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基于靶向代谢组学研究黄柏与知母药对治疗良性前列腺增生的配伍效应

Compatibility effects of herb pair Phellodendri chinensis cortex and Anemarrhenae rhizoma on benign prostatic hyperplasia using targeted metabolomics.

作者信息

Zhao Xiaoning, Li Yiran, Huai Jiaxin, Cheng Congcong, Zhang Teng, Xie Linlin, Wang Siqi, Zhang Meng, Dai Ronghua

机构信息

Shenyang Pharmaceutical University, School of Pharmacy, Shenyang, China.

出版信息

Biomed Chromatogr. 2018 Oct;32(10):e4296. doi: 10.1002/bmc.4296. Epub 2018 Jun 28.

DOI:10.1002/bmc.4296
PMID:29808482
Abstract

Phellodendri chinensis cortex (P. C. cortex) and Anemarrhenae rhizoma (A. rhizoma) herb pair is a core component of traditional Chinese medicines used to treat inflammation and benign prostatic hyperplasia (BPH). The present study was designed to profile the arachidonic acid (AA) metabolomic characteristics in rat plasma and prostate after being treated with P. C. cortex and A. rhizoma as well as their combination. Plasma and prostate samples from sham group, BPH model group, herb pair group and two single herb groups were collected on days 7, 14, 21 and 28. Then, a systemic metabolomic analysis based on UFLC-MS/MS was employed to quantify AA and its cyclooxygenase and lipoxygenase pathway metabolites (15-HETE, 12-HETE, 5-HETE, AA, PGI , PGF , 8-HETE, PGD , PGE and LTB ). The results demonstrated that BPH led a significant increase of 10 biomarkers in plasma and tissue (p < 0.05). The clusters of herb pair group and single herb groups showed a tendency to return to the initial space, and the AA and its metabolites from those groups were differently downregulated to a healthier level, with the combination of single herbs most obvious. The present study demonstrated that P. C. cortex-A. rhizoma herb pair might produce synergistic or complementary compatibility effects on suppressing inflammatory processes occurring in BPH.

摘要

黄柏(P. C. cortex)与知母(A. rhizoma)药对是用于治疗炎症和良性前列腺增生(BPH)的传统中药的核心成分。本研究旨在剖析大鼠血浆和前列腺在接受黄柏、知母及其组合处理后的花生四烯酸(AA)代谢组学特征。在第7、14、21和28天收集假手术组、BPH模型组、药对组和两个单味药组的血浆和前列腺样本。然后,采用基于超高效液相色谱-串联质谱(UFLC-MS/MS)的系统代谢组学分析来定量AA及其环氧化酶和脂氧合酶途径代谢物(15-羟基二十碳四烯酸、12-羟基二十碳四烯酸、5-羟基二十碳四烯酸、AA、前列环素、前列腺素F、8-羟基二十碳四烯酸、前列腺素D、前列腺素E和白三烯B)。结果表明,BPH导致血浆和组织中10种生物标志物显著增加(p < 0.05)。药对组和单味药组的聚类显示出回到初始状态的趋势,且这些组中的AA及其代谢物不同程度地下调至更健康水平,单味药组合最为明显。本研究表明,黄柏-知母药对在抑制BPH中发生的炎症过程方面可能产生协同或互补的配伍效应。

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