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首页> 外文期刊>Evidence-based complementary and alternative medicine: eCAM >Potential Mechanisms of an Antiadenomyosis Chinese Herbal Formula Shaoyao-Gancao Decoction in Primary Cell Culture Model
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Potential Mechanisms of an Antiadenomyosis Chinese Herbal Formula Shaoyao-Gancao Decoction in Primary Cell Culture Model

机译:中草原中草原芍药型芍药 - 芍药汤中原发性细胞培养模型的潜在机制

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摘要

Background. Shaoyao-Gancao Decoction (SGD), a well-known traditional Chinese medicine prescription, has been widely used to treat adenomyosis, dysmenorrhea, abdominal pain, and inflammation in Asia. However, the mechanism underlying the effectiveness of SGD in the treatment of adenomyosis still remains elusive. The present study aimed to investigate the bioactivity of SGD and its underlying molecular mechanisms using cultured human adenomyosis-derived cells. Methods. Human adenomyosis-derived cells were treated with SGD and its major constituents (paeoniflorin and liquiritin) in vitro. Effects of SGD, paeoniflorin, and liquiritin on cell proliferation and apoptosis were examined by MTT assay and flow cytometry analyses. The effects of SGD, paeoniflorin, and liquiritin on the production of PGE_2 and PGF_2a were assayed using ELISA. ER-alpha and OTR mRNA expression levels were also evaluated by real-time qRT-PCR. Results. SGD, paeoniflorin, and liquiritin inhibited proliferation and induced apoptosis of human adenomyosis-derived cells in a dose-dependent manner. SGD and paeoniflorin significantly reduced the PGE_2 and PGF_2alpha production. Furthermore, they remarkably decreased the mRNA levels of ER-? and OTR. Conclusions. The results of this study provide possible mechanisms for the bioactivity of SGD for treating adenomyosis and contribute to the ethnopharmacological knowledge about this prescription.
机译:背景。邵涛 - 甘达汤(SGD)是一种着名的中医处方,已被广泛用于治疗腺弥抑,痛经,腹痛和亚洲炎症。然而,在治疗腺小症治疗中,SGD的有效性的机制仍然难以捉摸。本研究旨在研究SGD的生物活性及其使用培养的人腺细胞腺细胞症衍生细胞的潜在分子机制。方法。用SGD及其主要成分(PaeOniflorin和Liquiritin)在体外处理人腺细胞症衍生的细胞。 SGD,PaeOniflorin和Liyiritin对细胞增殖和细胞凋亡的影响和流式细胞术分析。使用ELISA测定SGD,PaeOniflorin和Liquiritin对PGE_2和PGF_2A的产生的影响。通过实时QRT-PCR评估ER-α和OTR mRNA表达水平。结果。 SGD,PaeOniflorin和Lialiritin以剂量依赖性方式抑制了人腺胚胎衍生细胞的增殖和诱导的凋亡。 SGD和PaeOniflorin显着降低了PGE_2和PGF_2Alpha生产。此外,它们显着降低了er-的mR-?和otr。结论。该研究的结果为治疗腺型症的生物活性提供了可能的机制,并有助于对该处方的民族医药知识。

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