首页> 外文期刊>Canadian journal of anesthesia: Journal canadien d'anesthesie >Preconditioning with prolonged oxygen exposure induces ischemic tolerance in the brain via oxygen free radical formation: (Le preconditionnement relevant d'une exposition prolongee a l'oxygene induit une tolerance ischemique dans le cerveau par la fo
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Preconditioning with prolonged oxygen exposure induces ischemic tolerance in the brain via oxygen free radical formation: (Le preconditionnement relevant d'une exposition prolongee a l'oxygene induit une tolerance ischemique dans le cerveau par la fo

机译:长期暴露于氧气中的预处理会通过形成氧自由基来诱导脑缺血耐受:

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PURPOSE: To determine if 100% oxygen (O(2)) inhalation induces ischemic tolerance to focal cerebral ischemia and if the effect is induced via O(2) free radical formation. METHODS: Experiment 1: 36 rats were randomly assigned to four groups (n = 9 each): Group A, control rats inhaled air for 24 hr; Groups B, C and D animals inhaled 100% O(2) for six hours, 12 hr and 24 hr respectively. Experiment 2: 32 rats were randomly assigned to four groups (n = 8 each): Groups E and F rats received normal saline (5 mL*kg(-1) intraperitoneally) and then inhaled air (Group E) or 100% O(2) (Group F) for 24 hr; Groups G and H animals received 10% dimethylthiourea (500 mg*kg(-1) intraperitoneally) and then inhaled 100% O(2) (Group G) or air (Group H) for 24 hr. Twenty-four hours after the treatments, the right middle cerebral artery was occluded in all rats for 120 min. The neurologic deficit scores (NDS) and brain infarct volumes were evaluated at 24 hr after reperfusion. RESULTS: Experiment 1: the infarct volume and NDS of Group D were smaller than in controls (P = 0.004 and 0.042 respectively). The infarct volume was reduced by 47% in Group D. There was no statistical difference among Groups A, B and C. Experiment 2: the infarct volume and NDS in Group F were less than in controls (Group E; P = 0.001 and 0.036 respectively). The infarct volume was reduced by 60% in Group F. There was no difference among Groups E, G and H. CONCLUSION: Our study demonstrates that preconditioning with 100% O(2) for 24 hr can induce ischemic tolerance via formation of O(2) free radicals in transient focal cerebral ischemia in rats.
机译:目的:确定是否100%氧气(O(2))吸入诱导局部脑缺血的局部缺血耐受,以及是否通过O(2)自由基形成诱导该作用。方法:实验1:将36只大鼠随机分为4组,每组9只。 B,C和D组动物分别吸入100%O(2)六个小时,12小时和24小时。实验2:将32只大鼠随机分为四组(每组n = 8):E和F组的大鼠腹腔注射生理盐水(5 mL * kg(-1)),然后吸入空气(E组)或100%O( 2)(F组)24小时; G组和H组动物腹膜内接受10%二甲基硫脲(500 mg * kg(-1)),然后吸入100%O(2)(G组)或空气(H组)24小时。治疗后二十四小时,所有大鼠的右大脑中动脉闭塞120分钟。再灌注后24小时评估神经功能缺损评分(NDS)和脑梗死体积。结果:实验1:D组的梗死体积和NDS均小于对照组(分别为P = 0.004和0.042)。 D组梗死体积减少了47%。A,B和C组之间无统计学差异。实验2:F组梗死体积和NDS小于对照组(E组; P = 0.001和0.036分别)。 F组梗死体积减少了60%。E,G和H组之间没有差异。结论:我们的研究表明,用100%O(2)预处理24小时可以通过形成O( 2)自由基在大鼠短暂性局灶性脑缺血中的作用。

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