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首页> 外文期刊>Clinical pharmacokinetics >Influence of Morbid Obesity on the Pharmacokinetics of Morphine, Morphine-3-Glucuronide, and Morphine-6-Glucuronide
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Influence of Morbid Obesity on the Pharmacokinetics of Morphine, Morphine-3-Glucuronide, and Morphine-6-Glucuronide

机译:病态肥胖对吗啡,吗啡-3-葡糖苷和吗啡-6-葡糖醛酸的药代动力学的影响

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摘要

Abstract Introduction Obesity is associated with many pathophysiological changes that may result in altered drug metabolism. The aim of this study is to investigate the influence of obesity on the pharmacokinetics of morphine, morphine-3-glucuronide (M3G), and morphine-6-glucuronide (M6G) through a combined analysis in morbidly obese patients and non-obese healthy volunteers. Methods In this analysis, data from 20 morbidly obese patients [mean body mass index 49.9?kg/m 2 (range 37.6–78.6?kg/m 2 ) and weight 151.3?kg (range 112–251.9?kg)] and 20 healthy volunteers [mean weight 70.6?kg (range 58–85?kg)] were included. Morbidly obese patients received 10?mg of intravenous (I.V.) morphine after gastric bypass surgery, with additional morphine I.V. doses as needed. Healthy volunteers received an I.V. bolus of morphine of 0.1?mg/kg followed by an infusion of 0.030?mg?kg ?1 ?h ?1 for 1?h. Population pharmacokinetic modeling was performed using NONMEM 7.2. Results In morbidly obese patients, elimination clearance of M3G and M6G was decreased substantially compared with healthy volunteers ( p ? p ? p ? Conclusion Metabolism of morphine is not altered in morbidly obese patients. However, decreased elimination of both M3G and M6G is evident, resulting in a substantial increase in exposure to these two metabolites. A rational explanation of this finding is that it results from alterations in membrane transporter function and/or expression in the liver. ClinicalTrials.gov identifier: NCT01097148.
机译:摘要引言肥胖与许多可能导致药物代谢改变的病理生理学变化有关。本研究的目的是通过病态肥胖患者和非肥胖健康志愿者的组合分析来研究肥胖症对吗啡,吗啡-3-葡糖苷(M3G)和吗啡-6-葡糖醛酸酯(M6G)对吗啡药代动力学的影响。该分析中的方法,来自20例病态肥胖患者的数据[平均体重指数49.9吗?kg / m 2(范围37.6-78.6 kg / m 2)和重量151.3 kg(范围112-251.9 kg)和20个健康志愿者[平均重量70.6?kg(范围58-85 kg)]。胃旁路手术后,病态肥胖患者在胃旁路手术后接受10μmγγγγ吗啡。根据需要剂量。健康的志愿者收到I.v.吗啡的推注0.1?mg / kg,然后输注0.030?kg?1?H?1持续1μlΩ。使用非血液7.2进行人口药代动力学建模。结果在病态肥胖的患者中,与健康志愿者相比,M3G和M6G的消除清除率降低了(P?P?P?结论吗啡的代谢在病态肥胖患者中没有改变。然而,减少了M3G和M6G的消除,显而易见,导致暴露于这两个代谢物的大幅增加。对该发现的理性解释是它是由膜转运蛋白功能的改变和/或肝脏中表达的改变。ClinicalTrials.gov标识符:NCT01097148。

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