Xu Weifan, Jiang Tao, Ding Luying, Jiang Yiping, Zhang Lichao, Xia Tianshuang, Xin Hailiang
Department of Pharmacy, Fujian University of Traditional Chinese Medicine, Fuzhou, 350122, Fujian, China.
Department of Pharmacognosy, School of Pharmacy, Naval Medical University, Shanghai, 200433, China.
J Nat Med. 2024 Jun;78(3):488-504. doi: 10.1007/s11418-024-01779-1. Epub 2024 Mar 26.
Osteoporosis (OP) is closely related to iron overload. Bajitianwan (BJTW) is a traditional Chinese medicine formulation used for treating senile diseases such as dementia and osteoporosis. Modern pharmacological researches have found that BJTW has beneficial effect on bone loss and memory impairment in aging rats. This paper aimed to explore the role and mechanism of BJTW in ameliorating iron overload-induced bone loss. Furthermore, BJTW effectively improved the bone micro-structure of the femur in mice, and altered bone metabolism biomarkers alkaline phosphatase (ALP) and osteocalcin (OCN) in serum, as well as oxidative indexes superoxide dismutase (SOD), catalase (CAT), glutathione reductase (GR) glutathione (GSH) and malondialdehyde (MDA) in liver. As for network pharmacology, 73 components collected from BJTW regulated 99 common targets merged in the BJTW and OP. The results of RNA-seq indicated that there were 418 potential targets in BJTW low dose group (BJTW-L) and 347 potential targets in BJTW high dose group (BJTW-H). Intriguingly, both PI3K-AKT signaling pathway and the AGEs-RAGE signaling pathway were contained in the KEGG pathways enrichment results of network pharmacology and transcriptomics, which were considered as the potential mechanism. Additionally, we verified that BJTW regulated the expression of related proteins in RAGE/PI3K-AKT pathways in MC3T3-E1 cells. In summary, BJTW has potent effect on protecting against iron overload-induced OP, and its mechanism may be related to the activation of the RAGE/PI3K-AKT signaling pathways.
骨质疏松症(OP)与铁过载密切相关。八味添髓丸(BJTW)是一种用于治疗痴呆和骨质疏松症等老年疾病的中药制剂。现代药理学研究发现,BJTW对衰老大鼠的骨质流失和记忆障碍具有有益作用。本文旨在探讨BJTW在改善铁过载诱导的骨质流失中的作用及机制。此外,BJTW有效改善了小鼠股骨的骨微结构,并改变了血清中骨代谢生物标志物碱性磷酸酶(ALP)和骨钙素(OCN),以及肝脏中的氧化指标超氧化物歧化酶(SOD)、过氧化氢酶(CAT)、谷胱甘肽还原酶(GR)、谷胱甘肽(GSH)和丙二醛(MDA)。在网络药理学方面,从BJTW中收集的73种成分调节了BJTW和OP中合并的99个共同靶点。RNA测序结果表明,BJTW低剂量组(BJTW-L)有418个潜在靶点,BJTW高剂量组(BJTW-H)有347个潜在靶点。有趣的是,PI3K-AKT信号通路和AGEs-RAGE信号通路都包含在网络药理学和转录组学的KEGG通路富集结果中,这被认为是潜在机制。此外,我们验证了BJTW调节MC3T3-E1细胞中RAGE/PI3K-AKT通路相关蛋白的表达。综上所述,BJTW对预防铁过载诱导的OP具有显著作用,其机制可能与激活RAGE/PI3K-AKT信号通路有关。