Division of Pharmacology and Therapeutics, Graduate School of Pharmaceutical Sciences, Kumamoto University, Kumamoto, Japan.
Department of Molecular Medicine, Graduate School of Pharmaceutical Sciences, Kumamoto University, Kumamoto, Japan.
Sci Rep. 2020 Mar 9;10(1):4313. doi: 10.1038/s41598-020-61148-2.
Melinjo seed extract (MSE) contains large amounts of polyphenols, including dimers of trans-resveratrol (e.g. gnetin C, L, gnemonoside A, B and D), and has been shown to potentially improve obesity. However, there is no clinical evidence regarding the anti-obesity effects of MSE, and its mechanisms are also unclear. We investigated the hypothesis that MSE supplementation increases the adiponectin (APN) multimerization via the up-regulation of disulfide bond A oxidoreductase-like protein (DsbA-L) under either or both physiological and obese conditions. To investigate the effect of MSE on the physiological condition, 42 healthy young volunteers were enrolled in a randomized, double-blind placebo-controlled clinical trial for 14 days. The participants were randomly assigned to the MSE 150 mg/day, MSE 300 mg/day or placebo groups. Furthermore, in order to investigate the effect of MSE on APN levels under obese conditions, we administered MSE powder (500 or 1000 mg/kg/day) to control-diet- or high-fat-diet (HFD)-fed C57BL/6 mice for 4 weeks. All participants completed the clinical trial. The administration of MSE 300 mg/day was associated with an increase in the ratio of HMW/total APN in relation to the genes regulating APN multimerization, including DsbA-L. Furthermore, this effect of MSE was more pronounced in carriers of the DsbA-L rs191776 G/T or T/T genotype than in others. In addition, the administration of MSE to HFD mice suppressed their metabolic abnormalities (i.e. weight gain, increased blood glucose level and fat mass accumulation) and increased the levels of total and HMW APN in serum and the mRNA levels of ADIPOQ and DsbA-L in adipose tissue. The present study suggests that MSE may exert beneficial effects via APN multimerization in relation to the induction of DsbA-L under both physiological and obese conditions.
美藤果提取物(MSE)含有大量多酚,包括反式白藜芦醇二聚体(如 Gnetin C、L、 gnemonoside A、B 和 D),并已被证明可能有助于改善肥胖。然而,目前尚无关于 MSE 抗肥胖作用的临床证据,其机制也不清楚。我们假设,在生理和肥胖两种情况下,MSE 通过上调二硫键 A 氧化还原酶样蛋白(DsbA-L)增加脂联素(APN)多聚体化。为了研究 MSE 对生理状态的影响,我们招募了 42 名健康的年轻志愿者,进行了为期 14 天的随机、双盲、安慰剂对照临床试验。参与者被随机分配到 MSE 150mg/天、MSE 300mg/天或安慰剂组。此外,为了研究 MSE 在肥胖状态下对 APN 水平的影响,我们给正常饮食喂养或高脂肪饮食(HFD)喂养的 C57BL/6 小鼠喂食 MSE 粉末(500 或 1000mg/kg/天)4 周。所有参与者均完成了临床试验。与调节 APN 多聚化的基因相关,MSE 300mg/天的给药与 HMW/total APN 比值的增加有关,包括 DsbA-L。此外,在 DsbA-L rs191776 G/T 或 T/T 基因型携带者中,MSE 的这种作用更为明显。此外,MSE 对 HFD 小鼠的给药抑制了它们的代谢异常(即体重增加、血糖水平升高和脂肪量积累增加),并增加了血清中总 APN 和 HMW APN 的水平,以及脂肪组织中 ADIPOQ 和 DsbA-L 的 mRNA 水平。本研究表明,MSE 可能通过诱导 DsbA-L 介导 APN 多聚化,在生理和肥胖两种情况下发挥有益作用。