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重组腺相关病毒介导的甲基苯丙胺抗体表达减轻小鼠的甲基苯丙胺诱导的过度活动。

Recombinant Adeno-Associated Virus-Mediated Expression of Methamphetamine Antibody Attenuates Methamphetamine-Induced Hyperactivity in Mice.

机构信息

Department of Life Science, Fu-Jen Catholic University, New Taipei City, Taiwan.

Center for Neuropsychiatric Research, National Health Research Institutes, Zhunan, Taiwan.

出版信息

Sci Rep. 2017 Apr 7;7:46301. doi: 10.1038/srep46301.

Abstract

Methamphetamine (Meth) is one of the most frequently abused drugs worldwide. Recent studies have indicated that antibodies with high affinity for Meth reduce its pharmacological effects. The purpose of this study was to develop a technique for virus-based passive immunization against Meth effects. We generated a recombinant adeno-associated virus serotype-8 vector (AAV-MethAb) carrying the gene for a Meth-specific monoclonal antibody (MethAb). Infection of 293 cells with AAV-MethAb resulted in the expression and secretion of antibodies which bind to Meth. The viral vector was then examined in adult ICR mice. Systemic administration of AAV-MethAb resulted in long-term expression of MethAb in the serum for up to 29 weeks. Serum collected from the animals receiving AAV-MethAb retained a high specificity for (+)-Meth. Animals were challenged with Meth five weeks after viral injection. Meth levels in the brain and serum were reduced while Meth-induced locomotor activity was significantly attenuated. In conclusion, AAV-MethAb administration effectively depletes Meth from brain and serum while reducing the behavioral response to Meth, and thus is a potential therapeutic approach for Meth abuse.

摘要

甲基苯丙胺(冰毒)是世界上滥用最频繁的毒品之一。最近的研究表明,对冰毒具有高亲和力的抗体可以降低其药理作用。本研究旨在开发一种基于病毒的针对冰毒作用的被动免疫技术。我们生成了携带冰毒特异性单克隆抗体(MethAb)基因的重组腺相关病毒血清型 8 载体(AAV-MethAb)。AAV-MethAb 感染 293 细胞导致表达和分泌与冰毒结合的抗体。然后在成年 ICR 小鼠中检查了该病毒载体。AAV-MethAb 的全身给药导致 MethAb 在血清中的长期表达长达 29 周。从接受 AAV-MethAb 的动物收集的血清对(+)-冰毒保持高特异性。在病毒注射后五周,动物接受冰毒挑战。大脑和血清中的冰毒水平降低,而冰毒诱导的运动活性显著减弱。总之,AAV-MethAb 给药可有效清除大脑和血清中的冰毒,同时降低对冰毒的行为反应,因此是治疗冰毒滥用的潜在方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c565/5384190/3500936e93f9/srep46301-f1.jpg

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