaires M AD - Department of Biological Sciences, College of Science, King Faisal University, Al-Ahsa, Saudi Arabia. FAU - Abdel-Moneim, Ashraf M AU - Abdel-Moneim AM AD - Department of Biological Sciences, College of Science, King Faisal University, Al-Ahsa, Saudi Arabia. AD - Department of Zoology, Faculty of Science, Alexandria University, Alexandria, Egypt. FAU - Khalil, Mahmoud AU - Khalil M AD - Department of Zoology, Faculty of Science, Alexandria University, Alexandria, Egypt. AD - Department of Biological Sciences, Faculty of Science, Beirut Arab University, Beirut, Lebanon. LA - eng PT - Journal Article PL - England TA - Redox Rep JT - Redox report : communications in free radical research JID - 9511366 RN - 0 (Antioxidants) RN - 0 (Flavanones) RN - EC 1.15.1.1 (Superoxide Dismutase) RN - N7TD9J649B (naringin) RN - YL5FZ2Y5U1 (Methotrexate) SB - IM MH - Animals MH - Antioxidants/metabolism MH - *Flavanones/pharmacology/therapeutic use MH - Male MH - *Methotrexate/toxicity MH - Oxidative Stress MH - Rats MH - Rats, Wistar MH - Superoxide Dismutase/metabolism MH - Testis/metabolism PMC - PMC9310850 OTO - NOTNLM OT - Methotrexate OT - antioxidants OT - naringin OT - nitric oxide OT - oxidative stress OT - testicular toxicity OT - testosterone OT - ultrastructure COIS- No potential conflict of interest was reported by the author(s). EDAT- 2022/07/22 06:00 MHDA- 2022/07/23 06:00 PMCR- 2022/07/21 CRDT- 2022/07/21 07:24 PHST- 2022/07/21 07:24 [entrez] PHST- 2022/07/22 06:00 [pubmed] PHST- 2022/07/23 06:00 [medline] PHST- 2022/07/21 00:00 [pmc-release] AID - 2101832 [pii] AID - 10.1080/13510002.2022.2101832 [doi] PST - ppublish SO - Redox Rep. 2022 Dec;27(1):158-166. doi: 10.1080/13510002.2022.2101832.