Department of Public Health Sciences, BK21PLUS Program in Embodiment: Health-Society Interaction, Graduate School, Korea University, Seoul 02841, Korea.
Department of Pharmaceutics and Pharmaceutical Chemistry, University of Utah, Salt Lake City, UT 84112, USA.
Nutrients. 2019 Dec 12;11(12):3035. doi: 10.3390/nu11123035.
Since arginase has been shown to compete with nitric oxide (NO) synthase, emerging evidence has reported that arginase inhibition improves obesity by increasing NO production. Semen cuscutae (SC), which is a well-known Chinese medicine, has multiple biological functions such as anti-oxidant function and immune regulation. In this study, we investigated whether the SC as a natural arginase inhibitor influences hepatic lipid abnormalities and whole-body adiposity in high-fat diet (HFD)-induced obese mice. The lipid accumulation was significantly reduced by SC treatment in oleic acid-induced hepatic steatosis in vitro. Additionally, SC supplementation substantially lowered HFD-induced increases in arginase activity and weights of liver and visceral fat tissue, while increasing hepatic NO. Furthermore, elevated mRNA expressions of sterol regulatory element-binding transcription factor 1 (SREBP-1c), fatty-acid synthase (FAS), peroxisome proliferator-activated receptor-gamma (PPAR-γ)1, and PPAR-γ2 in HFD-fed mice were significantly attenuated by SC supplementation. Taken together, SC, as a novel natural arginase inhibitor, showed anti-obesity properties by modulating hepatic arginase and NO production and metabolic pathways related to hepatic triglyceride (TG) metabolism.
由于精氨酸酶已被证明与一氧化氮(NO)合酶竞争,新出现的证据表明,通过增加 NO 的产生,精氨酸酶抑制可以改善肥胖。菟丝子(SC)是一种众所周知的中药,具有多种生物学功能,如抗氧化功能和免疫调节。在这项研究中,我们研究了作为天然精氨酸酶抑制剂的 SC 是否会影响高脂肪饮食(HFD)诱导肥胖小鼠的肝脏脂质异常和全身肥胖。SC 处理可显著减少体外油酸诱导的肝脂肪变性中的脂质堆积。此外,SC 补充可显著降低 HFD 诱导的精氨酸酶活性和肝脏及内脏脂肪组织重量的增加,同时增加肝脏中的 NO。此外,HFD 喂养小鼠中固醇调节元件结合转录因子 1(SREBP-1c)、脂肪酸合酶(FAS)、过氧化物酶体增殖物激活受体-γ(PPAR-γ)1 和 PPAR-γ2 的 mRNA 表达水平显著降低,而 SC 补充可显著降低 SREBP-1c、FAS、PPAR-γ1 和 PPAR-γ2 的 mRNA 表达水平。总之,SC 作为一种新型天然精氨酸酶抑制剂,通过调节肝脏精氨酸酶和 NO 的产生以及与肝脏三酰甘油(TG)代谢相关的代谢途径,显示出抗肥胖特性。