K(ATP)(+) channels, nitric oxide, and adenosine are not required for local metabolic coronary vasodilation

scientific article

K(ATP)(+) channels, nitric oxide, and adenosine are not required for local metabolic coronary vasodilation is …
instance of (P31):
scholarly articleQ13442814

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P356DOI10.1152/AJPHEART.2001.280.2.H868
P698PubMed publication ID11158988

P2093author name stringM W Gorman
E O Feigl
J D Tune
K N Richmond
P2860cites workCoronary physiologyQ28265074
Endogenous adenosine mediates coronary vasodilation during exercise after K(ATP)+ channel blockadeQ34195568
Role of K+ ATP channels and adenosine in the regulation of coronary blood flow during exercise with normal and restricted coronary blood flowQ37352052
ATP-sensitive K+ channels, adenosine, and nitric oxide-mediated mechanisms account for coronary vasodilation during exerciseQ41714306
K+ATP channels and adenosine are not necessary for coronary autoregulationQ42445079
Quantitative relation between interstitial adenosine concentration and coronary blood flowQ42522368
Hypoxic dilation of coronary arteries is mediated by ATP-sensitive potassium channelsQ46218245
A method for repeated high-fidelity micromanometer measurement of intracardiac pressuresQ50105243
Influence of chronic nitric oxide inhibition of coronary blood flow regulation: a study of the role of endogenous adenosine in anesthetized, open-chested dogs.Q51515968
Role of K(ATP)(+) channels and adenosine in the control of coronary blood flow during exercise.Q52075780
Adenosine is not responsible for local metabolic control of coronary blood flow in dogs during exercise.Q52082669
Comparison of myocardial ATP, blood flow, and cytosolic adenosine in demand ischemia and coronary occlusion.Q52331953
Comprehensive model of transport and metabolism of adenosine and S-adenosylhomocysteine in the guinea pig heart.Q52414826
Coronary reactive hyperemia and adenosine-induced vasodilation are mediated partially by a glyburide-sensitive mechanism.Q53850369
Inhibition of nitric oxide synthesis increases adenosine production via an extracellular pathway through activation of protein kinase C.Q53964309
Adenosine kinetics in canine coronary circulation.Q53989170
A sheath for repetitive insertion of high-fidelity micromanometer-tipped catheters.Q54343142
P433issue2
P304page(s)H868-75
P577publication date2001-02-01
P1433published inAmerican Journal of Physiology Heart and Circulatory PhysiologyQ3193662
P1476titleK(ATP)(+) channels, nitric oxide, and adenosine are not required for local metabolic coronary vasodilation
P478volume280

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cites work (P2860)
Q36732021A pharmacological analysis of the possible role of vasoactive mediators in compensatory coronary blood flow
Q44633432Aging-related changes in myocardial purine metabolism and ischemic tolerance
Q26998655Bang-bang model for regulation of local blood flow
Q33727584Contribution of BK(Ca) channels to local metabolic coronary vasodilation: Effects of metabolic syndrome.
Q37595589Contribution of hydrogen sulfide to the control of coronary blood flow
Q44362053Coronary blood flow regulation in exercising swine involves parallel rather than redundant vasodilator pathways
Q46230060Coronary microvascular Kv1 channels as regulatory sensors of intracellular pyridine nucleotide redox potential.
Q40351732Effects of combined inhibition of ATP-sensitive potassium channels, nitric oxide, and prostaglandins on hyperemia during moderate exercise
Q33901706Enzymatic function of hemoglobin as a nitrite reductase that produces NO under allosteric control
Q36886654Exercise hyperaemia: is anything obligatory but the hyperaemia?
Q44951858F0F1 ATP synthase activity is differently modulated by coronary reactive hyperemia before and after ischemic preconditioning in the goat.
Q36699621Fractal regional myocardial blood flows pattern according to metabolism, not vascular anatomy
Q28345462Functional characterization of coronary vascular adenosine receptors in the mouse
Q33351391Giant sucking sound: can physiology fill the intellectual void left by the reductionists?
Q44358444Glyburide decreases myocardial oxygen pressure in dogs
Q47625681Hydrogen sulfide as an oxygen sensor in trout gill chemoreceptors
Q37185110Impaired vascular KATP function attenuates exercise capacity in obese zucker rats
Q39306627Kv1.3 channels facilitate the connection between metabolism and blood flow in the heart
Q35819031Matching coronary blood flow to myocardial oxygen consumption.
Q35048663Mediators of coronary reactive hyperaemia in isolated mouse heart
Q34295446Metabolic hyperemia requires ATP-sensitive K+ channels and H2O2 but not adenosine in isolated mouse hearts
Q44183002Metabolic regulation of coronary vascular tone: role of endothelin-1.
Q36518520Nitrite as a vascular endocrine nitric oxide reservoir that contributes to hypoxic signaling, cytoprotection, and vasodilation
Q41886769Nitrite regulates hypoxic vasodilation via myoglobin-dependent nitric oxide generation
Q57469985Paradoxical Arteriole Constriction Compromises Cytosolic and Mitochondrial Oxygen Delivery in the Isolated Saline-Perfused Heart
Q38111280Peripheral circulation
Q37399536Regulating myocardial blood flow in health and disease
Q50949282Regulation of Coronary Blood Flow.
Q37216075Regulation of coronary blood flow during exercise
Q37950830Regulation of coronary resistance vessel tone in response to exercise
Q27001180Regulation of increased blood flow (hyperemia) to muscles during exercise: a hierarchy of competing physiological needs
Q36832399Requisite Role of Kv1.5 Channels in Coronary Metabolic Dilation
Q39195631Smooth Muscle Ion Channels and Regulation of Vascular Tone in Resistance Arteries and Arterioles
Q37827645Ten questions about systems biology
Q40518120The human paracellin-1 gene (hPCLN-1): renal epithelial cell-specific expression and regulation
Q41959243Unveiling the Mechanism of Coronary Metabolic Vasodilation: Voltage-Gated Potassium Channels and Hydrogen Peroxide

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