Department of Endocrinology, Affiliated Hospital of Shandong University of Traditional Chinese Medicine, Jinan, Shandong, PR China.
Department of Cardiovascular, Affiliated Hospital of Shandong University of Traditional Chinese Medicine, Jinan, Shandong, PR China.
Pharm Biol. 2021 Dec;59(1):382-390. doi: 10.1080/13880209.2021.1898648.
CONTEXT: (Willd.) Ohwi (Fabaceae) root extract can lower blood glucose levels; however, whether root polysaccharide (PLP) possesses these effects is still unknown. OBJECTIVE: This study evaluates the therapeutic effect of PLP on diabetic metabolic syndrome. MATERIALS AND METHODS: The db/m mice were assigned to normal control group (NC), db/db mice were divided into four groups randomly (n = 8). The db/db mice received rosiglitazone (10 mg/kg BW) or PLP (100 or 200 mg/kg BW) via oral gavage for 6 weeks. Afterward, blood glucose, insulin, and glycogen content were assayed, and insulin tolerance test (ITT), oral glucose tolerance test (OGTT) were performed. Glucose and lipid metabolism-related parameters and gene expression levels were assayed by ELISA and RT-PCR, respectively. RESULTS: After treatment with HPLP, the values of body weight, epididymal fat, subcutaneous fat, fasting blood glucose, insulin, and HOMA-IR decreased to 45.89 ± 1.66 g, 1.65 ± 0.14 g, 1.97 ± 0.16 g, 14.84 ± 1.52 mM, 9.35 ± 0.98 mU/L, and 5.56 ± 1.26, respectively; the levels of TG, TC, LDL-C, and FFA decreased to 1.67 ± 0.11 mmol/L, 6.23 ± 0.76 mmol/L, 1.29 ± 0.07 mmol/L, and 1.71 ± 0.16 mmol/L, respectively. HPLP down-regulated PEPCK, G6PC, FOXO1, SREBP-1, and ACC mRNA expression ( < 0.01), and up-regulated GS, Akt2, PI3K, GLUT2, PPARα, and LDLR mRNA expression in the liver ( < 0.01). DISCUSSION AND CONCLUSION: PLP exerts antidiabetic effects via activating the PI3K/AKT signalling pathway, thus improving insulin resistance, glucose, and lipid metabolism in db/db mice. Thus, PLP may be considered as a potential antidiabetic agent in clinical therapy.
背景:(Willd.)Ohwi(豆科)根提取物可降低血糖水平;然而,根多糖(PLP)是否具有这些作用尚不清楚。 目的:本研究评估 PLP 对糖尿病代谢综合征的治疗作用。 材料和方法:将 db/m 小鼠分为正常对照组(NC),db/db 小鼠随机分为 4 组(n=8)。db/db 小鼠经口灌胃给予罗格列酮(10mg/kg BW)或 PLP(100 或 200mg/kg BW)6 周。测定血糖、胰岛素和肝糖原含量,进行胰岛素耐量试验(ITT)和口服葡萄糖耐量试验(OGTT)。用 ELISA 和 RT-PCR 分别测定葡萄糖和脂质代谢相关参数和基因表达水平。 结果:经 HPLP 治疗后,体重、附睾脂肪、皮下脂肪、空腹血糖、胰岛素和 HOMA-IR 分别降至 45.89±1.66g、1.65±0.14g、1.97±0.16g、14.84±1.52mM、9.35±0.98mU/L 和 5.56±1.26;TG、TC、LDL-C 和 FFA 水平分别降至 1.67±0.11mmol/L、6.23±0.76mmol/L、1.29±0.07mmol/L 和 1.71±0.16mmol/L。HPLP 下调 PEPCK、G6PC、FOXO1、SREBP-1 和 ACC mRNA 表达( <0.01),上调肝内 GS、Akt2、PI3K、GLUT2、PPARα 和 LDLR mRNA 表达( <0.01)。 讨论与结论:PLP 通过激活 PI3K/AKT 信号通路发挥抗糖尿病作用,从而改善 db/db 小鼠的胰岛素抵抗、葡萄糖和脂质代谢。因此,PLP 可作为临床治疗的潜在抗糖尿病药物。
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