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静脉内治疗实验性帕金森病的 IgG-GDNF 融合蛋白在穿透血脑屏障的小鼠中。

Intravenous treatment of experimental Parkinson's disease in the mouse with an IgG-GDNF fusion protein that penetrates the blood-brain barrier.

机构信息

Department of Medicine, UCLA, Los Angeles, CA 90024, USA.

出版信息

Brain Res. 2010 Sep 17;1352:208-13. doi: 10.1016/j.brainres.2010.06.059. Epub 2010 Jun 30.

Abstract

Glial-derived neurotrophic factor (GDNF) is a trophic factor for the nigra-striatal tract in experimental Parkinson's disease (PD). The neurotrophin must be administered by intra-cerebral injection, because GDNF does not cross the blood-brain barrier (BBB). In the present study, GDNF was re-engineered to enable receptor-mediated transport across the BBB following fusion of GDNF to the heavy chain of a chimeric monoclonal antibody (MAb) against the mouse transferrin receptor (TfR), and this fusion protein is designated cTfRMAb-GDNF. This fusion protein had been previously shown to retain low nM binding constants for both the GDNF receptor and the mouse TfR, and to rapidly enter the mouse brain in vivo following intravenous administration. Experimental PD in mice was induced by the intra-striatal injection of 6-hydroxydopamine, and mice were treated with either saline or the cTfRMAb-GDNF fusion protein every other day for 3 weeks, starting 1 h after toxin injection. Fusion protein treatment caused a 44% decrease in apomorphine-induced rotation, a 45% reduction in amphetamine-induced rotation, a 121% increase in the vibrissae-elicited forelimb placing test, and a 272% increase in striatal tyrosine hydroxylase (TH) enzyme activity at 3 weeks after toxin injection. Fusion protein treatment caused no change in TH enzyme activity in either the contralateral striatum or the frontal cortex. In conclusion, following fusion of GDNF to a BBB molecular Trojan horse, GDNF trophic effects in brain in experimental PD are observed following intravenous administration.

摘要

胶质细胞源性神经营养因子(GDNF)是实验性帕金森病(PD)黑质纹状体束的营养因子。神经营养因子必须通过脑内注射给药,因为 GDNF 不能穿过血脑屏障(BBB)。在本研究中,通过将 GDNF 融合到针对小鼠转铁蛋白受体(TfR)的嵌合单克隆抗体(MAb)的重链上,对 GDNF 进行了再工程设计,从而使 GDNF 能够在融合蛋白 cTfRMAb-GDNF 融合蛋白融合后,通过受体介导的方式穿过 BBB。该融合蛋白先前已被证明对 GDNF 受体和小鼠 TfR 均保留低 nM 的结合常数,并且在静脉内给药后可迅速进入体内的小鼠大脑。通过纹状体注射 6-羟多巴胺诱导小鼠实验性 PD,并在毒素注射后 1 小时开始,每隔一天用生理盐水或 cTfRMAb-GDNF 融合蛋白治疗小鼠 3 周。融合蛋白治疗可使阿扑吗啡诱导的旋转减少 44%,安非他命诱导的旋转减少 45%,触须诱发的前肢放置试验增加 121%,纹状体酪氨酸羟化酶(TH)酶活性增加 272%,在毒素注射后 3 周。融合蛋白治疗在对侧纹状体或额皮质中均未引起 TH 酶活性的变化。总之,在将 GDNF 融合到 BBB 分子木马之后,在实验性 PD 中静脉内给予 GDNF 后可观察到脑内的营养作用。

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