Astragaloside IV improves renal function and alleviates renal damage and inflammation in rats with chronic glomerulonephritis.

Turkish journal of biology = Turk biyoloji dergisi Pub Date : 2022-12-09 eCollection Date: 2023-01-01 DOI:10.55730/1300-0152.2641
Dong Zhang, ZongYing Li, Yuan Gao, HaiLing Sun
{"title":"Astragaloside IV improves renal function and alleviates renal damage and inflammation in rats with chronic glomerulonephritis.","authors":"Dong Zhang,&nbsp;ZongYing Li,&nbsp;Yuan Gao,&nbsp;HaiLing Sun","doi":"10.55730/1300-0152.2641","DOIUrl":null,"url":null,"abstract":"<p><p>From <i>Astragalus membranaceus</i> (Fisch.) Bge.var. mongholicus (Bge.) Hsiao, astragaloside IV (AS-IV), a saponin can be purified and is considered traditional Chinese medicine. The purpose of this study was to evaluate the AS-IV-mediated mechanism on chronic glomerulonephritis (CGN). A cationic bovine serum albumin-induced CGN rat model was established and 10, 15, or 20 mg/kg of AS-IV was administered to measure renal function and inflammatory infiltration. Influences of AS-IV on proliferation, cell cycle, and inflammation of LPS-induced rat mesangial cells (RMCs) were determined. The results demonstrated that AS-IV alleviated renal dysfunction, renal lesions, and inflammation in CGN rats. AS-IV prolonged the G0-G1 phase, shortened the S phase, and inhibited cell proliferation and inflammation in RMCs. AS-IV can promote miR-181d-5p expression to inhibit CSF1. miR-181d-5p promotion or CSF1 suppression could further enhance the therapeutic role of AS-IV in CGN rats, while miR-181d-5p silencing or CSF1 overexpression abolished the effect of AS-IV. In conclusion, AS-IV by mediating the miR-181d-5p/CSF1 axis protects against CGN.</p>","PeriodicalId":23375,"journal":{"name":"Turkish journal of biology = Turk biyoloji dergisi","volume":"47 1","pages":"61-73"},"PeriodicalIF":0.0000,"publicationDate":"2022-12-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10387845/pdf/","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Turkish journal of biology = Turk biyoloji dergisi","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.55730/1300-0152.2641","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2023/1/1 0:00:00","PubModel":"eCollection","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 1

Abstract

From Astragalus membranaceus (Fisch.) Bge.var. mongholicus (Bge.) Hsiao, astragaloside IV (AS-IV), a saponin can be purified and is considered traditional Chinese medicine. The purpose of this study was to evaluate the AS-IV-mediated mechanism on chronic glomerulonephritis (CGN). A cationic bovine serum albumin-induced CGN rat model was established and 10, 15, or 20 mg/kg of AS-IV was administered to measure renal function and inflammatory infiltration. Influences of AS-IV on proliferation, cell cycle, and inflammation of LPS-induced rat mesangial cells (RMCs) were determined. The results demonstrated that AS-IV alleviated renal dysfunction, renal lesions, and inflammation in CGN rats. AS-IV prolonged the G0-G1 phase, shortened the S phase, and inhibited cell proliferation and inflammation in RMCs. AS-IV can promote miR-181d-5p expression to inhibit CSF1. miR-181d-5p promotion or CSF1 suppression could further enhance the therapeutic role of AS-IV in CGN rats, while miR-181d-5p silencing or CSF1 overexpression abolished the effect of AS-IV. In conclusion, AS-IV by mediating the miR-181d-5p/CSF1 axis protects against CGN.

Abstract Image

Abstract Image

Abstract Image

黄芪甲苷改善慢性肾小球肾炎大鼠肾功能,减轻肾损害和炎症。
从黄芪(Fisch.)Bge.var.mongholicus(Bge.)Hsiao、黄芪甲苷IV(AS-IV)中可以纯化出一种皂苷,被认为是中药。本研究的目的是评估AS IV介导的慢性肾小球肾炎(CGN)的机制。建立阳离子牛血清白蛋白诱导的CGN大鼠模型,并给予10、15或20mg/kg的AS-IV以测量肾功能和炎症浸润。测定AS-IV对LPS诱导的大鼠系膜细胞(RMCs)增殖、细胞周期和炎症的影响。结果表明,AS-IV减轻了CGN大鼠的肾功能障碍、肾损伤和炎症。AS-IV延长RMCs的G0-G1期,缩短S期,并抑制细胞增殖和炎症。AS-IV可以促进miR-181d-5p的表达以抑制CSF1。miR-181d-5p的促进或CSF1的抑制可以进一步增强AS-IV在CGN大鼠中的治疗作用,而miR-181d-5 p的沉默或CSF1过表达消除了AS-IV的作用。总之,AS-IV通过介导miR-181d-5p/CSF1轴来保护CGN。
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