Department of Toxicology, Jai Research Foundation, Valvada 396108, Gujarat, India.
Environ Toxicol Pharmacol. 2013 Nov;36(3):769-78. doi: 10.1016/j.etap.2013.07.011. Epub 2013 Jul 24.
The present study examined the protective effect of sulindac on bleomycin-induced lung fibrosis in rats. Animals were divided into saline group, bleomycin group (single intra-tracheal instillation of bleomycin) and bleomycin+sulindac (orally from day 1 to day 20). Bleomycin administration reduced the body weight, altered antioxidant status (such as superoxide dismutase, catalase, glutathione peroxidase, glutathione reductase and glutathione) while it increased the lung weight, hydroxyproline content, collagen deposition and lipid peroxidation. However, simultaneous administration of sulindac improved the body weight, antioxidant status and decreased the collagen deposition in lungs. Moreover, the levels of inflammatory cytokine tumour necrosis factor-α increased in bleomycin-induced group, whereas, on treatment with sulindac the levels of tumour necrosis factor-α were found reduced. Finally, histological evidence also supported the ability of sulindac to inhibit bleomycin-induced lung fibrosis. The results of the present study indicate that sulindac can be used as an agent against bleomycin-induced pulmonary fibrosis.
本研究探讨了舒林酸对博来霉素诱导的大鼠肺纤维化的保护作用。动物分为生理盐水组、博来霉素组(单次气管内滴注博来霉素)和博来霉素+舒林酸组(从第 1 天到第 20 天口服)。博来霉素给药降低了体重,改变了抗氧化状态(如超氧化物歧化酶、过氧化氢酶、谷胱甘肽过氧化物酶、谷胱甘肽还原酶和谷胱甘肽),同时增加了肺重量、羟脯氨酸含量、胶原沉积和脂质过氧化。然而,舒林酸的同时给药改善了体重、抗氧化状态,并减少了肺部的胶原沉积。此外,博来霉素诱导组中肿瘤坏死因子-α 的水平增加,而在用舒林酸治疗时发现肿瘤坏死因子-α的水平降低。最后,组织学证据也支持舒林酸抑制博来霉素诱导的肺纤维化的能力。本研究的结果表明,舒林酸可作为对抗博来霉素诱导的肺纤维化的药物。