INHIBITION OF NEUTRAL AMINO-ACID-TRANSPORT ACROSS THE HUMAN BLOOD-BRAIN-BARRIER BY PHENYLALANINE

被引:0
|
作者
SHULKIN, BL
BETZ, AL
KOEPPE, RA
AGRANOFF, BW
机构
[1] UNIV MICHIGAN,SCH MED,DEPT INTERNAL MED,DIV NUCL MED,ANN ARBOR,MI 48109
[2] UNIV MICHIGAN,SCH MED,DEPT PEDIAT,ANN ARBOR,MI
[3] UNIV MICHIGAN,SCH MED,DEPT SURG NEUROSURG,ANN ARBOR,MI
[4] UNIV MICHIGAN,SCH MED,DEPT NEUROL,ANN ARBOR,MI
[5] UNIV MICHIGAN,SCH MED,DEPT PSYCHIAT,ANN ARBOR,MI
[6] UNIV MICHIGAN,SCH MED,DEPT BIOL CHEM,ANN ARBOR,MI 48109
[7] UNIV MICHIGAN,SCH MED,MENTAL HLTH RES INST,ANN ARBOR,MI 48109
关键词
AMINOCYCLOHEXANECARBOXYLATE; POSITRON EMISSION TOMOGRAPHY; L-SYSTEM TRANSPORTER; ESSENTIAL AMINO ACIDS;
D O I
暂无
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
The delivery of large neutral amino acids (LNAAs) to brain across the blood-brain barrier (BBB) is mediated by the L-type neutral amino acid transporter present in the membranes of the brain capillary endothelial cell. In experimental animals, the L-system transporter is saturated under normal conditions, and therefore an elevation in the plasma concentration of one LNAA will reduce brain uptake of others. In this study, we used positron emission tomography (PET) to determine the effect of elevated plasma phenylalanine concentrations on the uptake of an artificial neutral amino acid, [C-11]-aminocyclohexanecarboxylate ([C-11]ACHC), in human brain. PET scans were performed on six normal male subjects after an overnight fast and again 60 min after oral administration of 100 mg/kg of phenylalanine. The plasma phenylalanine concentration increased by an average of 11-fold between the first and second scans. This increase produced a reduction in [C-11]ACHC uptake in all brain regions but not in scalp. The mean +/- SD influx rate constant for whole brain decreased after phenylalanine ingestion from 0.036 +/- 0.002 to 0.019 +/- 0.004 ml/gl min. Kinetic analysis of the effect of plasma phenylalanine concentration on the rate of [C-11]ACHC uptake is compatible with a model of competitive inhibition so that large increases in the concentration of one LNAA in plasma will reduce the brain uptake of other LNAAs across the human BBB.
引用
收藏
页码:1252 / 1257
页数:6
相关论文
共 50 条
  • [31] INHIBITION OF THIAMINE TRANSPORT ACROSS THE BLOOD-BRAIN-BARRIER BY THIAMINE ANALOGS
    GREENWOOD, J
    PRATT, OE
    JOURNAL OF PHYSIOLOGY-LONDON, 1981, 317 (AUG): : P65 - P65
  • [32] NEUTRAL AMINO-ACID TRANSPORT AT THE HUMAN-BLOOD BRAIN BARRIER
    HARGREAVES, KM
    PARDRIDGE, WM
    CLINICAL RESEARCH, 1989, 37 (01): : A140 - A140
  • [33] AGING EFFECT ON NEUTRAL AMINO-ACID-TRANSPORT AT THE BLOOD-BRAIN-BARRIER MEASURED WITH L-[2-F-18]-FLUOROPHENYLALANINE AND PET
    ITO, H
    HATAZAWA, J
    MURAKAMI, M
    MIURA, S
    IIDA, H
    BLOOMFIELD, PM
    KANNO, I
    FUKUDA, H
    UEMURA, K
    JOURNAL OF NUCLEAR MEDICINE, 1995, 36 (07) : 1232 - 1237
  • [34] PENTOBARBITAL-ANESTHESIA - INFLUENCE ON AMINO-ACID TRANSPORT ACROSS THE BLOOD-BRAIN-BARRIER
    SAGE, JI
    DUFFY, TE
    JOURNAL OF NEUROCHEMISTRY, 1979, 33 (04) : 963 - 965
  • [35] PHENYLALANINE TRANSPORT AT THE HUMAN BLOOD-BRAIN-BARRIER - STUDIES WITH ISOLATED HUMAN-BRAIN CAPILLARIES
    CHOI, TB
    PARDRIDGE, WM
    JOURNAL OF BIOLOGICAL CHEMISTRY, 1986, 261 (14) : 6536 - 6541
  • [36] PHENYLALANINE TRANSPORT AT THE HUMAN BLOOD-BRAIN-BARRIER (BBB) - STUDIES WITH ISOLATED BRAIN CAPILLARIES
    CHOI, TB
    YANG, J
    PARDRIDGE, WM
    CLINICAL RESEARCH, 1986, 34 (01): : A57 - A57
  • [37] PHENYLALANINE TRANSPORT AT THE HUMAN BLOOD-BRAIN-BARRIER (BBB) - STUDIES WITH ISOLATED BRAIN CAPILLARIES
    CHOI, TB
    JING, Y
    PARDRIDGE, WM
    DIABETES, 1986, 35 : A196 - A196
  • [38] TRANSPORT OF IONS ACROSS THE BLOOD-BRAIN-BARRIER
    BETZ, AL
    FEDERATION PROCEEDINGS, 1986, 45 (07) : 2050 - 2054
  • [39] SELECTIVE TRANSPORT ACROSS THE BLOOD-BRAIN-BARRIER
    BANKS, WA
    KASTIN, AJ
    MICHALS, EA
    ANNALS OF INTERNAL MEDICINE, 1986, 105 (03) : 472 - 472
  • [40] DEVELOPMENTS IN AMINO-ACID TRANSPORT, ILLUSTRATED FOR THE BLOOD-BRAIN-BARRIER
    CHRISTENSEN, HN
    BIOCHEMICAL PHARMACOLOGY, 1979, 28 (13) : 1989 - 1992