In vivo dynamic distribution of 131I-glucagon-like peptide-1 (7-36) amide in the rat studied by gamma camera

被引:54
作者
Hassan, M
Eskilsson, A
Nilsson, C
Jonsson, C
Jacobsson, H
Refai, E
Larsson, S
Efendic, S
机构
[1] Karolinska Pharm, S-10401 Stockholm, Sweden
[2] Huddinge Univ Hosp, Dept Med Lab Sci & Technol, Div Clin Pharmacol, Huddinge, Sweden
[3] BMC, Uppsala, Sweden
[4] Karolinska Hosp, Dept Diagnost Radiol, S-10401 Stockholm, Sweden
[5] Karolinska Hosp, Dept Hosp Phys, S-10401 Stockholm, Sweden
[6] Karolinska Inst, Inst Biochem, Stockholm, Sweden
[7] Karolinska Inst, Inst Mol Med, Stockholm, Sweden
关键词
GLP-1; pharmacokinetics; distribution; glucagon-like peptide; diabetes; gamma camera;
D O I
10.1016/S0969-8051(98)00121-8
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
The in vivo distribution of glucagon-like peptide-1 (7-36) amide (GLP-1) was studied in a rat model using radiolabeled GLP-1 (I-131-GLP-1) depicted by a gamma-camera. The dynamic scan showed a rapid clearance from the blood circulation after an intravenous (IV) injection of I-131-GLP-1. After 10 min, the major part of the radioactivity was accumulated in the kidneys, whereas about 9% (of the blood value) was found in the brain. The pharmacokinetic study using I-125-GLP-1 demonstrated a rapid elimination from plasma, with a half-life of 3.3 +/- 0.6 min, a clearance of 117 +/- 15 mL/min, and a distribution volume of 557 +/- 61 mL. The elimination half-lives for the intact I-125-GLP-1 in lungs and kidneys were determined to 3.7 and 3.9 min, respectively. The metabolite GLP-1 (9-36) amide was followed in blood, lung, and kidney. All other organs assumed to contain low molecular weight fragments of GLP-1. The present study suggest that GLP-1 and/or its labeled metabolites cross the blood-brain barrier. Also the kidney plays an essential role in GLP-1 elimination after an IV administration, which can be of clinical interest especially in patients with kidney insufficiency who are treated with GLP-1. NUCL MED BIOL 26;4:413-420, 1999. (C) 1999 Elsevier Science Inc. All rights reserved.
引用
收藏
页码:413 / 420
页数:8
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