Mohamed Enas Ahmed, Kassem Hussien H
Department of Anatomy and Embryology, Faculty of Medicine, Cairo University, Cairo, Egypt.
Department of Cardiology, Faculty of Medicine, Cairo University, Cairo, Egypt.
Arch Med Sci. 2018 Oct;14(6):1450-1458. doi: 10.5114/aoms.2018.79008. Epub 2018 Oct 23.
The cardiotoxicity of doxorubicin is incompletely understood. We investigated the prophylactic effect of nebivolol on doxorubicin-induced cardiac toxicity.
Thirty rats were divided into a control group, doxorubicin-treated group and nebivolol + doxorubicin-treated group. The specimens were examined using H + E and Masson's trichrome, caspase 3, endothelial nitric oxide synthase (eNOS), inducible nitric oxide synthase (iNOS) and tumor necrosis factor factor-α (TNF-α). The mean area percentage of collagen fiber content, caspase-3, eNOS, iNOS and TNF-α immunoactivities was measured.
The doxorubicin-treated group showed marked myocyte distortion and fragmentation, congestion and cytoplasmic lysis in most fibers. These changes were less intense in the nebivolol-treated group. The mean area percentage of collagen fiber in the nebivolol-treated group was non-significantly smaller ( = 0.07) than that in the doxorubicin-treated group. The expression of caspase-3 ( = 0.03), eNOS ( ≤ 0.001), iNOS ( < 0.001) and TNF-α ( = 0.003) immunoreactivity was improved in the nebivolol-treated group.
Nebivolol exerted a significant protective effect from doxorubicin toxicity. The protective effect appears to be mediated mainly through caspase-3, eNOS, iNOS and TNF-α modulation.
阿霉素的心脏毒性尚未完全明确。我们研究了奈必洛尔对阿霉素诱导的心脏毒性的预防作用。
将30只大鼠分为对照组、阿霉素治疗组和奈必洛尔+阿霉素治疗组。使用苏木精-伊红染色和马松三色染色、半胱天冬酶3、内皮型一氧化氮合酶(eNOS)、诱导型一氧化氮合酶(iNOS)和肿瘤坏死因子-α(TNF-α)对标本进行检测。测量胶原纤维含量、半胱天冬酶-3、eNOS、iNOS和TNF-α免疫活性的平均面积百分比。
阿霉素治疗组显示大多数纤维出现明显的心肌细胞变形和破碎、充血和细胞质溶解。在奈必洛尔治疗组中,这些变化不那么明显。奈必洛尔治疗组胶原纤维的平均面积百分比比阿霉素治疗组略小(=0.07),差异无统计学意义。奈必洛尔治疗组半胱天冬酶-3(=0.03)、eNOS(≤0.001)、iNOS(<0.001)和TNF-α(=0.003)免疫反应性的表达有所改善。
奈必洛尔对阿霉素毒性具有显著的保护作用。这种保护作用似乎主要通过半胱天冬酶-3、eNOS、iNOS和TNF-α的调节来介导。