Zheng Xi-Geng, Li Xin-Wang, Yang Xiao-Yan, Sui Nan
Brain and Behavior Research Center, Institute of Psychology, Chinese Academy of Sciences, Beijing 100101, China.
Acta Pharmacol Sin. 2002 May;23(5):477-80.
To investigate effects of morphine on acquisition process of rats a nd interactions of opioid and cholinergic systems by Morris water maze performance.
Morris water maze was used to measure the latency of rats with drug s treatment to find the covert platform.
Chronic morphine administration (10 mg/kg) impaired the acquisition process of rats in Morris water maze task. Appreciable difference was identified with morphine 10 mg/k g group compared with morphine 3 mg/kg group. Co-administration of morphine (10 mg/kg) and scopolamine (3 mg/kg) aggravated acquisition impairment induced by morphine 1 0 mg/kg or scopolamine alone, though scopolamine itself induced no salient changes in acquisition capabilities of rats. In addition, physostigmine (0.1 mg/kg) could appreciably attenuate morphine-induced acquisition impairment.
Morphine 10 mg/kg evidently impaired acquisition process of rats. There was a close relationship between the acquisition capabilities of morphine-treated rats and the functions of cholinergic system.