Yue Ting, Xu He-Lin, Chen Pian-Pian, Zheng Lei, Huang Qun, Sheng Wen-Shuang, Zhuang Yuan-Di, Jiao Li-Zhuo, Chi Ting-Ting, ZhuGe De-Li, Liu Jin-Jin, Zhao Ying-Zheng, Lan Li
Department of Radiology, The First Affiliated Hospital, Wenzhou Medical University, Wenzhou, Zhejiang Province 325035, China.
School of Pharmaceutical Sciences, Wenzhou Medical University, Wenzhou, Zhejiang Province 325035, China.
Int J Pharm. 2017 Aug 7;528(1-2):664-674. doi: 10.1016/j.ijpharm.2017.06.070. Epub 2017 Jun 19.
Diabetic nephropathy (DN) is one of the most common and lethal microvascular complications of diabetes. This study aimed to explore whether coenzymeQ10 (CoQ10) as an antioxidant combined with ultrasound-targeted microbubble destruction (UTMD) could reverse the progress of early diabetic nephropathy (DN). CoQ10 has great potential to treat early DN. However, the clinical application of CoQ10 has been limited because of its low aqueous solubility and non-specific distribution. Therefore, CoQ10-loaded liposomes (CoQ10-lip) were prepared and combined with ultrasound microbubbles for the early theranostics of DN. CoQ10-lip exhibited a good round morphology with a diameter of 183±1.7nm and a negative zeta potential of -25.3mV, which was capable of prolonging the release of the encapsulated CoQ10. The early DN rat models were induced by streptozotocin (STZ) and confirmed by contrast-enhanced ultrasound (CEUS) and 24-h urinary albumin. After the administration of CoQ10-lip combined with the UTMD technique to rats with early DN, the morphology and function of the kidney were evaluated by ultrasonography, histological and molecular analyses. The renal hemodynamics were significantly improved, moreover, 24-h urinary protein, and oxidative stress indexes were modulated after treatment with CoQ10-lip+UTMD indicating recovery of renal function. An elevated level of Nphs2 protein and reduced caspase 3 level indicated the preservation of podocytes and inhibition of cell apoptosis after CoQ10-lip+UTMD treatment. The molecular mechanism was associated with the upregulation of Bcl-2 and the downregulation of Bax. Moreover, the combination of CoQ10-lip and ultrasound microbubbles demonstrated a better protective effect on the damaged kidney than the other groups (free CoQ10 or CoQ10-lip+/- UTMD). Conclusively, CoQ10-lip in combination with ultrasound microbubbles might be a potential strategy to reverse the progress of early DN.
糖尿病肾病(DN)是糖尿病最常见且致命的微血管并发症之一。本研究旨在探讨作为抗氧化剂的辅酶Q10(CoQ10)联合超声靶向微泡破坏(UTMD)能否逆转早期糖尿病肾病(DN)的进展。CoQ10在治疗早期DN方面具有巨大潜力。然而,由于其水溶性低和分布不具有特异性,CoQ10的临床应用受到限制。因此,制备了负载CoQ10的脂质体(CoQ10-lip)并与超声微泡联合用于DN的早期诊疗。CoQ10-lip呈现出良好的圆形形态,直径为183±1.7nm,ζ电位为-25.3mV,能够延长包封的CoQ10的释放。早期DN大鼠模型通过链脲佐菌素(STZ)诱导,并通过超声造影(CEUS)和24小时尿白蛋白进行确认。对早期DN大鼠给予CoQ10-lip联合UTMD技术后,通过超声检查、组织学和分子分析评估肾脏的形态和功能。肾脏血流动力学得到显著改善,此外,CoQ10-lip + UTMD治疗后,24小时尿蛋白和氧化应激指标得到调节,表明肾功能恢复。Nphs2蛋白水平升高和半胱天冬酶3水平降低表明CoQ10-lip + UTMD治疗后足细胞得以保留且细胞凋亡受到抑制。分子机制与Bcl-2上调和Bax下调有关。此外,CoQ10-lip与超声微泡的联合对受损肾脏的保护作用优于其他组(游离CoQ10或CoQ10-lip + / - UTMD)。总之,CoQ10-lip与超声微泡联合可能是逆转早期DN进展的一种潜在策略。