• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

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

丙戊酸诱导大鼠产生的阶段依赖性骨骼畸形

Stage-dependent skeletal malformations induced by valproic acid in rat.

作者信息

Menegola E, Broccia M L, Prati M, Giavini E

机构信息

Department of Biology, University of Milan, Italy.

出版信息

Int J Dev Biol. 1998 Jan;42(1):99-102.

PMID:9496792
Abstract

In this work we study the skeletal teratogenic response in rats exposed to NaVP at different embryonic stages. Crl:CD female rats were treated subcutaneously with 400 mg/Kg b.w. NaVP at presomitic stage (group II) or nearly at 2, 6, 10, 14, 18 or 22 somites (groups III-VIII). The females on group I were treated with saline and served as controls. No treatment-related effects were observed at the level of resorptions, live fetuses and fetal or placental weight. The skeletal examination showed characteristic patterns of malformations strictly related to the period of treatment. In particular, groups II and III showed a significant increase of alterations of cervical vertebrae (mainly 1st to 3rd segment) and a decrease of the frequency of extra lumbar ribs in comparison to control. Group IV showed severe abnormalities localized at the 4th to 7th cervical segment and at the level of the 1st and 2nd thoracic segments, including duplications of thoracic segments 1, 2 or 3. The fetuses of group V were characterized by several alterations of the thoracic segments distributed without a clear specificity. In group VI, the thoracic region was also affected with some specificity at the level of the segments 4th to 9th; in group VII, last thoracic and lumbar segments were affected (mainly duplications) and in group VIII only lumbo-sacral abnormalities were recorded. These results confirm the specific effect of NaVP at the level of the axial skeleton and suggest a possible interaction with the expression of genes identifying the vertebral segments.

摘要

在本研究中,我们探究了在不同胚胎阶段暴露于戊烯醇钠(NaVP)的大鼠的骨骼致畸反应。将Crl:CD雌性大鼠在体节形成前阶段皮下注射400 mg/Kg体重的NaVP(II组),或在大约2、6、10、14、18或22体节时注射(III - VIII组)。I组雌性大鼠用生理盐水处理作为对照。在吸收、活胎以及胎儿或胎盘重量方面未观察到与处理相关的影响。骨骼检查显示出与处理时期严格相关的特征性畸形模式。具体而言,与对照组相比,II组和III组显示颈椎改变(主要是第1至3节段)显著增加,额外腰椎肋骨频率降低。IV组显示严重异常集中在第4至7颈椎节段以及第1和第2胸椎节段水平,包括第1、2或3胸椎节段的重复。V组胎儿的特征是胸椎节段有多种改变,分布无明显特异性。在VI组中,胸椎区域在第4至9节段水平也受到一些特异性影响;在VII组中,最后胸椎和腰椎节段受到影响(主要是重复),而在VIII组中仅记录到腰骶部异常。这些结果证实了NaVP在轴骨骼水平的特定作用,并提示其可能与确定椎骨节段的基因表达存在相互作用。

相似文献

1
Stage-dependent skeletal malformations induced by valproic acid in rat.丙戊酸诱导大鼠产生的阶段依赖性骨骼畸形
Int J Dev Biol. 1998 Jan;42(1):99-102.
2
Morphological alterations induced by sodium valproate on somites and spinal nerves in rat embryos.丙戊酸钠对大鼠胚胎体节和脊神经诱导的形态学改变。
Teratology. 1999 Feb;59(2):110-9. doi: 10.1002/(SICI)1096-9926(199902)59:2<110::AID-TERA5>3.0.CO;2-2.
3
Axial skeletal and Hox expression domain alterations induced by retinoic acid, valproic acid, and bromoxynil during murine development.维甲酸、丙戊酸和溴苯腈在小鼠发育过程中诱导的轴向骨骼和Hox表达域改变。
J Biochem Mol Toxicol. 2003;17(6):346-56. doi: 10.1002/jbt.10098.
4
Teratogenic effects of sodium valproate in mice and rats at midgestation and at term.丙戊酸钠在小鼠和大鼠妊娠中期及足月时的致畸作用。
Teratog Carcinog Mutagen. 1996;16(2):97-108. doi: 10.1002/(SICI)1520-6866(1996)16:2<97::AID-TCM4>3.0.CO;2-A.
5
Teratogenic effects of vigabatrin in TO mouse fetuses.氨己烯酸对TO小鼠胎儿的致畸作用。
Teratology. 1997 Mar;55(3):165-76. doi: 10.1002/(SICI)1096-9926(199703)55:3<165::AID-TERA1>3.0.CO;2-1.
6
Effects of hyperthermia and boric acid on skeletal development in rat embryos.高温和硼酸对大鼠胚胎骨骼发育的影响。
Birth Defects Res B Dev Reprod Toxicol. 2005 Jun;74(3):268-76. doi: 10.1002/bdrb.20047.
7
NTP technical report on the toxicity studies of Dibutyl Phthalate (CAS No. 84-74-2) Administered in Feed to F344/N Rats and B6C3F1 Mice.美国国家毒理学计划关于邻苯二甲酸二丁酯(化学物质登记号84 - 74 - 2)经饲料给予F344/N大鼠和B6C3F1小鼠的毒性研究技术报告。
Toxic Rep Ser. 1995 Apr;30:1-G5.
8
Axial skeletal malformations induced by acetazolamide in rabbits.乙酰唑胺诱导家兔轴向骨骼畸形。
Teratology. 1992 Jun;45(6):629-36. doi: 10.1002/tera.1420450607.
9
Developmental toxicity study with triethylene glycol given by gavage to CD rats and CD-1 mice.采用灌胃方式给予CD大鼠和CD-1小鼠三甘醇的发育毒性研究。
J Appl Toxicol. 2005 Sep-Oct;25(5):418-26. doi: 10.1002/jat.1089.
10
Embryotoxic effects of CKD-602, a new camptothecin anticancer agent, in rats.新型喜树碱类抗癌药CKD-602对大鼠的胚胎毒性作用
Reprod Toxicol. 2005 May-Jun;20(1):165-73. doi: 10.1016/j.reprotox.2005.01.004.

引用本文的文献

1
Chromatin Imbalance as the Vertex Between Fetal Valproate Syndrome and Chromatinopathies.染色质失衡:胎儿丙戊酸综合征与染色质病之间的关联点
Front Cell Dev Biol. 2021 Apr 20;9:654467. doi: 10.3389/fcell.2021.654467. eCollection 2021.
2
Inhibition of Valproic Acid-Induced Prenatal Developmental Abnormalities with Antioxidants in Rats.抗氧化剂对丙戊酸诱导的大鼠产前发育异常的抑制作用
ACS Omega. 2020 Mar 2;5(10):4953-4961. doi: 10.1021/acsomega.9b03792. eCollection 2020 Mar 17.
3
Evo-Devo of the Human Vertebral Column: On Homeotic Transformations, Pathologies and Prenatal Selection.
人类脊柱的演化发育生物学:同源异型转化、病理学与产前选择
Evol Biol. 2012 Dec;39(4):456-471. doi: 10.1007/s11692-012-9196-1. Epub 2012 Aug 18.