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Biologically active withanolides from <i>Physalis peruviana</i>.

Physalis peruviana由来の生理活性ウィタノリド (機械翻訳の邦題)

Pharmaceutical biology2025Sang-Ngern M, Fukuchi A, Kondratyuk TP, et al.
研究デザインその他の原著論文
対象動物

記録の確認項目

研究デザイン
その他の原著論文
対象
動物
出版年
2025
出典
doi.org
抄録の表示
表示あり
出版状態
有効な記録
状態確認日
2026/08/17
収集日
2026/08/03
鮮度
確認期限内
確認段階
自動処理
記録状態
公開

日本語要約(機械生成)

Physalis peruviana(ポハ)の伝統的がん治療への利用に着目し、その化学成分と薬理活性を検討した。新鮮果実と地上部から抽出し、果実から新規ウィタノリド(physaperuvin K)を、地上部から希少な塩素化ウィタノリドを含む7種のウィタノリドを単離した。NMRやX線回折で構造決定し、酢酸誘導体も調製した。抗炎症活性評価では、化合物1、2、3がTNF-α誘導NF-κB活性をIC50 10、60、40 nMで阻害し、細胞毒性は50 μMで認められなかった。また、これらはNO産生もIC50 0.32〜13.3 μMで抑制した。アセチル化は活性に大きな影響を与えなかったが、化合物4ではNF-κBとNOアッセイのIC50がそれぞれ11.0から0.33 μM、1.8から0.24 μMに低下した。最も活性の高いphysaperuvin Kは食用果実に含まれることが判明した。

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抄録

Context: Physalis peruviana L. (Solanaceae), also known as Poha, has been used in traditional medicine since pre-Columbian times, particularly in treating cancer.Objective: To study the chemical composition and potential medicinal properties of Poha.Materials and methods: The fresh fruits and aerial parts of Poha were extracted. The isolation of extract yields a novel withanolide (physaperuvin K; 1) from the edible fruit, and seven withanolides (2-8), including a rare chlorinated withanolide (physalolactone; 2) from the aerial parts. Structure elucidation/determination was performed, some acetate derivatives were prepared (2a-6a), and the compounds were evaluated with in vitro assays indicative of anti-inflammatory activity.Results: The structure of 1 was elucidated through NMR spectroscopic analyses. The absolute configuration of compound 2 was determined using single-crystal X-ray diffraction. Compounds 1, 2, and 3 exhibited inhibition of tumor necrosis factor-α-induced nuclear factor-kappa B (NF-κB) activity with IC50 values of 10, 60, and 40 nM, respectively, without causing cytotoxicity at a concentration of 50 μM. Furthermore, compounds 1-3 reduced nitric oxide (NO) production in lipopolysaccharide-activated RAW 264.7 mouse macrophage cells with IC50 values ranging from 0.32 to 13.3 μM without overt cytotoxicity. Overall, acetylation did not significantly impact activity, except for compound 4, wherein the IC50 values in the NF-κB and NO assays were reduced from 11.0 to 0.33 μM, and 1.8 to 0.24 μM, respectively.Conclusions: These findings enhance our understanding of Poha's constituents and potential medicinal properties. One of the most bioactive compounds identified in this study, physaperuvin K, is found in edible fruit.

MeSH

AnimalsAnti-Inflammatory AgentsDose-Response Relationship, DrugFruitMacrophagesMiceNF-kappa BNitric OxidePhysalisPlant Components, AerialPlant ExtractsRAW 264.7 CellsTumor Necrosis Factor-alphaWithanolides

DOI 10.1080/13880209.2025.2488136

PMID 40285658

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