Desensitization of sulphonylurea- and nutrient-induced insulin secretion following prolonged treatment with glibenclamide

被引:22
作者
Ball, AJ [1 ]
Flatt, PR [1 ]
McClenaghan, NH [1 ]
机构
[1] Univ Ulster, Sch Biomed Sci, Coleraine BT52 1SA, Londonderry, North Ireland
关键词
glibenclamide; tolbutamide; desensitization; clonal pancreatic beta-cell; insulin release; K-ATP channel;
D O I
10.1016/S0014-2999(00)00782-2
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Functional effects of prolonged exposure to the sulphonylurea glibenclamide were examined in a popular clonal pancreatic p-cell line, denoted as BRIN-BD11. In acute 20-min incubations, 200 muM of tolbutamide or glibenclamide stimulated insulin release from non-depolarized and depolarized cells, which was dramatically reduced following 18-h culture with 100 muM glibenclamide. Sulphonylurea desensitization in non-depolarized cells was reversed following 6-36-h subsequent culture in the absence of glibenclamide. However, desensitization of insulinotropic effects of sulphonylureas in depolarized cells following glibenclamide culture and associated decline in cellular insulin content was not fully reversible. Culture with 100 muM glibenclamide also markedly reduced the acute insulinotropic actions of glucose, L-alanine, L-arginine, 2-ketoisocaproic acid (KIC) and KCl. These effects were almost completely reversed following 18-h culture in the absence of the sulphonylurea. (C) 2000 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:327 / 333
页数:7
相关论文
共 43 条
[1]   Molecular biology of adenosine triphosphate-sensitive potassium channels [J].
Aguilar-Bryan, L ;
Bryan, J .
ENDOCRINE REVIEWS, 1999, 20 (02) :101-135
[2]   Identification of the high-affinity tolbutamide site on the SUR1 subunit of the KATP channel [J].
Ashfield, R ;
Gribble, FM ;
Ashcroft, SJH ;
Ashcroft, FM .
DIABETES, 1999, 48 (06) :1341-1347
[3]  
Ball AJ, 1999, DIABETOLOGIA, V42, pA244
[4]  
BORG HLA, 1980, ACTA DIABETOL LAT, V18, P65
[5]   INTERNALIZATION OF GLIBENCLAMIDE-H-3 IN PANCREATIC-ISLET CELLS [J].
CARPENTIER, JL ;
SAWANO, F ;
RAVAZZOLA, M ;
MALAISSE, WJ .
DIABETOLOGIA, 1986, 29 (04) :259-261
[6]   ATP-sensitive potassium channels and efaroxan-induced insulin release in the electrofusion-derived BRIN-BD11 β-cell line [J].
Chapman, JC ;
McClenaghan, NH ;
Cosgrove, KE ;
Hashmi, MN ;
Shepherd, RM ;
Giesberts, AN ;
White, SJ ;
Ämmälä, C ;
Flatt, PR ;
Dunne, MJ .
DIABETES, 1999, 48 (12) :2349-2357
[7]   ATP-SENSITIVE K+ CHANNELS IN PANCREATIC BETA-CELLS - SPARE-CHANNEL HYPOTHESIS [J].
COOK, DL ;
SATIN, LS ;
ASHFORD, MLJ ;
HALES, CN .
DIABETES, 1988, 37 (05) :495-498
[8]  
DeFronzo R.A., 1998, CURRENT THERAPY DIAB
[9]   INHIBITORY EFFECT OF TOLBUTAMIDE AND GLIBENCLAMIDE (GLYBURIDE) ON PANCREATIC-ISLETS OF NORMAL ANIMALS [J].
DUNBAR, JC ;
FOA, PP .
DIABETOLOGIA, 1974, 10 (01) :27-35
[10]   Signaling and sites of interaction for RX-871024 and sulfonylurea in the stimulation of insulin release [J].
Efanov, AM ;
Zaitsev, SV ;
Efanova, IB ;
Zhu, SS ;
Östenson, CG ;
Berggren, PO ;
Efendic, S .
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, 1998, 274 (04) :E751-E757