Folic acid reverses endothelial dysfunction induced by inhibition of tetrahydrobiopterin biosynthesis

被引:41
作者
Moat, SJ
Clarke, ZL
Madhavan, AK
Lewis, MJ
Lang, D
机构
[1] Univ Cardiff Wales, Wales Coll Med, Wales Heart Res Inst, Cardiff CF14 4XN, S Glam, Wales
[2] Univ Wales Hosp, Dept Med Biochem, Cardiff CF14 4XN, S Glam, Wales
基金
英国惠康基金;
关键词
folic acid; endothelium; tetrahydrobiopterin; endothelial dysfunction;
D O I
10.1016/j.ejphar.2005.11.047
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
While folic acid has been shown to reverse endothelial dysfunction, the exact underlying mechanism remains elusive. Here, folic acid reversed both the endothelial dysfunction and increased production of superoxide following depiction of rabbit aortic ring tetrahydrobiopterin (BH4) levels with 2,4-diamino-6-hydroxy-pyrimidine (DAHP) and N-acetyl-5-hydroxy-tryptamine (NAS). Incubation with L-nitroarginine methyl ester also attenuated the production of superoxide. DAHP and NAS reduced BH4 concentrations in both aorta and cultured porcine aortic endothelial cells. Folic acid had no effect on BH4 concentrations in either preparation. The superoxide anion scavenger Tiron but not folic acid reversed the endothelial dysfunction produced in aortic rings by inhibition of copper-zinc superoxide dismutase with diethyldithiocarbamic acid. Neither folic acid nor its metabolite 5-methyltetrahydrofolate prevented the in vitro oxidation of BH4. This study demonstrates that folic acid reverses the endothelial dysfunction induced by BH4 depletion independently of either the regeneration or stabilization of BH4 or an antioxidant effect. (c) 2005 Elsevier B.V All rights reserved.
引用
收藏
页码:250 / 258
页数:9
相关论文
共 29 条
[11]   Interaction of 5-methyltetrahydrofolate and tetrahydrobiopterin on endothelial function [J].
Hyndman, ME ;
Verma, S ;
Rosenfeld, RJ ;
Anderson, TJ ;
Parsons, HG .
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 2002, 282 (06) :H2167-H2172
[12]   Tetrahydrobiopterin synthesis inhibitors induce nitric oxide synthesis in rat aorta [J].
Joly, GA ;
Kilbourn, RG .
GENERAL PHARMACOLOGY-THE VASCULAR SYSTEM, 1997, 28 (03) :475-480
[13]   Free radical scavenging behavior of folic acid: Evidence for possible antioxidant activity [J].
Joshi, R ;
Adhikari, S ;
Patro, BS ;
Chattopadhyay, S ;
Mukherjee, T .
FREE RADICAL BIOLOGY AND MEDICINE, 2001, 30 (12) :1390-1399
[14]   SOME METABOLIC RELATIONSHIPS BETWEEN BIOPTERIN AND FOLATE - IMPLICATIONS FOR THE METHYL TRAP HYPOTHESIS [J].
KAUFMAN, S .
NEUROCHEMICAL RESEARCH, 1991, 16 (09) :1031-1036
[15]   Dysfunction of endothelial nitric oxide synthase and atherosclerosis [J].
Kawashima, S ;
Yokoyama, M .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2004, 24 (06) :998-1005
[16]   Pivotal role for endothelial tetrahydrobiopterin in pulmonary hypertension [J].
Khoo, JP ;
Zhao, L ;
Alp, NJ ;
Bendall, JK ;
Nicoli, T ;
Rockett, K ;
Wilkins, MR ;
Channon, KM .
CIRCULATION, 2005, 111 (16) :2126-2133
[17]   Inhibition of tetrahydrobiopterin biosynthesis impairs endothelium-dependent relaxations in canine basilar artery [J].
Kinoshita, H ;
Milstien, S ;
Wambi, C ;
Katusic, ZS .
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 1997, 273 (02) :H718-H724
[18]   Homocysteine-induced inhibition of endothelium-dependent relaxation in rabbit aorta - Role for superoxide anions [J].
Lang, D ;
Kredan, MB ;
Moat, SJ ;
Hussain, SA ;
Powell, CA ;
Bellamy, MF ;
Powers, HJ ;
Lewis, MJ .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2000, 20 (02) :422-427
[19]   Treatment of coronary heart disease with folic acid: is there a future? [J].
Moat, SJ ;
Doshi, SN ;
Lang, D ;
McDowell, IFW ;
Lewis, MJ ;
Goodfellow, J .
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 2004, 287 (01) :H1-H7
[20]   Folate, homocysteine, endothelial function and cardiovascular disease [J].
Moat, SJ ;
Lang, D ;
McDowell, IFW ;
Clarke, ZL ;
Madhavan, AK ;
Lewis, MJ ;
Goodfellow, J .
JOURNAL OF NUTRITIONAL BIOCHEMISTRY, 2004, 15 (02) :64-79