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来自前扣带皮层到伏隔核和腹侧被盖区的投射有助于大鼠的神经病理性疼痛诱发厌恶。

The projections from the anterior cingulate cortex to the nucleus accumbens and ventral tegmental area contribute to neuropathic pain-evoked aversion in rats.

机构信息

Department of Neurobiology, College of Basic Medical Science, Chongqing Key Laboratory of Neurobiology, Army Medical University, Chongqing 400038, China; Shigatse Branch, Xinqiao Hospital, Army 953 Hospital, Army Medical University, Shigatse 857000, China.

Shigatse Branch, Xinqiao Hospital, Army 953 Hospital, Army Medical University, Shigatse 857000, China.

出版信息

Neurobiol Dis. 2020 Jul;140:104862. doi: 10.1016/j.nbd.2020.104862. Epub 2020 Apr 3.

Abstract

Although the anterior cingulate cortex (ACC) plays a vital role in neuropathic pain-related aversion, the underlying mechanisms haven't been fully studied. The mesolimbic dopamine system encodes reward and aversion, and participates in the exacerbation of chronic pain. Therefore, we investigated whether the ACC modulates aversion to neuropathic pain via control of the mesolimbic dopamine system, in a rat model of chronic constriction injury (CCI) to the sciatic nerve. Using anterograde and retrograde tracings, we confirmed that a subgroup of ACC neurons projected to the nucleus accumbens (NAc) and ventral tegmental area (VTA), which are two crucial nodes of the mesolimbic dopamine system. Combining electrophysiology in juvenile rats 7 days post-CCI, we found that the NAc/VTA-projecting neurons were hyperexcitable after CCI. Chemogenetic inhibition of these projections induced conditioned place preference in young adult rats 10-14 days post-CCI, without modulating the evoked pain threshold, whereas activation of these projections in sham rats mimicked aversive behavior. Furthermore, the function of the ACC projections was probably mediated by NAc D2-type medium spiny neurons and VTA GABAergic neurons. Taken together, our findings suggest that projections from the ACC to the NAc and VTA mediate neuropathic pain-related aversive behavior.

摘要

尽管前扣带皮层(ACC)在神经性疼痛相关的厌恶反应中起着至关重要的作用,但相关的潜在机制尚未得到充分研究。中脑边缘多巴胺系统编码奖励和厌恶,参与慢性疼痛的加剧。因此,我们通过控制中脑边缘多巴胺系统,在坐骨神经慢性缩窄性损伤(CCI)的大鼠模型中,研究了 ACC 是否调节对神经性疼痛的厌恶。通过顺行和逆行示踪,我们证实了 ACC 的亚群神经元投射到伏隔核(NAc)和腹侧被盖区(VTA),这两个是中脑边缘多巴胺系统的两个关键节点。结合电生理学在 CCI 后 7 天的幼年大鼠中的应用,我们发现 CCI 后 NAc/VTA 投射神经元过度兴奋。这些投射物的化学遗传抑制在 CCI 后 10-14 天的成年大鼠中引起条件性位置偏好,而不调节诱发的疼痛阈值,而在假手术大鼠中激活这些投射物则模拟了厌恶行为。此外,ACC 投射的功能可能是由 NAc D2 型中间神经元和 VTA GABA 能神经元介导的。总之,我们的发现表明,ACC 到 NAc 和 VTA 的投射介导了神经性疼痛相关的厌恶行为。

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