Laboratory of Translational Medicine, Gachon University Lee Gil Ya Cancer and Diabetes Institute, Incheon, Korea.
J Gastroenterol Hepatol. 2012 Apr;27 Suppl 3:13-22. doi: 10.1111/j.1440-1746.2012.07065.x.
Cysteamine is a reducing aminothiol used for inducing duodenal ulcer through mechanisms of oxidative stress related to thiol-derived H(2)O(2) reaction. Cochinchina momordica saponins have been suggested to be protective against various gastric diseases based on their cytoprotective and anti-inflammatory mechanisms. This study was aimed to document the preventive effects of Cochinchina momordica seed extract against cysteamine-induced duodenal ulcer as well as the elucidation of its pharmacological mechanisms.
Cochinchina momordica seed extract (50, 100, 200 mg/kg) was administrated intragastrically before cysteamine administration, after which the incidence of the duodenal ulcer, ulcer size, serum gastrin level, and the ratio of reduced glutathione (GSH)/oxidized glutathione disulfide (GSSG) as well as biochemical and molecular measurements of cytoplasmic phospholipase A(2) (cPLA(2)), cyclooxygenase-2 (COX-2), 5-lipoxygenase and the expression of proinflammatory genes including IL-1β, IL-6, COX-2 were measured in rat model. Additional experiments of electron spin resonance measurement and the changes of glutathione were performed.
Cochinchina momordica seed extract effectively prevented cysteamine-induced duodenal ulcer in a dose-dependent manner as reflected with significant decreases in either duodenal ulcerogenesis or perforation accompanied with significantly decreased in serum gastrin in addition to inflammatory mediators including cPLA(2), COX-2, and 5-lipoxygenase. Cochinchina momordica seed extract induced the expression of γ-glutamylcysteine synthetase (γ-GCS)-related glutathione synthesis as well as significantly reduced the expression of cPLA(2). Cochinchina momordica seed extract preserved reduced glutathione through increased expressions of γ-GCS.
Cochinchina momordica seed extracts exerted significantly protective effect against cysteamine-induced duodenal ulcer by either cPLA2 inhibition or glutathione preservation.
半胱胺是一种还原型硫醇,可通过与硫醇衍生的 H2O2 反应相关的氧化应激机制诱导十二指肠溃疡。根据其细胞保护和抗炎机制,三叶木通皂苷已被证明对各种胃病具有保护作用。本研究旨在记录三叶木通种子提取物对半胱胺诱导的十二指肠溃疡的预防作用,并阐明其药理机制。
半胱胺给药前,三叶木通种子提取物(50、100、200mg/kg)经胃内给药,然后测量十二指肠溃疡的发生率、溃疡大小、血清胃泌素水平以及还原型谷胱甘肽(GSH)/氧化型谷胱甘肽二硫化物(GSSG)的比值,以及细胞质磷脂酶 A2(cPLA2)、环氧化酶-2(COX-2)、5-脂氧合酶的生化和分子测量,以及包括白细胞介素-1β(IL-1β)、白细胞介素-6(IL-6)、COX-2 在内的促炎基因的表达。还进行了电子顺磁共振测量和谷胱甘肽变化的附加实验。
三叶木通种子提取物以剂量依赖的方式有效预防半胱胺诱导的十二指肠溃疡,表现为十二指肠溃疡形成或穿孔明显减少,同时血清胃泌素显著降低,以及包括 cPLA2、COX-2 和 5-脂氧合酶在内的炎症介质减少。三叶木通种子提取物诱导与谷胱甘肽合成相关的γ-谷氨酰半胱氨酸合成酶(γ-GCS)的表达,并显著降低 cPLA2 的表达。三叶木通种子提取物通过增加 γ-GCS 的表达来保存还原型谷胱甘肽。
三叶木通种子提取物通过抑制 cPLA2 或保存谷胱甘肽,对半胱胺诱导的十二指肠溃疡具有显著的保护作用。