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胰蛋白酶抑制剂具有抗氧化活性,可抑制A549细胞增殖,并提高活性氧清除酶的活性。

Trypsin inhibitors demonstrate antioxidant activities, inhibit A549 cell proliferation, and increase activities of reactive oxygen species scavenging enzymes.

作者信息

Shamsi Tooba Naz, Parveen Romana, Fatima Sadaf

机构信息

Department of Biotechnology, Jamia Millia Islamia, New Delhi, India.

出版信息

Indian J Pharmacol. 2017 Mar-Apr;49(2):155-160. doi: 10.4103/ijp.IJP_553_16.

DOI:10.4103/ijp.IJP_553_16
PMID:28706328
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5497437/
Abstract

OBJECTIVES

Protease inhibitors are one of the most promising and investigated subjects for their role in pharmacognostical and pharmacological studies. This study aimed to investigate antineoplastic and antioxidant activity of trypsin inhibitors (TIs) isolated from three plant sources and their inhibitory role in the cell line.

MATERIALS AND METHODOLOGY

TIs were obtained from different plant sources. Antineoplastic potential on adenocarcinoma human alveolar basal epithelial cell line (A549) and normal Human Embryonic Kidney (HEK) was determined using MTT assay. Activities of antioxidant enzyme, nitric oxide scavenger, superoxide dismutase, glutathione S-transferase, and glutathione peroxidase were assessed in cell lines incubated with and without TIs. The outcome was analyzed by spectrophotometer.

RESULTS

TIs showed the higher cytotoxicity on A549 cells as compared to normal HEK cell line. TIs exhibited fair increase in antioxidant enzyme activity in A549 cells as compared to control. This might be one of the strategies of antineoplastic effect in cancer cells.

CONCLUSIONS

This study has reported the antioxidant and antineoplastic properties of these TIs for the first time in A549 cells (to the best of our knowledge). The results show that TIs possess ability to prevent cancer and diseases caused due to oxidative stress. Therefore, we conclude that TIs can be used as supplements along with the conventional drugs for increased efficacy in the treatment of diseases such as cardiovascular disease, atherosclerosis, and cancer.

摘要

目的

蛋白酶抑制剂因其在生药学和药理学研究中的作用,是最具前景且研究最多的课题之一。本研究旨在探究从三种植物来源分离得到的胰蛋白酶抑制剂(TIs)的抗肿瘤和抗氧化活性及其在细胞系中的抑制作用。

材料与方法

TIs 从不同植物来源获得。使用 MTT 法测定其对人肺泡基底上皮腺癌细胞系(A549)和正常人胚肾(HEK)细胞的抗肿瘤潜力。在有和没有 TIs 的情况下孵育的细胞系中评估抗氧化酶、一氧化氮清除剂、超氧化物歧化酶、谷胱甘肽 S - 转移酶和谷胱甘肽过氧化物酶的活性。通过分光光度计分析结果。

结果

与正常 HEK 细胞系相比,TIs 对 A549 细胞显示出更高的细胞毒性。与对照相比,TIs 在 A549 细胞中使抗氧化酶活性有明显增加。这可能是癌细胞抗肿瘤作用的策略之一。

结论

据我们所知,本研究首次报道了这些 TIs 在 A549 细胞中的抗氧化和抗肿瘤特性。结果表明,TIs 具有预防癌症和由氧化应激引起的疾病的能力。因此,我们得出结论,TIs 可与传统药物一起用作补充剂,以提高在治疗心血管疾病、动脉粥样硬化和癌症等疾病中的疗效。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/110e/5497437/8b68465fb21a/IJPharm-49-155-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/110e/5497437/24c823bdbc63/IJPharm-49-155-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/110e/5497437/cd98bd648ab4/IJPharm-49-155-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/110e/5497437/f87d6aa71416/IJPharm-49-155-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/110e/5497437/d22e55b76345/IJPharm-49-155-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/110e/5497437/8b68465fb21a/IJPharm-49-155-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/110e/5497437/24c823bdbc63/IJPharm-49-155-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/110e/5497437/cd98bd648ab4/IJPharm-49-155-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/110e/5497437/f87d6aa71416/IJPharm-49-155-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/110e/5497437/d22e55b76345/IJPharm-49-155-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/110e/5497437/8b68465fb21a/IJPharm-49-155-g005.jpg

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