Tetrahydrobiopterin, nitric oxide and regulation of cerebral arterial tone

被引:34
作者
Kinoshita, H
Tsutsui, M
Milstien, S
Katusic, ZS
机构
[1] MAYO CLIN & MAYO FDN, DEPT ANESTHESIOL, ROCHESTER, MN 55905 USA
[2] MAYO CLIN & MAYO FDN, DEPT PHARMACOL, ROCHESTER, MN 55905 USA
[3] NIMH, CELL BIOL LAB, NIH, BETHESDA, MD 20892 USA
关键词
D O I
10.1016/S0301-0082(97)00017-8
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Tetrahydrobiopterin is an essential cofactor required for activity of nitric oxide synthases. Existing evidence suggests that, during activation of constitutive and inducible isoforms of nitric oxide synthase, tetrahydrobiopterin is needed for allosteric and redox activation of enzymatic activity. However, precise mechanisms underlying the role of tetrahydrobiopterin in regulation of nitric oxide formation is not fully understood. In cerebral and peripheral arteries, increased availability of tetrahydrobiopterin can augment production of nitric oxide. In contrast, in arteries depleted of tetrahydrobiopterin, production of nitric oxide is impaired. Proinflammatory cytokines enhance mRNA expression of the rate-limiting enzyme of tetrahydrobiopterin biosynthesis, GTP cyclohydrolase I and stimulate production of tetrahydrobiopterin. The ability of vascular tissues to synthesize tetrahydrobiopterin plays an important role in regulation of nitric oxide synthase under physiological conditions as well as during inflammation and sepsis. More recent studies concerning expression and function of recombinant nitric oxide synthases suggest that availability of tetrahydrobiopterin is important for production of nitric oxide in genetically engineered blood vessels. In this review, mechanisms regulating availability of intracellular tetrahydrobiopterin and its role in control of vascular tone under physiological and pathological conditions will be discussed. (C) 1997 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:295 / 302
页数:8
相关论文
共 78 条
[21]   SUPEROXIDE ANION IS INVOLVED IN THE BREAKDOWN OF ENDOTHELIUM-DERIVED VASCULAR RELAXING FACTOR [J].
GRYGLEWSKI, RJ ;
PALMER, RMJ ;
MONCADA, S .
NATURE, 1986, 320 (6061) :454-456
[22]   GTP CYCLOHYDROLASE-1 MESSENGER-RNA IS INDUCED BY LPS IN VASCULAR SMOOTH-MUSCLE - CHARACTERIZATION, SEQUENCE AND RELATIONSHIP TO NITRIC-OXIDE SYNTHASE [J].
HATTORI, Y ;
GROSS, SS .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1993, 195 (01) :435-441
[23]   CA2+/CALMODULIN-DEPENDENT FORMATION OF HYDROGEN-PEROXIDE BY BRAIN NITRIC-OXIDE SYNTHASE [J].
HEINZEL, B ;
JOHN, M ;
KLATT, P ;
BOHME, E ;
MAYER, B .
BIOCHEMICAL JOURNAL, 1992, 281 :627-630
[24]   MACROPHAGE NITRIC-OXIDE SYNTHASE - RELATIONSHIP BETWEEN ENZYME-BOUND TETRAHYDROBIOPTERIN AND SYNTHASE ACTIVITY [J].
HEVEL, JM ;
MARLETTA, MA .
BIOCHEMISTRY, 1992, 31 (31) :7160-7165
[25]  
HEVEL JM, 1991, J BIOL CHEM, V266, P22789
[26]   Smoking impairs the activity of endothelial nitric oxide synthase in saphenous vein [J].
Higman, DJ ;
Strachan, AMJ ;
Buttery, L ;
Hicks, RCJ ;
Springall, DR ;
Greenhalgh, RM ;
Powell, JT .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 1996, 16 (04) :546-552
[27]   NITRIC-OXIDE SYNTHASE INHIBITION AND CEREBROVASCULAR REGULATION [J].
IADECOLA, C ;
PELLIGRINO, DA ;
MOSKOWITZ, MA ;
LASSEN, NA .
JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM, 1994, 14 (02) :175-192
[28]   Adenoviral-mediated transfer of the human endothelial nitric oxide synthase gene reduces acute hypoxic pulmonary vasoconstriction in rats [J].
Janssens, SP ;
Bloch, KD ;
Nong, ZX ;
Gerard, RD ;
Zoldhelyi, P ;
Collen, D .
JOURNAL OF CLINICAL INVESTIGATION, 1996, 98 (02) :317-324
[29]   Superoxide anion and endothelial regulation of arterial tone [J].
Katusic, ZS .
FREE RADICAL BIOLOGY AND MEDICINE, 1996, 20 (03) :443-448
[30]  
KATUSIC ZS, 1994, CAN J PHYSL PHARM, V72, P473