首页> 外文期刊>American Journal of Physiology >Ghrelin selectively reduces mechanosensitivity of upper gastrointestinal vagal afferents.
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Ghrelin selectively reduces mechanosensitivity of upper gastrointestinal vagal afferents.

机译:Ghrelin选择性降低上消化道迷走神经传入的机械敏感性。

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摘要

Ghrelin is a peptide released from gastric endocrine cells that has an orexigenic effect via a vagal pathway. Here we determine the effect of ghrelin on mechanosensitivity of upper-intestinal vagal afferent fibers in ferret and mouse. The responses of gastroesophageal vagal afferents to graded mechanical stimulation were determined in vitro before and during application of ghrelin to their peripheral endings. Three types of vagal afferent were tested: tension receptors responding to circumferential tension, mucosal receptors responding only to mucosal stroking, and tension/mucosal (TM) receptors in ferret esophagus that responded to both stimuli. In the mouse, ghrelin did not significantly affect the response of mucosal receptors to mucosal stroking with calibrated von Frey hairs. However, it significantly reduced responses of tension receptors to circumferential tension (P < 0.005; two-way ANOVA) by up to 40%. This inhibition was reversed by the ghrelin receptor antagonist [d-Lys-3]-growth hormone-releasing peptide (GHRP)-6. In the ferret, ghrelin significantly reduced the response of mucosal and TM receptors to mucosal stroking with calibrated von Frey hairs. Surprisingly, ghrelin did not significantly alter the response to circumferential tension in either tension or TM receptors. RT-PCR analysis indicated that both ghrelin and its receptor are expressed in vagal afferent cell bodies in mouse nodose ganglia. In conclusion, ghrelin selectively inhibits subpopulations of mechanically sensitive gastroesophageal vagal afferents; there is also potential for ghrelin release from vagal afferents. However, the subpopulation of afferents inhibited differs between species. These data have broad implications for ghrelin's role in food intake regulation and reflex control of gastrointestinal function.
机译:Ghrelin是从胃内分泌细胞释放的一种肽,具有通过迷走途径的致呕作用。在这里,我们确定ghrelin对雪貂和小鼠上肠道迷走神经传入纤维的机械敏感性的影响。在将ghrelin应用于其外周末端之前和期间,在体外确定胃食管迷走神经传入对分级机械刺激的反应。测试了三种类型的迷走神经传入:对周向张力响应的张力受体,仅对粘膜抚摸响应的粘膜受体以及在雪貂食管中对两种刺激都响应的张力/粘膜(TM)受体。在小鼠中,生长素释放肽没有显着影响粘膜受体对标定的冯·弗雷毛发粘膜抚摸的反应。但是,它显着降低了张力受体对周向张力的响应(P <0.005;双向ANOVA)达40%。 ghrelin受体拮抗剂[d-Lys-3]-生长激素释放肽(GHRP)-6逆转了这种抑制作用。在雪貂中,生长素释放肽显着降低了经校准的冯·弗雷毛对粘膜和TM受体的粘膜抚触反应。令人惊讶的是,生长素释放肽在张力或TM受体中均未显着改变对圆周张力的反应。 RT-PCR分析表明,生长素释放肽及其受体均在小鼠结节神经节的迷走神经传入细胞体中表达。总之,生长素释放肽选择性抑制机械敏感的胃食管迷走神经传入的亚群。 ghrelin也可能从迷走神经传入中释放出来。但是,传入子群受到抑制的物种之间有所不同。这些数据对生长素释放肽在食物摄入调节和胃肠功能反射控制中的作用具有广泛的意义。

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