Suppr超能文献

从丹皮中胰岛素模拟新型抑制物对 PEPCK 基因转录的药理学评价。

Pharmacological evaluation of insulin mimetic novel suppressors of PEPCK gene transcription from Paeoniae Rubra Radix.

机构信息

Division of Herbal Drugs and Natural Products, National Research Institute of Chinese Medicine, Taipei, Taiwan, ROC.

出版信息

J Ethnopharmacol. 2011 Sep 1;137(1):592-600. doi: 10.1016/j.jep.2011.06.007. Epub 2011 Jun 16.

Abstract

ETHNOPHARMACOLOGICAL RELEVANCE

Paeoniae Rubra Radix (root of Paeonia lactiflora) has been frequently employed in Traditional Chinese Medicine (TCM) as and anti-diabetic therapy to enhance blood circulation and dissipate stasis.

AIM OF THE STUDY

Previously, we identified a novel hypoglycemic action of a crude extract from Paeoniae Rubra Radix, which also suppressed phosphoenolpyruvate carboxykinase (PEPCK) gene transcription. Therefore, the current investigation intended to elucidate potential active bio-constituents of this herb and mechanisms of action.

MATERIALS AND METHODS

Glucocorticoid receptor (GR) nuclear localization, the PEPCK messenger (m)RNA level, pregnane X receptor (PXR) mRNA expression, cAMP-responsive element-binding protein (CREB) serine phosphorylation and DNA binding were evaluated in dexamethasone (Dex) and 8-bromo-cAMP (CA)-stimulated H4IIE cells, while efficacy of agents was assessed in a stable cell line containing a green fluorescent protein (GFP) reporter driven by the PEPCK promoter. HPLC profiling, colorimetric assays, and NMR analysis were employed for chemical characterization purpose.

RESULTS

An extract of Paeoniae Rubra Radix lacking the insulin mimetic compound, 1,2,3,4,6-penta-O-galloyl-beta-d-glucose (PGG), and termed the non-PGG fraction (NPF), consisting of tannin polymers, suppressed PEPCK expression in the presence of an insulin receptor antagonist (HNMPA-AM(3)), suggesting the action of this fraction is independent of the insulin receptor. Furthermore, Dex-stimulated GR nuclear localization and transactivation were prevented by the NPF. Similarly, CA-stimulated CREB serine phosphorylation and DNA binding were also inhibited by the NPF in H4IIE cells. Hence NPF antagonizes both signaling pathways that induce PEPCK gene transcription.

CONCLUSION

In conclusion, the current study proposes that the potent suppressive activity on PEPCK gene transcription observed with Paeoniae Rubra Radix extract, can be attributed to at least two distinct components, namely PGG and NPF.

摘要

民族药理学相关性

白芍(芍药的根)在中药(TCM)中常被用作抗糖尿病疗法,以促进血液循环和消散淤血。

研究目的

之前,我们发现白芍粗提取物具有新的降血糖作用,还能抑制磷酸烯醇丙酮酸羧激酶(PEPCK)基因转录。因此,本研究旨在阐明该草药的潜在活性生物成分及其作用机制。

材料和方法

在地塞米松(Dex)和 8-溴-cAMP(CA)刺激的 H4IIE 细胞中评估糖皮质激素受体(GR)核定位、PEPCK 信使(m)RNA 水平、妊娠相关蛋白 X 受体(PXR)mRNA 表达、环磷酸腺苷反应元件结合蛋白(CREB)丝氨酸磷酸化和 DNA 结合,同时在含有 GFP 报告基因的稳定细胞系中评估药物的功效。采用 HPLC 分析、比色法和 NMR 分析进行化学表征。

结果

白芍提取物中不含胰岛素模拟化合物 1,2,3,4,6-五-O-没食子酰基-β-D-葡萄糖(PGG),称为非 PGG 部分(NPF),由单宁聚合物组成,在胰岛素受体拮抗剂(HNMPA-AM(3))存在的情况下抑制 PEPCK 表达,表明该部分的作用独立于胰岛素受体。此外,NPF 还可防止 Dex 刺激的 GR 核定位和反式激活。同样,NPF 也可抑制 H4IIE 细胞中 CA 刺激的 CREB 丝氨酸磷酸化和 DNA 结合。因此,NPF 拮抗两种诱导 PEPCK 基因转录的信号通路。

结论

总之,本研究表明,白芍提取物对 PEPCK 基因转录的强烈抑制活性可归因于至少两种不同的成分,即 PGG 和 NPF。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验