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α-肾上腺素能诱导溶酶体酶穿越血脑屏障的转运

Alpha Adrenergic Induction of Transport of Lysosomal Enzyme across the Blood-Brain Barrier.

作者信息

Urayama Akihiko, Dohgu Shinya, Robinson Sandra M, Sly William S, Grubb Jeffery H, Banks William A

机构信息

Department of Neurology, University of Texas Medical School at Houston, Houston, TX, United States of America.

Department of Pharmaceutical Care and Health Sciences, Faculty of Pharmaceutical Sciences, Fukuoka, Japan.

出版信息

PLoS One. 2015 Nov 6;10(11):e0142347. doi: 10.1371/journal.pone.0142347. eCollection 2015.

Abstract

The impermeability of the adult blood-brain barrier (BBB) to lysosomal enzymes impedes the ability to treat the central nervous system manifestations of lysosomal storage diseases. Here, we found that simultaneous stimulation of the alpha1 and alpha2 adrenoreceptor restores in adult mice the high rate of transport for the lysosomal enzyme P-GUS that is seen in neonates but lost with development. Beta adrenergics, other monoamines, and acetylcholine did not restore this transport. A high dose (500 microg/mouse) of clonidine, a strong alpha2 and weak alpha1 agonist, was able to act as monotherapy in the stimulation of P-GUS transport. Neither use of alpha1 plus alpha2 agonists nor the high dose clonidine disrupted the BBB to albumin. In situ brain perfusion and immunohistochemistry studies indicated that adrengerics act on transporters already at the luminal surface of brain endothelial cells. These results show that adrenergic stimulation, including monotherapy with clonidine, could be key for CNS enzyme replacement therapy.

摘要

成年血脑屏障(BBB)对溶酶体酶的不可渗透性阻碍了治疗溶酶体贮积病中枢神经系统表现的能力。在此,我们发现同时刺激α1和α2肾上腺素能受体可使成年小鼠恢复新生儿期可见但随发育而丧失的溶酶体酶P-GUS的高转运速率。β肾上腺素能药物、其他单胺类物质和乙酰胆碱不能恢复这种转运。高剂量(500微克/小鼠)的可乐定,一种强效α2和弱效α1激动剂,能够作为单一疗法刺激P-GUS转运。使用α1加α2激动剂或高剂量可乐定都不会破坏BBB对白蛋白的屏障功能。原位脑灌注和免疫组织化学研究表明,肾上腺素能药物作用于脑内皮细胞腔面已有的转运体。这些结果表明,肾上腺素能刺激,包括可乐定单一疗法,可能是中枢神经系统酶替代疗法的关键。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2fda/4636227/956d548218f1/pone.0142347.g001.jpg

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