Chronic treatment with the thiazolidinedione, MCC-555, is associated with reductions in nitric oxide synthase activity and β-cell apoptosis in the pancreas of the Zucker Diabetic Fatty rat

被引:14
作者
Pickavance, LC
Widdowson, PS
Foster, JR
Williams, G
Wilding, JPH
机构
[1] Univ Liverpool, UCD, Dept Med, Diabet & Endocrinol Res Grp, Liverpool L69 3GA, Merseyside, England
[2] Syngenta Cent Toxicol Lab, Dept Pathol, Macclesfield, Cheshire, England
关键词
apoptosis; beta-cells; diabetes mellitus type 2; fatty acids; nitric oxide; pancreas; thiazolidinedione; ZDF rats;
D O I
10.1046/j.1365-2613.2003.00337.x
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
The Zucker Diabetic Fatty (ZDF) rat is a model of impaired insulin sensitivity arising from hyperphagia owing to a mutation in the leptin receptor. In time, young ZDF rats, which are not initially diabetic, develop impaired pancreatic beta-cell function leading to apoptotic cell death. This results in an inability to fully compensate for the reduction in insulin sensitivity with hypersecretion of insulin. Young, pre-diabetic ZDF rats were treated, over a 4-week period, with the thiazolidinedione compound MCC-555, and the islet morphology studied in comparison to ZDF rats not given MCC-555. In particular, changes in the apoptotic incidence, as measured using TUNEL staining to localize apoptotic cells, were studied over the 4-week period. Changes in the induction of nitric oxide synthase and in the accumulation of nitrate/nitrite within the pancreas were also studied during the time course of administration of MCC-555. The study has demonstrated that the administration of MCC-555 significantly decreases the apoptotic incidence in the islets of Langerhans of pre-diabetic ZDF rats given the compound, as compared to those not given MCC-555, as well as decreasing the accumulation of nitrate/nitrite within the pancreas.
引用
收藏
页码:83 / 89
页数:7
相关论文
共 24 条
[1]   Diabetes mellitus and genetically programmed defects in β-cell function [J].
Bell, GI ;
Polonsky, KS .
NATURE, 2001, 414 (6865) :788-791
[2]   NITRIC-OXIDE MEDIATES CYTOKINE-INDUCED INHIBITION OF INSULIN-SECRETION BY HUMAN ISLETS OF LANGERHANS [J].
CORBETT, JA ;
SWEETLAND, MA ;
WANG, JL ;
LANCASTER, JR ;
MCDANIEL, ML .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (05) :1731-1735
[3]   NITRIC-OXIDE MEDIATES GLUTAMATE NEUROTOXICITY IN PRIMARY CORTICAL CULTURES [J].
DAWSON, VL ;
DAWSON, TM ;
LONDON, ED ;
BREDT, DS ;
SNYDER, SH .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (14) :6368-6371
[4]  
Harris MI, 1996, DIABETIC MED, V13, pS9
[5]   Insulin resistance and its treatment by thiazolidinediones [J].
Lebovitz, HE ;
Banerji, MA .
RECENT PROGRESS IN HORMONE RESEARCH, VOL 56, 2001, 56 :265-294
[6]  
LOWRY OH, 1951, J BIOL CHEM, V193, P265
[7]  
McDaniel ML, 1996, P SOC EXP BIOL MED, V211, P24
[8]   A NEW ANTIDIABETIC AGENT, BRL-49653, REDUCES LIPID AVAILABILITY AND IMPROVES INSULIN ACTION AND GLUCOREGULATION IN THE RAT [J].
OAKES, ND ;
KENNEDY, CJ ;
JENKINS, AB ;
LAYBUTT, DR ;
CHISHOLM, DJ ;
KRAEGEN, EW .
DIABETES, 1994, 43 (10) :1203-1210
[9]   The insulin sensitizer, BRL 49653, reduces systemic fatty acid supply and utilization and tissue lipid availability in the rat [J].
Oakes, ND ;
Camilleri, S ;
Furler, SM ;
Chisholm, DJ ;
Kraegen, EW .
METABOLISM-CLINICAL AND EXPERIMENTAL, 1997, 46 (08) :935-942
[10]  
OHNEDA M, 1995, DIABETOLOGIA, V38, P173, DOI 10.1007/s001250050267