1. 广西中医药大学第一附属医院
2. 广西中医药大学
纸质出版:2016
移动端阅览
[1]孙平良,耿曙光,袁代解,杨光,付军,黄艳,文亦磊,肖振球.安肠汤对溃疡性结肠炎大鼠肠黏膜组织中内源性代谢物的影响[J].中医杂志,2016,57(19):1678-1683.
SUN Pingliang, GENG Shuguang, YUAN Daijie, et al. Impact of Anchang Decoction (安肠汤) on Endogenous Metabolites in Intestinal Mucosa Tissue of Ulcerative Colitis Rats[J]. Journal of Traditional Chinese Medicine2016, 57(19): 1678-1683.
[1]孙平良,耿曙光,袁代解,杨光,付军,黄艳,文亦磊,肖振球.安肠汤对溃疡性结肠炎大鼠肠黏膜组织中内源性代谢物的影响[J].中医杂志,2016,57(19):1678-1683. DOI: 10.13288/j.11-2166/r.2016.19.015.
SUN Pingliang, GENG Shuguang, YUAN Daijie, et al. Impact of Anchang Decoction (安肠汤) on Endogenous Metabolites in Intestinal Mucosa Tissue of Ulcerative Colitis Rats[J]. Journal of Traditional Chinese Medicine2016, 57(19): 1678-1683. DOI: 10.13288/j.11-2166/r.2016.19.015.
目的应用代谢组学方法探讨安肠汤治疗溃疡性结肠炎的可能作用机制。方法将76只Wistar大鼠随机分为空白组(4只)、模型组、丽珠肠乐组、美沙拉嗪组和安肠汤低、中、高剂量组各12只。除空白组外其余各组大鼠肛门注入246-三硝基苯磺酸液(90 mg/kg)建立溃疡性结肠炎大鼠模型。空白组和模型组大鼠每只均以生理盐水3 ml灌胃
丽珠肠乐组给予丽珠肠乐溶液0.5亿活菌/ml灌胃
每次0.12 ml
美沙拉嗪组给予美沙拉嗪混悬液5 mg/ml灌胃
每次0.35 ml
安肠汤低、中、高剂量组分别给予安肠汤浓缩液1、5、10 ml/(kg·d)灌胃
各组每次灌胃均为药液+生理盐水共3 ml。每日1次
共15天。于5、10、15天3个时间点对大鼠结肠黏膜组织进行气相色谱-质谱联用(GC-MS)技术的代谢组学方法检测
对采集数据进行多元统计分析(PCA
PLS-DA
OPLS-DA)
采用t检验并结合OPLS-DA模型第一主成分的VIP值来寻找差异性表达代谢物并对其相对含量及代谢途径进行分析。结果将得到的色谱图与质谱库进行匹配鉴定
最终得到准确定性的化合物48个。多元统计分析后得到的得分图显示模型组和空白组大鼠结肠组织的代谢表型有明显差异
样本点完全分离
且显示第10天时差异最大;安肠汤各剂量组相比丽珠肠乐组、美沙拉嗪组
与空白组差异较小
且安肠汤中剂量组比安肠汤低、高剂量组差异小。分析后最终得到11个潜在代谢标志物
分别为尿苷、牛磺酸、甘氨酸、苏氨酸、乳酸、β-丙氨酸、肌氨酸、甘露糖、木糖、葡萄糖、蔗果三糖。相对模型组
安肠汤各剂量组11种代谢物均显示表达回调(P<0.05)
且安肠汤中剂量组的回调幅度最优。结论安肠汤对11种代谢物的调节作用可能是其治疗溃疡性结肠炎的途径和机制。
Objective To explore the possible mechanism of Anchang Decoction treating ulcerative colitis( UC)adopting the method of metabolism. Methods Seventy-six Wistar rats were randomized into the blank group( n =4)
the model group( n = 12)
the Lizhu Changle( 丽珠肠乐) group( n = 12)
the mesalazine group
the low
medium and high dose Anchang Decoction groups( n = 12 in each group). Rats in other groups were given anal injection of 2 4 6-three nitrobenzene sulfonic acid solution( 90 mg / kg) to establish UC rat models except the blank group.Rats in the blank group and the model group were given normal saline 3 ml by gavage. The Lizhu Changle group was given Lizhu Changle solution 50 million viable organism / ml by gavage
0. 12 ml each time. The mesalazine group was given mesalazine suspension 5 mg / ml by gavage
0. 35 ml each time. The low
medium and high dose Anchang Decoction groups were respectively given Anchang Decoction concentrate 1
5 and 10 ml /( kg· d) by gavage. Rats in each group were given 3 ml of liquid medicine and normal saline by gavage
once every day. For 15 days. On the 5 th
10 th and 15 th day
rats’ colonic mucosa tissues were examined by the method of metabolism which adopted gas chromatography / mass spectrometry( GC-MS) technology. The data collected were made multivariate statistical analysis
including principal component analysis( PCA)
ciscriminant analysis by partial least squares( PLS-DA) and orthogonal partial least squares discriminant analysis( OPLS-DA). T-test combined with VIP value of OPLS-DA model first principal component were adopted to find the differentially expressed metabolites and to analyze its relative amount and the metabolic pathway. Results The obtained chromatogram map and the mass spectra database were made matching identification. At last
48 accurately characterized compounds were got. After multivariate statistical analysis
score plot showed that the difference of colonic tissue metabolic phenotype of rats in the model group and the blank group was significant. Sample points showed complete separation. The most significant difference was on the 10 th day. Compared with the Lizhu Changle group and the mesalazine group
the difference between the Anchang Decoction groups and the blank group was not significant. The difference in the medium dose Anchang Decoction group was less significant than in the low and high dose Anchang Decoction groups. After analysis
11 potential metabolic markers were found at last
which were uridine
ethylamine sulfonic acid
glycocoll
threonine
lactic acid
β-alanine
methyl glycosine
seminose
xylopyranose
glucose and kestose. Compared with the model group
11 metabolin in the Anchang Decoction groups all showed expression callback( P < 0. 05). The callback range in the medium dose Anchang Decoction group was the best. Conclusion The regulating effect of Anchang Decoction on 11 metabolin might be the pathway and mechanism to treat UC.
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