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酸枣仁汤的镇静催眠作用 总被引:43,自引:2,他引:41
目的对酸枣仁汤镇静催眠药理作用进行初探。方法采用镇静催眠实验观察酸枣仁汤对小鼠自主活动的影响 ,协同戊巴比妥钠对小鼠的催眠作用。结果酸枣仁汤能明显减少小鼠自主活动次数 ,增加阈下剂量戊巴比妥钠致小鼠睡眠只数 ,延长阈上剂量戊巴比妥钠致小鼠睡眠时间。结论酸枣仁汤有明显的镇静、催眠作用。 相似文献
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北五味子的镇静、催眠作用 总被引:28,自引:0,他引:28
目的对北五味子水提取物镇静、催眠药理作用进行初探。方法采用镇静、催眠实验观察北五味子水提取物对小鼠自主活动的影响 ,协同戊巴比妥钠对小鼠的催眠作用。结果北五味子水提取物能明显减少小鼠自主活动次数 ,增加阈下剂量戊巴比妥钠致小鼠睡眠只数 ,延长阈上剂量戊巴比妥钠致小鼠睡眠时间。结论北五味子水提取物有明显的镇静、催眠作用。 相似文献
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目的:通过药理实验观察复方杜仲片的镇静催眠作用。方法:观察药物对正常小鼠的自主活动的影响以评价复方杜仲片的镇静作用;观察复方杜仲片对小鼠戊巴比妥钠催眠阈剂量所致小鼠兴奋性活动的影响以探讨复方杜仲片的催眠作用,同时观察复方杜仲片对戊巴比妥钠的协同催眠作用和复方杜仲片对抗士的宁的中枢兴奋作用。结果:复方杜仲片能明显减弱小鼠自主活动,降低小鼠戊巴比妥钠催眠阈剂量,与戊巴比妥钠有较好的催眠协同作用,可延长小鼠睡眠时间,提高小鼠的入睡率,同时可使惊厥小鼠数减少,且惊厥率随剂量的增加而降低。结论:复方杜仲片具有明显的镇静催眠作用。 相似文献
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目的观察刺五加安睡丸对改善小鼠睡眠的影响。方法通过直接睡眠实验、延长戊巴比妥钠睡眠时间实验、戊巴比妥钠阈下剂量催眠实验、巴比妥钠睡眠潜伏期试验来测定动物直接睡眠时间、戊巴比妥钠诱导的睡眠时间及阈下剂量的睡眠发生率、巴比妥钠诱导的小鼠睡眠的潜伏时间。结果受试物可延长戊巴比妥钠催眠的中、高剂量组小鼠的睡眠时间,与对照组比较差异有统计学意义(P<0.05);可缩短巴比妥钠催眠中、高剂量组小鼠的入睡潜伏期,与对照组比较差异有统计学意义(P<0.05);该受试物对小鼠的体重增长无影响。结论刺五加安睡丸具有改善小鼠睡眠作用。 相似文献
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目的:观察复方安神液镇静催眠作用并与复方枣仁胶囊作比较.方法:采用抖笼换能器法、翻正反射法观察复方安神液的镇静催眠作用.结果:复方安神液高、低剂量组能抑制小鼠的自主活动强度,明显延长小鼠戊巴比妥钠阈上剂量睡眠时间,增加阈下剂量戊巴比妥钠引起的小鼠入睡数.结论:复方安神液具有较明显的镇静催眠作用. 相似文献
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目的 研究无糖型宁心安神糖浆(SNAS)的镇静、催眠作用.方法 采用自主活动试验、戊巴比妥钠阈上催眠剂量试验、睡眠试验、戊巴比妥钠阈下催眠剂量试验,每个试验均选择ICR小鼠60只,随机分为6组,每组10只,分别为空白对照组,安神补脑液组,蔗糖型宁心安神糖浆组,SNAS高、中、低剂量(100、50、25 mL/kg)组,观察SNAS对小鼠的镇静和催眠作用.结果 SNAS能明显减少小鼠的自主活动次数,增加阈下剂量戊巴比妥钠致小鼠入睡数量,延长小鼠睡眠时间,缩短入睡潜伏期.结论 无糖型宁心安神糖浆具有明显的镇静、催眠作用. 相似文献
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目的:观察参芎化瘀胶囊(SXHYC)的镇静催眠和镇痛作用及急性毒性。方法:通过小鼠扭体法和小鼠热板法观察镇痛作用;并采用戊巴比妥钠阈下剂量致小鼠睡眠法,观察药物的镇静催眠作用;通过检测小鼠的最大耐受剂量,考察SXHYC的急性毒性。结果:SXHYC能抑制醋酸致小鼠扭体反应,提高小鼠热板法痛阈值。另外,SXHYC能提高戊巴比妥钠阈下剂量小鼠睡眠率。小鼠对SXHYC一日最大耐受剂量相当于成人临床用量的384倍。结论:SXHYC具有明显的镇痛和镇静作用,且急性用药安全。 相似文献
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目的 探讨夜来香多糖对小鼠镇静催眠作用的影响.方法 将小鼠随机分为生理盐水组(戊巴比妥钠组)、1.0 mg/kg夜来香多糖组、2.0 mg/kg夜来香多糖组、4.0 mg/kg夜来香多糖组.观察夜来香多糖对小鼠自发活动的影响、对阈上剂量戊巴比妥钠小鼠睡眠时间的影响、对阈下剂量戊巴比妥钠小鼠睡眠时间的影响.结果 与生理盐水组比较,2.0、4.0 mg/kg的夜来香多糖能显著抑制小鼠自发活动(P<0.05,P<0.01);与戊巴比妥钠组比较,2.0、4.0 mg/kg的夜来香多糖能显著加速阈上剂量戊巴比妥钠的入睡时间和延长戊巴比妥钠的睡眠时间(P<0.05,P<0.01);与戊巴比妥钠组比较,1.0、2.0、4.0 mg/kg的夜来香多糖能显著加速阈下剂量戊巴比妥钠的入睡时间和延长戊巴比妥钠的睡眠时间(P<0.05,P<0.01,P<0.01).结论 夜来香多糖具有明显的镇静催眠作用. 相似文献
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目的研究安睡片的镇静催眠作用。方法安睡片高剂量(1200mg·kg^-1)、中剂量(900mg·kg^-1)、低剂量(600mg·kg^-1)给小鼠连续灌胃30天,观察安睡片对阈下剂量戊巴比妥钠催眠试验、阈剂量戊巴比妥钠催眠试验、巴比妥钠睡眠潜伏期试验的影响。结果安睡片高剂量能够提高小鼠睡眠发生率(58.33%);高、中剂量能显著够延长小鼠睡眠时间;高、低剂量能显著缩短小鼠的睡眠潜伏期。 相似文献
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Ferreira MA Nunes Odel R Leal LK Pessoa OD Lemos TL Viana GS 《Biological & pharmaceutical bulletin》2003,26(5):595-599
