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Kaempferol induces autophagic cell death via IRE1-JNK-CHOP pathway and inhibition of G9a in gastric cancer cells.山奈酚通过 IRE1-JNK-CHOP 通路和抑制胃癌细胞中的 G9a 诱导自噬细胞死亡。
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2
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3
Drug resistance in Plasmodium.疟原虫的耐药性。
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Antiplasmodial activity of Mezoneuron benthamianum leaves and identification of its active constituents.本氏红叶藤叶的抗疟活性及其活性成分的鉴定
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Kaempferol Modulates DNA Methylation and Downregulates DNMT3B in Bladder Cancer.山奈酚调节膀胱癌中的DNA甲基化并下调DNMT3B
Cell Physiol Biochem. 2017;41(4):1325-1335. doi: 10.1159/000464435. Epub 2017 Mar 8.
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Protein aggregation as a cellular response to oxidative stress induced by heme and iron.蛋白质聚集作为细胞对血红素和铁诱导的氧化应激的反应。
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9
Metabolic host responses to malarial infection during the intraerythrocytic developmental cycle.红细胞内发育周期中宿主对疟疾感染的代谢反应。
BMC Syst Biol. 2016 Aug 8;10(1):58. doi: 10.1186/s12918-016-0291-2.
10
Antiplasmodial, antioxidant and immunomodulatory activities of ethanol extract of Vernonia amygdalina del. Leaf in Swiss mice.扁桃斑鸠菊叶乙醇提取物对瑞士小鼠的抗疟原虫、抗氧化及免疫调节活性
Avicenna J Phytomed. 2016 Mar-Apr;6(2):236-47.

山柰酚及其与氯喹联用对小鼠感染的抗疟活性

Antimalarial Activity of Kaempferol and Its Combination with Chloroquine in Infection in Mice.

作者信息

Somsak Voravuth, Damkaew Awatsada, Onrak Pinanong

机构信息

School of Allied Health Sciences, Walailak University, Nakhon Si Thammarat 80161, Thailand.

Research Excellence Center for Innovation and Health Products, Walailak University, Nakhon Si Thammarat 80161, Thailand.

出版信息

J Pathog. 2018 Dec 2;2018:3912090. doi: 10.1155/2018/3912090. eCollection 2018.

DOI:10.1155/2018/3912090
PMID:30631601
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6304481/
Abstract

The search for new antimalarial drugs has become an urgent requirement due to resistance to the available drugs and the lack of an effective vaccine. In this respect, the present study aimed to evaluate the antimalarial activity of kaempferol against infection in mice as an model. Chronic toxicity and antimalarial activities of kaempferol alone and in combination with chloroquine were investigated in ANKA infected ICR mice using standard procedures. The results showed that chronic administration of 2,000 mg/kg of kaempferol resulted in no overt signs of toxicity as well as no hepatotoxicity, nephrotoxicity, or hematotoxicity. Interestingly, kaempferol exerted significant ( < 0.05) chemosuppressive, chemoprophylactic, and curative activities in a dose-dependent manner. The highest antimalarial activity was found at a dose of 20 mg/kg which resulted in a significantly ( < 0.05) prolonged survival of infected mice. Moreover, combination treatment of chloroquine and kaempferol also presented significant ( < 0.05) antimalarial effects, although the effects were not significantly different from the chloroquine treated group. From the results of the present study, it can be concluded that kaempferol possesses acceptable antimalarial activities. However, further investigation should be undertaken on the mechanism responsible for the observed antimalarial activity.

摘要

由于现有药物存在抗药性且缺乏有效的疫苗,寻找新的抗疟药物已成为一项紧迫需求。在这方面,本研究旨在评估山奈酚对小鼠感染作为[具体感染模型名称缺失]模型的抗疟活性。采用标准程序,在感染ANKA的ICR小鼠中研究了单独使用山奈酚以及山奈酚与氯喹联合使用的慢性毒性和抗疟活性。结果表明,以2000mg/kg的剂量长期给予山奈酚未产生明显的毒性迹象,也未出现肝毒性、肾毒性或血液毒性。有趣的是,山奈酚以剂量依赖性方式发挥了显著(P<0.05)的化学抑制、化学预防和治疗活性。在20mg/kg的剂量下发现了最高的抗疟活性,这导致感染小鼠的存活时间显著(P<0.05)延长。此外,氯喹和山奈酚的联合治疗也呈现出显著(P<0.05)的抗疟效果,尽管其效果与氯喹治疗组没有显著差异。从本研究结果可以得出结论,山奈酚具有可接受的抗疟活性。然而,应对观察到的抗疟活性的作用机制进行进一步研究。