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桦木酸通过坏死诱导克氏锥虫细胞死亡。

Betulinic acid induces cell death by necrosis in Trypanosoma cruzi.

作者信息

Sousa Paloma Leão, Souza Racquel Oliveira da Silva, Tessarolo Louise Donadello, de Menezes Ramon Róseo Paula Pessoa Bezerra, Sampaio Tiago Lima, Canuto Jader Almeida, Martins Alice Maria Costa

机构信息

Department of Clinical and Toxicological Analisis, Federal University of Ceará, Fortaleza, Ceará, Brazil.

Department of Physiology and Pharmacology, Federal University of Ceará, Fortaleza, Ceará, Brazil.

出版信息

Acta Trop. 2017 Oct;174:72-75. doi: 10.1016/j.actatropica.2017.07.003. Epub 2017 Jul 6.

Abstract

Chagas' disease is a neglected disease caused by the protozoan parasite Trypanosoma cruzi and constitutes a serious health problem worldwide. The treatment is limited, with variable efficacy of benznidazole and nifurtimox. Betulinic Acid (BA), a triterpene, can be found in medicinal herbs and has a wide variety of biological and pharmacological activities. The objective was to evaluate betulinic acid effects on the cell death mechanism in Trypanosoma cruzi strain Y. BA inhibited the growth of epimastigotes in periods of 24h (IC=73.43μM), 48h (IC=119.8μM) and 72h (IC=212.2μM) of incubation; of trypomastigotes (IC=51.88μM) in periods of 24h and intracellular amastigotes (IC=25.94μM) in periods of 24 and 48h of incubation, no toxicity on LLC-MK cells at the concentrations used. Analysis of the possible mechanism of parasite cell death showed alterations in mitochondrial membrane potential, alterations in cell membrane integrity, an increase in the formation of reactive oxygen species and increase swelling of the reservosomes. In conclusion, betulinic acid was be able to inhibition all developmental forms of Trypanosoma cruzi Y strain with necrotic mechanism and involvement of mitochondrial membrane potential alteration and increase in reactive oxygen species.

摘要

恰加斯病是一种由原生动物寄生虫克氏锥虫引起的被忽视的疾病,在全球范围内构成严重的健康问题。治疗方法有限,苯硝唑和硝呋替莫的疗效各异。桦木酸(BA)是一种三萜类化合物,存在于草药中,具有多种生物学和药理活性。目的是评估桦木酸对克氏锥虫Y株细胞死亡机制的影响。桦木酸在孵育24小时(IC = 73.43μM)、48小时(IC = 119.8μM)和72小时(IC = 212.2μM)期间抑制无鞭毛体的生长;在24小时期间抑制锥鞭毛体(IC = 51.88μM),在孵育24小时和48小时期间抑制细胞内无鞭毛体(IC = 25.94μM),在所使用的浓度下对LLC-MK细胞无毒性。对寄生虫细胞死亡可能机制的分析表明,线粒体膜电位发生改变、细胞膜完整性改变、活性氧形成增加以及储存泡肿胀增加。总之,桦木酸能够通过坏死机制抑制克氏锥虫Y株的所有发育形式,并涉及线粒体膜电位改变和活性氧增加。

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