吗啡戒断,Morphine withdrawal
1)Morphine withdrawal吗啡戒断
1.Effect of CCK receptor antagonists on CaMKⅡα mRNA and protein of neuron in hippocampus of morphine withdrawal rats;CCK受体拮抗剂对吗啡戒断大鼠海马神经元CaMKⅡα mRNA及蛋白表达的影响
2.Effect of melatonin on the blood follicle stimulating hormone, luteinizing hormone and testosterone of the morphine withdrawal mice.;褪黑素对吗啡戒断小鼠血液中卵泡刺激素、黄体生成素和睾酮的影响
3.Effect of acupuncture on emotion and level of amino acids after morphine withdrawal;针刺对吗啡戒断大鼠情绪及氨基酸水平的影响
英文短句/例句
1.Method: Abstinence syndrome of morphine dependent rats and the treatment effect of Bup were observed.方法··:观察吗啡戒断及经丁丙诺啡治疗大鼠的戒断体征 ;
2.EFFECT OF ACUPUNCTURE ON NITRIC OXIDE IN RATS WITH MORPHINE ABSTINENCE SYNDROME针刺对吗啡戒断大鼠一氧化氮的影响
3.THE EXPRESSION AND EFFECT OF EGR-1 GENE IN PC12 CELLS AFTER CHRONIC MORPHINE TREATMENT AND WITHDRAWAL吗啡慢性处理和吗啡戒断对PC12细胞Egr-1基因表达的影响
4.Experimental Study on the Effect of Reinforcing Body Resistance and Elimination Poison of Acupuncture on Morphine Abstinence Syndrome in Rats针刺对吗啡戒断大鼠祛毒扶正作用的实验研究
5.The Alteration of Nucleus Accumbens Neuronal Excitability during Morphine Withdrawal in Rats吗啡戒断大鼠伏核神经元兴奋性的改变
6.Effect of Electroacupuncture on Nitric Oxide Synthase mRNA Expression in Rats with Morphine Abstinence Syndrome针刺对吗啡戒断大鼠脑组织一氧化氮合酶基因表达的影响
7.Effects of Morphine Withdrawal on Locomotor Activity and Contextual Fear Conditioning in Mice;吗啡戒断对小鼠自发活动及场景性恐惧条件化的影响
8.Effects of PNS on CaMKⅡ and CREB in Hippocampus of Morphine Withdrawal Rats;三七总皂甙对吗啡戒断大鼠海马组织CaMKⅡ和CREB的影响
9.Changes of Nitric Oxide and Neuronal Nitric Oxide Synthase in Morphine Dependent and Abstinent Rats;吗啡依赖及戒断大鼠NO与nNOS的改变
10.The Change of CCK-8 Gene Expression in the Central Nervous System in Morphine Dependent and Withdrawal Rats;吗啡依赖及戒断大鼠中枢CCK-8基因表达的变化
11.Changes of cAMP and cGMP contents in the central nervous system in morphine dependent and withdrawal rats;吗啡依赖和戒断大鼠中枢cAMP和cGMP含量的变化
12.ESTABLISHMENT AND EVALUATION ON ANXIETY MODEL OF MORPHINE-WITHDRAWAL RATS大鼠吗啡依赖戒断后焦虑模型的建立和评价
13.Morphologic change of myelin sheath in amygdala of anxious symptom rats suffered from morphine withdrawal吗啡依赖戒断焦虑大鼠杏仁核髓鞘结构的改变
14.Effect of morphine addiction and withdrawal on the expression of P-CREB in CA1 area of hippocampus of the adult rat吗啡成瘾戒断对大鼠海马CA1区P-CREB表达的影响
