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首页> 外文期刊>International Journal of Pharmacy and Pharmaceutical Sciences >INVESTIGATION OF ANALGESIC ACTIVITY OF XANTHINE OXIDASE INHIBITOR ALLOPURINOL: AN EXPERIMENTAL STUDY
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INVESTIGATION OF ANALGESIC ACTIVITY OF XANTHINE OXIDASE INHIBITOR ALLOPURINOL: AN EXPERIMENTAL STUDY

机译:黄嘌呤氧化酶抑制剂Allopurinol止痛活性的实验研究

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摘要

Objectives: To investigate the analgesic activity of xanthine oxidase inhibitor, allopurinol in three graded doses and compare it with control and aspirin. Methods: Analgesic effect of allopurinol in three graded doses (100, 200, 400 mg/kg I. P.), aspirin in analgesic dose (100mg/kg I. P.) and tramadol was evaluated by using Radiant heat Tail-flick method and Acetic-acid induced writhing method in albino rats and mice respectively. The results were analyzed statistically by ANOVA followed by Dunnet’s test. Results: Allopurinol possesses significant analgesic activity in both models of analgesia . In Tail-flick method, in doses of 100mg/kg the percentage of tail flick elongation time with allopurinol is comparable with aspirin at all time intervals with maximum activity at 60 minutes. In doses of 200mg/kg, the percentage increase in reaction time is more than aspirin at 30, 90 & 120 minutes but this difference is not statistically significant. In doses of 400mg/kg, the percent increase in reaction time is more than aspirin but the difference is not statistically significant. In acetic acid induced writhing method, allopurinol in dose of 100mg/kg differ significantly than aspirin, latter being more effective. The analgesic activity of allopurinol in doses of 200mg/kg & 400mg/kg was comparable to aspirin. Conclusion: Allopurinol possesses significant analgesic activity comparable with aspirin in tail flick model as well as acetic acid induced model of nociception. And this drug should be further evaluated for this indication Keywords : Analgesic, Allopurinol, Purines, Tail-flick method, Xanthine oxidase inhibitor.
机译:目的:研究黄嘌呤氧化酶抑制剂别嘌醇在三种分级剂量下的镇痛作用,并将其与对照和阿司匹林进行比较。方法:采用辐射热甩尾法和醋酸诱导扭体法评估三种分级剂量(100、200、400 mg / kg IP),阿司匹林(100mg / kg IP)和曲马多的镇痛效果。方法分别用于白化病大鼠和小鼠。对结果进行了统计学分析,然后进行了Dunnet检验。结果:别嘌呤醇在两种镇痛模型中均具有显着的镇痛活性。在甩尾法中,在100mg / kg的剂量下,别嘌呤醇的甩尾伸长时间百分比在所有时间间隔均与阿司匹林相当,在60分钟时具有最大活性。在200mg / kg的剂量下,在30分钟,90分钟和120分钟时,反应时间增加的百分比大于阿司匹林,但这种差异在统计学上并不显着。在400mg / kg的剂量下,反应时间增加的百分比大于阿司匹林,但差异无统计学意义。在乙酸诱导扭体法中,别嘌呤醇100mg / kg的剂量与阿司匹林有显着差异,后者更为有效。 200mg / kg和400mg / kg剂量的别嘌醇的镇痛活性与阿司匹林相当。结论:别嘌呤醇在甩尾模型和乙酸诱导的伤害感受模型中均具有与阿司匹林相当的镇痛活性。并应进一步评估该药物的适应症。关键词:止痛药,别嘌醇,嘌呤,甩尾法,黄嘌呤氧化酶抑制剂。

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