Suppr超能文献

白藜芦醇及其他一些天然化合物对酪氨酸激酶活性和细胞溶解的影响。

Effect of resveratrol and some other natural compounds on tyrosine kinase activity and on cytolysis.

作者信息

Palmieri L, Mameli M, Ronca G

机构信息

Department of Human and Environmental Sciences, University of Pisa, Italy.

出版信息

Drugs Exp Clin Res. 1999;25(2-3):79-85.

Abstract

Resveratrol is a phytoalexin with several biological and pharmacological activities including the "French paradox". We investigated the effect of resveratrol on cytolytic activity by oxygen reactive species and on soluble and particulate tyrosine kinases from human placenta and human prostatic adenoma. These effects were compared with those of piceatannol, quercetin, catechin and epicatechin. Fifty percent of erythrocyte lysis due to H2O2-lactoperoxidase-KI incubation, in which I3-, OI- and oxygen singlet are produced, was obtained after 22 +/- 7 (SD) min in the absence of the tested compounds. The 50% lysis was obtained after 66 +/- 15, 129 +/- 35, 196 +/- 21, 240 +/- 63 and 420 +/- 80 min with 40 microM piceatannol, quercetin, resveratrol, epicatechin and catechin respectively. Protection was concentration dependent. The assay of tyrosine kinase activity was performed using two different substrates as follows: substrate A corresponded to the sequence 1-17 of gastrin, and substrate B to sequence 6-20 of cell division kinase p34cdc2. In all experiments, initial velocity was measured. When assayed with both substrates, tyrosine kinase activities from particulate and cytosolic fractions of placenta were more inhibited by piceatannol and quercetin. Resveratrol significantly inhibited the particulate fraction and the cytosolic fraction respectively when substrates A and B were employed: Catechin acted as an inhibitor with substrate A and particulate fraction while in the other experimental conditions it acted as an activator. Resveratrol inhibited the tyrosine kinase of particulate and cytosolic fractions of prostatic adenoma assayed with substrate A and B.

摘要

白藜芦醇是一种具有多种生物学和药理活性的植保素,其中包括“法国悖论”。我们研究了白藜芦醇对氧活性物质的细胞溶解活性以及对人胎盘和人前列腺腺瘤中可溶性和颗粒性酪氨酸激酶的影响。将这些影响与3,4,5-三甲氧基芪、槲皮素、儿茶素和表儿茶素的影响进行了比较。在不存在受试化合物的情况下,H2O2-乳过氧化物酶-KI孵育(其中产生I3-、OI-和单线态氧)导致红细胞50%溶解在22±7(标准差)分钟后出现。分别用40微摩尔的3,4,5-三甲氧基芪、槲皮素、白藜芦醇、表儿茶素和儿茶素时,50%溶解分别在66±15、129±35、196±21、240±63和420±80分钟后出现。保护作用呈浓度依赖性。酪氨酸激酶活性测定使用两种不同的底物如下:底物A对应胃泌素的1-17序列,底物B对应细胞分裂激酶p34cdc2的6-20序列。在所有实验中,均测量初始速度。当用两种底物进行测定时,胎盘颗粒和胞质部分的酪氨酸激酶活性受到3,4,5-三甲氧基芪和槲皮素的抑制作用更强。当使用底物A和B时,白藜芦醇分别显著抑制颗粒部分和胞质部分:儿茶素在底物A和颗粒部分时起抑制剂作用,而在其他实验条件下起激活剂作用。白藜芦醇抑制用底物A和B测定的前列腺腺瘤颗粒和胞质部分的酪氨酸激酶。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验