Horlock Duncan, Kaye David M, Winbanks Catherine E, Gao Xiao-Ming, Kiriazis Helen, Donner Daniel G, Gregorevic Paul, McMullen Julie R, Bernardo Bianca C
Baker Heart and Diabetes Institute, Melbourne, VIC 3004, Australia.
Department of Cardiology, Alfred Hospital, Melbourne, VIC 3004, Australia.
Pharmaceuticals (Basel). 2021 Mar 15;14(3):263. doi: 10.3390/ph14030263.
Cardiac fibrosis is associated with most forms of cardiovascular disease. No reliable therapies targeting cardiac fibrosis are available, thus identifying novel drugs that can resolve or prevent fibrosis is needed. Tilorone, an antiviral agent, can prevent fibrosis in a mouse model of lung disease. We investigated the anti-fibrotic effects of tilorone in human cardiac fibroblasts in vitro by performing a radioisotopic assay for [H]-proline incorporation as a proxy for collagen synthesis. Exploratory studies in human cardiac fibroblasts treated with tilorone (10 µM) showed a significant reduction in transforming growth factor-β induced collagen synthesis compared to untreated fibroblasts. To determine if this finding could be recapitulated in vivo, mice with established pathological remodelling due to four weeks of transverse aortic constriction (TAC) were administered tilorone (50 mg/kg, i.p) or saline every third day for eight weeks. Treatment with tilorone was associated with attenuation of fibrosis (assessed by Masson's trichrome stain), a favourable cardiac gene expression profile and no further deterioration of cardiac systolic function determined by echocardiography compared to saline treated TAC mice. These data demonstrate that tilorone has anti-fibrotic actions in human cardiac fibroblasts and the adult mouse heart, and represents a potential novel therapy to treat fibrosis associated with heart failure.
心脏纤维化与大多数形式的心血管疾病相关。目前尚无针对心脏纤维化的可靠治疗方法,因此需要鉴定能够解决或预防纤维化的新型药物。替洛隆是一种抗病毒药物,可在肺部疾病小鼠模型中预防纤维化。我们通过进行放射性同位素测定法检测[H]-脯氨酸掺入量(作为胶原合成的替代指标),在体外研究了替洛隆对人心脏成纤维细胞的抗纤维化作用。对用替洛隆(10 µM)处理的人心脏成纤维细胞进行的探索性研究表明,与未处理的成纤维细胞相比,转化生长因子-β诱导的胶原合成显著减少。为了确定这一发现是否能在体内得到重现,对因四周主动脉缩窄(TAC)而出现病理性重塑的小鼠,每隔一天腹腔注射替洛隆(50 mg/kg)或生理盐水,持续八周。与生理盐水处理的TAC小鼠相比,替洛隆治疗与纤维化减轻(通过Masson三色染色评估)、有利的心脏基因表达谱以及超声心动图测定的心脏收缩功能无进一步恶化相关。这些数据表明,替洛隆在人心脏成纤维细胞和成年小鼠心脏中具有抗纤维化作用,代表了一种治疗与心力衰竭相关纤维化的潜在新型疗法。