Chen Tao, Li Jing, Feng Ban, Hui Rui, Dong Yu-Lin, Huo Fu-Quan, Zhang Ting, Yin Jun-Bin, Du Jian-Qing, Li Yun-Qing
Department of Anatomy, Histology and Embryology, K. K. Leung Brain Research Centre, The Fourth Military Medical University, Xi'an, 710032, China.
Department of Physiology and Pathophysiology, College of Medicine, Xi'an Jiaotong University, Xi'an, 710061, China.
Mol Neurobiol. 2016 Apr;53(3):2036-2053. doi: 10.1007/s12035-015-9159-5. Epub 2015 Apr 16.
The ventrolateral periaqueductal gray (vlPAG) is an important brain area, in which 5-HTergic neurons play key roles in descending pain modulation. It has been proposed that opioid peptides within the vlPAG can excite the 5-HTergic neurons by alleviating tonic inhibition from GABAergic neurons, the so-called disinhibitory effect. However, no direct morphological evidence has been observed for the micro-circuitry among the opioid peptide-, GABA-, and 5-HT-immunoreactive (ir) profiles nor for the functional involvement of the opioid peptides in the intrinsic properties of GABAergic and 5-HTergic neurons. In the present study, through microscopic observation of triple-immunofluorescence, we firstly identified the circuitry among the endomorphin-1 (EM1, an endogenous ligand for the μ-opioid receptor)-ir terminals and GABA-ir and 5-HT-ir neurons within the rat vlPAG. The synaptic connections of these neurons were further confirmed by electron microscopy. Through the in vitro whole-cell patch-clamp method, we showed that EM1 has strong inhibitory effects on the spiking of GABAergic neurons. However, although the resting membrane potential was hyperpolarized, EM1 actually increased the firing of 5-HTergic neurons. More interestingly, EM1 strongly inhibited the excitatory input to GABAergic neurons, as well as the inhibitory input to 5-HTergic neurons. Finally, behavioral results showed that pretreatment with a GABA(A) receptor antagonist potentiated the analgesic effect of EM1, while treatment with a GABA(A) receptor agonist blocked its analgesic effect. In summary, by utilizing morphological and functional methods, we found that the analgesic effect of EM1 is largely dependent on its potent inhibition on the inhibitory inputs to 5-HTergic neurons, which overwhelms EM1's direct inhibitory effect on 5-HTergic neurons.
腹外侧导水管周围灰质(vlPAG)是一个重要的脑区,其中5-羟色胺能神经元在下行性疼痛调制中起关键作用。有人提出,vlPAG内的阿片肽可通过减轻来自γ-氨基丁酸能神经元的紧张性抑制来兴奋5-羟色胺能神经元,即所谓的去抑制效应。然而,尚未观察到阿片肽、γ-氨基丁酸和5-羟色胺免疫反应性(ir)成分之间的微环路的直接形态学证据,也未观察到阿片肽在γ-氨基丁酸能和5-羟色胺能神经元固有特性中的功能参与情况。在本研究中,通过三重免疫荧光显微镜观察,我们首先确定了大鼠vlPAG内脑啡肽-1(EM1,μ-阿片受体的内源性配体)-ir终末与γ-氨基丁酸-ir和5-羟色胺-ir神经元之间的环路。这些神经元的突触连接通过电子显微镜进一步得到证实。通过体外全细胞膜片钳方法,我们发现EM1对γ-氨基丁酸能神经元的放电有强烈抑制作用。然而,尽管静息膜电位超极化,但EM1实际上增加了5-羟色胺能神经元的放电。更有趣的是,EM1强烈抑制对γ-氨基丁酸能神经元的兴奋性输入以及对5-羟色胺能神经元的抑制性输入。最后,行为学结果表明,用γ-氨基丁酸A受体拮抗剂预处理可增强EM1的镇痛作用,而用γ-氨基丁酸A受体激动剂处理则可阻断其镇痛作用。总之,通过形态学和功能学方法,我们发现EM1的镇痛作用很大程度上依赖于其对5-羟色胺能神经元抑制性输入的有效抑制作用大于EM1对5-羟色胺能神经元的直接抑制作用。