Nitric oxide is significantly reduced in ex vivo porcine arteries during reverse flow because of increased superoxide production

被引:90
作者
Lu, X [1 ]
Kassab, GS [1 ]
机构
[1] Univ Calif Irvine, Dept Biomed Engn, Rockwell Engn Ctr, Irvine, CA 92697 USA
来源
JOURNAL OF PHYSIOLOGY-LONDON | 2004年 / 561卷 / 02期
关键词
D O I
10.1113/jphysiol.2004.075218
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Oscillatory and negative flows occur normally in the cardiovascular system, which predispose those regions to atherosclerosis. Nitric oxide (NO) production increases in proportion to the magnitude of flow and is known to be athero-protective. What is not known, however, is the effect of flow reversal on NO concentration ([NO]). The hypothesis of the present study is that [NO] is reduced in reverse flow. An additional hypothesis is that the reduction in [NO] is mediated through an increase in superoxide production during flow reversal. These hypotheses were tested in an ex vivo preparation of porcine elastic and muscular arteries. The flow of a physiological solution through the vessels was regulated in the forward and reverse direction and the effluent was assayed for nitrite levels using a combination of a diazo coupling method and high performance liquid chromatography. Our results show that [NO] is significantly reduced during reverse flow. Furthermore, addition of tempol (superoxide dismutase-mimetic) which is a superoxide scavenger returns the [NO] during reverse flow to mirror those of forward flow. These results have important implications since the action of superoxide is implicated in many cardiovascular diseases, and the present finding suggests that flow reversal should be added to the list.
引用
收藏
页码:575 / 582
页数:8
相关论文
共 47 条
[31]   Role of hyaluronic acid glycosaminoglycans in shear-induced endothelium-derived nitric oxide release [J].
Mochizuki, S ;
Vink, H ;
Hiramatsu, O ;
Kajita, T ;
Shigeto, F ;
Spaan, JAE ;
Kajiya, F .
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 2003, 285 (02) :H722-H726
[32]   PULSATILE VELOCITY-MEASUREMENTS IN A MODEL OF THE HUMAN ABDOMINAL-AORTA UNDER RESTING CONDITIONS [J].
MOORE, JE ;
KU, DN .
JOURNAL OF BIOMECHANICAL ENGINEERING-TRANSACTIONS OF THE ASME, 1994, 116 (03) :337-346
[33]  
Oshinski JN, 1995, JMRI-J MAGN RESON IM, V5, P640
[34]   In vivo wall shear stress measured by magnetic resonance velocity mapping in the normal human abdominal aorta [J].
Oyre, S ;
Pedersen, EM ;
Ringgaard, S ;
Boesiger, P ;
Paaske, WP .
EUROPEAN JOURNAL OF VASCULAR AND ENDOVASCULAR SURGERY, 1997, 13 (03) :263-271
[35]  
Pedersen EM, 1999, SCAND CARDIOVASC J, V33, P206
[36]   THE INTIMA - SOIL FOR ATHEROSCLEROSIS AND RESTENOSIS [J].
SCHWARTZ, SM ;
DEBLOIS, D ;
OBRIEN, ERM .
CIRCULATION RESEARCH, 1995, 77 (03) :445-465
[37]   Wall shear stress and early atherosclerosis: A review [J].
Shaaban, AM ;
Duerinckx, AJ .
AMERICAN JOURNAL OF ROENTGENOLOGY, 2000, 174 (06) :1657-1665
[38]   Unidirectional and oscillatory shear stress differentially modulate NOSIII gene expression [J].
Silacci, P ;
Formentin, K ;
Bouzourène, K ;
Daniel, F ;
Brunner, HR ;
Hayoz, D .
NITRIC OXIDE-BIOLOGY AND CHEMISTRY, 2000, 4 (01) :47-56
[39]  
SMIESKO V, 1993, NEWS PHYSIOL SCI, V8, P34
[40]   Characteristics of arterial wall shear stress which cause endothelium-dependent vasodilatation in the anaesthetized dog [J].
Snow, HM ;
Markos, F ;
O'Regan, D ;
Pollock, K .
JOURNAL OF PHYSIOLOGY-LONDON, 2001, 531 (03) :843-848