Li Kai, Kuang Hai-Xue, Yin Yue, Zhang Jie-Yu, Wang Zhi, Zhang Qiu-Yue, Wang Jian-Wei
Heilongjiang University of Chinese Medicine, Harbin 150040, China.
Harbin Food and Drug Administration, Harbin 150036, China.
Zhongguo Zhong Yao Za Zhi. 2017 Mar;42(5):970-981. doi: 10.19540/j.cnki.cjcmm.20170121.016.
To evaluate the effect of Tongxie Yaofang on cardiac endogenous metabolism in irritable bowel syndrome(IBS) rats by using metabolomics method, find its potential biomarkers, analyze the metabolic pathways, and explore the pharmacological effects, mechanisms of action and syndrome essence of syndrome model. Forty Wistar rats were used to establish IBS models, and then randomly divided into four groups: model control group and Tongxie Yaofang treatment groups (high, medium, low dose). Another 10 rats were used as normal group. The rats in Tongxie Yaofang-treated(low, medium and high dose) groups were orally administrated with Tongxie Yaofang extracts once a day for 2 weeks, respondingly with the doses of 0.203,0.406,0.812 g•mL⁻¹. The rats in normal group and model control group were given with equal volume of saline once a day for 2 weeks. On the 0 and 15th days, serum was collected and each sample extract was analyzed by UPLC-Q-TOF-MS. Eight potential biomarkers were identified and 8 major metabolic pathways were found to be related with IBS diseases neurotransmitter metabolism, inflammatory immunity, brain function and energy metabolism, etc. Tongxie Yaofang had certain pharmacological effects on IBS, and its mechanism may be related to serotonergic synapse, tryptophan metabolism, cysteine and methionine metabolism, glycerophospholipid metabolism, nicotinate and nicotinamide metabolism and so on, which might be the biological basis of IBS liver-spleen deficiency syndrome.
采用代谢组学方法评价痛泻要方对肠易激综合征(IBS)大鼠心脏内源性代谢的影响,寻找其潜在生物标志物,分析代谢途径,探讨该方对综合征模型的药理作用、作用机制及证候本质。将40只Wistar大鼠用于建立IBS模型,然后随机分为四组:模型对照组和痛泻要方治疗组(高、中、低剂量)。另取10只大鼠作为正常组。痛泻要方治疗(低、中、高剂量)组大鼠每天灌胃给予痛泻要方提取物1次,连续2周,相应剂量分别为0.203、0.406、0.812 g•mL⁻¹。正常组和模型对照组大鼠每天给予等体积生理盐水,连续2周。在第0天和第15天采集血清,各样本提取物采用超高效液相色谱-四极杆飞行时间质谱联用仪进行分析。鉴定出8种潜在生物标志物,发现8条主要代谢途径与IBS疾病的神经递质代谢、炎症免疫、脑功能和能量代谢等有关。痛泻要方对IBS有一定药理作用,其机制可能与5-羟色胺能突触、色氨酸代谢、半胱氨酸和甲硫氨酸代谢、甘油磷脂代谢、烟酸和烟酰胺代谢等有关,这些可能是IBS肝脾虚弱证的生物学基础。