Mechanisms of metabolic coronary flow regulation

被引:69
作者
Deussen, Andreas [1 ]
Ohanyan, Vahagn [2 ]
Jannasch, Anett [3 ]
Yin, Liya [2 ]
Chilian, William [2 ]
机构
[1] Tech Univ Dresden, Med Fac Carl Gustav, Dept Physiol, D-01307 Dresden, Germany
[2] NE Ohio Med Univ, Dept Integrat Med Sci, Rootstown, OH 44272 USA
[3] Heart Ctr Dresden, Cardiosurg Lab, D-01307 Dresden, Germany
关键词
Coronary blood flow; Oxygen; Carbon dioxide; Reactive oxygen species; Adenosine; Nitric oxide; Prostaglandins; Ion channels; K-ATP CHANNELS; SENSITIVE POTASSIUM CHANNELS; MYOCARDIAL BLOOD-FLOW; GUINEA-PIG HEART; NITRIC-OXIDE; HYPERCAPNIC ACIDOSIS; ARTERIOLAR DILATION; HYDROGEN-PEROXIDE; MICROVASCULAR DILATION; SPATIAL HETEROGENEITY;
D O I
10.1016/j.yjmcc.2011.10.001
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Coronary blood flow is tightly adjusted to the oxygen requirements of the myocardium. The underlying control mechanisms keep coronary venous pO(2) at a rather constant level around 20 mm Hg under a variety of physiological conditions. Because coronary flow may increase more than 5-fold during exercise without any signs of under- or overperfusion, coronary flow must be controlled, at least in part, in a feed forward manner. Likely metabolic factors contributing to feed forward control are carbon dioxide and reactive oxygen species. Adaptation of coronary flow to exercise under physiological conditions involves in addition to metabolic control feed forward neuronal and endothelium-dependent control. Under pathological conditions, e.g. vessel stenosis or anemia, or specific environmental conditions, e.g. high altitude exposure, cardiac oxygenation may become critical, especially if oxygen demand is increased during physical exercise. Under such conditions the fall of coronary pO(2) may directly result in opening of oxygen sensitive potassium or closure of calcium channels. Furthermore the fall of pO(2) results in the production of vasoactive metabolites, e.g. adenosine, nitric oxide or prostaglandins, and in proton accumulation. All of these adaptations support a reduction of coronary vessel resistance. This article is part of a Special Issue entitled "Coronoray Blood Flow". (C) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码:794 / 801
页数:8
相关论文
共 105 条
  • [1] ATP-SENSITIVE POTASSIUM CHANNELS ARE INVOLVED IN ADENOSINE A(2) RECEPTOR-MEDIATED CORONARY VASODILATATION IN THE DOG
    AKATSUKA, Y
    EGASHIRA, K
    KATSUDA, Y
    NARISHIGE, T
    UENO, H
    SHIMOKAWA, H
    TAKESHITA, A
    [J]. CARDIOVASCULAR RESEARCH, 1994, 28 (06) : 906 - 911
  • [2] EFFECT OF BLOCKADE OF THE ATP-SENSITIVE POTASSIUM CHANNEL ON METABOLIC CORONARY VASODILATION IN THE DOG
    AVERSANO, T
    OUYANG, P
    SILVERMAN, H
    ZIEGELSTEIN, RC
    GIPS, S
    [J]. PHARMACOLOGY, 1993, 47 (06) : 360 - 368
  • [3] A P-31-NMR STUDY OF THE EFFECTS OF REFLOW ON THE ISCHEMIC RAT-HEART
    BAILEY, IA
    SEYMOUR, AML
    RADDA, GK
    [J]. BIOCHIMICA ET BIOPHYSICA ACTA, 1981, 637 (01) : 1 - 7
  • [4] Bassenge E, 1990, Rev Physiol Biochem Pharmacol, V116, P77
  • [5] CARDIAC NUCLEOTIDES IN HYPOXIA - POSSIBLE ROLE IN REGULATION OF CORONARY BLOOD FLOW
    BERNE, RM
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY, 1963, 204 (02): : 317 - &
  • [6] SYNERGISTIC ACTION OF MYOCARDIAL OXYGEN AND CARBON-DIOXIDE IN CONTROLLING CORONARY BLOOD-FLOW
    BROTEN, TP
    ROMSON, JL
    FULLERTON, DA
    VANWINKLE, DM
    FEIGL, EO
    [J]. CIRCULATION RESEARCH, 1991, 68 (02) : 531 - 542
  • [7] ROLE OF NITRIC-OXIDE IN HYPOXIC CORONARY VASODILATATION IN ISOLATED PERFUSED GUINEA-PIG HEART
    BROWN, IP
    THOMPSON, CI
    BELLONI, FL
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY, 1993, 264 (03): : H821 - H829
  • [8] THE ROLE OF PROSTAGLANDINS IN THE ENDOTHELIUM-MEDIATED VASODILATORY RESPONSE TO HYPOXIA
    BUSSE, R
    FORSTERMANN, U
    MATSUDA, H
    POHL, U
    [J]. PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY, 1984, 401 (01): : 77 - 83
  • [9] REGIONAL MYOCARDIAL FLOW AND CAPILLARY PERMEABILITY-SURFACE AREA PRODUCTS ARE NEARLY PROPORTIONAL
    CALDWELL, JH
    MARTIN, GV
    RAYMOND, GM
    BASSINGTHWAIGHTE, JB
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY, 1994, 267 (02): : H654 - H666
  • [10] HETEROGENEOUS MICROVASCULAR CORONARY ALPHA-ADRENERGIC VASOCONSTRICTION
    CHILIAN, WM
    LAYNE, SM
    EASTHAM, CL
    MARCUS, ML
    [J]. CIRCULATION RESEARCH, 1989, 64 (02) : 376 - 388