Yuan Haisheng, Xu Guoquan, Liu Jingran, Yan Yan, Zhao Shimin, Cai Fujuan, Yu Xiuling, Wang Yuzhen, Li Minhui
College of Life Sciences, Inner Mongolia Agricultural University, Hohhot, 010018, China.
Inner Mongolia Tianqi Biotechnology Co., Ltd., Chifeng, 024000, China.
J Tradit Complement Med. 2024 May 24;15(3):274-285. doi: 10.1016/j.jtcme.2024.05.007. eCollection 2025 May.
has been widely used in traditional Chinese medicine to treat diabetes and a variety of other diseases. This study aims to evaluate the alleviating effects and mechanisms of Polysaccharide (mAPS) against diet combined with streptozotocin (STZ)-induced Type 2 Diabetes Mellitus (T2DM).
T2DM rats were orally administrated either with 200 mg/kg mAPS or 300 mg/kg Metformin (MET) once daily for four weeks. Body weight and Fasting Blood Glucose (FBG) were detected every 6 days. Serum fasting insulin (FINS) was measured by ELISA and the homeostatic model assessment of insulin resistance (HOMA-IR) was calculated accordingly. Histological change was studied by Hematoxylin and eosin (HE) staining. 16S rDNA sequencing was used to detect the changes in gut microbiota.
Oral administration of mAPS significantly decreased body weight, FBG, and HOMA-IR in T2DM rats (<0.05). Moreover, HE staining showed that mAPS could alleviate histological distortion in the liver and pancreas. Treatment with mAPS elevated the hepatic levels of phosphatidylinositol-3 kinase (PI3K), phospho-protein kinase B (AKT), and glucose transporter type 4 (GLUT4), while reducing phospho-nuclear factor kappa-B (NF-κB), Toll-like receptor 4 (TLR4), tumor necrosis factor-α (TNF-α), interleukin-6 (IL-6), and interleukin-1β (IL-1β) (<0.05). Furthermore, mAPS supplementation could reverse the ratio of / (F/B) and reduce the abundance of and (<0.05). These results indicate that mAPS have the potential to enhance insulin sensitivity in diabetic rats by modifying gut microbiota and controlling the hepatic glycolipid metabolism and inflammation.
已广泛应用于中医治疗糖尿病及多种其他疾病。本研究旨在评估多聚糖(mAPS)对饮食联合链脲佐菌素(STZ)诱导的2型糖尿病(T2DM)的缓解作用及机制。
将T2DM大鼠每日口服200mg/kg mAPS或300mg/kg二甲双胍(MET),持续四周。每6天检测一次体重和空腹血糖(FBG)。通过酶联免疫吸附测定法(ELISA)测量血清空腹胰岛素(FINS),并据此计算胰岛素抵抗稳态模型评估(HOMA-IR)。采用苏木精-伊红(HE)染色研究组织学变化。利用16S rDNA测序检测肠道微生物群的变化。
口服mAPS可显著降低T2DM大鼠的体重、FBG和HOMA-IR(<0.05)。此外,HE染色显示mAPS可减轻肝脏和胰腺的组织学畸变。mAPS治疗可提高肝脏中磷脂酰肌醇-3激酶(PI3K)、磷酸化蛋白激酶B(AKT)和葡萄糖转运蛋白4(GLUT4)的水平,同时降低磷酸化核因子κB(NF-κB)、Toll样受体4(TLR4)、肿瘤坏死因子-α(TNF-α)、白细胞介素-6(IL-6)和白细胞介素-1β(IL-1β)(<0.05)。此外,补充mAPS可逆转/(F/B)比值并降低和的丰度(<0.05)。这些结果表明,mAPS有可能通过调节肠道微生物群以及控制肝脏糖脂代谢和炎症来增强糖尿病大鼠的胰岛素敏感性。