Department of Pathophysiology, Faculty of Medicine, University of Szeged, Hungary.
Department of Pathophysiology, Faculty of Medicine, University of Szeged, Hungary.
Brain Res. 2019 Mar 1;1706:41-47. doi: 10.1016/j.brainres.2018.10.028. Epub 2018 Oct 26.
The aim of the present study was to investigate the participation of corticotropin-releasing factor (CRF) receptors (CRF1 and CRF2) in the alterations of the dorsal and ventral striatal dopamine release and the vertical and horizontal locomotor activity observed in rats following chronic nicotine treatment and consequent acute withdrawal. In this purpose, male Wistar rats were exposed to repeated intraperitoneal (ip) injection with nicotine or saline solution for 7 days. On the 8th day or the 9th day the rats were injected intracerebroventricularly (icv) with selective CRF1 antagonist antalarmin or selective CRF2 antagonist astressin or saline solution. Thirty minutes after the icv injection the changes of the horizontal and vertical locomotor activity were recorded in an in vivo conducta system. Immediately after the behavioral recordings the changes of the dorsal and ventral striatal dopamine release were determined in an in vitro superfusion system. On the 8th day, the horizontal and vertical locomotor activities and the dorsal and ventral striatal dopamine releases increased significantly in nicotine-treated rats, compared to the saline-treated ones. On the 9th day, the horizontal locomotor activity and the dorsal striatal dopamine release increased significantly, whereas the vertical locomotor activity and the ventral striatal dopamine release decreased significantly in nicotine-treated rats, compared to the saline-treated ones. All the changes observed were attenuated significantly by antalarmin, but not astressin. The present study demonstrates that the changes of striatal dopamine release and locomotor activity observed following chronic nicotine treatment and consequent acute withdrawal are mediated by CRF1, but not CRF2, receptor.
本研究旨在探讨促肾上腺皮质素释放因子(CRF)受体(CRF1 和 CRF2)在慢性尼古丁处理和随后的急性戒断后大鼠背侧和腹侧纹状体多巴胺释放改变以及垂直和水平运动活动中的作用。为此,雄性 Wistar 大鼠接受了为期 7 天的腹膜内(ip)注射尼古丁或生理盐水。第 8 天或第 9 天,大鼠脑室内(icv)注射选择性 CRF1 拮抗剂 antalarmin 或选择性 CRF2 拮抗剂 astressin 或生理盐水。icv 注射后 30 分钟,在体内行为系统中记录水平和垂直运动活动的变化。行为记录后立即,在体外灌注系统中测定背侧和腹侧纹状体多巴胺的释放变化。第 8 天,与生理盐水处理的大鼠相比,尼古丁处理的大鼠的水平和垂直运动活动以及背侧纹状体多巴胺释放明显增加。第 9 天,与生理盐水处理的大鼠相比,尼古丁处理的大鼠的水平运动活动和背侧纹状体多巴胺释放明显增加,而垂直运动活动和腹侧纹状体多巴胺释放明显减少。antalarmin 显著减弱了所有观察到的变化,但 astressin 没有。本研究表明,慢性尼古丁处理和随后的急性戒断后观察到的纹状体多巴胺释放和运动活动的变化是由 CRF1 介导的,而不是 CRF2 受体介导的。