Laboratory of Metabolism, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, Maryland (D.P.P., T.Y., D.K., H.B.D., K.W.K., S.K., F.J.G.) and Laboratory of Cellular Biophysics and Inflammation, Pontifical Catholic University of Rio Grande do Sul, Rio Grande do Sul, Brazil (H.B.D.).
Laboratory of Metabolism, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, Maryland (D.P.P., T.Y., D.K., H.B.D., K.W.K., S.K., F.J.G.) and Laboratory of Cellular Biophysics and Inflammation, Pontifical Catholic University of Rio Grande do Sul, Rio Grande do Sul, Brazil (H.B.D.)
J Pharmacol Exp Ther. 2019 Nov;371(2):360-374. doi: 10.1124/jpet.119.256792. Epub 2019 Aug 16.
Nonalcoholic steatohepatitis (NASH) is the progressive stage of nonalcoholic fatty liver disease that highly increases the risk of cirrhosis and liver cancer, and there are few therapeutic options available in the clinic. Withaferin A (WA), extracted from the ayurvedic medicine , has a wide range of pharmacological activities; however, little is known about its effects on NASH. To explore the role of WA in treating NASH, two well defined NASH models were used, the methionine-choline-deficient diet and the 40 kcal% high-fat diet (HFD). In both NASH models, WA treatment or control vehicle was administered to evaluate its hepatoprotective effects. As assessed by biochemical and histologic analyses, WA prevented and therapeutically improved liver injury in both models, as revealed by lower serum aminotransaminases, hepatic steatosis, liver inflammation, and fibrosis. In the HFD-induced NASH model, both elevated serum ceramides and increased hepatic oxidative stress were decreased in the WA-treated group compared with the control vehicle-treated group. To further explore whether WA has an anti-NASH effect independent of its known action in leptin signaling associated with obesity, leptin signaling-deficient ob/ob mice maintained on an HFD were used to induce NASH. WA therapeutically reduced NASH in HFD-treated leptin-deficient ob/ob mice, thus demonstrating a leptin-independent hepatoprotective effect. This study revealed that WA treatment could be an option for NASH treatment.
非酒精性脂肪性肝炎(NASH)是一种非酒精性脂肪肝的进行性阶段,它极大地增加了肝硬化和肝癌的风险,而临床上可供选择的治疗方法很少。从印度草医学中提取的醉茄素 A(WA)具有广泛的药理活性;然而,人们对其在 NASH 中的作用知之甚少。为了探索 WA 治疗 NASH 的作用,我们使用了两种明确的 NASH 模型,即蛋氨酸-胆碱缺乏饮食和 40%高果糖饮食(HFD)。在这两种 NASH 模型中,给予 WA 治疗或对照载体,以评估其对肝脏的保护作用。通过生化和组织学分析评估,WA 预防和治疗了两种模型中的肝损伤,表现为血清转氨酶降低、肝脂肪变性、肝炎症和纤维化减轻。在 HFD 诱导的 NASH 模型中,与对照组相比,WA 治疗组的血清神经酰胺水平升高和肝氧化应激增加均降低。为了进一步探讨 WA 是否具有独立于其与肥胖相关的瘦素信号作用的抗 NASH 作用,我们使用瘦素信号缺陷 ob/ob 小鼠维持在 HFD 上诱导 NASH。WA 治疗可减少 HFD 治疗的瘦素缺陷 ob/ob 小鼠的 NASH,从而显示出瘦素非依赖性的肝脏保护作用。本研究表明,WA 治疗可能是 NASH 治疗的一种选择。