Ide Soichiro, Yamamoto Ryuta, Takeda Hiroshi, Minami Masabumi
Department of Pharmacology, Graduate School of Pharmaceutical Sciences, Hokkaido University, Sapporo, Japan.
Addictive Substance Project, Tokyo Metropolitan Institute of Medical Science, Tokyo, Japan.
Neuropsychopharmacol Rep. 2018 Mar;38(1):37-43. doi: 10.1002/npr2.12004. Epub 2018 Feb 6.
Although the important roles of bidirectional interactions between the brain and gut in stress and emotional responses have long been recognized, the underlying neuronal mechanisms remain unclear. The bed nucleus of the stria terminalis (BNST) is a limbic structure involved in stress responses and negative affective states, such as anxiety and depression. We have previously demonstrated that noradrenergic transmission within the ventral part of the BNST (vBNST) plays a crucial role in anxiety-like behaviors and pain-induced aversion.
This study aimed to examine the involvement of noradrenergic transmission via β-adrenoceptors within the vBNST in bidirectional brain-gut interactions.
We measured the gastric distention (GD)-induced noradrenaline release within the vBNST of freely moving rats using an in vivo microdialysis technique. Gastric emptying and intestinal transit were examined following intra-vBNST injections of isoproterenol, a β-adrenoceptor agonist, in the absence or presence of the coadministration of timolol, a β-adrenoceptor antagonist.
Gastric distention at a higher pressure (45 mm Hg) but not at a lower pressure (25 mm Hg) resulted in a significant increase in extracellular noradrenaline levels within the vBNST. Intra-vBNST injections of isoproterenol (30 nmol/side) induced significant reductions in gastric emptying and small intestinal transit, both of which were reversed by the coadministration of timolol (30 nmol/side).
Noradrenergic transmission via β-adrenoceptors within the vBNST was involved in bidirectional brain-gut interactions. These findings suggest that gastric dysfunction may induce negative affective states via the enhanced release of noradrenaline within the vBNST which, in turn, may cause gastrointestinal impairments.
尽管大脑与肠道之间双向相互作用在应激和情绪反应中的重要作用早已得到认可,但其潜在的神经元机制仍不清楚。终纹床核(BNST)是一个边缘结构,参与应激反应和负面情绪状态,如焦虑和抑郁。我们之前已经证明,BNST腹侧部分(vBNST)内的去甲肾上腺素能传递在焦虑样行为和疼痛引起的厌恶中起关键作用。
本研究旨在探讨vBNST内通过β-肾上腺素能受体的去甲肾上腺素能传递在脑-肠双向相互作用中的作用。
我们使用体内微透析技术测量自由活动大鼠vBNST内胃扩张(GD)诱导的去甲肾上腺素释放。在不存在或存在β-肾上腺素能受体拮抗剂噻吗洛尔共同给药的情况下,在vBNST内注射β-肾上腺素能受体激动剂异丙肾上腺素后,检测胃排空和肠道转运情况。
较高压力(45毫米汞柱)而非较低压力(25毫米汞柱)的胃扩张导致vBNST内细胞外去甲肾上腺素水平显著升高。vBNST内注射异丙肾上腺素(30纳摩尔/侧)导致胃排空和小肠转运显著减少,而噻吗洛尔(30纳摩尔/侧)共同给药可逆转这两种情况。
vBNST内通过β-肾上腺素能受体的去甲肾上腺素能传递参与脑-肠双向相互作用。这些发现表明,胃功能障碍可能通过vBNST内去甲肾上腺素释放增强诱导负面情绪状态,进而可能导致胃肠道损伤。