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刺五加中独特的潜在贝壳杉烯二萜——刺五加酸:药理学、分子机制和结构修饰的综述。

Acanthoic acid, unique potential pimaradiene diterpene isolated from Acanthopanax koreanum Nakai (Araliaceae): A review on its pharmacology, molecular mechanism, and structural modification.

机构信息

Key Laboratory of Traditional Chinese Korean Medicine Research (Yanbian University), State Ethnic Affairs Commission, College of Pharmacy, Yanbian University, Yanji, Jilin Province, 133002, China.

Key Laboratory of Traditional Chinese Korean Medicine Research (Yanbian University), State Ethnic Affairs Commission, College of Pharmacy, Yanbian University, Yanji, Jilin Province, 133002, China; Clinical Research Center, Affiliated Hospital of Yanbian University, Yanji, Jilin Province, 133002, China.

出版信息

Phytochemistry. 2022 Aug;200:113247. doi: 10.1016/j.phytochem.2022.113247. Epub 2022 May 18.

DOI:10.1016/j.phytochem.2022.113247
PMID:35597316
Abstract

Acanthoic acid (AA) is a pimaradiene diterpene isolated from the root bark of Acanthopanax koreanum Nakai (Araliaceae) with a wide range of pharmacological activities, including anti-cancer, anti-inflammatory, anti-diabetes, liver protection, gastrointestinal protection, and cardiovascular protection. In addition, AA promotes its pharmacological effects by targeting liver X receptors (LXRs), nuclear factor-kappa B (NF-κB), Toll-Like Receptor 4 (TLR4) and IL-1 receptor-associated kinase (IRAK) signaling pathways, or AMP-activated protein kinase (AMPK) signaling pathway, etc. Also, some studies focus on the structural modification of AA to improve its pharmacological activities. The review summarizes the pharmacological activities, molecular mechanism, and the structural modification of AA, which might supply information for the development of AA in the future.

摘要

刺囊酸(AA)是一种从刺五加根皮(五加科)中分离得到的枞烷二萜,具有广泛的药理活性,包括抗癌、抗炎、抗糖尿病、肝脏保护、胃肠道保护和心血管保护。此外,AA 通过靶向肝 X 受体(LXRs)、核因子-κB(NF-κB)、Toll 样受体 4(TLR4)和白细胞介素 1 受体相关激酶(IRAK)信号通路或 AMP 激活蛋白激酶(AMPK)信号通路等来促进其药理作用等。此外,一些研究还集中在 AA 的结构修饰上,以提高其药理活性。本综述总结了 AA 的药理活性、分子机制和结构修饰,为其未来的开发提供了信息。

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1
Acanthoic acid, unique potential pimaradiene diterpene isolated from Acanthopanax koreanum Nakai (Araliaceae): A review on its pharmacology, molecular mechanism, and structural modification.刺五加中独特的潜在贝壳杉烯二萜——刺五加酸:药理学、分子机制和结构修饰的综述。
Phytochemistry. 2022 Aug;200:113247. doi: 10.1016/j.phytochem.2022.113247. Epub 2022 May 18.
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Acanthoic acid, a diterpene in Acanthopanax koreanum, ameliorates the development of liver fibrosis via LXRs signals.刺五加酸,一种朝鲜刺五加中的二萜类化合物,通过肝X受体信号改善肝纤维化的发展。
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Acanthoic acid modulates lipogenesis in nonalcoholic fatty liver disease via FXR/LXRs-dependent manner.阿坎酸通过 FXR/LXRs 依赖性途径调节非酒精性脂肪性肝病中的脂肪生成。
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Acanthoic acid inhibits IL-8 production via MAPKs and NF-kappaB in a TNF-alpha-stimulated human intestinal epithelial cell line.棘酸通过丝裂原活化蛋白激酶(MAPKs)和核因子κB(NF-κB)抑制肿瘤坏死因子α(TNF-α)刺激的人肠上皮细胞系中白细胞介素8(IL-8)的产生。
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Acanthoic acid inhibits LPS-induced inflammatory response by activating LXRα in human umbilical vein endothelial cells.刺鼠酸通过激活人脐静脉内皮细胞中的肝X受体α(LXRα)来抑制脂多糖(LPS)诱导的炎症反应。
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Acanthoic acid ameliorates lipopolysaccharide-induced acute lung injury.棘酸可改善脂多糖诱导的急性肺损伤。
Eur J Pharmacol. 2015 Mar 5;750:32-8. doi: 10.1016/j.ejphar.2015.01.023. Epub 2015 Jan 23.
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Assessing the Efficacy of Acanthoic Acid Isolated from Nakai in Male Infertility: An In Vivo and In Silico Approach.评估从 Nakai 中分离出的刺酸对男性不育症的疗效:体内和计算机模拟方法。
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Acanthoic acid, a diterpene in Acanthopanax koreanum, protects acetaminophen-induced hepatic toxicity in mice.刺五加中的二萜化合物刺囊酸可保护小鼠的乙酰氨基酚诱导的肝毒性。
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Inhibition of trypsin-induced mast cell activation by acanthoic acid.刺酸对胰蛋白酶诱导的肥大细胞活化的抑制作用。
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Assessing the Efficacy of Acanthoic Acid Isolated from Nakai in Male Infertility: An In Vivo and In Silico Approach.评估从 Nakai 中分离出的刺酸对男性不育症的疗效:体内和计算机模拟方法。
Curr Issues Mol Biol. 2024 Jul 13;46(7):7411-7429. doi: 10.3390/cimb46070440.
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Antimicrobial Activity and Molecular Docking Studies of the Biotransformation of Diterpene Acanthoic Acid Using the Fungus sp.
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