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作 者:段秋霞 杨丹丹[1] 彭晓燕 郭菲菲[1] 徐珞[1]
机构地区:[1]青岛大学医学院病理生理学教研室,山东青岛266021 [2]青岛市第三人民医院,山东青岛266021
出 处:《现代生物医学进展》2017年第29期5628-5632,共5页Progress in Modern Biomedicine
基 金:国家自然科学基金项目(81470815;81270460;81500414);山东省优秀中青年科学基金项目(BS2014YY009);青岛市科技局项目(14-2-3-3-nsh)
摘 要:目的:探讨ARC orexin-A对胃传入信息以及胃运动的调控及机制。方法:采用细胞外放电记录方法,鉴定ARC orexin胃牵张敏感神经元(Gastric distention sensitive neurons,GD),并探讨ARC内orexin-A对GD神经元放电活动的影响及机制;采用ARC微量注射orexin-A和及其受体阻断剂SB334867,观察大鼠胃收缩幅度和频率的改变。结果:大鼠ARC共记录到149个GD神经元,其中GD-E神经元91个,GD-I神经元58个。ARC微量注射orexin-A,62个(62/91,68.1%)GD-E神经元兴奋性显著增加,其放电频率由4.27±0.58 Hz增加到8.46±0.95 Hz(P<0.01);39个(39/58,67.2%)GD-I神经元兴奋性也显著增强,其放电频率由4.02±0.53 Hz增加到5.43±0.57 Hz(P<0.05)。然而,ARC给予大鼠orexin-A受体拮抗剂SB334867,再给予orexin-A,orexin-A兴奋效应完全被阻断(P>0.05)。胃运动实验结果显示:在ARC注射不同浓度orexin-A,大约5 min后,大鼠胃收缩幅度和频率呈剂量依赖性增加(P<0.05~0.01)。ARC注射SB334867,可完全消除orexin-A对大鼠胃运动的兴奋效应(P<0.05)。结论:ARC orexin-A对大鼠GD神经元和胃运动有调控作用,该作用可能通过调控Orexin A受体活动实现的。Objective: To investigate the regulation and mechanism of ARC orexin-A on gastric afferent information and gastric motility. Methods: The extracellular discharge recording method: identification of ARC orexin gastric stretch sensitive neurons (Gastric distention, sensitive neurons, GD), and to explore the effect of orexin-A on ARC activity of GD neurons and its mechanism; antagonist SB334867 by ARC microinjection of orexin-A and its receptor, observe the rat gastric conlTaction amplitude and frequency change. Results: A total of 149 GD neurons were recorded in ARC rats, of which GD-E neurons were and GD-I neurons were 58. ARC microin- jection of orexin-A, 62 (62/91, 68.1%) significantly increased the excitability of GD-E neurons, the discharge frequency from 4.27±0.58 Hz to 8.46±0.95 Hz (P〈0.01); 39 (39/58, 67.2%) the excitability of GD-I neurons also increased significantly, the discharge frequency from 4.02±0.53 Hz to 5.43±0.57 Hz (P〈0.05). However, ARC was given to rat orexin-A receptor antagonist SB334867, and then given orexin-A, the orexin-A effect was completely blocked (P〉0.05). The results of gastric motility test showed that the amplitude and fre- quency of gastric contraction in rats were increased in a dose-dependent manner (P〈0.05 ~ 0.01) after ARC injection at different concen- trations of orexin-A (about 5 rain). The effect of orexin-A on gastric motility in rats was completely eliminated by ARC injection of SB334867 (P〈0.05). Conclusion: ARC orexin-A may regulate the activity of GD neurons and gastric motility in rats, which may be mediated by the regulation of Orexin A receptor activity.
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