Luczynski Pauline, Tramullas Monica, Viola Maria, Shanahan Fergus, Clarke Gerard, O'Mahony Siobhain, Dinan Timothy G, Cryan John F
APC Microbiome Institute, University College Cork, Cork, Ireland.
Department of Psychiatry and Neurobehavioural Science, University College Cork, Cork, Ireland.
Elife. 2017 Jun 20;6:e25887. doi: 10.7554/eLife.25887.
The perception of visceral pain is a complex process involving the spinal cord and higher order brain structures. Increasing evidence implicates the gut microbiota as a key regulator of brain and behavior, yet it remains to be determined if gut bacteria play a role in visceral sensitivity. We used germ-free mice (GF) to assess visceral sensitivity, spinal cord gene expression and pain-related brain structures. GF mice displayed visceral hypersensitivity accompanied by increases in Toll-like receptor and cytokine gene expression in the spinal cord, which were normalized by postnatal colonization with microbiota from conventionally colonized (CC). In GF mice, the volumes of the anterior cingulate cortex (ACC) and periaqueductal grey, areas involved in pain processing, were decreased and enlarged, respectively, and dendritic changes in the ACC were evident. These findings indicate that the gut microbiota is required for the normal visceral pain sensation.
内脏痛觉的感知是一个涉及脊髓和高级脑结构的复杂过程。越来越多的证据表明,肠道微生物群是大脑和行为的关键调节因子,但肠道细菌是否在内脏敏感性中发挥作用仍有待确定。我们使用无菌小鼠(GF)来评估内脏敏感性、脊髓基因表达和与疼痛相关的脑结构。GF小鼠表现出内脏超敏反应,同时脊髓中Toll样受体和细胞因子基因表达增加,通过用来自常规定植(CC)的微生物群进行出生后定植可使其恢复正常。在GF小鼠中,参与疼痛处理的前扣带回皮质(ACC)和导水管周围灰质的体积分别减小和增大,并且ACC中的树突变化明显。这些发现表明,正常的内脏痛觉需要肠道微生物群。