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曲马多预处理对氯胺酮抗抑郁作用的影响
引用本文:徐世霞,杨 春,刘向六,杨建军,周志强. 曲马多预处理对氯胺酮抗抑郁作用的影响[J]. 药学与临床研究, 2011, 19(5): 426-428
作者姓名:徐世霞  杨 春  刘向六  杨建军  周志强
作者单位:南京大学医学院临床学院/南京军区南京总医院麻醉科,南京,210002
摘    要:
目的:观察曲马多预处理对氯胺酮抗抑郁作用的影响。方法:32只Wistar大鼠随机分为生理盐水组(S组)、曲马多组(T组)、氯胺酮组(K组)、曲马多+氯胺酮组(T+K组)。药物预处理前1天大鼠强迫游泳15 min;预处理当天各组分别腹腔注射1 mL容积的生理盐水、曲马多5 mg.kg-1、生理盐水、曲马多5 mg.kg-1;30 min后,各组分别注射生理盐水、生理盐水、氯胺酮10 mg.kg-1、氯胺酮10 mg.kg-1;再经30 min后,行强迫游泳试验并记录其不动时间,取海马组织测定脑源性神经营养因子(BDNF)及酪氨酸受体激酶B(TrkB)的含量。结果:与S组相比,K组、T+K组强迫游泳试验不动时间减少,海马BDNF及TrkB表达增加(P<0.05);与K组相比,T+K组强迫游泳试验不动时间减少,海马BDNF及TrkB表达增加(P<0.05)。结论:曲马多预处理能增强氯胺酮的抗抑郁作用,这可能与大鼠海马BDNF及TrkB表达上调有关。

关 键 词:曲马多  氯胺酮  抑郁  BDNF  TrkB
收稿时间:2011-04-12
修稿时间:2011-08-02

Effects of Tramadol Pretreatment on Ketamine-induced Antidepressant Action
XU Shi-xi,YANG Chun,LIU Xiang-liu,YANG Jian-jun and ZHOU Zhi-qiang. Effects of Tramadol Pretreatment on Ketamine-induced Antidepressant Action[J]. Pharmacertical and Clinical Research, 2011, 19(5): 426-428
Authors:XU Shi-xi  YANG Chun  LIU Xiang-liu  YANG Jian-jun  ZHOU Zhi-qiang
Affiliation:XU Shi-xia,YANG Chun,LIU Xiang-liu,YANG Jian-jun,ZHOU Zhi-qiang Department of Anesthesiology,School of Medicine,Nanjing University/Nanjing General Hospital of Nanjing Military Command,PLA,Nanjing 210002,China
Abstract:
Objective: To observe the effects of tramadol pretreatment on ketamine-induced antidepressant action. Methods: Thirty-two Wistar rats were randomly divided into saline group (S group), tramadol group (T group), ketamine group (K group) and tramadol+ketamine group (T+K group). One day before drug pretreatment, rats were insulted in the forced swimming test (FST) for 15 min. At the day of drug pretreatment, rats were intraperitoneally injected with 1 ml of saline, tramadol 5 mg·kg-1, saline and tramadol 5 mg·kg-1, respectively; Thirty minutes later, rats were intraperitoneally injected with saline, saline, ketamine 10 mg·kg-1 and ketamine 10 mg·kg-1, respectively. Another 30 min later, FST was conducted and the immobility time was recorded. Rat hippocampus was harvested and the levels of brain-derived neurotrophic factor (BDNF) and tyrosine receptor kinases B(TrkB) were detected. Results: Compared with S group, the immobility time of rats receiving FST decreased and the expression of hippocampal BDNF and TrkB increased in K and T+K groups (P<0.05). Compared with K group, the immobility time decreased and the expression of hippocampal BDNF and TrkB increased in T+K group. Conclusion: Tramadol pretreatment can reinforce the antidepressant action of ketamine, which may be attributed to the increase in the expression of hippocampal BDNF and TrkB.
Keywords:Tramadol  Ketamine  Depression  BDNF  TrkB  
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