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一种改良的苏泰焕配方可改善 VCD 诱导的更年期小鼠模型的更年期焦虑、抑郁和心脏肥大。

A Modified Formulation of Sutaehwan Ameliorates Menopausal Anxiety, Depression and Heart Hypertrophy in the VCD-Induced Menopausal Mouse Model.

机构信息

Department of Korean Medicine, Graduate School of Dongguk University.

Department of Neuropsychiatry, Graduate School of Oriental Medicine, Dongguk University.

出版信息

Biol Pharm Bull. 2019;42(9):1471-1481. doi: 10.1248/bpb.b19-00056.

Abstract

Sutaehwan (STH) has been used in Korean medicine for the treatment of abortus habitualis such as fetal restlessness in the uterus. Previously, we reported that a modified formulation of STH, Sutaehwan-Gami, has phytoestrogen-like properties in an ovariectomized menopausal rat model. However, the therapeutic effects of STH and the precise mechanisms by which STH affects various menopausal symptoms remain poorly understood. The current study was designed to explore the effects of a modified form of STH on menopausal anxiety, depression and heart hypertrophy and its mechanisms in 4-vinylcyclohexene diepoxide (VCD)-induced menopausal mouse models. VCD-induced menopausal model mice were fed a modified form of STH, which contained water extract of 3 herbs (called STH_KP17001) at a dose of 100 or 300 mg/kg/d or as a positive control, estradiol at a dose of 0.2 mg/kg/d with standard mouse pellets for 13 weeks. The results show that STH_KP17001 significantly restored the VCD-induced weight reduction of uterine and ovary through the phosphorylation of extracellular signal-regulated kinase (ERK) and protein kinase B (AKT) in the uterus and ovary. Moreover, STH_KP17001 showed slight proliferative effects and estrogen receptor α phosphorylation in MCF-7 cells. Treatment with STH_KP17001 reversed VCD-induced anxiety and depression through AMP-activated protein kinase (AMPK) activation and brain-derived neurotrophic factor (BDNF) expression in the cerebral cortex, while improving heart hypertrophy through inactivation of inhibitor of kappaB α (IκBα) in the heart. The results indicate that STH_KP17001 improves menopause-induced anxiety, depression and heart hypertrophy, implying its protective role for the management of menopausal symptoms.

摘要

苏泰焕(STH)在韩国医学中被用于治疗习惯性流产等胎儿不安于子宫的病症。此前,我们报道了一种苏泰焕的改良配方,即苏泰焕-加米,在去卵巢绝经大鼠模型中具有植物雌激素样特性。然而,苏泰焕的治疗效果以及它影响各种绝经症状的确切机制仍知之甚少。本研究旨在探讨改良形式的苏泰焕对 4-乙烯环己烯二氧化物(VCD)诱导的绝经小鼠模型中绝经焦虑、抑郁和心脏肥大的影响及其机制。VCD 诱导的绝经模型小鼠用改良形式的苏泰焕(包含 3 种草药的水提取物,称为 STH_KP17001)喂养,剂量为 100 或 300mg/kg/d,或作为阳性对照,用 0.2mg/kg/d 的雌二醇和标准小鼠颗粒喂养 13 周。结果表明,STH_KP17001 通过子宫和卵巢中细胞外信号调节激酶(ERK)和蛋白激酶 B(AKT)的磷酸化,显著恢复了 VCD 诱导的子宫和卵巢重量减轻。此外,STH_KP17001 在 MCF-7 细胞中表现出轻微的增殖作用和雌激素受体α磷酸化。用 STH_KP17001 治疗可通过大脑皮质中 AMP 激活蛋白激酶(AMPK)的激活和脑源性神经营养因子(BDNF)的表达,逆转 VCD 诱导的焦虑和抑郁,同时通过心脏中抑制κBα(IκBα)的失活改善心脏肥大。结果表明,STH_KP17001 改善了绝经引起的焦虑、抑郁和心脏肥大,表明其对管理绝经症状具有保护作用。

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