Huo Fu-Quan, Chen Tao, Lv Bo-Chang, Wang Jing, Zhang Ting, Qu Chao-Ling, Li Yun-Qing, Tang Jing-Shi
Department of Physiology and Pathophysiology, Key Laboratory of Environment and Genes Related to Diseases, Ministry of Education, Xi'an Jiaotong University School of Medicine, Xi'an 710061, PR China.
Cereb Cortex. 2009 Jun;19(6):1263-72. doi: 10.1093/cercor/bhn169. Epub 2008 Nov 2.
The ventrolateral orbital cortex (VLO) is part of an endogenous analgesic system, consisting of the spinal cord-thalamic nucleus submedius-VLO periaqueductal gray (PAG)-spinal cord loop. The present study examined morphological connections of GABAergic (gamma-aminobutyric acidergic) neurons and serotonergic projection terminals from the dorsal raphe nucleus (DR), as well as the relationship between GABAergic terminals and VLO neurons projecting to the PAG, by using anterograde and retrograde tracing combined with immunofluorescence, immunohistochemistry, and electron microscopy methods. Results indicate that the majority (93%) of GABAergic neurons in the VLO also express the 5-HT(1A) (5-hydroxytryptamine 1A) receptor, and serotonergic terminals originating from the DR nucleus made symmetrical synapses with GABAergic neuronal cell bodies and dendrites within the VLO. GABAergic terminals also made symmetrical synapses with neurons expressing GABA(A) receptors and projecting to the PAG. These results suggest that a local neuronal circuit, consisting of 5-HTergic terminals, GABAergic interneurons, and projection neurons, exists in the VLO, and provides morphological evidence for the hypothesis that GABAergic modulation is involved in 5-HT(1A) receptor activation-evoked antinociception.
腹外侧眶额皮质(VLO)是内源性镇痛系统的一部分,该系统由脊髓-丘脑中介核-VLO-导水管周围灰质(PAG)-脊髓环路组成。本研究采用顺行和逆行追踪结合免疫荧光、免疫组织化学和电子显微镜方法,研究了来自中缝背核(DR)的γ-氨基丁酸能(GABA能)神经元和5-羟色胺能投射终末的形态学联系,以及GABA能终末与投射至PAG的VLO神经元之间的关系。结果表明,VLO中大多数(93%)GABA能神经元也表达5-HT(1A)(5-羟色胺1A)受体,源自DR核的5-羟色胺能终末与VLO内GABA能神经元的胞体和树突形成对称突触。GABA能终末也与表达GABA(A)受体并投射至PAG的神经元形成对称突触。这些结果表明,VLO中存在由5-羟色胺能终末、GABA能中间神经元和投射神经元组成的局部神经回路,并为GABA能调制参与5-HT(1A)受体激活诱发的抗伤害感受这一假说提供了形态学证据。