Abarikwu Sunny O, Okonkwo Chinedu J, Ezim Ogechukwu E, Obinna Victoria C, Nebeolisa Chisom E, Ndufeiya-Kumasi Lauritta C
Department of Biochemistry, Faculty of Science, University of Port Harcourt, Choba, Nigeria.
Reproductive Biology & Molecular Toxicology Research Laboratory, Department of Biochemistry, University of Port Harcourt, Choba, Nigeria.
Naunyn Schmiedebergs Arch Pharmacol. 2024 Dec 14. doi: 10.1007/s00210-024-03699-z.
This study evaluated the long-term protective effect of gallic acid (GAL) against testicular lesions induced by busulfan (BUSLF) in Wistar rats. Thirty (30) male rats weighing 60-70 g were randomized into three groups of ten in each group: control (2 ml kg body weight (b.w) olive oil), BUSLF (10 mg kg b.w), and BUSLF + GAL (10 mg kg b.w BUSLF + 20 mg kg b.w GAL). BUSLF was injected (intraperitoneally) concurrently with GAL (oral gavage) on day 1 but GAL administration continues for 12 weeks in the BUSLF + GAL animals. At the end of the study, all animals did not show relevant changes in body weights, but absolute testis weight and gonado-somatic index were decreased in the BUSLF-treated animals compared to the control values (p < 0.05). These biometric data remained unchanged in the BUSLF + GAL group relative to the control but were higher than the BUSLF values (p < 0.05). GAL co-treatment counteracted BUSLF-induced decrease in glutathione peroxidase activity and an increase in hydrogen peroxide, malondialdehyde, and carbonyl protein concentrations in the testis. Changes in testicular sorbitol and lactate dehydrogenases and myeloperoxidase activities in BUSLF-treated animals were ameliorated in the BUSLF + GAL-treated animals. GAL co-treatment also prevented BUSLF-induced decrease in testosterone and sialic acid concentrations and sperm quality. The spermatogenesis score index and histological changes induced by BUSLF were also abated in the BUSLF + GAL group. GAL has been established as an effective treatment regimen for the gonadal side effects of BUSLF in a rat model.
本研究评估了没食子酸(GAL)对白消安(BUSLF)诱导的Wistar大鼠睾丸损伤的长期保护作用。将30只体重60 - 70克的雄性大鼠随机分为三组,每组10只:对照组(2毫升/千克体重(b.w)橄榄油)、BUSLF组(10毫克/千克b.w)和BUSLF + GAL组(10毫克/千克b.w BUSLF + 20毫克/千克b.w GAL)。在第1天,BUSLF(腹腔注射)与GAL(灌胃)同时给药,但在BUSLF + GAL组动物中,GAL给药持续12周。研究结束时,所有动物体重均未出现相关变化,但与对照组相比,BUSLF处理组动物的睾丸绝对重量和性腺 - 体质量指数降低(p < 0.05)。BUSLF + GAL组的这些生物测量数据相对于对照组保持不变,但高于BUSLF组的值(p < 0.05)。GAL联合治疗抵消了BUSLF诱导的睾丸中谷胱甘肽过氧化物酶活性降低以及过氧化氢、丙二醛和羰基蛋白浓度升高。在BUSLF + GAL处理的动物中,BUSLF处理动物睾丸中山梨醇和乳酸脱氢酶以及髓过氧化物酶活性的变化得到改善。GAL联合治疗还预防了BUSLF诱导的睾酮和唾液酸浓度降低以及精子质量下降。BUSLF + GAL组中BUSLF诱导的精子发生评分指数和组织学变化也有所减轻。在大鼠模型中,GAL已被确立为治疗BUSLF性腺副作用的有效治疗方案。