Miwa H, Koseki J, Oshima T, Hattori T, Kase Y, Kondo T, Fukui H, Tomita T, Ohda Y, Watari J
Division of Gastroenterology, Department of Internal Medicine, Hyogo College of Medicine, Hyogo, Japan.
Tsumura Research Laboratories, Tsumura & Co., Ibaraki, Japan.
Neurogastroenterol Motil. 2016 May;28(5):765-78. doi: 10.1111/nmo.12775. Epub 2016 Feb 2.
Psychological stress has been shown to impair gastric accommodation (GA), but its mechanism has not been elucidated. This study was conducted to clarify the role of 5-HT2B receptors in a guinea pig model of stress-induced impairment of GA.
Gastric accommodation was evaluated by measuring the intrabag pressure in the proximal stomach after administration of a liquid meal. The guinea pigs were subjected to water-avoidance stress. The role of 5-HT2B receptors in impairment of GA was investigated by administering a 5-HT2B receptor agonist (BW723C86) or antagonist (SB215505), the traditional Japanese medicine rikkunshito (RKT), a muscarinic M3 receptor antagonist (1,1-dimethyl-4-diphenylacetoxypiperidium iodide [4-DAMP]), or a nitric oxide synthase inhibitor (Nω -nitro-L-arginine [L-NNA]).
In normal animals, liquid meal-induced GA was inhibited by BW723C86, but was not affected by SB215505. The inhibition of GA by BW723C86 was reversed by co-administration of 4-DAMP. Compared to normal animals, GA in stressed animals was significantly inhibited. SB215505 and RKT significantly suppressed stress-induced impairment of GA. After meal administration, the level of cyclic guanosine monophosphate in gastric fundus tissue increased by approximately twofold in normal animals, but did not change in stressed animals. The inhibition of GA by L-NNA was suppressed by SB215505 or RKT. At a dose that did not affect GA in normal animals, BW723C86 exacerbated the impairment of GA in stressed animals.
Stress-induced impairment of GA may be mediated by an increased responsiveness of 5-HT2B receptors, and activation of the 5-HT2B receptor signaling pathway may have an inhibitory effect on nitric oxide function.
心理应激已被证明会损害胃容纳功能(GA),但其机制尚未阐明。本研究旨在阐明5-HT2B受体在应激诱导的GA损害豚鼠模型中的作用。
通过测量给予流食后胃近端袋内压力来评估胃容纳功能。对豚鼠施加禁水应激。通过给予5-HT2B受体激动剂(BW723C86)或拮抗剂(SB215505)、传统日本药物理气剂(RKT)、毒蕈碱M3受体拮抗剂(1,1-二甲基-4-二苯乙酰氧基碘化哌啶[4-DAMP])或一氧化氮合酶抑制剂(Nω-硝基-L-精氨酸[L-NNA])来研究5-HT2B受体在GA损害中的作用。
在正常动物中,BW723C86抑制流食诱导的GA,但不受SB215505影响。4-DAMP共同给药可逆转BW723C86对GA的抑制作用。与正常动物相比,应激动物的GA受到显著抑制。SB215505和RKT显著抑制应激诱导的GA损害。进食后,正常动物胃底组织中环磷酸鸟苷水平增加约两倍,但应激动物中未改变。SB215505或RKT可抑制L-NNA对GA的抑制作用。在不影响正常动物GA的剂量下,BW723C86加剧了应激动物的GA损害。
应激诱导的GA损害可能由5-HT2B受体反应性增加介导,5-HT2B受体信号通路的激活可能对一氧化氮功能有抑制作用。