In previous studies in vitro we showed that the quinone fraction (QF) from the heartwood of Auxemma oncocalyx TAUB. presented antiplatelet and antioxidant activities. In the present work, the QF antioxidant property was evaluated in models of CCl(4)-induced hepatotoxicity in rats, and prolongation of pentobarbital-induced sleeping time in mice. Our results showed that levels of plasma glutamate-pyruvate-transaminase (GPT), as well as glutamate-oxalate-transaminase (GOT), were increased by the administration of CCl(4). On the other hand, only GPT levels were reduced by the QF treatment. Pentobarbital sleeping time was prolonged by the administration of CCl(4) and reduced by the QF treatment. Moreover, QF did not alter the pentobarbital-induced sleeping time. In conclusion, we showed that QF, represented mainly by oncocalyxone A, has hepatoprotective activity, and this effect is at least in part due to the antioxidant activity of this quinone. 相似文献
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Previous studies have indicated that acute exposure to ambient concentrations of ozone (O3) as low as 196 micrograms/m3 (0.1 ppm) increases pentobarbital (PEN)-induced sleeping time in female mice. To elucidate potential mechanisms involved, additional studies were performed. A 3 h exposure to 9800 micrograms O3/m3 (5 ppm) did not affect brain concentrations of PEN at time of awakening, even though sleeping time was increased. Exposure for 3 h to 9800 micrograms O3/m3 (5 ppm) did not alter the pattern of brain or plasma metabolites of PEN. Pentobarbital clearance followed first-order kinetics with a one-compartment model. Mice exposed to 9800 micrograms O3/m3 (5 ppm) for 3 h had a 106% increase in the plasma half-life of pentobarbital; at 1960 micrograms O3/m3 (1 ppm) for 3 h, a 71% increase was observed. It therefore appears possible that PEN-induced sleeping time might be increased due to an decrease in hepatic metabolism of PEN. 相似文献
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K Sasaki M Saitoh G Takayanagi 《Nihon yakurigaku zasshi. Folia pharmacologica Japonica》1979,75(6):543-550
Antitumor activity and lethality of cyclophosphamide alone and in combination with several drugs were investigated in male ddY mice. The antitumor activity was estimated by weighing the solid tumor on the 15th day after Ehrlich ascites cell inoculation. Pentobarbital induced sleeping time for monitoring the activity of hepatic drug-metabolizing enzymes was defined as the time between the loss and the recovery of the righting reflex. Consecutive administration of pentobarbital shortened the pentobarbital sleeping time and increased the antitumor activity after cyclophosphamide. On the contrary, a single administration of SKF 525A or cycloheximide prolonged the pentobarbital sleeping time