低氧预处理间充质干细胞的分泌组能改善 2 型糖尿病大鼠的高血糖症状

Wita Widyaningsih, Agung Putra, Sri Priyantini, A. Muhar, Titiek Sumarawati, S. Trisnadi, N. Amalina, I. Alif, Ardi Prasetio, Risky Chandra Satria Irawan
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摘要

简介2 型糖尿病(T2DM)是一种常见的糖尿病,影响着 90% - 95% 的糖尿病患者。胰岛素增敏剂和胰岛素外源供应可暂时缓解高血糖,但同时也会产生副作用。因此,需要新的方法来同时解决胰岛素抵抗和β细胞再生问题。缺氧间充质干细胞(SH-MSCs)的分泌组含有各种生长因子和抗炎细胞因子,有可能增强胰岛素抵抗和改善胰腺功能。研究目的在本研究中,我们通过输注 SH-MSCs 来改善 HFD 诱导的 T2DM 大鼠高血糖。方法我们采用高脂饮食(HFD)和链脲佐菌素(STZ)联合给药的方法建立了 T2DM 大鼠模型。然后,我们注射了 250 微升和 500 微升剂量的 SH-间充质干细胞,并评估了 SH-MSCs 的治疗效果。我们还研究了其中潜在的内在机制。结果注射 SH-MSCs 可改善 T2DM 大鼠的高血糖症状。500微升剂量的SH-间充质干细胞输注可降低胰岛素抵抗的静态模型评估(HOMA-IR)。组织学分析表明,注射 SH-MSCs 可减轻胰腺的形态损伤。注射 SH-MSCs 还能抑制 IL-6 水平,促进 CD163 2 型巨噬细胞的表达。结论我们的研究结果表明,SH-间充质干细胞具有改善高血糖的潜力,并对 T2DM 大鼠具有保护作用。组织学分析表明 SH-MSCs 对胰腺形态有保护作用SH-MSCs 有望改善 TD2M 大鼠的高血糖、胰岛素抵抗并提供保护作用GGRAPHICAL ABSTRACT
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Secretome of Hypoxia-Preconditioned Mesenchymal Stem Cells Ameliorates Hyperglycemia in Type 2 Diabetes Mellitus Rats
          Introduction: Type 2 diabetes mellitus (T2DM) is a prevalent form of diabetes that affects 90 - 95 % of all diabetic patients. Insulin sensitizers and insulin exogenous supply could temporarily ameliorate hyperglycaemia; however, they are accompanied by side effects. As a result, new approaches are required to address insulin resistance and regenerate beta cells simultaneously. The secretome of hypoxic mesenchymal stem cells (SH-MSCs) contains various growth factors and anti-inflammatory cytokines that could potentially enhance insulin resistance and improve pancreatic function. Objectives: In this study, we performed SH-MSCs infusion to ameliorate HFD-induced hyperglycaemia in T2DM rats. Methods: We created a T2DM rat model using a combination of a high-fat diet (HFD) and streptozotocin (STZ) administration. Then, we administered SH-MSCs injection at doses of 250 and 500 µL and assessed the therapeutic effects of SH-MSCs. We also investigated the potential underlying mechanisms involved. Results: The administration of SH-MSCs improved hyperglycemia in rats with T2DM. Infusion of SH-MSCs at 500 µL dose decreased homeostatic model assessment for insulin resistance (HOMA-IR). Histological analysis revealed that injection of SH-MSCs alleviated morphological damage of pancreas. SH-MSCs administration also inhibit the level of IL-6 and promote the expression of CD163 type 2 macrophage. Conclusion: The results of our study indicate that SH-MSCs have the potential to improve hyperglycemia and exert a protective effect on T2DM rats. HIGHLIGHTS   Administration of SH-MSCs effectively improved hyperglycemia and decreased insulin resistance in TD2M rats through modulation of IL-6 levels and promotes the expression of CD163 type 2 macrophage Histological analysis demonstrated the protective effect of SH-MSCs on pancreatic morphology SH-MSCs hold promise for improving hyperglycemia, insulin resistance, and providing a protective effect in TD2M GRAPHICAL ABSTRACT
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