Shastri Sonia, Shinde Tanvi, Woolley Krystel L, Smith Jason A, Gueven Nuri, Eri Rajaraman
Gut Health Laboratory, School of Health Sciences, College of Health and Medicine, University of Tasmania, Launceston, TAS, Australia.
Centre for Food Innovation, Tasmanian Institute of Agriculture, University of Tasmania, Launceston, TAS, Australia.
Front Pharmacol. 2021 Aug 23;12:709973. doi: 10.3389/fphar.2021.709973. eCollection 2021.
Ulcerative colitis (UC) is characterised by chronic, relapsing, idiopathic, and multifactorial colon inflammation. Recent evidence suggests that mitochondrial dysfunction plays a critical role in the onset and recurrence of this disease. Previous reports highlighted the potential of short-chain quinones (SCQs) for the treatment of mitochondrial dysfunction due to their reversible redox characteristics. We hypothesised that a recently described potent mitoprotective SCQ (UTA77) could ameliorate UC symptoms and pathology. In a dextran sodium sulphate- (DSS-) induced acute colitis model in C57BL/6J mice, UTA77 substantially improved DSS-induced body weight loss, disease activity index (DAI), colon length, and histopathology. UTA77 administration also significantly increased the expression of tight junction (TJ) proteins occludin and zona-occludin 1 (ZO-1), which preserved intestinal barrier integrity. Similar responses were observed in the spontaneous Winnie model of chronic colitis, where UTA77 significantly improved DAI, colon length, and histopathology. Furthermore, UTA77 potently suppressed elevated levels of proinflammatory cytokines and chemokines in colonic explants of both DSS-treated and Winnie mice. These results strongly suggest that UTA77 or its derivatives could be a promising novel therapeutic approach for the treatment of human UC.
溃疡性结肠炎(UC)的特征是慢性、复发性、特发性和多因素引起的结肠炎症。最近的证据表明,线粒体功能障碍在该疾病的发病和复发中起关键作用。先前的报道强调了短链醌(SCQ)因其可逆的氧化还原特性而具有治疗线粒体功能障碍的潜力。我们假设,一种最近被描述的强效线粒体保护SCQ(UTA77)可以改善UC症状和病理状况。在C57BL/6J小鼠的葡聚糖硫酸钠(DSS)诱导的急性结肠炎模型中,UTA77显著改善了DSS诱导的体重减轻、疾病活动指数(DAI)、结肠长度和组织病理学。给予UTA77还显著增加了紧密连接(TJ)蛋白闭合蛋白和闭合蛋白1(ZO-1)的表达,从而维持了肠道屏障的完整性。在慢性结肠炎的自发性Winnie模型中也观察到了类似的反应,其中UTA77显著改善了DAI、结肠长度和组织病理学。此外,UTA77强烈抑制了DSS处理的小鼠和Winnie小鼠结肠外植体中促炎细胞因子和趋化因子的升高水平。这些结果强烈表明,UTA77或其衍生物可能是治疗人类UC的一种有前景的新型治疗方法。