Effect of non-steroidal anti-inflammatory drugs on behavioral actions of diazepam in mice

被引:0
作者
Almaghour, Hind G. [1 ]
Sherif, Fathi M. [2 ]
机构
[1] Al Fateh Univ Med Sci, Biotechnol Res Ctr, Tripoli, Libya
[2] Al Fateh Univ Med Sci, Fac Pharm, Dept Pharmacol, Tripoli, Libya
关键词
RECEPTOR SUBTYPE; BENZODIAZEPINES; RESPONSES; EXTRACT; DISEASE; PROFILE; SLEEP;
D O I
暂无
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objectives: To investigate the behavioral pharmacological interactions of diazepam with non steroidal anti-inflammatory drugs. Methods: Non selective cyclooxygenase enzyme inhibitors (100 mg/kg acetylsalicylic acid, 10 mg/kg indomethacin, and 10 mg/kg diclofenac), a selective cyclooxygnase-1 inhibitor (10 mg/kg acetylsalicylic acid), and a selective cyclooxygnase-2 inhibitor (10 mg/kg celecoxib) of non steroidal anti-inflammatory drugs were individually pretreated to 15 and 24 groups of Albino mice for dose and time dependent models (n=8, each treatment) before sleeping induced by diazepam (20 mg/kg, intraperitoneally). In 6 groups using an open field and 4 groups using traction test models (n = 10), 5 and 10 mg/kg of diazepam, intraperitoneally were given to induce sedation and muscle relaxation, and 2 mg/kg to induce anxiolytic action after treatment with acetylsalicylic acid (10 mg/kg) to 4 groups (n = 6). This study was carried out at the Al-Fateh Medical Science University, Tripoli, Libya between February and May 2009. Results: In dose and time dependent models non selective cyclooxygenase and selective cyclo-oxygnase-1 inhibitors significantly reduced the duration of sleep induced by diazepam in mice by 60-75%, while the selective cyclooxygnase-2 inhibitor did not (p>0.05). However, anxiolyric, muscle relaxant, and sedative effects of diazepam were unchanged by acetylsalicylic acid. Conclusion: Non-steroidal anti-inflammatory drugs, most likely cyclooxygenase selective-1 inhibitors reduced the duration of sleep induced by diazepam, and this interaction could be of a pharmacodynamic type.
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页码:84 / 89
页数:6
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