Role of endothelium-derived hyperpolarizing factor in endothelial dysfunction during diabetes

被引:39
作者
Fitzgerald, SM
Kemp-Harper, BK
Tare, M
Parkington, HC
机构
[1] Monash Univ, Dept Physiol, Melbourne, Vic 3800, Australia
[2] Monash Univ, Dept Pharmacol, Melbourne, Vic 3800, Australia
关键词
endothelial dysfunction; endothelium-derived hyperpolarizing factor; resistance vessels; type; 1; diabetes; 2;
D O I
10.1111/j.1440-1681.2005.04216.x
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
1. Under normal conditions, the endothelium plays a major role in the maintenance of vasodilatory tone via the production of endothelium-derived vasodilator agents, such as prostacyclin, nitric oxide and endothelium-derived hyperpolarizing factor (EDHF). Inhibition of endothelium-dependent relaxation features prominently in a range of cardiovascular diseases, including hypertension, coronary artery disease and diabetes. 2. Endothelium-derived hyperpolarizing factor is a prominent vasodilator, particularly in smaller arteries and arterioles. There is now emerging evidence to suggest that EDHF may play a role in the endothelial dysfunction in diabetes. 3. Since the first description of endothelium-dependent hyperpolarization some 20 years ago, it has emerged that EDHF is heterogeneous in nature, consisting of diffusible factors and contact-mediated mechanisms. The specific identity of EDHF in any particular vascular bed may influence the impact of diabetes on vascular function. 4. There is accumulating evidence in diabetic rat models and humans showing impaired EDHF activity in small resistance vessels. In contrast, studies in mice suggest that EDHF activity is actually enhanced under diabetic conditions. 5. It is clear that alterations in EDHF activity may have an important contribution in diabetes, more specifically in contributing to microvascular complications observed under diabetic conditions.
引用
收藏
页码:482 / 487
页数:6
相关论文
共 60 条
[1]   Diabetes impairs endothelium-dependent relaxation of human penile vascular tissues mediated by NO and EDHF [J].
Angulo, J ;
Cuevas, P ;
Fernández, A ;
Gabancho, S ;
Allona, A ;
Martín-Morales, A ;
Moncada, I ;
Videla, S ;
de Tejada, IS .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2003, 312 (04) :1202-1208
[2]   Exercise enhances vasorelaxation in experimental obesity associated hypertension [J].
Arvola, P ;
Wu, XM ;
Kähönen, M ;
Mäkynen, H ;
Riutta, A ;
Mucha, I ;
Solakivi, T ;
Kainulainen, H ;
Pörsti, I .
CARDIOVASCULAR RESEARCH, 1999, 43 (04) :992-1002
[3]   Hydrogen peroxide relaxes porcine coronary arteries by stimulating BKCa channel activity [J].
Barlow, RS ;
White, RE .
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 1998, 275 (04) :H1283-H1289
[4]   Endothelium-independent relaxation and hyperpolarization to C-type natriuretic peptide in porcine coronary arteries [J].
Barton, M ;
Bény, JL ;
d'Uscio, LV ;
Wyss, T ;
Noll, G ;
Lüscher, TF .
JOURNAL OF CARDIOVASCULAR PHARMACOLOGY, 1998, 31 (03) :377-383
[5]   MECHANISMS OF ACTION OF NORADRENALINE AND CARBACHOL ON SMOOTH-MUSCLE OF GUINEA-PIG ANTERIOR MESENTERIC-ARTERY [J].
BOLTON, TB ;
LANG, RJ ;
TAKEWAKI, T .
JOURNAL OF PHYSIOLOGY-LONDON, 1984, 351 (JUN) :549-572
[6]   EDHF:: bringing the concepts together [J].
Busse, R ;
Edwards, G ;
Félétou, M ;
Fleming, I ;
Vanhoutte, PM ;
Weston, AH .
TRENDS IN PHARMACOLOGICAL SCIENCES, 2002, 23 (08) :374-380
[7]   Endothelium-derived hyperpolarizing factors and vascular cytochrome P450 metabolites of arachidonic acid in the regulation of tone [J].
Campbell, WB ;
Harder, DR .
CIRCULATION RESEARCH, 1999, 84 (04) :484-488
[8]   Release of C-type natriuretic peptide accounts for the biological activity of endothelium-derived hyperpolarizing factor [J].
Chauhan, SD ;
Nilsson, H ;
Ahluwalia, A ;
Hobbs, AJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (03) :1426-1431
[9]   Central role of heterocellular gap junctional communication in endothelium-dependent relaxations of rabbit arteries [J].
Chaytor, AT ;
Evens, WH ;
Griffith, TM .
JOURNAL OF PHYSIOLOGY-LONDON, 1998, 508 (02) :561-573
[10]   ACETYLCHOLINE RELEASES ENDOTHELIUM-DERIVED HYPERPOLARIZING FACTOR AND EDRF FROM RAT-BLOOD VESSELS [J].
CHEN, G ;
SUZUKI, H ;
WESTON, AH .
BRITISH JOURNAL OF PHARMACOLOGY, 1988, 95 (04) :1165-1174