Permeability of the blood-brain barrier to a novel satiety molecule nesfatin-1

被引:149
作者
Price, Tulin O. [1 ,2 ]
Samson, Willis K. [3 ]
Niehoff, Michael L. [1 ,2 ]
Banks, William A. [1 ,2 ,3 ]
机构
[1] Vet Affairs Med Ctr, John Cochran Div, GRECC, St Louis, MO 63106 USA
[2] St Louis Univ, Sch Med, Dept Internal Med, Div Geriatr, St Louis, MO 63106 USA
[3] St Louis Univ, Sch Med, Dept Pharmacol & Physiol Sci, St Louis, MO 63104 USA
关键词
nesfatin-1; anorexigenic pepticle; blood-brain barrier; unidirectional influx rate;
D O I
10.1016/j.peptides.2007.10.008
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Nesfatin-1 has recently been identified as a hypothalamic and brain stem peptide that regulates feeding behavior. Here, we determined the ability of nesfatin-1 to cross the blood-brain barrier (BBB) of mice. We used multiple-regression analysis to determine that radioactively labeled nesfatin-1 injected intravenously entered the brain. The entry rate (K-i) of I-131-nesfatin-1 from blood-to-brain was 0.20 +/- 0.02 mu l/g min. This modest rate of entry was not inhibited by the administration of nonradioactive nesfatin-1, suggesting that BBB transport of nesfatin-1 into the brain is by a nonsaturable mechanism. High performance liquid chromatography (HPLC) and acid precipitation showed that most of the injected radiolabeled nesfatin-1 reached the brain as intact peptide, and capillary depletion with vascular washout revealed that 67% of I-131-nesfatin-1 crossed the BBB to reach the brain parenchyma. Efflux of labeled nesfatin-1 from brain back into blood was by way of bulk flow. These findings demonstrate that nesfatin-1 crosses the BBB in both the blood-to-brain and brain-to-blood directions by nonsaturable mechanisms. Published by Elsevier Inc.
引用
收藏
页码:2372 / 2381
页数:10
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