和胃健脾颗粒缓解非糜糜性反流病内脏超敏反应内皮相互作用分子1/瞬时受体电位香草蛋白亚家族成员1通路

Cheng Yuan, Zhang Xiaosi, L I Junxiang, Zhang Liming, Dai Yi, Xie Chune, Shi Lei, L I Xiaohong, Kou Fushun
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引用次数: 0

摘要

目的:探讨和胃健脾颗粒是否通过基质相互作用分子1 (STIM1)/瞬时受体电位香草蛋白亚家族成员1 (TRPV1)通路调节食管超敏反应。方法:采用高效液相色谱法和气相色谱法对黄芩苷进行定性分析。在体内,通过果糖摄入和抑制应激建立非糜烂性反流病(NERD)动物模型。药物干预组灌胃给予HWJNG和奥美拉唑。通过病理改变、PH值测试、机械足戒断阈值、热戒断潜伏期和肥大细胞(MCs)脱颗粒分析反流和内脏超敏反应。体外将P物质(SP)诱导的P815细胞与背根神经节(DRG)细胞共培养。通过酶联免疫吸附试验、定量实时聚合酶链反应(qRT-PCR)和Western blot验证小鼠和细胞中STIM1、TRPV1和食管内脏超敏相关胃肠道神经化学物质的表达。此外,通过对STIM1的过表达和小干扰RNA来验证HWJNG在DRG细胞中的作用。结果:HWJNG显著抑制NERD小鼠细胞间隙增宽、线粒体损伤、MCs脱肉芽肿、机械性异常痛和热神经性感觉,并显著升高食管黏膜pH值。HWJNG抑制食管黏膜内脏超敏相关胃肠道神经化学物质表达,激活P815细胞,激活DRG和DRG细胞中STIM1、TRPV1及相关神经递质表达。STIM1 siRNA和HWJNG均能降低P815细胞对DRG细胞的粘附和Ca2+流入DRG细胞的细胞质空间。此外,HWJNG可以逆转STIM1过表达诱导的TRPV1上调。结论:HWJNG通过astim1 /TRPV1通路调节内脏超敏反应,抑制NERD小鼠细胞间隙增宽,稳定MCs,恢复神经元高兴奋性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Hewei Jiangni granule alleviates visceral hypersensitivity of non-erosive reflux diseasestromal interaction molecule 1/transient receptor potential vanilloid subfamily member 1 pathway.

Objective: To explore if Hewei Jiangni granule (, HWJNG) could regulate esophageal hypersensitivity via stromal interaction molecule 1 (STIM1)/transient receptor potential vanilloid subfamily member 1 (TRPV1) pathway.

Methods: Qualitative analysis of HWJNG was analysis by high performance of liquid and gas chromatography. In vivo, animal model of non-erosive reflux disease (NERD) was established by fructose intake and restraint stress. HWJNG and Omeprazole were administered by gavage to the drug intervention group. Reflux and visceral hypersensitivity were analyzed by pathological changes, PH value test, mechanical paw withdrawal threshold, thermal withdrawal latency and mast cells (MCs) degranulation. In vitro, substance P (SP)-induced P815 cells and dorsal root ganglion (DRG) cells were co-cultured. Expression in both mice and cells of STIM1, TRPV1, and esophageal visceral hypersensitivity-related gastrointestinal neurochemicals were validated by enzyme linked immunosorbent assays, quantitative real-time polymerase chain reaction (qRT-PCR) and Western blot. Moreover, overexpression and small interfering RNA against STIM1 were utilized to verify of the role of HWJNG in DRG cells.

Results: HWJNG significantly suppressed intercellular space widening, injury of mitochondrial, MCs degranulation, mechanical allodynia and heat neuropathic sensory and increased pH value of esophageal mucosa in NERD mice. HWJNG inhibited expression of visceral hypersensitivity-related gastrointestinal neurochemicals in esophageal mucosa and activated P815 cells, and expression of the STIM1, TRPV1 and related neurotransmitters in DRG and DRG cells. STIM1 siRNA and HWJNG both reduced P815 cells adhesion to DRGs cells and Ca2+ flow into the cytoplasmic space of DRG cells. Furthermore, HWJNG could reversed STIM1 overexpression induced upregulation of TRPV1.

Conclusion: HWJNG suppressed intercellular space widening in NERD mice, stabilized MCs and restored neuronal hyperexcitability by regulating visceral hypersensitivity viaSTIM1/TRPV1 pathway.

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