Nitric Oxide and the Cardiovascular System

被引:44
作者
Bohlen, Harold Glenn [1 ]
机构
[1] Indiana Univ Sch Med, Dept Cellular & Integrat Physiol, Indianapolis, IN 46202 USA
关键词
PROTEIN-KINASE-C; FLOW-INDUCED DILATION; VASCULAR SMOOTH-MUSCLE; SPONTANEOUSLY HYPERTENSIVE-RATS; CEREBRAL-ARTERY OCCLUSION; OPTIC-NERVE HEAD; ENDOTHELIUM-DEPENDENT VASODILATION; MESENTERIC RESISTANCE ARTERIES; EXTRACELLULAR-SODIUM SALT; GUINEA-PIG MESENTERY;
D O I
10.1002/cphy.c140052
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Nitric oxide (NO) generated by endothelial cells to relax vascular smooth muscle is one of the most intensely studied molecules in the past 25 years. Much of what is known about NO regulation of NO is based on blockade of its generation and analysis of changes in vascular regulation. This approach has been useful to demonstrate the importance of NO in large scale forms of regulation but provides less information on the nuances of NO regulation. However, there is a growing body of studies on multiple types of in vivo measurement of NO in normal and pathological conditions. This discussion will focus on in vivo studies and how they are reshaping the understanding of NO's role in vascular resistance regulation and the pathologies of hypertension and diabetes mellitus. The role of microelectrode measurements in the measurement of [NO] will be considered because much of the controversy about what NO does and at what concentration depends upon the measurement methodology. For those studies where the technology has been tested and found to be well founded, the concept evolving is that the stresses imposed on the vasculature in the form of flow-mediated stimulation, chemicals within the tissue, and oxygen tension can cause rapid and large changes in the NO concentration to affect vascular regulation. All these functions are compromised in both animal and human forms of hypertension and diabetes mellitus due to altered regulation of endothelial cells and formation of oxidants that both damage endothelial cells and change the regulation of endothelial nitric oxide synthase. (C) 2015 American Physiological Society.
引用
收藏
页码:803 / 828
页数:26
相关论文
共 280 条
[111]   Hypoxia and persistent sodium current [J].
Harnmarström, AKM ;
Gage, PW .
EUROPEAN BIOPHYSICS JOURNAL WITH BIOPHYSICS LETTERS, 2002, 31 (05) :323-330
[112]   Temporal Development of Retinal Arteriolar Endothelial Dysfunction in Porcine Type 1 Diabetes [J].
Hein, Travis W. ;
Potts, Luke B. ;
Xu, Wenjuan ;
Yuen, Josh Z. ;
Kuo, Lih .
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2012, 53 (13) :7943-7949
[113]   Divergent Roles of Nitric Oxide and Rho Kinase in Vasomotor Regulation of Human Retinal Arterioles [J].
Hein, Travis W. ;
Rosa, Robert H., Jr. ;
Yuan, Zhaoxu ;
Roberts, Elizabeth ;
Kuo, Lih .
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2010, 51 (03) :1583-1590
[114]   Estrogen maintains nitric oxide synthesis in arterioles of female hypertensive rats [J].
Huang, A ;
Sun, D ;
Kaley, G ;
Koller, A .
HYPERTENSION, 1997, 29 (06) :1351-1356
[115]   Molecular Strategy to Reduce In Vivo Collagen Barrier Promotes Entry of NCX1 Positive Inducible Pluripotent Stem Cells (iPSCNCX1+) into Ischemic (or Injured) Myocardium [J].
Huang, Wei ;
Dai, Bo ;
Wen, Zhili ;
Millard, Ronald W. ;
Yu, Xi-Yong ;
Luther, Kristin ;
Xu, Meifeng ;
Zhao, Ting C. ;
Yang, Huang-Tian ;
Qi, Zhihua ;
LaSance, Kathleen ;
Ashraf, Muhammad ;
Wang, Yigang .
PLOS ONE, 2013, 8 (08)
[116]   Nitric oxide from neuronal NOS plays critical role in cerebral capillary flow response to hypoxia [J].
Hudetz, AG ;
Shen, H ;
Kampine, JP .
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 1998, 274 (03) :H982-H989
[117]   Amino acids, arginase and nitric oxide in vascular health [J].
Huynh, NN ;
Chin-Dusting, J .
CLINICAL AND EXPERIMENTAL PHARMACOLOGY AND PHYSIOLOGY, 2006, 33 (1-2) :1-8
[118]   Direct in vivo measurement of flow-dependent nitric oxide production in mesenteric resistance arteries [J].
Hyre, CE ;
Unthank, JL ;
Dalsing, MC .
JOURNAL OF VASCULAR SURGERY, 1998, 27 (04) :726-732
[119]  
Iantorno M, 2014, J BIOL REG HOMEOS AG, V28, P169
[120]   NITRIC-OXIDE - A NOVEL SIGNAL TRANSDUCTION MECHANISM FOR TRANSCELLULAR COMMUNICATION [J].
IGNARRO, LJ .
HYPERTENSION, 1990, 16 (05) :477-483