首页> 外文期刊>International Journal of Basic & Clinical Pharmacology >Evaluation of the analgesic activity of single and multiple oral doses of teneligliptin (20 mg/day), using hot air analgesiometer in healthy human volunteers: a randomized, double blind, placebo controlled, cross over study
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Evaluation of the analgesic activity of single and multiple oral doses of teneligliptin (20 mg/day), using hot air analgesiometer in healthy human volunteers: a randomized, double blind, placebo controlled, cross over study

机译:评价单次口服剂量的镇痛活性(20毫克/天),在健康人志愿者中使用热空气镇痛仪:随机,双盲,安慰剂控制,交叉过研究

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Background DPP-4 inhibitors showed analgesic and anti-inflammatory activity in human and animal-studies. DPP-4 inhibitors improved nerve function and thermal nociception in animal models. Aim of the study was to explore analgesic activity of single and multiple doses of teneligliptin 20 mg/day using hot air analgesiometer in healthy human volunteers. Methods: After IEC approval and informed consent, subjects were randomized to receive either teneligliptin 20 mg or placebo in double-blinded manner with standard breakfast. Mean pain threshold and tolerance(sec) using hot air analgesiometer were recorded at baseline and 1 hr, 2 hrs post drug on day 1, for single dose study. Subsequently drugs were administered under supervision daily for 6 days and same procedure repeated on day8 for multiple-dose study. After 2 weeks washout, subjects crossed over in period 2 to receive other formulation and same procedure repeated to determine study parameters. Fasting blood-sugar (FBS) was monitored, ADRs recorded in CRF. Statistical analysis done with SPSS20.0. Results: Twelve-healthy subjects (8 males, 4 females) with mean age 33.08±4.69 years, mean BMI 22.6±1.37kg/m2 participated. Single dose teneligliptin produced significant increase in pain threshold (35.9%) and pain tolerance (25.1%) (p0.001) at 1hour compared to baseline. With multiple doses, pain threshold increased by 37.1% and pain tolerance by 25.4% (p0.001) at 1hour compared to baseline. The increase in pain threshold and tolerance values at 1 and 2 hours were similar. There was no significant change in pain threshold(p=0.4135) and tolerance (p=0.4476) at baseline on day1 and day 8. Placebo showed non-significant change in study parameters. Both treatments well tolerated. FBS of volunteers within normal limits during treatment period and no hypoglycemia reported. Conclusions: Results of our study suggest that teneligliptin20mg in healthy subjects demonstrated modest analgesic activity compared to baseline and placebo. Its role in painful diabetic conditions may be further explored.
机译:背景技术DPP-4抑制剂在人类和动物研究中显示出镇痛和抗炎活性。 DPP-4抑制剂改善了动物模型中的神经功能和热伤害。该研究的目的是利用健康人类志愿者中的热空气镇痛计探索单一和多剂量的Teneligliptin 20mg /天的镇痛活性。方法:在IEC批准和知情同意后,受访者随机地以双盲的方式接收Teneligliptin 20 Mg或安慰剂,并用标准的早餐。使用热空气镇痛计的平均疼痛阈值和耐受性(秒)在基线和1小时,第1天,2小时后药物,用于单剂量研究。随后在每天在监督下给药6天,并在DAY8中对多剂量研究重复相同的程序。 2周后冲洗后,在期间2的受试者交叉以接受其他配方和相同的程序重复以确定研究参数。监测空腹血糖(FBS),ADR在CRF中记录。使用SPSS20.0进行统计分析。结果:12家健康科目(8名男性,4名女性),平均年龄为33.08±4.69岁,平均BMI 22.6±1.37kg / m2参加。与基线相比,单剂量Teneligliptin在1小时的疼痛阈值(35.9%)和疼痛耐受性(35.9%)(25.1%)(p <0.001)中产生显着增加。与基线相比,多剂量,疼痛阈值增加37.1%(p <0.001)增加37.1%,疼痛耐受性。疼痛阈值和1和2小时的耐受性的增加是相似的。在第1天和第8天的基线下,疼痛阈值(p = 0.4135)和耐受性(p = 0.4476)没有显着变化.paulobo显示出研究参数的非显着变化。这两种治疗都很好。治疗期间正常限制内的志愿者的FBS,没有报告过血糖。结论:我们的研究结果表明,与基线和安慰剂相比,健康受试者的Teneligliptin20mg表现出适度的镇痛活动。它在痛苦的糖尿病条件中的作用可能会进一步探索。

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