首页|Nesfatin-1对IBS-D模型大鼠结肠动力及CRF信号通路的影响

Nesfatin-1对IBS-D模型大鼠结肠动力及CRF信号通路的影响

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目的 探讨Nesfatin-1对腹泻型肠易激综合征(IBS-D)模型大鼠结肠动力和促肾上腺激素释放因子(CRF)信号通路的影响.方法 将雄性SD大鼠分为对照组、IBD-D组、Nesfatin-1组1、Nesfatin-1组2及Nes-fatin-1 组3,除对照组外各组大鼠均制成IBS-D模型.Nesfatin-1组1~3于大鼠左侧迷走神经复合体注射0.5、5.0、50.0 μmol/L Nesfatin-1溶液,对照组、IBS-D组予等量0.9%氯化钠溶液.比较各组大鼠的结肠转运功能、小肠推进率;ELISA法检测各组大鼠脑、结肠组织中血管活性肠肽(VIP)水平;免疫组化法检测结肠组织cajal间质细胞(ICC)标记物c-kit和辣椒素受体1(TRPV1)表达;蛋白免疫印迹法检测促肾上腺激素释放因子(CRF)、CRF受体(CRF-R)1及CRF-R2蛋白表达水平.结果 IBS-D组大鼠的玻璃球排出时间短于对照组(P<0.05),脑、结肠组织中VIP水平和结肠组织CRF-R2蛋白表达均低于对照组(均P<0.05),小肠推进率、结肠组织c-kit、TRPV1平均光密度值和CRF、CRF-R1蛋白表达均高于对照组(均P<0.05).Nesfatin-1组1~3大鼠玻璃球排出时间均长于IBS-D组(均P<0.05),脑、结肠组织中VIP水平和结肠组织CRF-R2蛋白表达均高于IBS-D组(均P<0.05),小肠推进率、结肠组织c-kit、TRPV1平均光密度值和CRF、CRF-R1蛋白表达均低于IBS-D组(均P<0.05).结论 Nesfatin-1可以改善IBS-D大鼠的肠推进程度,可能与VIP水平提高、ICC水平和CRF信号通路活性抑制有关.
Effects of Nesfatin-1 on colonic motility and CRF signaling pathway in IBS-D rats
Objective To explore the effects of Nesfatin-1 on colonic motility and corticotropin-releasing factor(CRF)signaling pathway in rats with irritable bowel syndrome with predominant diarrhea(IBS-D).Methods Male SD rats were divided into control group,IBD-D group,Nesfatin-11 group,Nesfatin-12 group and Nesfatin-13 group.Except control group,rats in the other groups were made into IBS-D models.The rats inall the Nesfatin-1 groups were injected with Nesfatin-1(0.5,5.0,50.0 μmol/L)into the left vagus nerve complex,while those in control group and IBS-D group were given with the same volume of 0.9%sodium chloride solution.The colon transport function and small intestine propulsion rate of each group of rats was compared.The level of vasoactive intestinal peptide(VIP)in brain and colon tissues was detected by ELISA.The expressions of interstitial cells of cajal(ICC)marker c-kit and capsaicin receptor 1(TRPV1)in colon tissues were detected by immunohistochemistry.The expression levels of CRF,CRF-R1 and CRF-R2 proteins were detected by Western blot.Results The efflux time of glass ball in IBS-D group was shorter than that in control group(P<0.05).VIP level in brain and colon tissues,and expression of CRF-R2 protein in colon tissues were lower than those in control group(all P<0.05).The small intestine propulsion rate,av-erage optical density of c-kit and TRPV1 in colon tissues,and expressions of CRF and CRF-R1 proteins were higher than those in control group(all P<0.05).The efflux time of glass ball in all the Nesfatin-lgroups was longer than that in IBS-D group(all P<0.05).VIP level in brain and colon tissues,and expression of CRF-R2 protein in colon tissues were higher than those in IBS-D group(all P<0.05).The small intestine propulsion rate,average optical density of c-kit and TRPV1 in colon tissues,and expressions of CRF and CRF-R1 proteins were lower than those in control group(all P<0.05).Conclusions Nesfatin-1 can improve intestinal propulsion in IBS-D rats,which may be related to increasing VIP level,inhibiting ICC level and the activity of CRF signaling pathway.

Irritable bowel syndromeDiarrhea typeNesfatin-1Colonic motilityCorticotropin-releasing factor

谢碧云、邵喆、李硕君

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311400 杭州,杭州市富阳区第一人民医院

肠易激综合征 腹泻型 Nesfatin-1 结肠动力 促肾上腺激素释放因子

杭州市富阳区科技计划

2019SK018

2024

现代实用医学
宁波市医学会

现代实用医学

影响因子:0.652
ISSN:1671-0800
年,卷(期):2024.36(4)
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