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Effect of buspirone: An anxiolytic drug on blood glucose in humans

机译:丁螺环酮:抗焦虑药对人体血糖的影响

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摘要

The present study investigated the effect of an antianxiety drug, buspirone on blood glucose and plasma insulin level concerning the role of 5-HT1A receptors in blood glucose regulation in healthy humans. Twelve healthy male volunteers were administered single oral doses of buspirone (10 mg) or placebo, in a randomized, crossover way, followed by oral glucose load (75 gm in 200 ml) at reported Tmax i.e. the time of peak plasma concentration of the respective administered drug. The blood samples were collected as predose, postdose and post oral glucose load at 0.5, 1.0, 1.5, 2.0, 2.5 and 3.0 hr to investigate the effect of buspirone or placebo at basal blood glucose and plasma insulin level and after oral glucose load induced (postprandial) blood glucose and plasma insulin level. Blood glucose and plasma insulin concentrations were estimated by glucose hexokinase method and enzyme linked immunosorbent assay (ELISA) method respectively. The concentration of blood glucose was significantly (p<0.05) decreased after oral glucose load following administration of buspirone in comparison with placebo however no significant change was observed in the fasting blood glucose and plasma insulin (fasting and oral glucose load induced) level. In conclusions, the present study findings show that buspirone produced a significant alteration in blood glucose level in healthy humans. In addition, study results also indicate that the involvement of serotonergic (5-HT, receptors) mechanism of blood glucose regulation in humans is different from animals.
机译:本研究调查了抗焦虑药丁螺环酮对5-HT1A受体在健康人血糖调节中的作用对血糖和血浆胰岛素水平的影响。以随机,交叉的方式向12名健康的男性志愿者单口服口服丁螺环酮(10 mg)或安慰剂,然后以报告的Tmax口服葡萄糖负荷(200毫升中75毫克),即各自的血浆峰值浓度时间给药。分别在服药前,服药后和口服葡萄糖负荷后0.5、1.0、1.5、2.0、2.5和3.0小时采集血样,以研究丁螺环酮或安慰剂对基础血糖和血浆胰岛素水平以及口服葡萄糖负荷诱导后的影响(餐后)血糖和血浆胰岛素水平。分别通过葡萄糖己糖激酶法和酶联免疫吸附法(ELISA)评估血糖和血浆胰岛素浓度。与安慰剂相比,服用丁螺环酮后口服葡萄糖负荷后血糖浓度显着降低(p <0.05),但空腹血糖和血浆胰岛素水平(空腹和口服葡萄糖负荷诱导)水平未见明显变化。总之,本研究发现表明,丁螺环酮在健康人体内会引起血糖水平的显着改变。另外,研究结果还表明,人体内血糖调节的血清素能(5-HT,受体)机制与动物不同。

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