Rengasamy A, Ravichandran L V, Reikersdorfer C G, Johns R A
Department of Anesthesiology, University of Virginia Health Sciences Center, Charlottesville, USA.
J Pharmacol Exp Ther. 1995 May;273(2):599-604.
Inhalational anesthetics inhibit the nitric oxide (NO)-soluble guanylate cyclase signaling pathway in vascular and neuronal tissues and it has been proposed that this inhibition is due to several mechanisms, which include a direct inhibition of NO synthase. To determine the direct interaction of anesthetics with NO synthase, the effects of halothane, isoflurane and enflurane on NO synthase activity of bovine and rat brains and cultured bovine aortic endothelial cells were investigated. Halothane and enflurane at 1% to 3% concentrations produced no significant effect on crude bovine brain NO synthase activity, as measured by the conversion of L-[3H]arginine to L-[3H]citrulline. Similarly, crude rat brain NO synthase activity was not affected by exposure to 1% to 4% halothane or isoflurane. The effects of inhalational anesthetics on the crude bovine brain NO synthase activity were not altered when assayed at two different temperatures (22 degrees C and 37 degrees C). Halothane and isoflurane produced no significant effects on the activity of partially purified rat brain NO synthase at different concentrations of L-[3H]arginine in the reaction mixture. Partially purified endothelial NO synthase, when equilibrated with halothane or isoflurane (0.5-2%), exhibited no significant alteration in enzyme activity. This study suggests that the effects of inhalational anesthetics on NO synthesis in rat and bovine brains and in vascular endothelial cells are not due to their direct interaction with NO synthase.
吸入性麻醉药可抑制血管和神经组织中的一氧化氮(NO)-可溶性鸟苷酸环化酶信号通路,有人提出这种抑制作用是由多种机制引起的,其中包括对一氧化氮合酶的直接抑制。为了确定麻醉药与一氧化氮合酶的直接相互作用,研究了氟烷、异氟烷和恩氟烷对牛和大鼠大脑以及培养的牛主动脉内皮细胞中一氧化氮合酶活性的影响。通过将L-[3H]精氨酸转化为L-[3H]瓜氨酸来测量,1%至3%浓度的氟烷和恩氟烷对粗制牛脑一氧化氮合酶活性没有显著影响。同样,暴露于1%至4%的氟烷或异氟烷不会影响粗制大鼠脑一氧化氮合酶活性。在两个不同温度(22℃和37℃)下测定时,吸入性麻醉药对粗制牛脑一氧化氮合酶活性的影响没有改变。在反应混合物中不同浓度的L-[3H]精氨酸条件下,氟烷和异氟烷对部分纯化的大鼠脑一氧化氮合酶活性没有显著影响。当与氟烷或异氟烷(0.5 - 2%)平衡时,部分纯化的内皮型一氧化氮合酶的酶活性没有显著变化。这项研究表明,吸入性麻醉药对大鼠和牛大脑以及血管内皮细胞中一氧化氮合成的影响并非由于它们与一氧化氮合酶的直接相互作用。