Gardmark M, Karlsson M O, Jonsson F, Hammarlund-Udenaes M
Division of Biopharmaceutics and Pharmacokinetics, Department of Pharmacy, Uppsala University, Box 580, S-751 23 Uppsala, Sweden.
J Pharm Sci. 1998 Jul;87(7):813-20. doi: 10.1021/js980056f.
The objective of this study was to quantify the influence of morphine-3-glucuronide (M3G) on the morphine antinociceptive effect (ANE) and respiratory effects in the rat. Three groups of rats were pretreated with either saline or M3G at two different rates. Morphine infusion of 10 mg/h/kg (group A) or 20 mg/h/kg (group B) was administered to each pretreatment group for 3 h. The ANE was measured by the electrical stimulation vocalization method, and blood gas parameters (pCO2, pO2, and pH) were assessed. Independent of pretreatment all groups displayed a concurrent increase in the ANE. The maximal effect diverged between pretreatments. Acute tolerance was observed, but no rebound effect was detected. To characterize the ANE, an effect compartment model and an indirect response model were selected, both capable of describing the observed features. In both models incorporation of M3G led to a better explanation of the data. On the basis of the parameters obtained in the fits, naturally occurring M3G would reduce the antinociceptive effect during a morphine infusion (plasma concentration 15 microM) by 15-20%. The exposure of M3G did not significantly change the respiratory response following the morphine treatment.
本研究的目的是量化吗啡-3-葡萄糖醛酸苷(M3G)对大鼠吗啡镇痛作用(ANE)和呼吸效应的影响。三组大鼠分别以两种不同速率用生理盐水或M3G进行预处理。对每个预处理组以10 mg/h/kg(A组)或20 mg/h/kg(B组)的速率输注吗啡,持续3小时。通过电刺激发声法测量ANE,并评估血气参数(pCO2、pO2和pH)。与预处理无关,所有组的ANE均同时增加。预处理之间的最大效应有所不同。观察到急性耐受性,但未检测到反跳效应。为了表征ANE,选择了效应室模型和间接反应模型,二者均能够描述观察到的特征。在两个模型中纳入M3G都能更好地解释数据。根据拟合得到的参数,内源性M3G会使吗啡输注期间(血浆浓度15 microM)的镇痛作用降低15%-20%。M3G的暴露并未显著改变吗啡治疗后的呼吸反应。