Investigation of sanguinarine and chelerythrine effects on CYP1A1 expression and activity in human hepatoma cells

血桂碱 白屈菜红碱 菲咯烷 化学 生物化学 细胞色素P450 生物碱 分子生物学 药理学 生物 立体化学 蛋白激酶C
作者
Adela Zdarilova,Radim Vrzal,M Rypka,Jitka Ulrichová,Zdenek Dvorak
出处
期刊:Food and Chemical Toxicology [Elsevier]
卷期号:44 (2): 242-249 被引量:32
标识
DOI:10.1016/j.fct.2005.07.006
摘要

Quaternary benzo[c]phenanthridine alkaloids (QBA) sanguinarine and chelerythrine exhibit a wide spectrum of biological activities whence they are used in dental care products. Recent studies indicated that cytochrome P450 CYP1A attenuates sanguinarine toxicity both in vivo [Williams, M.K., Dalvi, S., Dalvi, R.R., 2000. Influence of 3-methylcholanthrene pretreatment on sanguinarine toxicity in mice. Vet. Hum. Toxicol. 42, 196-198] and in vitro [Vrba, J., Kosina, P., Ulrichová, J., Modrianský, M., 2004. Involvement of cytochrome P450 1A in sanguinarine detoxication. Toxicol. Lett. 151, 375-387]. However, CYP1A converts sanguinarine to the products that form DNA adducts [Stiborová, M., Simánek, V., Frei, E., Hobza, P., Ulrichová, J., 2002. DNA adduct formation from quaternary benzo[c]phenanthridine alkaloids sanguinarine and chelerythrine as revealed by the 32P-postlabeling technique. Chem. Biol. Interact. 140, 231-242]. In our work we examined the effects of sanguinarine and chelerythrine on CYP1A1 expression and catalytic activity in human hepatoma cells-HepG2. Sanguinarine and chelerythrine did not affect basal and dioxin-inducible expression of CYP1A1 mRNA and protein in HepG2 cells. The enzymatic activity of CYP1A1 was assessed by the fluorescent measurement of 7-ethyxoresorufin-O-deethylase (EROD) activity. We observed a slight decrease of dioxin-induced EROD activity in HepG2 cells by sanguinarine and chelerythrine. This decrease was attributed to the inhibition of CYP1A1 catalytic activity, as revealed by enzyme kinetic studies on recombinant CYP1A1 protein. The IC50 values for the inhibition of CYP1A1 by sanguinarine and chelerythrine were 2.1 and 1.9muM, respectively. In conclusion, albeit the CYP1A modulates QBA cytotoxicity and genotoxicity, the QBA themselves do not affect CYP1A1 expression. The data indicate that studied alkaloids do not have specific cellular target and their biological effects are rather pleiotropic.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
更新
PDF的下载单位、IP信息已删除 (2025-6-4)

科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
sinn17完成签到,获得积分10
刚刚
2秒前
可爱的冷霜完成签到,获得积分10
3秒前
田様应助王文静采纳,获得10
3秒前
4秒前
老魏完成签到,获得积分10
4秒前
脑洞疼应助SuperFAN采纳,获得10
5秒前
___赵完成签到,获得积分10
7秒前
7秒前
8秒前
Miraitowa完成签到 ,获得积分10
8秒前
李爱国应助景笑天采纳,获得10
9秒前
10秒前
12秒前
12秒前
13秒前
Morning发布了新的文献求助10
13秒前
13秒前
Owen应助swallow采纳,获得10
14秒前
14秒前
16秒前
HOLLYWOO发布了新的文献求助10
18秒前
小包谷发布了新的文献求助10
19秒前
19秒前
嘻嘻哈哈应助yty采纳,获得10
20秒前
紫色茄子应助yty采纳,获得10
20秒前
爆米花应助yty采纳,获得10
20秒前
20秒前
20秒前
21秒前
22秒前
AL完成签到,获得积分10
22秒前
fyukgfdyifotrf完成签到,获得积分10
22秒前
小药同学发布了新的文献求助10
23秒前
24秒前
24秒前
汉堡包应助jorjames采纳,获得10
25秒前
勤劳尔丝完成签到 ,获得积分10
25秒前
素简发布了新的文献求助20
27秒前
LunminBao完成签到,获得积分10
27秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
FUNDAMENTAL STUDY OF ADAPTIVE CONTROL SYSTEMS 500
微纳米加工技术及其应用 500
Nanoelectronics and Information Technology: Advanced Electronic Materials and Novel Devices 500
Performance optimization of advanced vapor compression systems working with low-GWP refrigerants using numerical and experimental methods 500
Constitutional and Administrative Law 500
PARLOC2001: The update of loss containment data for offshore pipelines 500
热门求助领域 (近24小时)
化学 材料科学 医学 生物 工程类 有机化学 生物化学 物理 纳米技术 计算机科学 内科学 化学工程 复合材料 物理化学 基因 遗传学 催化作用 冶金 量子力学 光电子学
热门帖子
关注 科研通微信公众号,转发送积分 5295559
求助须知:如何正确求助?哪些是违规求助? 4445074
关于积分的说明 13835332
捐赠科研通 4329472
什么是DOI,文献DOI怎么找? 2376680
邀请新用户注册赠送积分活动 1371973
关于科研通互助平台的介绍 1337270