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Coronary Vascular Effects In Vivo

Halothane has variable effects on coronary blood flow and coronary vascular resistance in vivo that occur


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concomitant with changes in MVO2 .[242] [243] [244] [245] Decreases in MVO2 cause declines in coronary blood flow with relative maintenance or modest increases in coronary vascular resistance during halothane anesthesia.[14] [246] [247] Despite the decreases in coronary blood flow, halothane increases coronary sinus oxygen tension and decreases oxygen extraction, [243] [245] indicating that halothane is a relatively weak coronary vasodilator. Like halothane, isoflurane variably alters coronary blood flow in vivo.[19] [248] [249] [250] [251] Isoflurane reduces MVO2 and simultaneously decreases oxygen extraction, indicating direct coronary vasodilation. [249] Isoflurane can also produce mild and transient increases in blood flow independent of changes in MVO2 and autonomic nervous system activity during inhalational induction of anesthesia. [252] Perfusion of the left anterior descending coronary artery with blood previously equilibrated with isoflurane dramatically increases coronary blood flow,[253] but only mild coronary vasodilation occurs after a period of anesthetic equilibration in a similar experimental model.[250] Isoflurane-induced increases in coronary blood flow are not accompanied by epicardial coronary artery dilation, indicating that isoflurane predominantly dilates small coronary arteries.[254] However, adenosine, a potent coronary vasodilator, causes considerably greater vasodilation in coronary microvessels than does isoflurane.[255] The effects of enflurane on the coronary circulation in vivo are somewhat controversial. [232] [238] [239] [240] Enflurane produces greater reductions in MVO2 than does isoflurane concomitant with metabolically determined declines in coronary blood flow.[256] [257] However, isoflurane produces more profound decreases in myocardial oxygen extraction than does enflurane, indicating that isoflurane is a more potent coronary vasodilator than its structural isomer.[257]

The influence of the new volatile anesthetics on coronary blood flow in the intact cardiovascular system has been incompletely examined. Desflurane and isoflurane caused similar increases in the ratio of oxygen delivery to consumption and decreases in oxygen extraction, consistent with coronary vasodilation.[258] However, the increases in coronary blood flow produced by desflurane, but not isoflurane, are attenuated by pharmacologic blockade of the autonomic nervous system, suggesting that isoflurane causes greater direct coronary vasodilation in vivo than does desflurane. [16] Sevoflurane does not appear to produce any significant degree of coronary vasodilation,[46] [241] [259] [260] [261] in contrast to the findings with other volatile agents.

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