Department of Physiology, Kagoshima University Graduate School of Medical and Dental Science, Kagoshima, 890-8544, Japan.
Department of Molecular Pharmacology and Neurobiology, Yokohama City University Graduate School of Medicine, Yokohama, 236-0004, Japan.
Mol Brain. 2020 Apr 14;13(1):60. doi: 10.1186/s13041-020-00600-w.
The roles of serotonergic and noradrenergic signaling in nociceptive processing in the central nervous system are well known. However, dopaminergic signaling is also relevant to various physical functions, including nociception. The zona incerta is a subthalamic nucleus in which the A13 dopaminergic cell group resides, but how this A13 group affects nociceptive processing remains unknown. Recently, we showed that acute nociceptive stimuli rapidly induce the activity of A10 (ventral tegmental area) dopamine neurons via fiber photometry. In this study, we measured the activity of A13 dopaminergic neurons in response to acute nociceptive stimuli using the same system. Adeno-associated viruses (AAV-CAG-FLEX-G-CaMP6 and AAV-CAG-FLEX-mCherry) were unilaterally injected into the A13 site in transgenic mice carrying a dopamine transporter promotor-regulated Cre recombinase transgene to specifically introduce G-CaMP6/mCherry into A13 dopaminergic cell bodies through site-specific infection. We measured G-CaMP6/mCherry fluorescence intensity in the A13 site to acute nociceptive stimuli (pinch stimulus and heat stimulus). These stimuli significantly induced a rapid increase in G-CaMP6 fluorescence intensity, but non-nociceptive control stimuli did not. In contrast, mCherry fluorescence intensity was not significantly changed by nociceptive stimuli or non-nociceptive stimuli. Our finding is the first report to measure the activity of A13 dopaminergic neurons to aversive stimuli. A13 dopaminergic neurons project to the periaqueductal gray and the central nucleus of the amygdala, which are both well known as key regions in nociceptive processing. Therefore, together with our A10 study, our results indicate that A13 dopaminergic neurons play important roles in nociceptive processing.
众所周知,血清素能和去甲肾上腺素能信号在中枢神经系统的痛觉处理中起着重要作用。然而,多巴胺能信号也与各种生理功能有关,包括痛觉。未定带是一个丘脑下核,其中包含 A13 多巴胺能细胞群,但该 A13 群如何影响痛觉处理尚不清楚。最近,我们通过光纤光度法显示,急性痛觉刺激会迅速诱导 A10(腹侧被盖区)多巴胺神经元的活动。在这项研究中,我们使用相同的系统测量了急性痛觉刺激对 A13 多巴胺能神经元活性的影响。腺相关病毒(AAV-CAG-FLEX-G-CaMP6 和 AAV-CAG-FLEX-mCherry)被单侧注射到携带多巴胺转运蛋白启动子调节 Cre 重组酶转基因的转基因小鼠的 A13 部位,通过特异性感染将 G-CaMP6/mCherry 特异性引入 A13 多巴胺能神经元体。我们测量了 A13 部位对急性痛觉刺激(捏刺激和热刺激)的 G-CaMP6/mCherry 荧光强度。这些刺激显著诱导 G-CaMP6 荧光强度的快速增加,但非痛觉控制刺激则没有。相比之下,痛觉刺激或非痛觉刺激均未显著改变 mCherry 荧光强度。我们的发现是首次报道测量 A13 多巴胺能神经元对厌恶刺激的活性。A13 多巴胺能神经元投射到导水管周围灰质和杏仁中央核,这两个核团都是痛觉处理的关键区域。因此,结合我们的 A10 研究结果表明,A13 多巴胺能神经元在痛觉处理中发挥重要作用。