Department of Pharmacology, School of Life Science and Biopharmaceutics, Shenyang Pharmaceutical University, Shenyang 110016, China.
Key Laboratory for TCM Material Basis Study and Innovative Drug Development of Shenyang City, School of Traditional Chinese Materia Medica, Shenyang Pharmaceutical University, Shenyang 110016, China.
Fitoterapia. 2023 Jun;167:105497. doi: 10.1016/j.fitote.2023.105497. Epub 2023 Apr 3.
As the incidence of Alzheimer's disease (AD) continues to rise in recent years, there are few therapeutic drugs for AD treatment with limited efficacy. AD occurs twice as often in women as that in men, partially due to the low estrogen level in women after menopause. Phytoestrogens (PEs), similar to endogenous estrogens in chemical structure with neuroprotection and fewer side effects, have good development and application prospects in AD-treatment. Loureirin C is an active ingredient isolated from Chinese Dragon's Blood (CDB) with a similar structure to 17β-E2. In our study, we found that loureirin C targeted to ERα and had partial-agonistic activity using molecular docking prediction and dual-luciferase reporter assay. However, it is still unclear whether loureirin C has estrogenic effects in body, and whether exerts anti-AD effect through ERα. In this paper, the ERα selective inhibitor MPP or ERα specific small interfering RNA (siERα) mediated gene silencing technology were used. Besides,E-SCREEN method were used to evaluate the estrogen effects of loureirin C in vivo and in vitro. MTT assay, Western blot, real-time PCR technology and behaver tests was used to investigate the neuroprotective effect, cognitive function and the underlying mechanism. We found that loureirin C possessed estrogenic activity, had neuroprotective effects in AD cells and improved cognitive impairment in AD mice via ERα. Loureirin C may be a potential candidate for AD.
近年来,阿尔茨海默病(AD)的发病率不断上升,而治疗 AD 的疗效有限的治疗药物却寥寥无几。女性患 AD 的几率是男性的两倍,部分原因是女性绝经后雌激素水平较低。植物雌激素(PEs)在化学结构上与内源性雌激素相似,具有神经保护作用且副作用较少,在 AD 治疗方面具有良好的开发和应用前景。龙血素 C 是从中国龙血竭(CDB)中分离出来的一种具有类似 17β-E2 结构的活性成分。在我们的研究中,我们发现龙血素 C 靶向 ERα,通过分子对接预测和双荧光素酶报告基因检测具有部分激动活性。然而,目前尚不清楚龙血素 C 在体内是否具有雌激素作用,以及是否通过 ERα 发挥抗 AD 作用。在本文中,我们使用了 ERα 选择性抑制剂 MPP 或 ERα 特异性小干扰 RNA(siERα)介导的基因沉默技术。此外,我们还使用了 E-SCREEN 方法来评估龙血素 C 在体内和体外的雌激素作用。MTT 检测、Western blot、实时 PCR 技术和行为学测试用于研究其神经保护作用、认知功能和潜在机制。我们发现龙血素 C 具有雌激素活性,通过 ERα 对 AD 细胞具有神经保护作用,并改善 AD 小鼠的认知障碍。龙血素 C 可能是 AD 的潜在候选药物。