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作 者:鲍捷[1] 陈湉[1] 王莉[1] 孙煦[1] 黄腾[1] 孟晶[2]
机构地区:[1]徐州医学院麻醉学院,2005级4班江苏徐州221004 [2]徐州医学院麻醉药理学教研室
出 处:《徐州医学院学报》2009年第3期171-172,共2页Acta Academiae Medicinae Xuzhou
基 金:江苏省高校自然科学基础研究项目(07KJD310219);徐州医学院课题(07KJ029)
摘 要:目的测定氯胺酮抗硝酸士的宁小鼠惊厥的ED50。方法将昆明种小鼠随机分为6组,每组10只,分别腹腔注射生理盐水(NS)或氯胺酮24.5、35.0、50.0、71.4、102.0mg/kg,5min后分别腹腔注射硝酸士的宁1.5mg/kg,观察小鼠的惊厥发生率、潜伏期、强直持续期和死亡率,用序贯法、点斜法测定氯胺酮抗硝酸士的宁小鼠惊厥的ED50。结果与NS组比较,K50.0组、K71.4组和K102.0组惊厥发生率均降低(P〈0.05或P〈0.01),如K35.0、K50.0、K71.4和K102.0组小鼠死亡率均降低(P〈0.05或P〈0.01),各组惊厥潜伏期均延长(P〈0.05或P〈0.01),且呈剂量依赖性(r=0.9740,P〈0.01)。氯胺酮抗士的宁惊厥的点斜法ED50的95%可信区间是44.8~64.3mg/kg。序贯法ED50的95%可信区间是39.3—74.8mg/kg。结论氯胺酮的抗士的宁小鼠惊厥ED50的95%可信区间分别为44.8~64.3mg/kg和39.3—74.8mg/kg,其机制可能与甘氨酸受体有关。Objective To determine the effects of ketamine and its 50% effective dose ( ED50 ) during its therapeutic use against strychnine - induced convulsions in mice. Methods Kunming mice randomly divided into six groups (n =10) were given intraperitoneal injection of saline 0. 1 ml/10 g or doses of ketamine (24.5, 35.0, 50. 0, 71.4 and 102.0 mg/kg), respectively. 5 minutes later, 0.1 ml/kg of 1.5 mg/kg strychnine nitrate was administered i.p. to observe the incidence of seizures in mice, latency, duration of tonic state and mortality, and to determine the anticonvulsant ED50 of ketamine against strychnine - induced convulsions in mice using sequential method and spot - slope method. Results Compared with the NS group, the incidences of seizures decreased in K50.0, K71.4 and K102.0 groups ( P 〈 0.05, P 〈 0.01 ) ; the mortalities significantly decreased in K35. 0, K50 .0, K71.4 and K102.0 groups (P 〈 0.05, P 〈 0.01 ), the sei- zure latencies were prolonged in all groups ( P 〈 0.05, P 〈 0.01 ) ; in a dose - dependent manner each group can be shortened seizure latency (P 〈 0.05, P 〈 0.01 ), and a dose - dependent manner ( r = 0. 9740, P 〈 0.01 ). The 95% authentic range of ketamine EDs0 against strychnine convulsion was 44.8 - 64.3 mg/kg by the grouping method and 39.3 - 74.8 mg/kg by the sequential method. Conclusion The anticonvulsant mechanisms of ketamine may, be associated with glycin receptor.
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