Hunter M A, Vangelisti G R, Olsen G D
Department of Physiology and Pharmacology, Oregon Health Sciences University School of Medicine, Portland, USA.
Biol Neonate. 1997;72(5):293-304. doi: 10.1159/000244496.
This study was done to determine if chronic intermittent in utero exposure to morphine (MOR) during the last half of gestation results in hypoventilation and decreased ventilatory sensitivity to CO2 in the neonate. Pregnant guinea pigs were randomly assigned to once-daily treatment with saline and 1.5, 5.0, or 15.0 mg/kg MOR. Neonates were studied for 3 weeks. Prenatal exposure to 5.0 and 15.0 mg/kg MOR significantly increased neonatal minute ventilation and central inspiratory drive on day 7 while breathing room air or 5% CO2. The increase in minute ventilation was part of a withdrawal syndrome that included increased locomotor activity, but was not due to an increase in metabolic rate or sensitivity to CO2. We conclude that neonatal guinea pigs exposed once daily to MOR during the last half of gestation hyperventilate during the 1st week after birth. These changes are neither permanent nor followed by hypoventilation or depressed sensitivity to CO2.
本研究旨在确定妊娠后半期子宫内慢性间歇性暴露于吗啡(MOR)是否会导致新生儿通气不足以及对二氧化碳的通气敏感性降低。将怀孕的豚鼠随机分为每日一次接受生理盐水以及1.5、5.0或15.0mg/kg吗啡治疗的组。对新生儿进行了3周的研究。产前暴露于5.0和15.0mg/kg吗啡显著增加了出生第7天新生儿在呼吸空气或5%二氧化碳时的分钟通气量和中枢吸气驱动。分钟通气量的增加是戒断综合征的一部分,该综合征包括运动活动增加,但并非由于代谢率增加或对二氧化碳的敏感性增加。我们得出结论,在妊娠后半期每天暴露于吗啡一次的新生豚鼠在出生后第1周会出现通气过度。这些变化既不是永久性的,也不会随后出现通气不足或对二氧化碳的敏感性降低。