加味逍遥汤镇痛作用的分子机制研究:一项网络药理学研究
An Investigation of the Molecular Mechanisms Underlying the Analgesic Effect of Jakyak-Gamcho Decoction: A Network Pharmacology Study.
作者信息
Lee Ho-Sung, Lee In-Hee, Kang Kyungrae, Park Sang-In, Kwon Tae-Wook, Lee Dae-Yeon
机构信息
The Fore, 87 Ogeum-ro, Songpa-gu, Seoul 05542, Republic of Korea.
Forest Hospital, 129 Ogeum-ro, Songpa-gu, Seoul 05549, Republic of Korea.
出版信息
Evid Based Complement Alternat Med. 2020 Dec 1;2020:6628641. doi: 10.1155/2020/6628641. eCollection 2020.
Herbal drugs have drawn substantial interest as effective analgesic agents; however, their therapeutic mechanisms remain to be fully understood. To address this question, we performed a network pharmacology study to explore the system-level mechanisms that underlie the analgesic activity of Jakyak-Gamcho decoction (JGd; Shaoyao-Gancao-Tang in Chinese and Shakuyaku-Kanzo-To in Japanese), an herbal prescription consisting of Pallas and Fischer. Based on comprehensive information regarding the pharmacological and chemical properties of the herbal constituents of JGd, we identified 57 active chemical compounds and their 70 pain-associated targets. The JGd targets were determined to be involved in the regulation of diverse biological activities as follows: calcium- and cytokine-mediated signalings, calcium ion concentration and homeostasis, cellular behaviors of muscle and neuronal cells, inflammatory response, and response to chemical, cytokine, drug, and oxidative stress. The targets were further enriched in various pain-associated signalings, including the PI3K-Akt, estrogen, ErbB, neurotrophin, neuroactive ligand-receptor interaction, HIF-1, serotonergic synapse, JAK-STAT, and cAMP pathways. Thus, these data provide a systematic basis to understand the molecular mechanisms underlying the analgesic activity of herbal drugs.
草药作为有效的镇痛剂已引起了广泛关注;然而,其治疗机制仍有待充分了解。为了解决这个问题,我们进行了一项网络药理学研究,以探索芍药甘草汤(JGd;中文为芍药甘草汤,日文为芍药甘草汤)镇痛活性背后的系统水平机制,该草药方剂由芍药和甘草组成。基于有关JGd草药成分的药理和化学性质的全面信息,我们鉴定出57种活性化合物及其70个与疼痛相关的靶点。JGd靶点被确定参与多种生物活性的调节,如下所示:钙和细胞因子介导的信号传导、钙离子浓度和稳态、肌肉和神经元细胞的细胞行为、炎症反应以及对化学、细胞因子、药物和氧化应激的反应。这些靶点进一步富集于各种与疼痛相关的信号传导中,包括PI3K-Akt、雌激素、ErbB、神经营养因子、神经活性配体-受体相互作用、HIF-1、5-羟色胺能突触、JAK-STAT和cAMP途径。因此,这些数据为理解草药镇痛活性的分子机制提供了系统依据。
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