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作 者:赵健[1] 韦慧[1] 李贺[2] 韩平平[3] 戴体俊[2] 邵东华[4] 杭黎华[4]
机构地区:[1]徐州医学院临床医学系,江苏徐州221002 [2]徐州医学院麻醉学院,江苏徐州221002 [3]徐州医学院药学院,江苏徐州221002 [4]镇江市第一人民医院麻醉科,江苏镇江212001
出 处:《华西药学杂志》2013年第6期579-582,共4页West China Journal of Pharmaceutical Sciences
基 金:国家自然科学基金资助项目(批准号:30872432;30471657;39970715);江苏省社会发展科技计划项目(BS 200054);徐州医学院药学院研究生科研创新计划项目(2010YKYCX011)
摘 要:目的探讨吗啡对家兔定量药物脑电图(QPEEG)B:频段的影响及其与阿片受体的关系。方法取42只成年家兔随机均分为Ns组(1mL·kg-1生理盐水)、吗啡低(LD)、中(MD)、高(HD)剂量组(0.5、1、2mg·kg-1吗啡)、Na组(200μg·kg-1纳洛酮)、NSM组(1mL·kg-1生理盐水+2mg·kg-1吗啡)和NAM组(200μg·kg-1纳洛酮+2mg·kg-1吗啡),应用QPEEG,采用功率谱分析家兔在iv药物前后β2频段功率百分比的变化。结果与给药前比较,Ns组、N组和LD组中家兔的p。频段功率百分比无明显变化;MD组和HD组中的B:频段功率百分比在部分脑区0.5~5min时增加(P〈0.05,P〈0.01),此改变在0.5~5min与吗啡剂量呈正相关(r=0.407~0.694,P〈0.01);NAM组的家兔在给吗啡前后,β2频段功率百分比无明显变化,部分脑区低于NSM组的(P〈0.05)。结论吗啡以剂量依赖方式增加兔QPEEGp:频段功率百分比,纳洛酮可拮抗之,表明吗啡在大脑皮层作用部位广泛,阿片受体介导了这一作用,提示β2频段可能成为反映镇痛程度的指标。OBJECTIVE To study the effect of Morphine on β2 - band of quantitative pharmaco - electroencephalogram (QPEEG) in the rabbits and the relation with opiate receptor. METHODS 42 grown rabbits were divided into 7 groups ( n = 6 ) : NS group ( normal saline 1 mL kg - l ) , LD group ( Morphine 0.5 mg- kg - 1 ) , MD group ( Morphine 1 mg kg - 1 ) , HD group ( Morphine 2 mg. kg - 1 ) , Na group ( Naloxone 200 μg kg - 1 ) , NSM group ( normal saline 1 mL- kg - 1 + Morphine 2 rag. kg - 1 ) and NAM group ( Naloxone 200 μg kg-1 + Morphine 2 mg kg-1 ). QPEEG activity was processed with power spectral analysis in order to analyze the change of 132 - band power percentage before and after the rabbits' being administrated drugs. RESULTS Compared with the previous administration, there was no obvious change in β2 - band power percentage of NS group, N group and LD group. In MD group and HD group,β2 - band power percentage had an increased in several brain regions during 0.5 -5 min(P 〈0. 05,P 〈0.01 ). The change of β2- band power percentage during 0.5 -5 rain had a positive correlation with Morphine dose( r = 0. 407 - 0. 694,P 〈 0.01 ). In NAM group,there was no obvious change in β2 - band power percentage before and after the rabbits' being administrated Morphine. β2 - band pow- er percentage of NAM group were even lower than that of NSM group in some brain regions (P 〈 0.05 ). CONCLUSION Morphine can increase β2- band power percentage of QPEEG in a dose dependant manner in rabbits, which can be antagonized by Naloxone. It indicates that Morphine affects the sites in cerebral cortex widely. Opiate receptor mediates this effect and β2- band may become an index that reflects analgesia degree.
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