Alteration of mercuric chloride-induced autoimmune glomerulonephritis in Brown-Norway rats by herring oil, evening primrose oil and OKY-046 a selective TXA-synthetase inhibitor

Nikolaos Papanikolaou
{"title":"Alteration of mercuric chloride-induced autoimmune glomerulonephritis in Brown-Norway rats by herring oil, evening primrose oil and OKY-046 a selective TXA-synthetase inhibitor","authors":"Nikolaos Papanikolaou","doi":"10.1016/0262-1746(87)90066-7","DOIUrl":null,"url":null,"abstract":"<div><p>Repeated subcutaneous (SC) injections of mercuric chloride (MC) in Brown Norway (BN) rats induce an autoimmune glomerulonephritis (GN) due to antiglomerular basement membrane (BM) antibody deposition in the glomeruli. The aim of this study was to investigate the effects on MC-induced autoimmune GN of a) OKY-046,a selective TXA-synthetase inhibitor b) herring oil (HO), which is rich in eicosapentaenoic acid (EPA) (5.6%) precursor of the three series of prostaglandins (PGs) and of (inactive) thromboxane (TXA3),and c) evening primrose oil (EPO), which is rich in linoleic acid (LA) (72%) and gamma-linolenic acid (GLNA) (9%), precursors of the one series of PGs, mainly PGE1,and of (inactive) TXA1. The administration of OKY-046 significantly inhibited proteinuria, partially prevented fibrin thrombi (FT) formation in the glomeruli, decreased urinary TXB, enhanced 6ketoPGF excretion and, increased survival rate of the animals from 60% (group receiving only MC) to 86%. However, OKY-046 did not prevent body weight (BW) loss or the development and deposition of IgG in the glomeruli. Increased intake of HO (80 days prior and throughout the experiment) and avoidance of arachidonic acid (AA) intake prodused an effect comparable to that of OKY-046 in the rats. Furthermore, HO significantly inhibited the deposition of IgG in the glomeruli, increased the survival rate of the animals to 100% and further enhanced the increased urinary PGE excretion indused by MC. However, HO did not prevent BW loss in the animals. Increased intake of EPO and avoidance of AA intake prodused an effect comparable to that of HO. Additionally, EPO completely prevented BW loss induced by MC in these animals. These findings suggest that the metabolites of AA, EPA and GLNA play an important role either in the development or in the modulation of this model of MC indused GN.</p></div>","PeriodicalId":20720,"journal":{"name":"Prostaglandins, leukotrienes, and medicine","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"1987-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0262-1746(87)90066-7","citationCount":"14","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Prostaglandins, leukotrienes, and medicine","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/0262174687900667","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 14

Abstract

Repeated subcutaneous (SC) injections of mercuric chloride (MC) in Brown Norway (BN) rats induce an autoimmune glomerulonephritis (GN) due to antiglomerular basement membrane (BM) antibody deposition in the glomeruli. The aim of this study was to investigate the effects on MC-induced autoimmune GN of a) OKY-046,a selective TXA-synthetase inhibitor b) herring oil (HO), which is rich in eicosapentaenoic acid (EPA) (5.6%) precursor of the three series of prostaglandins (PGs) and of (inactive) thromboxane (TXA3),and c) evening primrose oil (EPO), which is rich in linoleic acid (LA) (72%) and gamma-linolenic acid (GLNA) (9%), precursors of the one series of PGs, mainly PGE1,and of (inactive) TXA1. The administration of OKY-046 significantly inhibited proteinuria, partially prevented fibrin thrombi (FT) formation in the glomeruli, decreased urinary TXB, enhanced 6ketoPGF excretion and, increased survival rate of the animals from 60% (group receiving only MC) to 86%. However, OKY-046 did not prevent body weight (BW) loss or the development and deposition of IgG in the glomeruli. Increased intake of HO (80 days prior and throughout the experiment) and avoidance of arachidonic acid (AA) intake prodused an effect comparable to that of OKY-046 in the rats. Furthermore, HO significantly inhibited the deposition of IgG in the glomeruli, increased the survival rate of the animals to 100% and further enhanced the increased urinary PGE excretion indused by MC. However, HO did not prevent BW loss in the animals. Increased intake of EPO and avoidance of AA intake prodused an effect comparable to that of HO. Additionally, EPO completely prevented BW loss induced by MC in these animals. These findings suggest that the metabolites of AA, EPA and GLNA play an important role either in the development or in the modulation of this model of MC indused GN.

鲱鱼油、月见草油和选择性txa合成酶抑制剂OKY-046对氯化汞诱导的褐挪威大鼠自身免疫性肾小球肾炎的影响
由于抗肾小球基底膜(BM)抗体在肾小球内沉积,多次皮下注射氯化汞(MC)可诱导自身免疫性肾小球肾炎(GN)。本研究的目的是探讨影响MC-induced自身免疫性GN) oky - 046,一种选择性TXA-synthetase抑制剂b)鲱鱼油(HO),富含二十碳五烯酸(EPA)(5.6%)三大系列的前身前列腺素(后卫)和(不活跃)的凝血恶烷(TXA3)和c)月见草油(EPO),富含亚油酸(LA)(72%)和gamma-linolenic酸(GLNA)(9%)、前兆的动力分配的一个系列,主要PGE1, TXA1(不活跃)。OKY-046显著抑制蛋白尿,部分阻止肾小球纤维蛋白血栓(FT)的形成,降低尿TXB,增加6ketoPGF的排泄,并将动物的存活率从60%(仅接受MC的组)提高到86%。然而,OKY-046并不能阻止体重(BW)下降或肾小球中IgG的形成和沉积。增加HO的摄入(80天前和整个实验期间)和避免花生四烯酸(AA)的摄入,在大鼠中产生了与OKY-046相当的效果。此外,HO显著抑制了肾小球中IgG的沉积,使动物的存活率提高到100%,并进一步增强了MC引起的尿PGE的增加,但HO并没有阻止动物的体重损失。增加EPO的摄入和避免AA的摄入所产生的效果与HO相当。此外,EPO完全阻止了MC引起的体重损失。这些发现表明,AA、EPA和GLNA的代谢物在MC诱导的GN模型的发生或调节中发挥了重要作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信