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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
6
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pubmed:dateCreated |
1988-4-15
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pubmed:abstractText |
It is becoming increasingly evident that peptides can cross the blood-brain barrier. The entry into the central nervous system of a commercially available analog of Peptide T, an octapeptide derived from the human immunodeficiency virus envelope glycoprotein 120, was studied in several experiments. It was found that 125I-Peptide T analog given intravenously in the periphery entered the brain in an intact form, as confirmed by HPLC, to a greater extent than did the labeled albumin control. This entry occurred despite the very low lipid solubility, measured by the octanol/buffer partition coefficient, for the iodinated analog. The rate of entry was decreased by unlabeled Peptide T analog, but not by iodo-tyrosine. Saturable transport out of the brain was not observed after intraventricular administration. Thus, results with 125I-Peptide T analog indicate that saturable systems can transport peptides from the blood into the central nervous system.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Dec
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pubmed:issn |
0361-9230
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
19
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
629-33
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:3440215-Animals,
pubmed-meshheading:3440215-Blood-Brain Barrier,
pubmed-meshheading:3440215-Chromatography, High Pressure Liquid,
pubmed-meshheading:3440215-Iodine Radioisotopes,
pubmed-meshheading:3440215-Kinetics,
pubmed-meshheading:3440215-Male,
pubmed-meshheading:3440215-Mice,
pubmed-meshheading:3440215-Mice, Inbred ICR,
pubmed-meshheading:3440215-Oligopeptides,
pubmed-meshheading:3440215-Peptide T,
pubmed-meshheading:3440215-Technetium Tc 99m Aggregated Albumin
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pubmed:year |
1987
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pubmed:articleTitle |
D-[Ala1]-peptide T-amide is transported from blood to brain by a saturable system.
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pubmed:affiliation |
Veterans Administration Medical Center, New Orleans, LA 70146.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, Non-P.H.S.
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