Validity of multiple-time regression analysis in measurement of tritiated and iodinated leptin crossing the blood-brain barrier: meaningful controls

被引:67
作者
Kastin, AJ
Akerstrom, V
Pan, WH [1 ]
机构
[1] VA Med Ctr, New Orleans, LA 70112 USA
[2] Tulane Univ, Sch Med, New Orleans, LA 70112 USA
关键词
blood-brain barrier; peptides; polypeptides; leptin; tritiation;
D O I
10.1016/S0196-9781(01)00569-1
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
Multiple-time regression analysis has been used to study the influx of radiolabeled peptides and polypeptides across the blood-brain barrier (BBB). This study used both tritiated and iodinated leptin to clarify several issues associated with these measurements. Recombinant murine leptin was radiolabeled with H-3 by derivatization or with I-125 by the iodobead method and each studied separately in mice. Intact H-3-leptin had a higher apparent influx rate from blood to brain than did intact I-125, correlating with its higher proportion of reversible association with the capillary lumen that would misleadingly appear to reflect entry. Yet the majority of H-3-leptin and I-125-leptin reached brain parenchyma. There was no significant difference in the influx rate between cerebral cortex and the subcortical regions, thus ruling out a predominant contribution of simple diffusion through the circumventricular organs or choroid plexuses outside the BBB. The influx of radiolabeled leptin, especially I-125-leptin, was decreased by excess unlabeled leptin, supporting the presence of a saturable transport system for leptin at the BBB. To identify the specificity of the transport system and determine whether it is shared by H-3-leptin and I-125-leptin, these radioactively labeled leptins were heat-denatured. Denaturation had no effect on the fast influx of H-3-leptin, but abolished the entry of I-125-leptin into brain; excess denatured leptin failed to inhibit the influx of either H-3-leptin or I-125-leptin. This indicates that the conformation of I-125-leptin is similar to that of native unlabeled leptin, so that iodination would be the better choice for investigating the interaction of leptin with the BBB. However, H-3-leptin can use the same transport system, as shown by inhibition of its influx by unlabeled leptin, whereas the derivatization procedure altered its biophysical properties such that its non-saturated influx was greatly enhanced. Finally, the rapid influx of radioactively labeled leptin contrasted greatly with that of the reference compounds Tc-99m-albumin and H-3-inulin which had no significant penetration of the BBB. Thus, with additional considerations such as stability and interactions with the vasculature, multiple-time regression analysis is sensitive and selective for study of the penetration of peptides across the BBB. (C) 2001 Elsevier Science Inc. All rights reserved.
引用
收藏
页码:2127 / 2136
页数:10
相关论文
共 34 条
  • [1] Partial saturation and regional variation in the blood-to-brain transport of leptin in normal weight mice
    Banks, WA
    Clever, CM
    Farrell, CL
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, 2000, 278 (06): : E1158 - E1165
  • [2] OPPOSITE DIRECTION OF TRANSPORT ACROSS THE BLOOD-BRAIN BARKER FOR TYR-MIF-1 AND MIF-1 - COMPARISON WITH MORPHINE
    BANKS, WA
    KASTIN, AJ
    [J]. PEPTIDES, 1994, 15 (01) : 23 - 29
  • [3] Leptin enters the brain by a saturable system independent of insulin
    Banks, WA
    Kastin, AJ
    Huang, WT
    Jaspan, JB
    Maness, LM
    [J]. PEPTIDES, 1996, 17 (02) : 305 - 311
  • [4] PEPTIDES AND THE BLOOD-BRAIN-BARRIER - THE STATUS OF OUR UNDERSTANDING
    BEGLEY, DJ
    [J]. MODELS OF NEUROPEPTIDE ACTION, 1994, 739 : 89 - 100
  • [5] TRANSPORT OF ALPHA-AMINOISOBUTYRIC-ACID ACROSS BRAIN CAPILLARY AND CELLULAR MEMBRANES
    BLASBERG, RG
    FENSTERMACHER, JD
    PATLAK, CS
    [J]. JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM, 1983, 3 (01) : 8 - 32
  • [6] BLASSBERG RG, 1980, ADV NEUROL, P255
  • [7] DAVSON H, 1995, PHYSL CSF BLOOD BRAI
  • [8] Bioavailability and transport of peptides and peptide drugs into the brain
    Egleton, RD
    Davis, TP
    [J]. PEPTIDES, 1997, 18 (09) : 1431 - 1439
  • [9] MURINE TUMOR-NECROSIS-FACTOR-ALPHA IS TRANSPORTED FROM BLOOD TO BRAIN IN THE MOUSE
    GUTIERREZ, EG
    BANKS, WA
    KASTIN, AJ
    [J]. JOURNAL OF NEUROIMMUNOLOGY, 1993, 47 (02) : 169 - 176
  • [10] Johanson C. E., 1995, NEUROSCIENCE MED, P171