Wang Ying, Wang Shuai, Bao Yongrui, Li Tianjiao, Chang Xin, Yang Guanlin, Meng Xiansheng
School of Pharmacy, Liaoning University of Traditional Chinese Medicine, Dalian, People's Republic of China.
Component Medicine Engineering Research Center of Liaoning Province, Dalian, People's Republic of China.
Pharmacogn Mag. 2017 Apr-Jun;13(50):209-215. doi: 10.4103/0973-1296.204550. Epub 2017 Apr 18.
Gastric ulcer is a common chronic disease in human digestive system, which is difficult to cure, easy to relapse, and endangers human health seriously. Compared with western medicine, traditional Chinese medicine has a unique advantage in improving the general situation, stablizing medical condition, and with little side effects. known as "king of all the medicine", has a range of pharmacological activities and is commonly used in a variety of proprietary Chinese medicines and formulations.
On the basis of explicit antiulcer effect of triterpenes, the molecular mechanisms of its therapeutic effect on acetic acid induced gastric ulcer in rats were explored.
Acetic acid induced gastric ulcer model in rats was established to evaluate the curing effect of triterpenes and all of the rats were randomised into six groups: Control group, model group, omeprazole group (0.8 mg/mL), triterpenes high dose group (378.0 mg/mL), triterpenes middle dose group (126.0 mg/mL), and triterpenes low dose group (42.0 mg/mL). All rats in groups were orally administered the active group solution 1.5 mL once daily (model and control groups with saline) for 7 days. HPLC-TOF-MS analysis method was performed to obtain the plasma metabolites spectrums of control group, model group, triterpenes high, middle and low dose groups.
A total of 11 differential endogenous metabolites related to the therapeutic effect of triterpenes were identified, including tryptophan, phingosine-1-phosphate, pantothenic acid, and so on, among which tryptophan and phingosine-1-phosphate are related with the calcium signaling pathway and arachidonic acid (AA) metabolism. At the same time, in order to verify the above results, quantitative real time polymerase chain reaction were performed to evaluate the expression of H-K-ATPase alpha mRNA and phospholipase a 2 mRNA in relational signaling pathways. Combined with statistical analysis of plasma metabolic spectrum and gene expression in tissue, it is suggested that triterpenes has antiulcer effect on gastric ulcer in rats.
triterpenes has a certain regulating effect on the metabolism of tryptophan, AA, sphingosine, and other endogenous metabolites, and we speculated that the antiulcer potential of triterpenes can be primarily attributed to its inhibiting gastric acid secretion, reducing the release of inflammatory mediators, and protecting gastric mucosa effects to prevent the further development of gastric ulcer.
can obviously relieve the symptoms of gastric ulcer, especially the low dose group. can effectively regulate the amount of small molecule metablism in gastric ulcer rats , including tryptophan, phingosine-1-phosphate, etc. resisting gastric ulcer is probably by regulating arachidonic acid metabolism, sphingosine metabolism, etc.Down-regulation of H+-K+-ATPase alpha subunit mRNA and up-regulation of PLA mRNA in gastric tissue of dose group validated the possible mechanisms of G. triterpenes for the treatment of gastric ulcer HP: Helicobacter pylori, ECL: enterochromaffinlike, TCM: Traditional Chinese medicine; HPLC: High Performance Liquid Chromatography, HPLC/MS: High Performance Liquid chromatography Mass Spectrometry, HPLC-TOF-MS: High Performance Liquid Chromatography and Tof Mass Spectrometry, SD: Sprague Dawley, PCDL: Personal Compound Database and Library, MPP: Mass Profiler Professiona; PCA: principal component analysis, RT-PCR: real time polymerase chain reaction, PGE 2: Prostaglandin E2, COX1: cyclooxygenase 1 S1P: Sphingosine-1-phosphate, AA: Arachidonic acid, 5-HT: 5- hydroxytryptamine.
胃溃疡是人类消化系统常见的慢性疾病,难以治愈,易复发,严重危害人类健康。与西药相比,中药在改善整体状况、稳定病情及副作用小等方面具有独特优势。某药被誉为“众药之王”,具有一系列药理活性,常用于多种中成药及制剂中。
在明确某三萜类化合物抗溃疡作用的基础上,探讨其对乙酸诱导的大鼠胃溃疡治疗作用的分子机制。
建立乙酸诱导的大鼠胃溃疡模型以评价某三萜类化合物的治疗效果,将所有大鼠随机分为6组:对照组、模型组、奥美拉唑组(0.8 mg/mL)、某三萜类化合物高剂量组(378.0 mg/mL)、某三萜类化合物中剂量组(126.0 mg/mL)、某三萜类化合物低剂量组(42.0 mg/mL)。各组大鼠均每日灌胃给予相应活性组溶液1.5 mL(模型组和对照组给予生理盐水),连续7天。采用高效液相色谱-飞行时间质谱分析方法获取对照组、模型组、某三萜类化合物高、中、低剂量组的血浆代谢物谱。
共鉴定出11种与某三萜类化合物治疗作用相关的差异内源性代谢物,包括色氨酸、鞘氨醇-1-磷酸、泛酸等,其中色氨酸和鞘氨醇-1-磷酸与钙信号通路及花生四烯酸(AA)代谢有关。同时,为验证上述结果,进行定量实时聚合酶链反应以评价相关信号通路中H⁺-K⁺-ATP酶α亚基mRNA和磷脂酶A2 mRNA的表达。结合血浆代谢谱和组织基因表达的统计分析,提示某三萜类化合物对大鼠胃溃疡有抗溃疡作用。
某三萜类化合物对色氨酸、AA、鞘氨醇等内源性代谢物的代谢有一定调节作用,推测某三萜类化合物的抗溃疡潜能主要归因于其抑制胃酸分泌、减少炎症介质释放及保护胃黏膜的作用,以防止胃溃疡进一步发展。
某药能明显缓解胃溃疡症状,尤其是低剂量组。某药能有效调节胃溃疡大鼠体内小分子代谢物的量,包括色氨酸、鞘氨醇-1-磷酸等,其抗胃溃疡作用可能是通过调节花生四烯酸代谢、鞘氨醇代谢等实现。某药剂量组胃组织中H⁺-K⁺-ATP酶α亚基mRNA下调及PLA mRNA上调验证了某三萜类化合物治疗胃溃疡的可能机制。 幽门螺杆菌(HP);肠嗜铬样细胞(ECL);中药(TCM);高效液相色谱(HPLC);高效液相色谱-质谱联用(HPLC/MS);高效液相色谱-飞行时间质谱联用(HPLC-TOF-MS);斯普拉格-道利大鼠(SD);个人化合物数据库和库(PCDL);质谱分析专业软件(MPP);主成分分析(PCA);实时聚合酶链反应(RT-PCR);前列腺素E2(PGE2);环氧化酶1(COX1);鞘氨醇-1-磷酸(S1P);花生四烯酸(AA);5-羟色胺(5-HT)
需注意,原文中存在一些未明确的指代,翻译时用“某”进行了替代,可能会影响对完整准确信息的理解。