Division of Herbal Drugs and Natural Products, National Research Institute of Chinese Medicine, Taipei, Taiwan, ROC.
J Ethnopharmacol. 2011 Sep 1;137(1):592-600. doi: 10.1016/j.jep.2011.06.007. Epub 2011 Jun 16.
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.
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.
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.
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.
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.
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。
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。
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。
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。
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。