Circulating neuroactive peptides and the blood-brain and blood-cerebrospinal fluid barriers.

Endocrinologia experimentalis Pub Date : 1990-03-01
B V Zlokovic, M B Segal, H Davson, M N Lipovac, S Hyman, J G McComb
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Abstract

Interactions of radiolabelled circulating neuroactive peptides: enkephalin-leucine (Enk-Leu), delta sleep inducing peptide (DSIP), thyrotropin-releasing hormone (TRH) and vasopressin-arginine (VP-Arg) with the blood-brain and blood-cerebrospinal fluid barriers were studied by mean of: 1. a vascular perfusion technique in the guinea-pig using multiple-time brain uptake analysis, 2. a vascular perfusion technique of the in situ isolated choroid plexus from sheep using single-circulation paired-tracer dilution or steady-state analysis. It has been demonstrated that Enk-Leu, DSIP and VP-Arg were taken up intact at the luminal side of the blood-brain barrier and blood-tissue interface of the blood-cerebrospinal fluid barrier by a saturable mechanism. On the other hand, a non-saturable mechanism as well as possible enzymatic degradation were shown during TRH interactions with either the blood-brain or blood-cerebrospinal fluid barriers. It is concluded that both, facilitated and simple diffusion, govern circulating neuroactive peptide uptake into the central nervous system.

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循环神经活性肽与血脑和血脑脊液屏障。
通过以下方法研究了放射性标记循环神经活性肽:脑啡肽-亮氨酸(Enk-Leu)、delta睡眠诱导肽(DSIP)、促甲状腺素释放激素(TRH)和加压素-精氨酸(VP-Arg)与血脑和血脑脊液屏障的相互作用:使用多次脑摄取分析的豚鼠血管灌注技术,2。利用单循环配对示踪剂稀释或稳态分析对绵羊原位离体脉络膜丛进行血管灌注技术。研究表明,Enk-Leu、DSIP和VP-Arg以饱和机制在血脑屏障的管腔侧和血脑脊液屏障的血组织界面被完整地吸收。另一方面,在TRH与血脑或血脑脊液屏障相互作用期间,显示了一种不饱和机制以及可能的酶降解。结论是,促进扩散和简单扩散都控制着循环神经活性肽进入中枢神经系统的摄取。
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