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儿茶酚胺的血脑屏障——再探讨。

The blood-brain barrier for catecholamines - revisited.

作者信息

Kostrzewa Richard M

机构信息

Department of Pharmacology, Quillen College of Medicine, East Tennessee State University, Johnson City, TN 37614, USA.

出版信息

Neurotox Res. 2007 Apr;11(3-4):261-71. doi: 10.1007/BF03033571.

Abstract

Although it is well-recognized that catecholamines are generally unable to penetrate the developed blood-brain barrier (BBB) to gain entry into brain, except at circumventricular sites where the BBB is absent or deficient, ontogenetic development of this barrier seems to have escaped systematic study. To explore BBB development, several approaches were used. In the first study rats were treated once on a specific day of postnatal ontogeny, as early as the day of birth, with the neurotoxin 6-hydroxydopamine (6-OHDA; 60 mg/kg), and then terminated in adulthood for regional analysis of endogenous norepinephrine (NE) content of brain. In another study, rats were treated once, on a specific day of postnatal ontogeny, with the BBB-permeable neurotoxin 6-hydroxydopa (6-OHDOPA; 60 mg/kg) following pretreatment with the BBB-impermeable amino acid decarboxylase inhibitor carbidopa (100 mg/kg IP), then terminated in adulthood for regional analysis of endogenous NE content of brain. In the third study rats were treated once, on a specific day of postnatal ontogeny, with the analog [3H]metaraminol, and terminated 1 hour later for determination of regional distribution of tritium in brain. On the basis of [3H]metaraminol distribution and NE depletions after neurotoxin treatments, it is evident that the BBB in neocortex, striatum, cerebellum and other brain regions forms in stages over a period of at least 2 weeks from birth. Moreover, because the BBB consists of several element (physical-, ion-restrictive-, and enzymatic-barrier), the method employed will derive data mainly applicable to the targeted aspect of the barrier, which may or may not necessarily coincide with elements of the barrier that have a different rate of ontogenetic development. Accordingly, it is evident that some aspects of physical- and ion-restrictive elements of the BBB form within approximately the first week after birth in rat neocortex and striatum, while enzymatic elements of the BBB form more than than 2 weeks later. Regardless, the BBB forms at earlier times in forebrain vs hindbrain regions.

摘要

尽管人们普遍认识到,除了在血脑屏障(BBB)不存在或有缺陷的室周部位外,儿茶酚胺通常无法穿透发育成熟的血脑屏障进入大脑,但这一屏障的个体发育似乎尚未得到系统研究。为了探索血脑屏障的发育,我们采用了几种方法。在第一项研究中,大鼠在出生后的特定发育日,最早在出生当天,用神经毒素6-羟基多巴胺(6-OHDA;60mg/kg)进行一次处理,然后在成年期处死,用于对脑内内源性去甲肾上腺素(NE)含量进行区域分析。在另一项研究中,大鼠在出生后的特定发育日,先用血脑屏障不可渗透的氨基酸脱羧酶抑制剂卡比多巴(100mg/kg腹腔注射)预处理,然后用可穿透血脑屏障的神经毒素6-羟基多巴(6-OHDOPA;60mg/kg)进行一次处理,然后在成年期处死,用于对脑内内源性NE含量进行区域分析。在第三项研究中,大鼠在出生后的特定发育日,用类似物[3H]间羟胺进行一次处理,并在1小时后处死,用于测定脑内氚的区域分布。根据神经毒素处理后[3H]间羟胺的分布和NE的耗竭情况,很明显,新皮层、纹状体、小脑和其他脑区的血脑屏障从出生起至少在2周的时间内分阶段形成。此外,由于血脑屏障由几个要素(物理屏障、离子限制屏障和酶屏障)组成,所采用的方法将得出主要适用于该屏障目标方面的数据,这可能与或不一定与具有不同个体发育速率的屏障要素一致。因此,很明显,血脑屏障的物理和离子限制要素的某些方面在大鼠新皮层和纹状体出生后的大约第一周内形成,而血脑屏障的酶要素则在2周多以后形成。无论如何,前脑区域的血脑屏障比后脑区域形成得更早。

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