15.The observation of PSD-95 immunohistochemistry in cerebral regions of morphine-withdrawal rats in different dependent time吗啡依赖戒断大鼠部分脑区PSD-95免疫组化观察
16.Changes of Preprodynor phine mRNA and μOpioid Receptor in Morphine Dependent and Abstinent Rats;吗啡成瘾及戒断大鼠前强啡肽原mRNA与μ阿片受体的改变
17.Therapeutic evaluation of" Ju Yan Bao Kang Keli" in detoxication therapy for morphine dependent rats菊延保康冲剂对吗啡依赖大鼠戒断治疗的作用评价
18.Expression of cAMP response element binding protein in some brain regions of morphine-dependence rats环磷酸腺苷反应元件结合蛋白在吗啡依赖及戒断大鼠脑区的表达
相关短句/例句
abstinence[英]["?bst?n?ns][美]["?bst?n?ns]吗啡戒断
3)morphine withdrawal syndromes吗啡戒断反应
1.The effects of central 5-HT_1,5-HT_2 receptors onmorphine withdrawal syndromes in rates;中枢5-HT_1、5-HT_2受体对吗啡戒断反应的影响
4)morphine withdrawal syndrome吗啡戒断症状
1.Effect of intracerebroventricular injection of glutamic acid/MK-801/ketamine onmorphine withdrawal syndrome in rats侧脑室注射谷氨酸、MK-801及氯氨酮对大鼠吗啡戒断症状的影响
2.Objective: To study the therapeutic effects of isoptin onmorphine withdrawal syndromes in infantile SD rats.结果··:给成瘾动物单次ip异博定 (10mg·kg-1)能明显缓解由纳洛酮诱发的吗啡戒断症状 ,并对吗啡戒断引起的体重下降有减轻作用。
5)morphine withdrawal rat吗啡戒断大鼠
1.The expression of μ-opioid receptor mRNA in the brain tissue ofmorphine withdrawal rats was examined by RT-PCR,and effects of EA at Zusanli(ST36) on the body weight and expression of μ-opioid receptor mRNA ofmorphine withdrawal rat were observed.方法建立自然吗啡戒断大鼠模型,运用RT-PCR方法测定脑组织μ受体mRNA的表达,观察电针足三里对吗啡戒断大鼠体重及μ受体mRNA表达的影响。
6)amorphinism[?"m?:f?,niz?m]吗啡断瘾状态
延伸阅读
盐酸吗啡,美施康定(吗啡控释片),美菲康,吗啡药物名称：吗啡英文名：Morphine别名：盐酸吗啡,美施康定(吗啡控释片),美菲康,吗啡外文名：Morphine ,Morphine Hydrochlride, Morphina, Morphinum适应症：1.镇痛：有强大的镇痛作用，对一切疼痛均有效，对持续性钝痛比间断性锐痛及内脏绞痛效果强。１次给药，镇痛作用持续４～８小时，故仅用于创伤、手术、烧伤、心肌梗塞等引起的剧痛。 2.镇静：在镇痛的同时有明显镇静作用，有时产生欣快感，可改善疼痛病人的紧张情绪。 3.抑制呼吸：可抑制呼吸中枢，降低呼吸中枢对二氧化碳的敏感性。 4.镇咳：可抑制咳嗽中枢，产生镇咳作用。因有成瘾性，并不适用于临床。 5.对平滑肌的作用：可使消化道平滑肌兴奋，致使便秘；并使胆道、输尿管、支气管平滑肌张力增加。 6.心血管系统：可促进内源性组胺的释放而使外周血管扩张、血压下降；使脑血管扩张，颅压增高。 7.镇吐：亦因有成瘾性而不适用于临床。 用量用法： 皮下注射或口服：每次５～１０ｍｇ，１日１～３次。极量：皮下注射，每次２０ｍｇ，１日６０ｍｇ；口服每次３０ｍｇ，１日１００ｍｇ。 注意事项： 1.连续使用可成瘾，需慎用。 2.婴儿及哺乳妇女忌用，临产妇女禁用（因可经乳腺排出及分布至胎盘，可抑制新生儿及婴儿呼吸）。 3.可引起眩晕、呕吐及便秘等不良反应。 4.慢性阻塞性肺疾患、支气管哮喘、肺原性心脏病禁用；急性左心衰竭晚期并出现呼吸衰竭时忌用。 5.颅内高压、颅脑损伤等病人禁用。 6.肝功能减退者忌用。 7.胆绞痛、肾绞痛需与阿托品合用，单用本品反而加剧疼痛。 8.在疼痛原因未明确前，忌用本品，以防掩盖症状，贻误诊治。 9.对呼吸抑制的程度与使用吗啡的剂量并行，过大剂量可致急性吗啡中毒病人出现昏睡、呼吸减慢、瞳孔缩小针尖样，进而可致呼吸麻痹而死亡。 规格：注射液：每支５ｍｇ（0.50ｍｌ）；１０ｍｇ（１ｍｌ）。 片剂：每片５ｍｇ；１０ｍｇ。 类别：镇痛药\阿片受体激动剂
