Bowen S R, Carpenter F G, Sowell J G
Br J Pharmacol. 1979 Mar;65(3):457-63. doi: 10.1111/j.1476-5381.1979.tb07851.x.
1 The disappearance of morphine from specially formulated pellets containing 75 mg morphine base was measured for 10 days after they were implanted into adult rats; the morphine content decreased at a rate of 5 mg pellet daily.2 From the 2nd to the 6th day of implantation the plasma morphine concentration increased but by the 10th day had declined to only one half the concentration found on day 6.3 Six and 24 h after the pellets were removed from 6 day implanted animals the plasma concentration of morphine amounted to only one quarter to one sixth of the amount in the plasma, respectively, of animals with pellets intact.4 The pulmonary minute volume of naive and implanted rats was depressed by morphine in proportion to the plasma morphine concentration. Less depression was produced by intravenous morphine in the implanted rats than in the naive animals; the greater morphine tolerance displayed by the implanted animals could be shown by the third day of implantation and appeared to be maintained to the 10th day.5 The pulmonary minute volume of implanted rats on the 6th day was much less than the pulmonary minute volume of naive rats. Six and 24 h after the pellets were removed the pulmonary minute volume increased as the plasma morphine concentration decreased.6 The effects on the pulmonary minute volume produced by the slow release of morphine from the implanted pellets was not changed by the development of tolerance while the effects of morphine produced by rapid injection were diminished by the development of tolerance; the different effects of morphine are accordingly linked to the mode of administration.7 We conclude that the action of morphine on the pulmonary minute volume in tolerant rats following rapid injection is fundamentally different from its action following its slow release from implanted pellets, possibly due to differences in access to an undefined neuronal site.
将含有75毫克吗啡碱的特制微丸植入成年大鼠体内后,对其吗啡消失情况进行了为期10天的测定;吗啡含量以每天5毫克/微丸的速度下降。
植入后的第2天至第6天,血浆吗啡浓度升高,但到第10天时已降至第6天浓度的一半。
从植入6天的动物体内取出微丸后6小时和24小时,吗啡的血浆浓度分别仅为微丸完整的动物血浆中吗啡含量的四分之一至六分之一。
未植入和植入微丸的大鼠的肺分钟通气量均因吗啡而降低,且与血浆吗啡浓度成比例。植入大鼠静脉注射吗啡产生的抑制作用比未植入大鼠小;植入动物在植入后第3天就表现出更大的吗啡耐受性,且这种耐受性似乎一直维持到第10天。
植入微丸第6天的大鼠肺分钟通气量远低于未植入大鼠。取出微丸后6小时和24小时,随着血浆吗啡浓度下降,肺分钟通气量增加。
植入微丸缓慢释放吗啡对肺分钟通气量的影响不会因耐受性的产生而改变,而快速注射吗啡产生的影响会因耐受性的产生而减弱;因此,吗啡的不同作用与给药方式有关。
我们得出结论,快速注射后吗啡对耐受性大鼠肺分钟通气量的作用与其从植入微丸中缓慢释放后的作用根本不同,这可能是由于到达未明确的神经元位点的途径不同所致。