Metabolic responses with endothelin antagonism in a model of insulin resistance

被引:11
作者
Berthiaume, N
Wessale, JL
Opgenorth, TJ
Zinker, BA [1 ]
机构
[1] Abbott Labs, Metab Dis Res, Global Pharmaceut Res & Dev Div, Abbott Pk, IL 60064 USA
[2] Abbott Labs, Integrat Pharmacol, Global Pharmaceut Res & Dev Div, Abbott Pk, IL 60064 USA
来源
METABOLISM-CLINICAL AND EXPERIMENTAL | 2005年 / 54卷 / 06期
基金
加拿大健康研究院;
关键词
D O I
10.1016/j.metabol.2004.12.019
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Atrasentan, an endothelin antagonist, would have beneficial effects on metabolic responses in a model of insulin resistance. Zucker lean or fatty rats were maintained either on regular (lean and fatty control, n = 12) or atrasentan-treated water (5 mg/kg/d, fatty atrasentan, n = 13) for 6 weeks. There was no significant difference in water intake and body weight with the atrasentan-treated group compared with fatty controls. Although atrasentan had no effect on 3-hour fasting glucose levels, it reduced fasting insulin levels between weeks 2 and 4 of treatment by 53% (fatty control vs fatty atrasentan, P < .01). Atrasentan decreased the incremental area under the plasma glucose response curve (Delta AUC) after a nutritionally complete meal tolerance test (MTT), by 28% in the atrasentan-treated group compared with fatty controls (P < .05), and decreased the MTT-induced insulin Delta AUC by 63% in treated animals compared with the fatty control group (P < .01). In addition, atrasentan significantly decreased the MTT-induced glucose-insulin index Delta AUC by 58% in treated rats compared with fatty controls (P < .01). In summary, in the Zucker fatty rat, atrasentan significantly reduces (1) 3-hour fasting insulin levels at 4 weeks, (2) glucose and insulin MTT-induced Delta AUCs, and (3) the MTT-induced glucose-insulin index Delta AUC. These results demonstrate an improvement in hyperinsulinemia as well as in glucose tolerance and insulin sensitivity with chronic endothelin antagonism in a model of insulin resistance and suggest that chronic endothelin antagonism may have benefits in the treatment of insulin resistance and/or diabetes. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:735 / 740
页数:6
相关论文
共 35 条
[31]   PRODUCTION OF ENDOTHELIN-1 FROM THE MESENTERIC-ARTERIES OF STREPTOZOTOCIN-INDUCED DIABETIC RATS [J].
TAKEDA, Y ;
MIYAMORI, I ;
YONEDA, T ;
TAKEDA, R .
LIFE SCIENCES, 1991, 48 (26) :2553-2556
[32]   Endothelin-1 infusion inhibits plasma insulin responsiveness in normal men [J].
Teuscher, AU ;
Lerch, M ;
Shaw, S ;
Pacini, G ;
Ferrari, P ;
Weidmann, P .
JOURNAL OF HYPERTENSION, 1998, 16 (09) :1279-1284
[33]  
WOLEVER TMS, 1986, AM J NUTR, V59, P331
[34]   Endothelin stimulates glucose uptake and GLUT4 translocation via activation of endothelin ETA receptor in 3T3-L1 adipocytes [J].
Wu-Wong, JSR ;
Berg, CE ;
Wang, JH ;
Chiou, WJ ;
Fissel, B .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (12) :8103-8110
[35]   A NOVEL POTENT VASOCONSTRICTOR PEPTIDE PRODUCED BY VASCULAR ENDOTHELIAL-CELLS [J].
YANAGISAWA, M ;
KURIHARA, H ;
KIMURA, S ;
TOMOBE, Y ;
KOBAYASHI, M ;
MITSUI, Y ;
YAZAKI, Y ;
GOTO, K ;
MASAKI, T .
NATURE, 1988, 332 (6163) :411-415