Hyperglycaemia alters the endothelium-dependent relaxation of canine coronary arteries

被引:0
作者
Kocsis, E
Pacher, P
Pósa, I
Nieszner, E
Pogátsa, G
Koltai, MZ
机构
[1] Gyorgy Gottsegen Natl Inst Cardiol, Res Dept, H-1096 Budapest, Hungary
[2] Semmelweis Univ, Dept Pharmacol, H-1085 Budapest, Hungary
[3] Haynal Imre Univ Med Sci, Ctr Cardiovasc, Budapest, Hungary
来源
ACTA PHYSIOLOGICA SCANDINAVICA | 2000年 / 169卷 / 03期
关键词
acetylcholine; coronary artery; dog; endothelium; experimental diabetes; hyperglycaemia; in vitro;
D O I
暂无
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
The aim of the present study was to investigate the effects of experimental diabetes and hyperglycaemia per se on the endothelium-dependent relaxation of isolated canine coronary arteries and to analyse the possible involvement of the cyclooxygenase pathway in the alterations induced by hyperglycaemia. Rings from the left anterior descending coronary arteries of 18 metabolically healthy, six alloxan-diabetic and six insulin-treated alloxan diabetic dogs were set up for isometric tension recording. Diabetic coronaries as well as healthy vessels subjected to in vitro hyperglycaemia (25.5 mmol L-1 glucose) showed impaired (P < 0.05) relaxation to acetylcholine (3 nmol L-1-10 mu mol L-1) compared with normoglycaemic, i.e. metabolically healthy and insulin-treated diabetic controls, either before or after indomethacin (3 mu mol L-1) administration. The maximal dilation elicited by acetylcholine was further decreased (P < 0.05) by the cyclooxygenase inhibitor in the diabetic coronaries only. Relaxation to sodium nitroprusside did not differ among groups. These results suggest that hyperglycaemia may result in impaired endothelium-dependent dilation of coronary arteries. Diminished relaxation of diabetic coronaries is worsened by the inhibition of the synthesis of vasodilator cyclooxygenase products.
引用
收藏
页码:183 / 187
页数:5
相关论文
共 23 条
[1]   TOPICAL HYPERGLYCEMIA RAPIDLY SUPPRESSES EDRF-MEDIATED VASODILATION OF NORMAL RAT ARTERIOLES [J].
BOHLEN, HG ;
LASH, JM .
AMERICAN JOURNAL OF PHYSIOLOGY, 1993, 265 (01) :H219-H225
[2]  
Cosentino F, 1997, CIRCULATION, V96, P25
[3]   THE INFLUENCE OF THE INITIAL STRETCH AND THE AGONIST-INDUCED TONE ON THE EFFECT OF BASAL AND STIMULATED RELEASE OF EDRF [J].
DAINTY, IA ;
MCGRATH, JC ;
SPEDDING, M ;
TEMPLETON, AGB .
BRITISH JOURNAL OF PHARMACOLOGY, 1990, 100 (04) :767-773
[4]   VASCULAR REACTIVITY IN DIABETES-MELLITUS - ROLE OF THE ENDOTHELIAL-CELL [J].
FORTES, ZB ;
LEME, JG ;
SCIVOLETTO, R .
BRITISH JOURNAL OF PHARMACOLOGY, 1983, 79 (03) :771-781
[5]  
GEBREMEDHIN D, 1987, ARCH INT PHARMACOD T, V288, P100
[6]   INFLUENCE OF EXPERIMENTAL DIABETES ON THE MECHANICAL RESPONSES OF CANINE CORONARY-ARTERIES - ROLE OF ENDOTHELIUM [J].
GEBREMEDHIN, D ;
KOLTAI, MZ ;
POGATSA, G ;
MAGYAR, K ;
HADHAZY, P .
CARDIOVASCULAR RESEARCH, 1988, 22 (08) :537-544
[7]  
GERRARD JM, 1980, J LAB CLIN MED, V95, P950
[8]   IMPAIRMENT OF ENDOTHELIUM-DEPENDENT RELAXATION AND CHANGES IN LEVELS OF CYCLIC-GMP IN AORTA FROM STREPTOZOTOCIN-INDUCED DIABETIC RATS [J].
KAMATA, K ;
MIYATA, N ;
KASUYA, Y .
BRITISH JOURNAL OF PHARMACOLOGY, 1989, 97 (02) :614-618
[9]  
Koltai MZ, 1997, CARDIOVASC RES, V34, P157
[10]   STRUCTURAL AND FUNCTIONAL ORIGINS OF SUPPRESSED ACETYLCHOLINE VASODILATION IN DIABETIC RAT INTESTINAL ARTERIOLES [J].
LASH, JM ;
BOHLEN, HG .
CIRCULATION RESEARCH, 1991, 69 (05) :1259-1268