Meligy Fatma Y, El-Deen Mohammed Hanan Sharaf, Mostafa Tarek M, Elfiky Mohamed M, El-Sayed Mohamed Ashry Israa, Abd-Eldayem Ahmed M, Rizk Nermin I, Sabry Dina, Abd Allah Eman S H, Ahmed Salwa Fares
Histology and Cell Biology Department, Faculty of Medicine, Assiut University, Assiut 71526, Egypt.
Internal Medicine_Critical Care Department, Faculty of Medicine, Assiut University, Assiut 71526, Egypt.
Pharmaceutics. 2022 Jun 22;14(7):1322. doi: 10.3390/pharmaceutics14071322.
This study compared the cardioprotective action of mesenchymal stem cells (MSCs) and PUFAs in a rat model of gentamicin (GM)-induced cardiac degeneration. Male Wistar albino rats were randomized into four groups of eight rats each: group I (control group), group II (gentamicin-treated rats receiving gentamicin intraperitoneally (IP) at dose of 100 mg/kg/day for 10 consecutive days), group III (gentamicin and PUFA group receiving gentamicin IP at dose of 100 mg/kg/day for 10 consecutive days followed by PUFAs at a dose of 100 mg/kg/day for 4 weeks), and group IV (gentamicin and MSC group receiving gentamicin IP at dose of 100 mg/kg/day followed by a single dose of MSCs (1 × 10)/rat IP). Cardiac histopathology was evaluated via light and electron microscopy. Immunohistochemical detection of proliferating cell nuclear antigen (PCNA), caspase-3 (apoptosis), Bcl2, and Bax expression was performed. Moreover, cardiac malonaldehyde (MDA) content, catalase activity, and oxidative stress parameters were biochemically evaluated. Light and electron microscopy showed that both MSCs and PUFAs had ameliorative effects. Their actions were mediated by upregulating PCNA expression, downregulating caspase-3 expression, mitigating cardiac MDA content, catalase activity, and oxidative stress parameters. MSCs and PUFAs had ameliorative effects against gentamicin-induced cardiac degeneration, with MSCs showing higher efficacy compared to PUFAs.
本研究在庆大霉素(GM)诱导的大鼠心脏退变模型中比较了间充质干细胞(MSCs)和多不饱和脂肪酸(PUFAs)的心脏保护作用。雄性Wistar白化大鼠被随机分为四组,每组八只:第一组(对照组),第二组(庆大霉素处理组,大鼠连续10天腹腔注射(IP)100mg/kg/天的庆大霉素),第三组(庆大霉素和PUFA组,大鼠连续10天腹腔注射100mg/kg/天的庆大霉素,随后4周每天腹腔注射100mg/kg/天的PUFAs),以及第四组(庆大霉素和MSC组,大鼠腹腔注射100mg/kg/天的庆大霉素,随后腹腔注射单剂量的MSCs(1×10⁶/只大鼠))。通过光学显微镜和电子显微镜评估心脏组织病理学。进行增殖细胞核抗原(PCNA)、半胱天冬酶-3(凋亡相关)、Bcl2和Bax表达的免疫组化检测。此外,还对心脏丙二醛(MDA)含量、过氧化氢酶活性和氧化应激参数进行了生化评估。光学显微镜和电子显微镜显示,MSCs和PUFAs均具有改善作用。它们的作用是通过上调PCNA表达、下调半胱天冬酶-3表达、减轻心脏MDA含量、过氧化氢酶活性和氧化应激参数来介导的。MSCs和PUFAs对庆大霉素诱导的心脏退变均有改善作用,其中MSCs的疗效高于PUFAs。