Ide Soichiro, Yamamoto Ryuta, Suzuki Hacchi, 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 Dec;38(4):182-188. doi: 10.1002/npr2.12032. Epub 2018 Sep 27.
The bed nucleus of the stria terminalis (BNST) is a limbic structure mediating autonomic and neuroendocrine responses and negative affective states such as anxiety and fear. We previously demonstrated that noradrenergic transmission via β-adrenoceptors within the ventral part of BNST (vBNST) is involved in bidirectional interactions between the brain and the upper gastrointestinal (GI) tract. The present study aimed to examine the roles of intra-vBNST noradrenergic transmission via β-adrenoceptors in bidirectional interactions between the brain and lower GI tract.
In vivo microdialysis experiments were performed to examine colorectal distention (CRD)-induced noradrenaline release within the vBNST of freely moving male Sprague-Dawley rats. Colonic transit and abdominal pain perception were examined following intra-vBNST injections of isoproterenol, a β-adrenoceptor agonist, with and without co-administration of timolol, a β-adrenoceptor antagonist.
CRD increased extracellular noradrenaline levels within the vBNST and evoked abdominal contractions in a pressure-dependent manner (30-60 mm Hg). Bilateral intra-vBNST injections of isoproterenol (30 nmol/side) significantly increased CRD (30 mm Hg)-induced abdominal contractions. Intra-vBNST injections of isoproterenol (30 nmol/side) significantly increased colonic transit, which was reversed by co-administration of timolol (30 nmol/side).
The results of this study suggest (a) the existence of a positive feedback loop between intra-vBNST noradrenaline release and abdominal pain perception, and (b) the modulation of colonic motility by intra-vBNST noradrenergic transmission via β-adrenoceptors. Dysfunction of the lower GI tract may increase noradrenaline release within the vBNST, which, in turn, may exacerbate impairment of its motility and pain perception.
终纹床核(BNST)是一个边缘系统结构,介导自主神经和神经内分泌反应以及焦虑和恐惧等负面情绪状态。我们之前证明,通过BNST腹侧部分(vBNST)内的β-肾上腺素能受体进行的去甲肾上腺素能传递参与了大脑与上消化道(GI)之间的双向相互作用。本研究旨在探讨通过β-肾上腺素能受体进行的vBNST内去甲肾上腺素能传递在大脑与下消化道双向相互作用中的作用。
进行体内微透析实验,以检测自由活动的雄性Sprague-Dawley大鼠vBNST内结肠扩张(CRD)诱导的去甲肾上腺素释放。在注射β-肾上腺素能受体激动剂异丙肾上腺素的情况下,无论是否同时给予β-肾上腺素能受体拮抗剂噻吗洛尔,均检测结肠转运和腹痛感知。
CRD增加了vBNST内细胞外去甲肾上腺素水平,并以压力依赖性方式(30 - 60 mmHg)诱发腹部收缩。双侧vBNST内注射异丙肾上腺素(30 nmol/侧)显著增加了CRD(30 mmHg)诱导的腹部收缩。vBNST内注射异丙肾上腺素(30 nmol/侧)显著增加了结肠转运,而同时给予噻吗洛尔(30 nmol/侧)可逆转这一作用。
本研究结果表明:(a)vBNST内去甲肾上腺素释放与腹痛感知之间存在正反馈回路;(b)通过β-肾上腺素能受体进行的vBNST内去甲肾上腺素能传递对结肠运动有调节作用。下消化道功能障碍可能会增加vBNST内去甲肾上腺素释放,进而可能加剧其运动和疼痛感知的损害。