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Biotech / Medical : Indications -- obesity/erectile dysfunction

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To: scaram(o)uche who started this subject8/19/2003 2:00:37 AM
From: Miljenko Zuanic  Read Replies (1) of 435
 
The Journal of Pharmacology And Experimental Therapeutics Fast Forward

First published on May 15, 2003; 10.1124/jpet.103.051821

JPET 306:948-953, 2003

ABSORPTION, DISTRIBUTION, METABOLISM, AND EXCRETION

Characterization of Blood-Brain Barrier Permeability to PYY3-36 in the Mouse
Naoko Nonaka, Seiji Shioda, Michael L. Niehoff, and William A. Banks
Oral Anatomy, School of Dentistry, Showa University, Tokyo, Japan (N.N.); First Anatomy, School of Medicine, Showa University, Tokyo, Japan (N.N., S.S.); Geriatric Research, Education, and Clinical Center, Veterans Affairs Medical Center-St. Louis and Division of Geriatrics, Department of Internal Medicine, St. Louis University School of Medicine, St. Louis, Missouri (N.N., M.L.N., W.A.B.)

Peptide YY3-36 (PYY) has emerged as an important signal in the gut-brain axis, with peripherally administered PYY affecting feeding and brain function. For these effects to be direct, PYY would have to cross the blood-brain barrier (BBB). Here, we determined the permeability of the BBB to PYY radioactively labeled with 131I (I-PYY). Multiple-time regression analysis showed the unidirectional influx rate (Ki) from blood-to-brain for I-PYY to be 0.49 ± 0.19 µl/g-min, a rate similar to that previously measured for leptin. Influx was not inhibited by 1 µg/mouse of unlabeled PYY, suggesting PYY crosses the BBB by transmembrane diffusion. About 0.176% of the i.v.-injected dose of I-PYY was taken up by brain, an amount similar to that for other peptides important in gut-brain communication. Capillary depletion showed that 69% of I-PYY crossed the BBB to enter the parenchymal space of the brain, and high-performance liquid chromatography demonstrated that the radioactivity in this space represented intact I-PYY. After intracerebroventricular injection, I-PYY crossed from brain to blood by the mechanism of bulk flow. We conclude that PYY crosses in both the blood-to-brain and brain-to-blood directions by nonsaturable mechanisms. Passage across the BBB provides a mechanism by which blood-borne PYY can affect appetite and brain function.

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Received March 18, 2003; accepted May 7, 2003.
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