Antelo M T, Fernández B, Kitchen I, Viveros M P
Departamento de Biología Animal II, Facultad de Biología, Universidad Complutense, 28040, Madrid, Spain.
Brain Res Dev Brain Res. 1998 Sep 10;110(1):127-30. doi: 10.1016/s0165-3806(98)00095-9.
The effect of a daily injection of the delta-selective opioid antagonist naltrindole (1 mg/kg), from birth to postnatal day 19, on the development of stress-induced-antinociception (SIA) and on the antinociceptive response to the mu-selective agonist alfentanil (65 microg/kg) in female rats was investigated. Functional blockade of the delta-receptor during the preweanling period markedly reduced the antinociceptive response to swim-stress in 25-day-old rats, and SIA was only mediated by delta-receptors at this age. In 20-day-old rats and in adults, SIA was predominantly mu-receptor mediated and unaffected by delta-receptor blockade. The lack of interference with mu-receptor function was confirmed as alfentanil responses were unaffected by preweanling naltrindole treatment. The data show independence of mu- and delta-receptors in the control of SIA during development and an impairment of delta- but not mu-mediated SIA after chronic delta-antagonist treatment.
研究了从出生到出生后第19天每天注射δ-选择性阿片类拮抗剂纳曲吲哚(1毫克/千克)对雌性大鼠应激诱导的抗伤害感受(SIA)发育以及对μ-选择性激动剂阿芬太尼(65微克/千克)的抗伤害感受反应的影响。断奶前时期δ-受体的功能阻断显著降低了25日龄大鼠对游泳应激的抗伤害感受反应,并且在这个年龄SIA仅由δ-受体介导。在20日龄大鼠和成年大鼠中,SIA主要由μ-受体介导且不受δ-受体阻断的影响。由于阿芬太尼反应不受断奶前纳曲吲哚治疗的影响,因此证实了对μ-受体功能没有干扰。数据表明在发育过程中μ-受体和δ-受体在控制SIA方面具有独立性,并且慢性δ-拮抗剂治疗后δ-介导的SIA受损,但μ-介导的SIA不受影响。