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聚焦于双重严重结核病治疗方法,研究从 Vernonia cinerea (L.) Less. 中提取的部分和物质的抗分枝杆菌和抗炎活性。

Antimycobacterial and anti-inflammatory activities of fractions and substances from Erythrina verna Vell focusing on dual severe TB treatment approach.

机构信息

Universidade Estadual do Norte Fluminense Darcy Ribeiro, Laboratório de Biologia do Reconhecer, Centro de Biociências e Biotecnologia, Av. Alberto Lamego, 2000, Parque Califórnia, 28013-602 Campos dos Goytacazes, RJ, Brazil.

Universidade Federal do Rio de Janeiro, Laboratório de Produtos Bioativos, Campus Macaé, Av. Aluizio da Silva Gomes, 50, Novo Cavaleiros, 27930-560 Macaé, RJ, Brazil.

出版信息

An Acad Bras Cienc. 2022 Oct 7;94(3):e20211032. doi: 10.1590/0001-3765202220211032. eCollection 2022.

Abstract

Tuberculosis remains a major health problem worldwide. Drug-resistant and hypervirulent Mycobacterium tuberculosis (Mtb) strains can lead to a hyperinflammatory response and necrotic pathology in hyper-reactive individuals that require adjunctive treatment. Plant-derived substances have been investigated for TB treatment, among which flavonoids stand out. We evaluate the anti-Mtb, anti-inflammatory and cytotoxicity activities of fractions and substances 1, 2 and 3 isolated from Erythrina verna through a bioassay guided fractionation. Seven fractions (1, 3-5 and 7-9) obtained from dichloromethane E. verna extract inhibited NO production (IC50 ≤ 15 μg/mL) with none or poor cytotoxic effect, while the fractions 4 and 5 notably reduced TNF-a production. Fractions 4, 6 and 9 suppressed Mycobacterium growth with MIC50 ≤ 20 μg/mL. Fraction 4 was the most potent due to dual biological activities. Erythratidinone and alpinumisoflavone inhibited the growth of Mtb H37Rv and hypervirulent strain in bacterial cultures (MIC50 ≤ 20 μg/mL), with erythratidinone standing out in reducing intracellular growth of Mtb H37Rv (5.8 ± 1.1 μg/mL). Alpinumisoflavone and erythratidinone were capable of inhibiting NO and TNF-α production besides showing significant inhibitory effects against Mycobacterium tuberculosis strains with low toxicity in macrophages. Both substances are promising for further studies focusing on an anti-TB dual treatment approach.

摘要

结核病仍然是全球主要的健康问题。耐药和高毒力结核分枝杆菌(Mtb)菌株可导致超反应个体发生过度炎症反应和坏死性病理,需要辅助治疗。植物衍生物质已被用于结核病治疗,其中黄酮类化合物尤为突出。我们通过生物活性指导的分步分离法,评估了从 Erythrina verna 中分离得到的化合物 1、2 和 3 及其相应的部分的抗 Mtb、抗炎和细胞毒性活性。从二氯甲烷 Erythrina verna 提取物中获得的七个部分(1、3-5 和 7-9)抑制了 NO 的产生(IC50≤15μg/mL),且没有或仅有轻微的细胞毒性作用,而部分 4 和 5 则明显降低了 TNF-a 的产生。部分 4、6 和 9 抑制了分枝杆菌的生长,MIC50≤20μg/mL。由于具有双重生物活性,部分 4 是最有效的。Erythratidinone 和 alpinumisoflavone 抑制了分枝杆菌 H37Rv 和高毒力菌株在细菌培养物中的生长(MIC50≤20μg/mL),其中 Erythratidinone 在降低分枝杆菌 H37Rv 的细胞内生长方面表现突出(5.8±1.1μg/mL)。Alpinumisoflavone 和 Erythratidinone 除了对巨噬细胞中的分枝杆菌菌株具有显著的抑制作用外,还能抑制 NO 和 TNF-α 的产生,而且毒性低。这两种物质都很有希望进一步研究,以关注抗结核的双重治疗方法。

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