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洛哌丁胺是一种止泻药,通过诱导细胞凋亡发挥抗肿瘤作用。

Loperamide, an antidiarrhea drug, has antitumor activity by inducing cell apoptosis.

机构信息

College of Food Science and Biotechnology, Zhejiang Gongshang University, Food Safety Key Lab of Zhejiang Province, Hangzhou 310035, China.

出版信息

Pharmacol Res. 2012 Mar;65(3):372-8. doi: 10.1016/j.phrs.2011.11.007. Epub 2011 Nov 22.

Abstract

Loperamide, an antidiarrhea drug, is a peripheral opiate agonist. Some other opiate agonists have been shown to promote cell apoptosis. In this research, we studied the apoptosis-inducing and cytotoxic activities of loperamide. MTT assay was used to determine its cytotoxicity on nine established human tumor cell lines. Cell apoptosis was detected by flow cytometry. Hypodiploid cells and cell cycles were analyzed by propidium iodide (PI) staining, while early apoptotic cells were detected by annexin V-FITC/PI staining. It was found that loperamide could inhibit the proliferation of the tested tumor cell lines. The IC₅₀ values for SMMC7721, MCF7, SPC-A1, SKOV3-DDP, H460, HepG2, SGC7901, U2OS, and ACHN cells were 24.2±2.1 μM, 23.6±2.5 μM, 25.9±3.1 μM, 27.1±2.5 μM, 41.4±2.1 μM, 23.7±1.3 μM, 35.4±3.5 μM, 11.8±2.8 μM, and 28.5±3.4 μM, respectively. Loperamide was more effective to the human osteosarcoma U2OS cells with an IC₅₀ value of 11.8±2.8 μM. Meanwhile, it could induce cell apoptosis and cause G2/M-phase cell cycle arrest. The apoptotic cells could be found when treating with loperamide for 6h and most of them belonged to early apoptosis. In loperamide-treated cells, activation of caspase-3 was found, namely that caspase-3 was involved in the loperamide-induced apoptosis. The results of these studies indicate that loperamide is a potential antitumor agent. To our knowledge, this is the first report on antitumor activity of loperamide.

摘要

洛哌丁胺是一种抗腹泻药物,属于外周阿片受体激动剂。其他一些阿片受体激动剂已被证明可促进细胞凋亡。本研究旨在探讨洛哌丁胺的诱导细胞凋亡和细胞毒性作用。采用 MTT 法检测洛哌丁胺对 9 种人肿瘤细胞系的细胞毒性。通过流式细胞术检测细胞凋亡。碘化丙啶(PI)染色分析亚二倍体细胞和细胞周期, Annexin V-FITC/PI 染色检测早期凋亡细胞。结果表明,洛哌丁胺可抑制所测肿瘤细胞系的增殖。SMMC7721、MCF7、SPC-A1、SKOV3-DDP、H460、HepG2、SGC7901、U2OS 和 ACHN 细胞的 IC₅₀值分别为 24.2±2.1 μM、23.6±2.5 μM、25.9±3.1 μM、27.1±2.5 μM、41.4±2.1 μM、23.7±1.3 μM、35.4±3.5 μM、11.8±2.8 μM 和 28.5±3.4 μM。洛哌丁胺对人骨肉瘤 U2OS 细胞的作用更明显,IC₅₀值为 11.8±2.8 μM。同时,洛哌丁胺可诱导细胞凋亡并导致 G2/M 期细胞周期阻滞。在洛哌丁胺处理 6 h 时可发现凋亡细胞,且大部分属于早期凋亡。在洛哌丁胺处理的细胞中,发现 caspase-3 被激活,即 caspase-3 参与了洛哌丁胺诱导的细胞凋亡。这些研究结果表明,洛哌丁胺是一种潜在的抗肿瘤药物。据我们所知,这是首次报道洛哌丁胺的抗肿瘤活性。

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