首页|雌激素和孕激素诱导的乳腺增生大鼠血清代谢组学研究

雌激素和孕激素诱导的乳腺增生大鼠血清代谢组学研究

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目的:基于液相色谱-质谱联用法(LC-MS)的血清代谢组学探究大鼠乳腺增生的发生机制以及潜在差异代谢物.方法:将12只SPF级8周龄Wistar雌性大鼠随机分为正常组(n=6)和模型组(n=6),模型组给予肌肉注射苯甲酸雌二醇(0.5 mg·kg-1·d-1),连续注射21 d,随后肌肉注射黄体酮(4 mg·kg-1·d-1),连续注射7 d,制备乳腺增生模型.测定大鼠体重和乳头直径,并观察乳腺组织病理形态变化.造模成功后,利用大鼠血清进行LC-MS代谢组学分析,采用主成分分析(PCA)和正交偏最小二乘判别分析法(PLS-DA)筛选正常组与模型组血清中的差异代谢物,并通过京都基因与基因组百科全书(KEGG)开放数据库对差异的标志物进行代谢通路分析.结果:与正常组大鼠相比,模型组大鼠体重无显著变化(P>0.05);乳头直径显著扩大(P<0.01);乳腺HE切片表现出典型的乳腺增生形态,表明造模成功.正常组与模型组血清样本的代谢模式存在显著差异,基于变量投影重要性(VIP)≥2.0和P<0.05的原则鉴定出30个差异代谢物,并且进一步进行ROC分析显示13种差异代谢物的AUC均大于0.9,表明这13种代谢物可能对乳腺增生的诊断具有较高的敏感度.经过KEGG通路富集分析显示,大部分差异代谢物主要富集在醛固酮的合成与分泌、鞘磷脂代谢、花生四烯酸代谢、细胞凋亡和胆固醇代谢等.结论:雌激素和孕激素诱导的乳腺增生大鼠的发病机制可能与改变胆汁酸及其衍生物代谢和脂质代谢途径有关.血清代谢组学鉴定出的13种敏感度较高的差异代谢物,可为乳腺增生疾病的诊断提供参考.
Serum metabolomics of estrogen-and progestogen-induced hyperplasia of mammary glands in rats
AIM:To investigate the mechanism of hyperplasia of mammary gland(HMG)and the potential differential metabolites in rats based on the serum metabolomics assessment by liquid chromatography-mass spectrometry(LC-MS).METHODS:Twelve specific-pathogen-free(SPF)-grade female Wistar rats were randomly and equally as-signed to the normal and model groups.The model group received intramuscular injections of estradiol benzoate(0.5 mg·kg-1·d-1)for 21 d,followed by intramuscular injections of progesterone(4 mg·kg-1·d-1)for 7 d for preparing the HMG model.The body weight and nipple diameter of the rats were measured,and the histopathological changes in their mamma-ry gland were monitored.After the successful establishment of the model,rat serum was collected for LC-MS metabolomics analysis,the differential metabolites in the serum of the normal and model group rats were analyzed by principal compo-nent analysis(PCA)and partial least squares discriminant analysis(PLS-DA),and the metabolic pathway analysis of dif-ferential markers through the Kyoto Encyclopedia of Genes and Genomes(KEGG)open database was performed.RE-SULTS:Compared with the normal rats in the control group,no significant change was observed in the body weight(P>0.05),the diameter of the nipple was significantly enlarged(P<0.01),the hematoxylin-eosin(HE)staining section of the mammary gland displayed typical HMG morphology,which together indicated that the modeling was successful.The metabolic patterns of the serum samples from both groups were significantly different,and 30 potentially differential metab-olites were identified based on the variable importance in projection(VIP)≥2.0 and P<0.05,mainly including 3-dehydro-cholic acid,alcoholic acid,glycocholate-3-sulfate,glycine-deoxycholan-3-sulfate,glycine-deoxycholan-3-sulfate,3a,7b,and 12a trihydroxycholan-3-sulfate,cholic acid,and glycolic acid.Further receiver operating characteristic(ROC)analysis revealed that the area under the curve(AUC)of the 13 metabolites was>0.9,implying the possible high sensitiv-ity for the diagnosis of HMG.According to the KEGG pathway enrichment analysis,most of the differential metabolites were mainly concentrated in aldosterone synthesis and secretion,sphingomyelin metabolism,arachidonic acid metabo-lism,apoptosis and cholesterol metabolism.CONCLUSION:The pathogenesis of estrogen-and progesterone-induced HMG in rats may be related to the altered bile acids,their derivatives metabolism,and the lipid metabolism pathways.The 13 differential metabolites identified by serum metabolomics with high sensitivity may thus provide a reference for the diagnosis of HMG.

hyperplasia of mammary glandpathogenesismetabolomicsbiomarkersmetabolic pathway

马茜茜、明慧、白雪、刘佳、张俊飞

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内蒙古民族大学公共卫生学院,内蒙古 通辽 028000

宁夏医科大学总医院医学实验中心,宁夏 银川 750000

宁夏医科大学总医院急诊科,宁夏 银川 750000

乳腺增生 发病机制 代谢组学 生物标志物 代谢通路

国家自然科学基金青年科学基金资助项目内蒙古自然科学基金资助项目内蒙古民族大学博士科研启动基金资助项目

822051162021BS08014BS619

2024

中国病理生理杂志
中国病理生理学会

中国病理生理杂志

CSTPCD北大核心
影响因子:1.065
ISSN:1000-4718
年,卷(期):2024.40(9)