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Relationship between morphine analgesia and cortical extracellular fluid levels of morphine and its metabolites in the rat: a microdialysis study

机译:吗啡镇痛作用与大鼠皮质吗啡及其代谢产物皮质细胞外液水平的关系:微透析研究

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1 The effect of morphine (10 mg kg~(-1), s.c.) on the analgesic response measured by the tail-flick method was determined in male Sprague-Dawley rats. The analgesic response to morphine was correlated with the levels of morphine and its metabolites collected by microdialysis from the cortical extracellular fluid (ECF). 2 The analgesic response to morphine lasted for 4 h. The concentration of morphine during a 4 h collection period was significantly higher than the metabolites concentration. The relative concentration of morphine and its metabolites during the 4 h period was 70 and 30% respectively. 3 The analgesic response during the first 2.25 h period accounted for more than 82% of the total analgesia as determined by the area under the time-response curve (AUC). The concentration of morphine and its metabolites during the same period were 78 and 22%, respectively, but they did not differ during the 2.25-4.0 h period (52 and 48%). 4 The half-life for morphine and its metabolites were similar, the maximal achievable concentration C_(max) and AUC_(0-4 h) were lower for metabolites but the time to reach maximum concentration was higher for morphine metabolites than for morphine. The ratio of the concentration of metabolites to the concentration of morphine in the cortical ECF increased with time whereas the analgesic response to morphine decreased with time. 5 At several time points following morphine injection even though the levels of morphine were the same, the concentration of metabolites (mainly M3G) differed and thus the ratio [metabolite/morphine]. A plot of [metabolite]/[morphine] vs. analgesia gave a high correlation coefficient. Since M3G has been shown to be antianalgesic and is the only metabolite of morphine in the rat, it is concluded that the levels of this metabolite may regulate the analgesic effect of morphine in the rat.
机译:1在雄性Sprague-Dawley大鼠中确定了吗啡(10 mg kg〜(-1),s.c.)对通过甩尾法测量的镇痛反应的影响。对吗啡的镇痛反应与通过皮质透析从皮质细胞外液(ECF)收集的吗啡及其代谢产物的水平相关。 2对吗啡的镇痛反应持续4小时。在4小时的收集时间内,吗啡的浓度显着高于代谢物的浓度。 4 h期间吗啡及其代谢产物的相对浓度分别为70%和30%。 3根据时间反应曲线(AUC)下的面积确定,在最初的2.25小时内,镇痛反应占总镇痛的82%以上。在同一时期,吗啡及其代谢产物的浓度分别为78%和22%,但是在2.25-4.0 h期间它们没有差异(52%和48%)。 4吗啡及其代谢物的半衰期相似,代谢物的最大可达到浓度C_(max)和AUC_(0-4 h)较低,但吗啡代谢物达到最大浓度的时间比吗啡长。皮质ECF中代谢物浓度与吗啡浓度的比率随时间增加,而对吗啡的镇痛反应随时间减少。 5在吗啡注射后的几个时间点,即使吗啡的水平相同,代谢物(主要是M3G)的浓度也不同,因此比例[代谢物/吗啡]。 [代谢物] / [吗啡]与镇痛的关系图具有较高的相关系数。由于已证明M3G具有止痛作用,并且是大鼠中吗啡的唯一代谢产物,因此可以得出结论,这种代谢产物的水平可能会调节吗啡在大鼠中的镇痛作用。

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