Tong Meng-Qi, Luo Lan-Zi, Xue Peng-Peng, Han Yong-Hui, Wang Li-Fen, Zhuge De-Li, Yao Qing, Chen Bin, Zhao Ying-Zheng, Xu He-Lin
Department of Pharmaceutics, School of Pharmaceutical Sciences, Wenzhou Medical University, Wenzhou City, Zhejiang Province 325035, China.
Department of Ultrasonography, the First Affiliated Hospital of Wenzhou Medical University, Wenzhou City, Zhejiang Province 325000, China.
Acta Biomater. 2021 Mar 1;122:111-132. doi: 10.1016/j.actbio.2021.01.007. Epub 2021 Jan 11.
Diabetic nephropathy (DN) is one of the most serious complications of diabetes mellitus. The combination of insulin (Ins) with liraglutide (Lir) has a greater potential for preventing DN than monotherapy. However, the renal protective effect of the combined Ins/Lir therapy is largely compromised due to their short half-lives after subcutaneous injection. Herein, a glucose-responsive hydrogel was designed in situ forming the dynamic boronic esters bonds between phenylboronic acid-grafted γ-Polyglutamic acid (PBA-PGA) and konjac glucomannan (KGM). It was hypothesized that the KGM/PBA-PGA hydrogel as the delivery vehicle of Ins/Lir would enhance the combinational effect of the latter on preventing the DN progress. Scan electronic microscopy and rheological studies showed that KGM/PBA-PGA hydrogel displayed good glucose-responsive property. Besides, the glucose-sensitive release profile of either Ins or Lir from KGM/PBA-PGA hydrogel was uniformly displayed at hyperglycemic level. Furthermore, the preventive efficacy of KGM/PBA-PGA hydrogel incorporating insulin and liraglutide (Ins/Lir-H) on DN progress was evaluated on streptozotocin-induced rats with diabetic mellitus (DM). At 6 weeks after subcutaneous injection of Ins/Lir-H, not only the morphology of kidneys was obviously recovered as shown by ultrasonography, but also the renal hemodynamics was significantly improved. Meanwhile, the 24-h urinary protein and albumin/creatinine ratio were well modulated. Inflammation and fibrosis were also largely inhibited. Besides, the glomerular NPHS-2 was obviously elevated after treatment with Ins/Lir-H. The therapeutic mechanism of Ins/Lir-H was highly associated with the alleviation of oxidative stress and activation of autophagy. Conclusively, the better preventive effect of the combined Ins/Lir via KGM/PBA-PGA hydrogel on DN progress was demonstrated as compared with their mixed solution, suggesting KGM/PBA-PGA hydrogel might be a potential vehicle of Ins/Lir to combat the progression of DN.
糖尿病肾病(DN)是糖尿病最严重的并发症之一。胰岛素(Ins)与利拉鲁肽(Lir)联合使用在预防DN方面比单一疗法具有更大的潜力。然而,由于皮下注射后Ins/Lir半衰期较短,联合治疗的肾脏保护作用在很大程度上受到损害。在此,设计了一种葡萄糖响应水凝胶,通过苯硼酸接枝的γ-聚谷氨酸(PBA-PGA)与魔芋葡甘聚糖(KGM)原位形成动态硼酸酯键。据推测,KGM/PBA-PGA水凝胶作为Ins/Lir的递送载体,将增强后者对预防DN进展的联合作用。扫描电子显微镜和流变学研究表明,KGM/PBA-PGA水凝胶具有良好的葡萄糖响应特性。此外,在高血糖水平下,Ins或Lir从KGM/PBA-PGA水凝胶中均呈现出葡萄糖敏感释放曲线。此外,在链脲佐菌素诱导的糖尿病(DM)大鼠中评估了包载胰岛素和利拉鲁肽的KGM/PBA-PGA水凝胶(Ins/Lir-H)对DN进展的预防效果。皮下注射Ins/Lir-H 6周后,不仅超声检查显示肾脏形态明显恢复,而且肾脏血流动力学也显著改善。同时,24小时尿蛋白和白蛋白/肌酐比值得到良好调节。炎症和纤维化也受到很大抑制。此外,Ins/Lir-H治疗后肾小球NPHS-2明显升高。Ins/Lir-H的治疗机制与氧化应激的减轻和自噬的激活高度相关。总之,与混合溶液相比,通过KGM/PBA-PGA水凝胶联合Ins/Lir对DN进展具有更好的预防效果,表明KGM/PBA-PGA水凝胶可能是Ins/Lir对抗DN进展的潜在载体。