significantly and decreased the antitumor activity after cyclophosphamide. Consecutive administration of aminopyrine, or chlorpromazine shortened the pentobarbital sleeping time and increased the antitumor activity after cyclophosphamide. These results indicate that aminopyrine and chlorpromazine may increase the levels of the hepatic drug-metabolizing components and may activate cyclophosphamide by conversion to an active form. Effect of a consecutive administration of morphine on the pentobarbital sleeping time and the antitumor activity was uncertain in individual cases.On the other hand, aminopyrine, chlorpromazine, or morphine in consecutive administration increased the lethality of cyclophosphamide. 相似文献
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目的观察神农丸对小白鼠胃粘膜损伤后有无止痛、保护作用以及对大白鼠胃液分泌有无调节作用。方法以醋酸致疼痛、乙醇致胃粘膜损伤两种小鼠模型和乙醇、去氧胆酸钠致慢性胃炎大鼠模型为实验对象,以小鼠扭体次数、溃疡指数、大鼠胃液游离酸度、胃蛋白酶活力、血活胃泌素量为指标,全面考察神农丸对胃粘膜损伤的保护作用和对胃液分泌的调节作用。结果神农丸能明显减少醋酸致疼痛模型小鼠的扭体次数,降低乙醇胃炎模型小鼠的溃疡指数,降低实验性慢性胃炎模型大鼠胃液中游离酸度,升高胃蛋白酶活力。结论神农丸对小白鼠胃粘膜损伤有止痛和保护作用,对大白鼠实验性慢性胃炎胃液分泌有调节作用。 相似文献
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The hepatotoxic effects of allyl alcohol with particular reference to mitochondrial morphology and function were compared in male CD1 mice and male CD rats 24 h after 0.05 ml/kg i.p. in corn oil. As already noted by others, allyl alcohol-treated rats usually showed histologic evidence of tissue necrosis when hematoxylin-eosin-stained tissue sections were examined whereas mouse tissue sections did not. The serum glutamic pyruvic transaminase (SGPT) activities were significantly elevated in both mice and rats but to a much greater extent in the latter. Pentobarbital sleeping time was significantly increased over that of corn oil control groups in rats but decreased in mice. In rats electron microscopy showed mitochondria which contained flocculent densities. State 4 respiration was not altered by allyl alcohol in rats, but state 3 respiration was significantly depressed indicating an absence of respiratory control and an inability to perform energy coupling. In allyl alcohol-treated mice the isolated mitochondria were found to be primarily in a condensed form. Except for the effect on pentobarbital sleeping time and SGPT, no other findings were different from those in control groups given only corn oil. When the dose of allyl alcohol in mice was increased to 0.15 ml/kg in an attempt to elicit more severe signs of hepatotoxicity, there was a high mortality in the first 24 h period without histologic evidence of liver necrosis. Thus, we confirm that at equivalent doses, male rats are more sensitive to the hepatotoxic effects of allyl alcohol than are male mice, and extend the generalization to the liver mitochondria of the 2 species. 相似文献
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