首页> 外文期刊>British Journal of Clinical Pharmacology >Effect of oral linezolid on the pressor response to intravenous tyramine.
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Effect of oral linezolid on the pressor response to intravenous tyramine.

机译:口服利奈唑胺对加压剂对静脉酪胺反应的影响。

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Aims To investigate the effect of monoamine oxidase A inhibition from a single oral dose of linezolid on the pressor response to intravenous (i.v.) tyramine, using positive and negative controls to validate the methodology. Methods This placebo-controlled, three-period crossover study was conducted in 12 healthy male volunteers. Each volunteer received either one oral dose of moclobemide (300 mg), linezolid (600 mg), or placebo tablet followed by an i.v. tyramine pressor test until an increase in systolic blood pressure of at least 30 mmHg above baseline occurred. Each study day was separated by a 7-day washout period. The dose of tyramine required to raise the blood pressure by 30 mmHg (TYR30) was calculated for each oral treatment by linear interpolation between log-transformed doses of i.v. tyramine. The influence of body mass index (BMI) on TYR30 was also investigated. Results The tyramine sensitivity factor (ratio of the geometric least square mean TYR30 for placebo and active oral treatment) was 1.8 [90% confidence interval (CI) 1.6, 2.0, P < 0.0001] for linezolid and 2.1 (90% CI 1.8, 2.4, P < 0.0001) for the positive control moclobemide. BMI had a statistically significant effect on TYR30. Conclusions There was a significant difference in the pressor response to i.v. tyramine between linezolid and placebo. Moclobemide (positive control) and linezolid have a similar pressor response to i.v. tyramine. The statistically significant effect of BMI on TYR30 underlines the advantage of within-individual comparisons of treatments in order to reduce variability and provide more accurate treatment estimates.
机译:目的为了研究单次口服利奈唑胺对单胺氧化酶A的抑制作用对加压剂对静脉(i.v.)酪胺的升压反应的影响,使用阳性和阴性对照来验证该方法。方法在12名健康男性志愿者中进行了安慰剂对照的三期交叉研究。每位志愿者接受口服一次口服莫洛贝米(300 mg),利奈唑胺(600 mg)或安慰剂片剂,然后接受静脉注射。进行酪胺加压试验,直到收缩压升高至少比基线高30 mmHg。每个研究日间隔7天的清除期。通过对数转化的静脉注射剂量之间的线性插值,为每次口服治疗计算出使血压升高30 mmHg(TYR30)所需的酪胺剂量。酪胺。还研究了体重指数(BMI)对TYR30的影响。结果对利奈唑胺的酪胺敏感性因子(安慰剂和积极口服治疗的几何最小二乘均值TYR30的比)为1.8 [90%置信区间(CI)1.6、2.0,P <0.0001]和2.1(90%CI 1.8、2.4 ,P <0.0001)为阳性对照莫洛贝米。 BMI对TYR30有统计学意义的影响。结论对i.v.的升压反应有显着差异。利奈唑胺和安慰剂之间的酪胺。莫氯贝胺(阳性对照)和利奈唑胺对静脉注射的升压反应相似。酪胺。 BMI对TYR30的统计学显着影响强调了个体内比较治疗的优势,以减少变异性并提供更准确的治疗估计。

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