Sheng-Jiang-Yi-You decoction inhibits the inflammatory response by down-regulating the p38MAPK signaling pathway to alleviate Helicobacter pylori-associated gastritis.

IF 2 4区 生物学 Q3 CELL BIOLOGY Histology and histopathology Pub Date : 2025-11-01 Epub Date: 2025-03-17 DOI:10.14670/HH-18-906
Ze Li, Ruirui Chen, Weihong Tang, Xiaoya Zheng, Xuefeng Jin, Zhongmin Wang, Qiao Wu
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Abstract

Background: Helicobacter pylori (HP)-associated gastritis is an important factor in development of stomach cancer. Components of Sheng-Jiang-Yi-You decoction (SJYYD) exert gastroprotective effects. However, the effects and mechanism of SJYYD in HP-associated gastritis remain uncertain.

Methods: HP bacterial solution (1×109 CFU/mL) was gavaged every other day for 14 days to construct an HP-associated gastritis mouse model. Male BALB/c mice were randomized into Sham, HP, HP+Standardized triple therapy (HP+Triplet), HP+SJYYD (0.4 mL/20 g), HP+Triplet+SJYYD, HP+anisomycin (ANI) (2.5 mg/kg/d, p38MAPK agonist, HP+ANI), and HP+SJYYD+ANI groups (n=6). Gastric mucosal injury detection and rapid urease test for HP infection were conducted. HE staining for pathological damage and ELISA for pro-inflammatory factors and immunoglobulin G (IgG) content were performed. Measurement of p38 mitogen-activated protein kinase (p38MAPK) pathway-related factor expression was performed by qRT-PCR and western blot.

Results: The increased IgG content and HP colonization rate indicated successful modeling. SJYYD caused attenuated gastric mucosal damage, with decreased ulcer index (UI), HP colonization rate, inflammatory cell infiltration, tumor necrosis factor-α (TNF-α), interleukin (IL)-6, and IL-1β levels in HP-associated gastritis mice. Moreover, SJYYD reduced p38MAPK, c-Jun N-terminal kinase (JNK), and extracellular regulated protein kinase (ERK) mRNA expression, as well as p-p38MAPK/p38MAPK, p-JNK/JNK, and p-ERK/ERK protein expression in gastric mucosa tissues of HP-associated gastritis mice. The above effects were reversed by further ANI treatment.

Conclusion: SJYYD may attenuate HP-associated gastritis by inhibiting inflammatory response by down-regulating p38MAPK pathway, providing scientific evidence for clinical application of SJYYD in HP-associated gastritis treatment and promoting the development of therapeutic approaches in HP-associated gastritis.

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生姜益友煎通过下调 p38MAPK 信号通路抑制炎症反应,从而缓解幽门螺旋杆菌相关性胃炎。
背景:幽门螺杆菌(HP)相关性胃炎是胃癌发生的重要因素。生姜益油汤各成分具有胃保护作用。然而,SJYYD在hp相关性胃炎中的作用和机制尚不清楚。方法:每隔一天灌胃一次HP菌液(1×109 CFU/mL),连续14 d建立HP相关性胃炎小鼠模型。雄性BALB/c小鼠随机分为Sham、HP、HP+标准化三联治疗(HP+Triplet)、HP+SJYYD、HP+Triplet+SJYYD (0.4 mL/20 g)、HP+大霉素(ANI) (2.5 mg/kg/d, p38MAPK激动剂,HP+ANI)和HP+SJYYD+ANI组(n=6)。进行HP感染的胃黏膜损伤检测和快速脲酶试验。采用HE染色检测病理损伤,ELISA检测促炎因子和免疫球蛋白G (IgG)含量。采用qRT-PCR和western blot检测p38丝裂原活化蛋白激酶(p38MAPK)通路相关因子的表达。结果:IgG含量升高,HP定殖率升高,表明造模成功。SJYYD可减轻HP相关性胃炎小鼠胃粘膜损伤,降低溃疡指数(UI)、HP定植率、炎症细胞浸润、肿瘤坏死因子-α (TNF-α)、白细胞介素(IL)-6和IL-1β水平。此外,SJYYD降低hp相关性胃炎小鼠胃黏膜组织中p38MAPK、c-Jun n -末端激酶(JNK)、细胞外调节蛋白激酶(ERK) mRNA表达以及p-p38MAPK/p38MAPK、p-JNK/JNK、p-ERK/ERK蛋白表达。通过进一步的ANI治疗,上述效果被逆转。结论:SJYYD可能通过下调p38MAPK通路抑制炎症反应,减轻hp相关性胃炎,为SJYYD在hp相关性胃炎治疗中的临床应用提供科学依据,促进hp相关性胃炎治疗途径的发展。
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来源期刊
Histology and histopathology
Histology and histopathology 生物-病理学
CiteScore
3.90
自引率
0.00%
发文量
232
审稿时长
2 months
期刊介绍: HISTOLOGY AND HISTOPATHOLOGY is a peer-reviewed international journal, the purpose of which is to publish original and review articles in all fields of the microscopical morphology, cell biology and tissue engineering; high quality is the overall consideration. Its format is the standard international size of 21 x 27.7 cm. One volume is published every year (more than 1,300 pages, approximately 90 original works and 40 reviews). Each volume consists of 12 numbers published monthly online. The printed version of the journal includes 4 books every year; each of them compiles 3 numbers previously published online.
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