Department of Woman and Child Health, Karolinska Institute, Stockholm, Sweden.
Adv Exp Med Biol. 2010;669:129-32. doi: 10.1007/978-1-4419-5692-7_26.
Search for physiological mechanisms which could antagonize the opioid-induced respiratory depression is of important clinical value. In this study, we investigated the acute effects of morphine on respiratory activity in genetically modified newborn (P2) mice with target deletion of the (Tac1 -/-) gene lacking substance P (SP) and neurokinin A (NKA). In vivo, as shown with whole-body flow barometric plethysmography technique, morphine induced significantly attenuated minute ventilation during intermittent hypoxia in control animals. In contrast, knockout mice revealed significant increase in minute ventilation. In vitro, in brainstem preparation, knockout mice demonstrated greater changes in burst frequency during intermittent anoxia challenge. The data suggest that hereditary deficiency in tachykinins, SP and NKA results in more robust hypoxic response in newborn Tac1-/- mice during respiratory depression induced by morphine.
寻找能够拮抗阿片类药物引起的呼吸抑制的生理机制具有重要的临床价值。在这项研究中,我们研究了吗啡对缺乏 P 物质(SP)和神经激肽 A(NKA)的(Tac1-/-)基因缺失的新生(P2)小鼠呼吸活动的急性影响。在体内,如全身流量描记术技术所示,吗啡在对照动物间歇性缺氧期间引起分钟通气量明显减弱。相比之下,敲除小鼠显示分钟通气量显著增加。在脑桥准备中,体外,敲除小鼠在间歇性缺氧挑战期间表现出更大的爆发频率变化。数据表明,速激肽、SP 和 NKA 的遗传缺失导致 Tac1-/- 新生小鼠在吗啡引起的呼吸抑制期间对缺氧的反应更加强烈。