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原儿茶酸通过抑制I相酶、减少细胞增殖和促进细胞凋亡来抑制二乙基亚硝胺诱导的肝前病变。

Protocatechuic acid suppresses diethylnitrosamine-induced hepatic preneoplastic lesions by inhibiting phase I enzymes, reducing cell proliferation, and promoting apoptosis.

作者信息

Punvittayagul Charatda, Taya Sirinya, Luangsuphabool Theerapat, Wongpoomchai Rawiwan

机构信息

Center of Veterinary Medical Diagnostic and Animal Health Innovation, Faculty of Veterinary Medicine, Chiang Mai University, Thailand.

Multidisciplinary Research Institute, Chiang Mai University, Thailand.

出版信息

J Toxicol Sci. 2025;50(8):387-397. doi: 10.2131/jts.50.387.

Abstract

Protocatechuic acid (PCA) is a phenolic compound naturally occurring in various plants. Although numerous studies have reported on its various biological activities, information on the anti-carcinogenic potential and its molecular mechanisms in animal models has never been conclusively determined. Therefore, this study aimed to study the inhibitory effect of PCA against diethylnitrosamine (DEN)-induced rat hepatocarcinogenesis. Rats received three intraperitoneal injections of 100 mg kg body weight of DEN to initiate hepatic preneoplastic lesions, and glutathione S-transferase placental form (GST-P)-positive foci were used as the end-point marker. Rats were treated with PCA at 40 mg kg body weight by oral gavage administration for 15 weeks to study its chemopreventive effect on the early stages of hepatocarcinogenesis. PCA treatment decreased the number and the area of hepatic GST-P-positive foci in DEN-induced rats. It inhibits the activity of cytochrome P450 reductase and reduces the expression of cytochrome P450 2E1 protein. It also suppresses cell proliferation by down-regulation of Cyclin D1 expression. Additionally, it induces apoptosis, as indicated by the up-regulation of pro-apoptotic genes, Bax and Bad, in DEN-induced rats. These findings suggest that PCA is an anti-cancer agent that inhibits hepatocarcinogenesis in DEN-treated rats.

摘要

原儿茶酸(PCA)是一种天然存在于多种植物中的酚类化合物。尽管众多研究已报道了其多种生物学活性,但关于其在动物模型中的抗癌潜力及其分子机制的信息尚未得到最终确定。因此,本研究旨在探讨PCA对二乙基亚硝胺(DEN)诱导的大鼠肝癌发生的抑制作用。大鼠接受三次腹腔注射,剂量为100 mg/kg体重的DEN,以引发肝脏癌前病变,谷胱甘肽S-转移酶胎盘型(GST-P)阳性灶用作终点标志物。通过口服灌胃给予大鼠40 mg/kg体重的PCA,持续15周,以研究其对肝癌发生早期阶段的化学预防作用。PCA处理降低了DEN诱导大鼠肝脏中GST-P阳性灶的数量和面积。它抑制细胞色素P450还原酶的活性,并降低细胞色素P450 2E1蛋白的表达。它还通过下调细胞周期蛋白D1的表达来抑制细胞增殖。此外,如在DEN诱导的大鼠中促凋亡基因Bax和Bad的上调所示,它诱导细胞凋亡。这些发现表明,PCA是一种抗癌剂,可抑制DEN处理大鼠的肝癌发生。

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