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与胃黏膜损伤相关的因素,如衰老、幽门螺杆菌感染和睡眠剥夺,会降低具有细胞保护作用的人三叶因子蛋白TFF2的昼夜节律。

The diurnal rhythm of the cytoprotective human trefoil protein TFF2 is reduced by factors associated with gastric mucosal damage: ageing, Helicobacter pylori infection, and sleep deprivation.

作者信息

Johns C Emma, Newton Julia L, Westley Bruce R, May Felicity E B

机构信息

Department of Pathology, University of Newcastle upon Tyne, Royal Victoria Infirmary, Queen Victoria Road, Newcastle upon Tyne, UK.

出版信息

Am J Gastroenterol. 2005 Jul;100(7):1491-7. doi: 10.1111/j.1572-0241.2005.41859.x.

Abstract

OBJECTIVES

To determine if the normal TFF2 diurnal rhythm is disrupted in those with increased risk of gastric morbidity. Trefoil proteins protect the gastrointestinal mucosa from damage and aid its repair. TFF2 is considered the major cytoprotective gastric trefoil protein. There is a marked circadian variation in gastric luminal TFF2 in young healthy volunteers with peak levels present during the night.

METHODS

Gastric juice was aspirated at two hourly intervals over a 24-h period via a nasogastric tube. TFF2 was measured by quantitative western transfer analysis. Helicobacter pylori (H. pylori) status was measured by C13 urea breath test and by serology. The effects of H. pylori infection, sleep deprivation, and ageing, which cause increased gastric morbidity, on the TFF2 circadian rhythm were tested.

RESULTS

H. pylori infection attenuated the increase in TFF2 that occurs during the night. The TFF2 diurnal rhythm was reduced in older people and both the TFF2 level reached and the time at which the maximum TFF2 concentration occurs were associated inversely with age (p < 0.005). Sleep deprivation delayed the normal night time increase in gastric TFF2 and resulted in an overall reduction in TFF2 secretion.

CONCLUSIONS

H. pylori infection, ageing, and sleep deprivation cause a reduction in the TFF2 diurnal rhythm. The demonstration that the TFF2 rhythm is impaired in cohorts of individuals known to suffer gastric symptoms suggests that interventions to restore the normal TFF2 rhythm in those with poor mucosal protection could reduce morbidity.

摘要

目的

确定胃发病风险增加者的三叶因子2(TFF2)正常昼夜节律是否被破坏。三叶因子可保护胃肠道黏膜免受损伤并促进其修复。TFF2被认为是主要的具有细胞保护作用的胃三叶因子。年轻健康志愿者的胃腔内TFF2存在明显的昼夜变化,夜间水平最高。

方法

通过鼻胃管在24小时内每隔两小时抽取胃液。采用定量western印迹分析测定TFF2。通过C13尿素呼气试验和血清学检测幽门螺杆菌(H. pylori)感染情况。测试了导致胃发病风险增加的幽门螺杆菌感染、睡眠剥夺和衰老对TFF2昼夜节律的影响。

结果

幽门螺杆菌感染减弱了夜间TFF2的升高。老年人的TFF2昼夜节律降低,TFF2达到的水平以及TFF2浓度最高时的时间均与年龄呈负相关(p < 0.005)。睡眠剥夺延迟了胃TFF2夜间的正常升高,并导致TFF2分泌总体减少。

结论

幽门螺杆菌感染、衰老和睡眠剥夺会导致TFF2昼夜节律降低。在已知有胃部症状的人群中TFF2节律受损的证据表明,对黏膜保护不良者采取干预措施恢复正常的TFF2节律可能会降低发病率。

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