相关实验视频
Updated: Sep 14, 2025

08:39
Murine Colitis Modeling using Dextran Sulfate Sodium DSS
Published on: January 19, 2010
50.2K
帕奇米酸在DSS诱导的性结肠炎小鼠模型中的保护作用
Hua Zhang1, Yunxia Wu1, Siyu Li1
1Department of Special Medical and Health Management, The First Affiliated Hospital of Xi'an Medical University, Xi'an, Shanxi, China.
Immunological investigations
|July 24, 2025
概括
帕奇米酸 (PA) 通过减少炎症和恢复肠道屏障,在小鼠模型中有效治疗性结肠炎 (UC). 这种天然化合物显示出UC治疗的前景.
科学领域:
- 药理学 药理学是指药理学的学科.
- 胃肠病学 胃肠病学
- 免疫学 免疫学 免疫学
背景情况:
- 性结肠炎 (UC) 是一种慢性炎症性肠病,其特征是结肠炎症和上皮屏障功能障碍.
- 目前对UC的治疗有局限性,需要探索新型治疗剂.
研究的目的:
- 为了研究帕奇米酸 (PA) 的保护作用,一种天然的三基,对硫酸 (DSS) 诱导的大肠炎在小鼠.
- 阐明PA改善结肠炎症和上皮损伤的潜在机制.
主要方法:
- 通过使用DSS诱导大肠炎的小鼠,并用PA治疗.
- 评估了疾病活动指数 (DAI),结肠组织学,粘液完整性,炎症性细胞因子,氧化应激标志物,DNA损伤 (γH2AX),紧结蛋白,亡调节器 (Bax/Bcl-2) 和NF-κB信号.
主要成果:
- 治疗PA显著降低了DAI得分,结肠缩短和组织学损伤,同时恢复了粘液层的完整性.
- 它抑制了促炎性细胞因子和氧化应激,增强了抗氧化活性,并减少了DNA损伤.
- PA恢复了紧结蛋白表达,调节了亡,并抑制了NF-κB信号传递.
结论:
- 帕奇米酸通过减轻结肠炎症和恢复表皮屏障功能,证明了性结肠炎的显著治疗潜力.
- PA的机制包括抗炎,抗氧化,DNA保护和肠道屏障恢复作用,突出其作为一种新型UC治疗的承诺.
相关概念视频
Pathophysiology of Peptic Ulcer Disease: Mucosal Defense Factors
580
Peptic ulcer disease, commonly called PUD, represents a multifaceted condition characterized by disruptions in the lining of the gastrointestinal (GI) tract. Central to the protection of the gastrointestinal lining is the mucosal-bicarbonate barrier. This physiological defense mechanism is a formidable shield against the corrosive effects of gastric acid and pepsin secretion in the stomach. Its role is pivotal in maintaining the structural integrity of the stomach's inner lining.
580
Drugs for Peptic Ulcer Disease: Sucralfate as Mucosal Protective Agents
694
In the intricate landscape of the gastric lumen, excessive acid secretion disrupts the natural defense mechanisms, weakening the mucus-bicarbonate barrier. This vulnerability allows pepsin to infiltrate epithelial cells, digesting mucosal proteins and triggering erosion, leading to ulcer formation.
In this scenario, mucosal protective agents like sucralfate play an essential role. Sucralfate, a complex of sulfated sucrose and aluminum hydroxide, demonstrates its usefulness in acidic conditions,...
In this scenario, mucosal protective agents like sucralfate play an essential role. Sucralfate, a complex of sulfated sucrose and aluminum hydroxide, demonstrates its usefulness in acidic conditions,...
694
Drugs for Treatment of Ulcerative Colitis in IBD
239
Ulcerative colitis is a chronic inflammatory condition primarily affecting the colon and rectum. The primary drugs used in the treatment of ulcerative colitis are aminosalicylates. They exhibit anti-inflammatory and immunosuppressive properties. They modulate inflammatory mediators and inhibit the activity of nuclear factor κB (NF-κB). Aminosalicylates also reduce inflammation by inhibiting prostaglandin and leukotriene production and decreasing neutrophil chemotaxis and superoxide...
239
Peptic Ulcer Disease I: Introduction
292
Peptic Ulcer Disease (PUD) is characterized by mucosal excavation in the esophagus, stomach, pylorus, or duodenum. It can manifest as acute or chronic based on the extent and duration of mucosal involvement.
An acute ulcer, marked by superficial erosion and minimal inflammation, swiftly resolves upon identifying and addressing the underlying cause. In contrast, a chronic ulcer persists, potentially eroding through the muscular wall and forming fibrous tissue.
Peptic ulcers can also be...
An acute ulcer, marked by superficial erosion and minimal inflammation, swiftly resolves upon identifying and addressing the underlying cause. In contrast, a chronic ulcer persists, potentially eroding through the muscular wall and forming fibrous tissue.
Peptic ulcers can also be...
292
Peptic Ulcer Disease II: Pathophysiology
856
Peptic Ulcer Disease (PUD) is characterized by the development of ulcers in the stomach or duodenal mucosa. Its pathophysiology is complex, involving a balance between damaging and protective elements.
Damaging agents such as Helicobacter pylori, gastric acid, pepsin, and nonsteroidal anti-inflammatory drugs (NSAIDs) can weaken the mucosal defense, allowing hydrogen ions to infiltrate back and harm epithelial cells.
Damaging agents such as Helicobacter pylori, gastric acid, pepsin, and nonsteroidal anti-inflammatory drugs (NSAIDs) can weaken the mucosal defense, allowing hydrogen ions to infiltrate back and harm epithelial cells.
856
Pathophysiology of Peptic Ulcer Disease: Injurious Factors
713
Peptic ulcers are sores on the stomach's inner lining and the upper small intestine, which are the result of disruptions in the mucosal layer that houses parietal cells which produce gastric acid, and chief cells which secrete pepsinogen.
In the antrum region, G cells secrete the gastrin hormone that binds to gastrin-cholecystokinin-B (CCK2) receptors on parietal and enterochromaffin-like (ECL) cells in the fundic glands. Simultaneously, the vagus nerve releases acetylcholine, which binds...
In the antrum region, G cells secrete the gastrin hormone that binds to gastrin-cholecystokinin-B (CCK2) receptors on parietal and enterochromaffin-like (ECL) cells in the fundic glands. Simultaneously, the vagus nerve releases acetylcholine, which binds...
713

