Lau Benjamin K, Vaughan Christopher W
Pain Management Research Institute, Kolling Institute for Medical Research, Northern Clinical School, University of Sydney at Royal North Shore Hospital, Sydney, NSW, Australia.
Pain Management Research Institute, Kolling Institute for Medical Research, Northern Clinical School, University of Sydney at Royal North Shore Hospital, Sydney, NSW, Australia.
Curr Opin Neurobiol. 2014 Dec;29:159-64. doi: 10.1016/j.conb.2014.07.010. Epub 2014 Jul 26.
Within the central nervous system, descending systems exist to endogenously modulate our perception of pain. Of particular interest is a descending pathway which projects via the midbrain periaqueductal grey (PAG) and rostral ventromedial medulla (RVM) to inhibit ascending nociceptive transmission at the spinal cord dorsal horn. This descending PAG-RVM system forms the circuitry that underlies the physiological phenomenon of stress-induced analgesia (SIA), which is mediated by parallel opioid and cannabinoid neurotransmitter systems in the PAG. At the cellular level, opioids and cannabinoids are hypothesised to activate descending analgesia through an indirect process of 'GABA disinhibition'-suppression of inhibitory GABAergic inputs onto output neurons which constitute the descending analgesic pathway. While there is much indirect evidence to support disinhibition, there are still questions regarding this model that remain unaddressed. Furthermore, there is growing evidence suggesting more complex models than originally proposed.
在中枢神经系统内,存在下行系统以内源性方式调节我们对疼痛的感知。特别值得关注的是一条下行通路,它通过中脑导水管周围灰质(PAG)和延髓头端腹内侧区(RVM)投射,以抑制脊髓背角的上行伤害性信息传递。这条下行的PAG-RVM系统构成了应激诱导镇痛(SIA)这一生理现象的基础电路,而SIA是由PAG中平行的阿片类和大麻素神经递质系统介导的。在细胞水平上,阿片类药物和大麻素被认为是通过“GABA去抑制”的间接过程来激活下行镇痛的,即抑制构成下行镇痛通路的输出神经元上的抑制性GABA能输入。虽然有很多间接证据支持去抑制作用,但关于这个模型仍有一些问题尚未得到解决。此外,越来越多的证据表明存在比最初提出的模型更为复杂的模型。