Department of Anesthesia and Critical Care, University of Würzburg, Würzburg, Germany.
J Cardiothorac Vasc Anesth. 2013 Jun;27(3):494-501. doi: 10.1053/j.jvca.2012.04.015. Epub 2012 Jun 9.
Nitric oxide synthases (NOSs) mediate the first window of anesthetic-induced preconditioning (APC). The authors tested the hypothesis that endothelial NOS (eNOS) mediates the first window and inducible NOS (iNOS) mediates the second window of APC.
Randomized, prospective, blinded laboratory investigation.
Experimental laboratory.
Mice.
Mice were subjected to a 45-minute coronary artery occlusion (CAO) and a 180-minute reperfusion. C57BL/6 mice received desflurane, 1.0 minimum alveolar concentration, for 30 minutes or 12, 24, 48, or 96 hours before CAO. In eNOS(-/-) and iNOS(-/-) mice, desflurane was given 30 minutes and 48 hours before CAO. In the control groups, no desflurane was administered. Myocardial infarct size (IS) was determined after staining with Evans blue and triphenyltetrazolium chloride.
The second window of APC was detectable at 48 hours but not at 12, 24, and 96 hours after preconditioning. In the control groups, IS was not different among the wild-type (50 ± 10%), eNOS(-/-) (52 ± 14%), and iNOS(-/-) (46 ± 10%) mice. The IS decreased significantly (p < 0.05) when desflurane was administered 30 minutes (10 ± 6%) or 48 hours (16 ± 7%) before CAO in wild-type mice, 48 hours (21 ± 13%) before CAO in eNOS(-/-) mice, and 30 minutes (13 ± 6%) before CAO in iNOS(-/-) mice. Desflurane given 30 minutes before CAO in eNOS(-/-) mice (60 ± 10%) and 48 hours before CAO in iNOS(-/-) mice (48 ± 21%) did not decrease the IS significantly compared with controls.
Endothelial NOS and iNOS work independently to mediate the first and second windows of APC, respectively. Endothelial NOS is not necessary to trigger the second window of APC.
一氧化氮合酶(NOS)介导麻醉诱导预处理(APC)的第一个窗口。作者测试了以下假设:内皮型一氧化氮合酶(eNOS)介导第一个窗口,诱导型一氧化氮合酶(iNOS)介导 APC 的第二个窗口。
随机、前瞻性、盲法实验室研究。
实验实验室。
小鼠。
小鼠接受 45 分钟的冠状动脉闭塞(CAO)和 180 分钟的再灌注。C57BL/6 小鼠在 CAO 前接受 30 分钟或 12、24、48 或 96 小时的 1.0 最低肺泡浓度的地氟醚。在 eNOS(-/-)和 iNOS(-/-)小鼠中,地氟醚在 CAO 前 30 分钟和 48 小时给予。在对照组中,没有给予地氟醚。用 Evans 蓝和三苯基四唑氯化物染色后确定心肌梗死面积(IS)。
APC 的第二个窗口在预处理后 48 小时可检测到,但在 12、24 和 96 小时后不可检测。在对照组中,野生型(50 ± 10%)、eNOS(-/-)(52 ± 14%)和 iNOS(-/-)(46 ± 10%)小鼠之间的 IS 无差异。当地氟醚在 CAO 前 30 分钟(10 ± 6%)或 48 小时(16 ± 7%)给予时,野生型小鼠的 IS 显著降低(p < 0.05),eNOS(-/-)小鼠的 IS 在 CAO 前 48 小时(21 ± 13%),iNOS(-/-)小鼠的 IS 在 CAO 前 30 分钟(13 ± 6%)。与对照组相比,地氟醚在 CAO 前 30 分钟给予 eNOS(-/-)小鼠(60 ± 10%)和 CAO 前 48 小时给予 iNOS(-/-)小鼠(48 ± 21%)并未显著降低 IS。
内皮型一氧化氮合酶和 iNOS 分别独立工作以介导 APC 的第一个和第二个窗口。内皮型一氧化氮合酶对于触发 APC 的第二个窗口不是必需的。