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Multifunctional Platinum@BSA–Rapamycin Nanocarriersfor the Combinatorial Therapy of Cerebral Cavernous Malformation

机译:多功能铂@ BSA–雷帕霉素纳米载体脑海绵状畸形的联合治疗

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摘要

Platinum nanoparticles (PtNPs) are antioxidant enzyme-mimetic nanomaterials with significant potential for the treatment of complex diseases related to oxidative stress. Among such diseases, Cerebral Cavernous Malformation (CCM) is a major cerebrovascular disorder of genetic origin, which affects at least 0.5% of the general population. Accumulated evidence indicates that loss-of-function mutations of the three known CCM genes predispose endothelial cells to oxidative stress-mediated dysfunctions by affecting distinct redox-sensitive signaling pathways and mechanisms, including pro-oxidant and antioxidant pathways and autophagy. A multitargeted combinatorial therapy might thereby represent a promising strategy for the effective treatment of this disease. Herein, we developed a multifunctional nanocarrier by combining the radical scavenging activity of PtNPs with the autophagy-stimulating activity of rapamycin (Rapa). Our results show that the combinatorial targeting of redox signaling and autophagy dysfunctions is effective in rescuing major molecular and cellular hallmarks of CCM disease, suggesting its potentialfor the treatment of this and other oxidative stress-related diseases.
机译:铂纳米颗粒(PtNPs)是抗氧化酶模拟的纳米材料,在治疗与氧化应激有关的复杂疾病方面具有巨大潜力。在这些疾病中,脑海绵状畸形(CCM)是遗传性的主要脑血管疾病,至少影响了总人口的0.5%。积累的证据表明,三个已知的CCM基因的功能丧失突变通过影响独特的氧化还原敏感信号传导途径和机制(包括促氧化剂和抗氧化剂途径以及自噬),使内皮细胞容易遭受氧化应激介导的功能障碍。因此,多靶点联合治疗可能代表一种有效治疗该疾病的有前途的策略。在这里,我们通过结合PtNPs的自由基清除活性和雷帕霉素(Rapa)的自噬刺激活性,开发了一种多功能纳米载体。我们的结果表明,氧化还原信号传导和自噬功能障碍的组合靶向可有效挽救CCM疾病的主要分子和细胞标志,表明其潜力用于治疗这种和其他与氧化应激相关的疾病。

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