Distribution and kinetics of amylin in humans

被引:26
作者
Clodi, M
Thomaseth, K
Pacini, G
Hermann, K
Kautzky-Willer, A
Waldhäusl, W
Prager, R
Ludvik, B
机构
[1] Univ Vienna, Dept Med 3, Div Endocrinol & Metab, A-1090 Vienna, Austria
[2] Inst Syst Sci & Biomed Engn, CNR, LADSEB, I-35127 Padua, Italy
来源
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM | 1998年 / 274卷 / 05期
关键词
pharmacokinetics; noncompartmental analysis; compartmental analysis; mathematical modeling;
D O I
10.1152/ajpendo.1998.274.5.E903
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The aim of the study was to determine the apparent volume of distribution (V-TOT), total body clearance (CL), fractional clearance, and mean residence time (MRT) of the beta-cell hormone amylin. We therefore performed an intravenous injection of 50 mu g of human synthetic amylin (amlintide) in nine healthy male subjects during suppression of endogenous amylin release by intravenous somatostatin (0.06 mu g.kg2(-1). min(-1)). The plasma levels of amylin concentrations over time were analyzed using three-exponential curves. V-TOT was 173 +/- 16 ml/kg and was not different from that of insulin reported in the literature (157 ml/kg). MRT was 27.7 +/- 2.1 min and thus two times the reported value for insulin (14.1 min) and C-peptide (16.4 min). CL and fractional CL were 6.2 +/- 0.2 ml.kg(-1).min(-1) and 0.038 +/- 0.003 min(-1), respectively. Fractional CL is therefore definitely lower than that reported for insulin (0.12-0.2 min(-1)) but is, however, in the range of that of C-peptide (0.05 min(-1)). In conclusion, clearance of amylin is similar to that reported for C-peptide and much slower than insulin, indicating that the commonly used molar insulin-to-amylin ratio does not reflect the correct relationship of the two peptides.
引用
收藏
页码:E903 / E908
页数:6
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