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紫苏提取液对小鼠急性酒精中毒的作用及机制 被引量:6
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作者 史继静 刘朝奇 +5 位作者 陈晶 王锦江 李斌 张伟 王雅琴 杨凡 《世界华人消化杂志》 CAS 北大核心 2008年第36期4098-4101,共4页
目的:探讨紫苏提取液(PLE)对小鼠急性酒精中毒的作用及机制.方法:用食用白酒(56度)灌胃昆明种小鼠,建立急性酒精中毒动物模型.选取小鼠40只,随机分为4组,每组10只,分别为空白对照组、PLE低剂量组(20g/kg)、PLE高剂量组(40g/kg)、模型组... 目的:探讨紫苏提取液(PLE)对小鼠急性酒精中毒的作用及机制.方法:用食用白酒(56度)灌胃昆明种小鼠,建立急性酒精中毒动物模型.选取小鼠40只,随机分为4组,每组10只,分别为空白对照组、PLE低剂量组(20g/kg)、PLE高剂量组(40g/kg)、模型组.各实验组给予相应的药物30min后,除空白组外其余各组分别灌胃实验用酒0.15mL/10g,空白组灌以等量的生理盐水.分别观察紫苏提取液对小鼠醉酒潜伏时间及肝组织形态的影响.Real-time PCR检测小鼠肝组织中IL-6、iNOS、TNF-α、Bax基因mRNA的表达水平.结果:酒前灌PLE可降低醉酒小鼠数量、延迟小鼠发生醉酒的时间,其中高浓度组小鼠发生醉酒的潜伏时间与对照组相比有显著性差异(47.00±6.04vs11.56±12.11,P<0.05).正常对照组小鼠肝脏小叶、汇管区结构正常,肝细胞无明显变性、坏死,无明显炎细胞浸润.与模型组相比,PLE高剂量组与低剂量组肝细胞变性、坏死,炎细胞浸润均有明显改善.与模型组相比PLE可明显下调IL-6、iNOS、TNF-α mRNA的表达(0.251±0.073,0.455±0.096vs1.58±0.124;0.381±0.043,0.345±0.067vs2.088±0.088;0.584±0.061,0.270±0.027vs2.025±0.056,P<0.05或0.01),同时Bax mRNA的表达亦下降但无统计学差异.结论:紫苏提取液可显著地延长小鼠的醉酒潜伏时间、拮抗乙醇引起的肝脏损伤,此作用可能与其下调肝组织中IL-6等基因的表达有关. 展开更多
关键词 紫苏提取液 急性酒精中毒 防醉作用 基因表达
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网状五层龙热水提取物醒酒作用的实验研究 被引量:1
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作者 宫德正 耿成燕 +2 位作者 刘军 姜丽萍 仲来福 《毒理学杂志》 CAS CSCD 北大核心 2005年第3期217-218,共2页
关键词 网状五层龙 热水提取物 醒酒防醉作用
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醒酒保肝胶囊对急性酒精性肝损伤的影响 被引量:4
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作者 苏德奇 马龙 +3 位作者 周晓辉 杨浩峰 刘涛 田丽婷 《新疆医科大学学报》 CAS 2005年第5期396-398,共3页
目的:探讨醒酒保肝胶囊的解酒、防醉以及对酒精性肝损伤的影响。方法:昆明种SPF级雄性小白鼠156只,建立急性酒精中毒动物模型,分别进行防醉、解酒,对急性酒精性肝损伤保护作用试验进行观察。结果:醒酒保肝胶囊可明显减少醉酒动物数目(P&... 目的:探讨醒酒保肝胶囊的解酒、防醉以及对酒精性肝损伤的影响。方法:昆明种SPF级雄性小白鼠156只,建立急性酒精中毒动物模型,分别进行防醉、解酒,对急性酒精性肝损伤保护作用试验进行观察。结果:醒酒保肝胶囊可明显减少醉酒动物数目(P<0.05),缩短醉酒动物的睡眠时间(P<0.05),而且可以抑制乙醇引起的小鼠肝组织中丙二醛(MDA)含量升高(P<0.05),提高肝组织中还原型谷胱甘肽(GSH)含量(P<0.05),抑制由乙醇引起的血清甘油三酯(TG)含量的升高(P<0.05)。结论:醒酒保肝胶囊具有防醉、解酒作用,且对乙醇引起的急性肝损伤具有一定的保护作用。 展开更多
关键词 醒酒保肝胶囊 酒精性肝损伤 防醉作用 解酒作用 抗氧化
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Study on the preventive effects of different drugs on reflux esophagitis in rats 被引量:1
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作者 汪涛 龚均 +4 位作者 陈杰 程鹏 常英 王进海 汪涛 《Journal of Medical Colleges of PLA(China)》 CAS 2004年第5期272-277,共6页
Objective: To observe the damage of mixed reflux to the rat esophageal mucosa, and investigate the preventive effects of cisapride, nabumetone and hydrotalcite on the damaged esophageal mucosa. Methods: Three hundred ... Objective: To observe the damage of mixed reflux to the rat esophageal mucosa, and investigate the preventive effects of cisapride, nabumetone and hydrotalcite on the damaged esophageal mucosa. Methods: Three hundred sixty-eight Sprague-Dawley rats were treated as esophagoduodenostomy and divided into four groups in random. Group Y: operation + saline as positive controls; Group P: operation + cisapride; Group R: operation + nabumetone; Group D: operation + hydrotalcite. Different drugs were perfused in the 1 st week after operation. The lesions of esophageal mucosa were observed in the 5th, 9th, 13th, 17th, 22nd, 28th, 35th and 40th week respectively, and evaluated the preventive effects of these drugs. Results: The lesions of esophageal mucosa in group Y were more severe than other three groups in different time (P < 0.05), and the incidence of Barrett's esophagus(BE), severe atypical hyperplasia and esophageal adenocarcinoma (EAC) in group Y were higher than others. After 22 weeks, the lesions in group P were more severe than group R and D, and there were obvious differences in different time ( P < 0.05); but the incidence of BE, severe atypical hyperplasia and EAC in group P had no significant difference with group R and group D( P > 0.05). Conclusion: BE, severe atypical hyperplasia and EAC could occur because of severe reflux esophagitis for a long term. Cisapride, nabumetone and hydrotalcite could reduce mucosa injury in reflux esophagitis and resist the development of BE, severe atypical hyperplasia and EAC.In addition, the curative effects of nabumetone and hydrotalcite were better than cisapride. 展开更多
关键词 reflux esophagitis CISAPRIDE NABUMETONE hydropride
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