Flow dependence and time constant of the change in nitric oxide concentration measured in the vascular media

被引:16
作者
Mochizuki, S
Goto, M
Chiba, Y
Ogasawara, Y
Kajiya, F
机构
[1] Kawasaki Med Sch, Dept Med Engn & Syst Cardiol, Kurashiki, Okayama 7010192, Japan
[2] Kawasaki Med Sch, Dept Plast & Reconstruct Surg, Kurashiki, Okayama 7010192, Japan
关键词
nitric oxide; vascular media; femoral artery; flow; shear stress; microelectrode;
D O I
10.1007/BF02513336
中图分类号
TP39 [计算机的应用];
学科分类号
081203 ; 0835 ;
摘要
It has been considered that the concentration of endothelium-derived nitric oxide (NO) in the arterial vascular wall changes in response to flow-induced shear stress. In the present study, using an NO-sensitive electrode, the aim was to directly evaluate the relationship between perfusion rate and NO concentration in the arterial vascular wall. The NO microelectrode (diameter: 100 mu m) was inserted into the vascular media of isolated canine femoral arteries, and the vessel was perfused with a Krebs-Henseleit buffer solution. A flow-related change in NO concentration in the vascular media was then evaluated by changing perfusion rate. NO concentration attained a peak value with a first-order time delay by a stepwise increase in perfusion rate, and the peak-level NO concentration was linearly correlated with perfusion rate in each vessel (10-154 pA at 2.1-72.3 ml min(-1); n = 7, r(2) = 0.89-0.99, p < 0.03). The average time constant for an increase in NO current with a stepwise increase in perfusion rate was 24 +/- 3 s (n = 5). NO production was increased by perfusing a solution containing 1 mmol l(-1) L-arginine and was attenuated by 100 mu mol l(-1) N-G-nitro-L-arginine, indicating the intactness of the endothelium, proper insertion of the NO electrode and selective detection of NO by the electrode. It is concluded that the NO microelectrode is applicable to NO measurement in the vascular media where NO controls vascular tone and that the concentration of NO in the arterial vascular media changes with perfusion rate in a rate-dependent manner as well as with a time constant of about 24s for a stepwise increase in flow.
引用
收藏
页码:497 / 503
页数:7
相关论文
共 41 条
[1]   Intracellular pH and tyrosine phosphorylation but not calcium determine shear stress-induced nitric oxide production in native endothelial cells [J].
Ayajiki, K ;
Kindermann, M ;
Hecker, M ;
Fleming, I ;
Busse, R .
CIRCULATION RESEARCH, 1996, 78 (05) :750-758
[2]   Arginase activity in endothelial cells: Inhibition by N-G-hydroxy-L-arginine during high-output NO production [J].
Buga, GM ;
Singh, R ;
Pervin, S ;
Rogers, NE ;
Schmitz, DA ;
Jenkinson, CP ;
Cederbaum, SD ;
Ignarro, LJ .
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 1996, 271 (05) :H1988-H1998
[3]  
BUSSE R, 1993, EUR HEART J, V14, P2
[4]   Role of nitric oxide in the local regulation of pulmonary vascular resistance in humans [J].
Cooper, CJ ;
Landzberg, MJ ;
Anderson, TJ ;
Charbonneau, F ;
Creager, MA ;
Ganz, P ;
Selwyn, AP .
CIRCULATION, 1996, 93 (02) :266-271
[5]   Phosphorylation of endothelial nitric oxide synthase in response to fluid shear stress [J].
Corson, MA ;
James, NL ;
Latta, SE ;
Nerem, RM ;
Berk, BC ;
Harrison, DG .
CIRCULATION RESEARCH, 1996, 79 (05) :984-991
[6]   ACTIVATION OF ENDOTHELIAL L-ARGININE PATHWAY IN RESISTANCE ARTERIES - EFFECT OF AGE AND HYPERTENSION [J].
DOHI, Y ;
THIEL, MA ;
BUHLER, FR ;
LUSCHER, TF .
HYPERTENSION, 1990, 16 (02) :170-179
[7]   INDUCIBLE NITRIC-OXIDE-SYNTHASE MESSENGER-RNA IS TRANSIENTLY EXPRESSED AND DESTROYED BY A CYCLOHEXIMIDE-SENSITIVE PROCESS [J].
EVANS, T ;
CARPENTER, A ;
COHEN, J .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1994, 219 (1-2) :563-569
[8]   Ca2+-independent activation of the endothelial nitric oxide synthase in response to tyrosine phosphatase inhibitors and fluid shear stress [J].
Fleming, I ;
Bauersachs, J ;
Fisslthaler, B ;
Busse, R .
CIRCULATION RESEARCH, 1998, 82 (06) :686-695
[9]  
GIBBONS GH, 1994, NEW ENGL J MED, V330, P1431
[10]   ANALYSIS OF NITRATE, NITRITE, AND [N-15]-LABELED NITRATE IN BIOLOGICAL-FLUIDS [J].
GREEN, LC ;
WAGNER, DA ;
GLOGOWSKI, J ;
SKIPPER, PL ;
WISHNOK, JS ;
TANNENBAUM, SR .
ANALYTICAL BIOCHEMISTRY, 1982, 126 (01) :131-138