McPhie A A, Barr G A
Biopsychology Doctoral Program, Department of Psychology, Hunter College, City University of New York, 695 Park Avenue, New York, NY 10021, USA.
Brain Res Dev Brain Res. 2000 Nov 30;124(1-2):73-80. doi: 10.1016/s0165-3806(00)00102-4.
Exposure to opiates such as morphine can lead to psychological and physical dependence in both adult and infant humans. Infant rats experience opiate withdrawal behaviors that are qualitatively different from the withdrawal behaviors displayed by adult rats. In the adult, withdrawal is largely mediated by the mu-opioid receptor. We sought to understand more about what role each opioid receptor (mu, kappa, and delta) plays in the display of the physical withdrawal in the infant rat. Beginning on postnatal day 1, infant rats were injected with morphine sulfate twice a day for 6.5 days. On the afternoon of the seventh day the infant rats were given an i.c. injection of a vehicle, the mu-opioid receptor antagonist CTOP, the kappa-opioid receptor antagonist nor-BNI, or the delta-opioid receptor antagonist naltrindole. CTOP precipitated withdrawal behaviors in the 7-day-old rat in a dose-dependent manner. Neither nor-BNI nor naltrindole induced any significant changes in the frequency of the withdrawal behaviors. These data suggest that in the infant rat control of certain behavioral withdrawal signs is modulated primarily by the mu-opioid receptor, as is the case in the adult rat.
接触吗啡等阿片类药物会导致成年和幼年人类产生心理和生理依赖。幼年大鼠会出现与成年大鼠表现出的戒断行为在性质上不同的阿片类药物戒断行为。在成年大鼠中,戒断主要由μ-阿片受体介导。我们试图更多地了解每种阿片受体(μ、κ和δ)在幼年大鼠身体戒断表现中所起的作用。从出生后第1天开始,每天给幼年大鼠注射硫酸吗啡两次,持续6.5天。在第7天下午,给幼年大鼠腹腔注射赋形剂、μ-阿片受体拮抗剂CTOP、κ-阿片受体拮抗剂nor-BNI或δ-阿片受体拮抗剂纳曲吲哚。CTOP以剂量依赖的方式促使7日龄大鼠出现戒断行为。nor-BNI和纳曲吲哚均未引起戒断行为频率的任何显著变化。这些数据表明,在幼年大鼠中,某些行为性戒断体征的控制主要由μ-阿片受体调节,成年大鼠也是如此。