在缺乏物质P受体的小鼠中,阿片类药物的有益作用是不存在的
P Murtra1, A M Sheasby, S P Hunt
1Instituto de Neurosciencias, Universidad Miguel Hernandez, Alicante, Spain.
Nature
|May 23, 2000
概括
破坏物质P受体会减少吗啡的含量.
科学领域:
- 神经科学是一个神经科学.
- 药理学 药理学是指药理学的学科.
- 成研究 研究成研究
背景情况:
- 物质P (SP) 是一种神经,与压力和情绪障碍有关.
- SP受体 (SPR) 存在于大脑中调节行为和奖励的区域.
- 在药物奖励的动机方面SPR的作用尚未完全被理解.
研究的目的:
- 调查物质P受体在调解阿片类药物的奖励作用中的特定作用.
- 为了确定SPR中断是否影响自然奖励或滥用其他药物的动机.
主要方法:
- 使用了缺乏物质P受体的基因工程小鼠 (SPR淘汰赛小鼠).
- 在野生型和SPR淘汰赛小鼠中评估了吗啡,可卡因和食物的奖励特性.
- 评估与阿片类药物戒断相关的身体反应.
主要成果:
- 在SPR淘汰的小鼠中,显著丧失了吗啡的奖励作用.
- 可卡因和食物的有益作用在SPR淘汰小鼠中保持不变.
- 在SPR淘汰赛小鼠中,阿片类药物的物理戒断症状减少了.
结论:
- 实物P在调解阿片类药物的激励性质方面发挥着特定的作用.
- 准物质P受体可能为管理阿片类成提供一种新的治疗策略.
- SPR调制为控制药物滥用提供了一个潜在的新药理学方法.
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