首页> 外文期刊>Iranian Journal of Basic Medical Sciences >EFFECT OF ACETYLCHOLINE RECEPTORS ON THE PAIN?RELATED ELECTRICAL ACTIVITIES IN THE HIPPOCAMPAL CA3 REGION OF MORPHINEADDICTED RATS
【24h】

EFFECT OF ACETYLCHOLINE RECEPTORS ON THE PAIN?RELATED ELECTRICAL ACTIVITIES IN THE HIPPOCAMPAL CA3 REGION OF MORPHINEADDICTED RATS

机译:乙酰胆碱受体对吗啡成瘾大鼠海马CA3区疼痛相关电活动的影响

获取原文
           

摘要

Objective (s): To determine the effect of acetylcholine (ACh), pilocarpine, and atropine on pain evoked responses of pain excited neurons (PEN) and pain inhibited neurons (PIN) in hippocampal CA3 region of morphine addicted rats.Materials and Methods: Female Wistar rats, weighing between 230 ? 260 g were used in this study.Morphine addicted rats were generated by subcutaneous injection of increasing concentrations of morphine hydrochloride for six days. Trains of electrical impulses applied to the sciatic nerve were used as noxious stimulation and the evoked electrical activities of PEN or PIN in hippocampal CA3 area were recorded using extracellular electrophysiological recording techniques in hippocampal slices.The effect of acetylcholine receptor stimulation by ACh, the muscarinic agonist pilocarpine, and the muscarinic antagonist atropine on the pain evoked responses of pain related electrical activities was analyzed in hippocampal CA3 area of morphine addicted rats.Results: Intra ? CA3 microinjection of ACh (2 m g/1 m l) or pilocarpine (2 m g/1 m l) decreased the discharge frequency and prolonged the firing latency of PEN, but increased the discharge frequency and shortened the firing inhibitory duration (ID) of PIN. The intra ? CA3 administration of atropine (0.5 m g/1 m l) produced opposite effect. The peak activity of cholinergic modulators was 2 to 4 min later in morphine addicted rats compared to peak activity previously observed in normal rats.Conclusion: ACh dependent modulation of noxious stimulation exists in hippocampal CA3 area of morphine addicted rats. Morphine treatment may shift the sensitivity of pain related neurons towards a delayed response to muscarinergic neurotransmission in hippocampal CA3 region.
机译:目的:确定乙酰胆碱(ACh),毛果芸香碱和阿托品对吗啡成瘾大鼠海马CA3区疼痛激发神经元(PEN)和疼痛抑制神经元(PIN)的疼痛诱发反应的影响。材料和方法:雌性Wistar鼠,体重在230到300之间。这项研究使用了260 g。通过皮下注射浓度不断增加的盐酸吗啡产生六天,从而产生了吗啡成瘾的大鼠。用一系列施加于坐骨神经的电脉冲作为有害刺激物,并利用细胞外电生理记录技术在海马切片中记录海马CA3区PEN或PIN诱发的电活动。分析了吗啡成瘾大鼠海马CA3区毛果芸香碱和毒蕈碱拮抗剂阿托品对疼痛相关电活动引起的疼痛的影响。 CA3微量注射ACh(2 m g / 1 ml)或毛果芸香碱(2 m g / 1 ml)会降低PEN的放电频率并延长点火时间,但会增加PIN的放电频率并缩短点火抑制时间(ID)。内? CA3给予阿托品(0.5 m g / 1 ml)产生相反的效果。与以前在正常大鼠中观察到的峰值活性相比,在吗啡成瘾的大鼠中胆碱能调节剂的峰值活性晚了2至4分钟。结论:吗啡成瘾的大鼠海马CA3区存在ACh依赖的有害刺激调节作用。吗啡治疗可能会使疼痛相关神经元的敏感性向海马CA3区对毒蕈碱能神经传递的延迟反应转移。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号