Graduate School of Biotechnology, College of Life Sciences, Kyung Hee University, Yongin-si 17104, Gyeonggi-do, Republic of Korea.
Hanbangbio Inc., Yongin-si 17104, Gyeonggi-do, Republic of Korea.
Int J Mol Sci. 2024 Jun 30;25(13):7247. doi: 10.3390/ijms25137247.
Postmenopausal osteoporosis, characterized by an imbalance between osteoclast-mediated bone resorption and osteoblast-driven bone formation, presents substantial health implications. In this study, we investigated the role of black goat extract (BGE), derived from a domesticated native Korean goat, estrogen-like activity, and osteoprotective effects in vitro. BGE's mineral and fatty acid compositions were analyzed via the ICP-AES method and gas chromatography-mass spectrometry, respectively. In vitro experiments were conducted using MCF-7 breast cancer cells, MC3T3-E1 osteoblasts, and RAW264.7 osteoclasts. BGE exhibits a favorable amount of mineral and fatty acid content. It displayed antimenopausal activity by stimulating MCF-7 cell proliferation and augmenting estrogen-related gene expression (ERα, , and ). Moreover, BGE positively impacted osteogenesis and mineralization in MC3T3-E1 cells through Wnt/β-catenin pathway modulation, leading to heightened expression of Runt-related transcription factor 2, osteoprotegerin, and collagen type 1. Significantly, BGE effectively suppressed osteoclastogenesis by curtailing osteoclast formation and activity in RAW264.7 cells, concurrently downregulating pivotal signaling molecules, including receptor activator of nuclear factor κ B and tumor necrosis factor receptor-associated factor 6. This study offers a shred of preliminary evidence for the prospective use of BGE as an effective postmenopausal osteoporosis treatment.
绝经后骨质疏松症的特征是破骨细胞介导的骨吸收和成骨细胞驱动的骨形成之间的失衡,对健康有重大影响。在这项研究中,我们研究了黑山羊提取物(BGE)的作用,该提取物源自一种国内的韩国山羊,具有雌激素样活性和体外护骨作用。通过电感耦合等离子体原子发射光谱法(ICP-AES)和气相色谱-质谱法分别分析了 BGE 的矿物质和脂肪酸组成。使用 MCF-7 乳腺癌细胞、MC3T3-E1 成骨细胞和 RAW264.7 破骨细胞进行了体外实验。BGE 表现出良好的矿物质和脂肪酸含量。它通过刺激 MCF-7 细胞增殖和增加雌激素相关基因表达(ERα、β和 GPER)来表现出抗绝经活性。此外,BGE 通过调节 Wnt/β-catenin 通路对 MC3T3-E1 细胞的成骨和矿化产生积极影响,导致 Runt 相关转录因子 2、骨保护素和胶原类型 1 的表达增加。值得注意的是,BGE 通过抑制 RAW264.7 细胞中的破骨细胞形成和活性有效抑制破骨细胞生成,同时下调关键信号分子,包括核因子κ B 受体激活物和肿瘤坏死因子受体相关因子 6。这项研究为 BGE 作为一种有效的绝经后骨质疏松症治疗方法的潜在用途提供了初步证据。