• 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

母体免疫激活模型中 C57BL/6J 小鼠的前脉冲抑制缺陷的种间差异。

Inter-breeder differences in prepulse inhibition deficits of C57BL/6J mice in a maternal immune activation model.

机构信息

Molecular Neurobiology, Brain Research Institute, Niigata University, Niigata, Japan.

Department of Molecular Brain Science, Graduate School of Life Sciences, Kumamoto University, Kumamoto, Japan.

出版信息

Neuropsychopharmacol Rep. 2021 Sep;41(3):416-421. doi: 10.1002/npr2.12178. Epub 2021 May 27.

DOI:10.1002/npr2.12178
PMID:34043885
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8411318/
Abstract

Genetic and environmental factors interact with each other to influence the risk of various psychiatric diseases; however, the intensity and nature of their interactions remain to be elucidated. We established a maternal infection model using polyinosinic-polycytidylic acid (Poly(I:C)) to determine the relationship between the maternal breeding environment and behavioral changes in the offspring. We purchased pregnant C57BL/6J mice from three breeders and administered Poly(I:C) (2 mg/kg) intravenously in their tail vein on gestation day 15. The offspring were raised to 8-12 weeks old and subjected to the acoustic startle tests to compare their startle response intensity, prepulse inhibition levels, and degree of the adaptation of the startle response. No statistical interaction between Poly(I:C) administration and sex was observed for prepulse inhibition; thus, male and female mice were analyzed together. There was a statistical interaction between the breeder origin of offspring and prepulse inhibition; the Poly(I:C) challenge significantly decreased prepulse inhibition levels of the offspring born to the pregnant dams from Breeder A but not those from the other breeders. However, we failed to detect significant inter-breeder differences in Poly(I:C) effects on startle response and on startle adaptation with the given number of mice examined. The rearing environment of mouse dams has a prominent effect on the Poly(I:C)-induced prepulse inhibition deficits in this maternal immune activation model.

摘要

遗传和环境因素相互作用,影响各种精神疾病的风险;然而,它们相互作用的强度和性质仍有待阐明。我们建立了一个母体感染模型,使用聚肌胞苷酸(Poly(I:C)) 来确定母体繁殖环境与后代行为变化之间的关系。我们从三个饲养员处购买了怀孕的 C57BL/6J 小鼠,并在妊娠第 15 天通过尾静脉给它们注射 2mg/kg 的 Poly(I:C)。将后代饲养至 8-12 周龄,并进行听觉惊跳测试,以比较它们的惊跳反应强度、前脉冲抑制水平和惊跳反应适应程度。前脉冲抑制没有观察到 Poly(I:C)给药和性别之间的统计学相互作用;因此,雄性和雌性小鼠一起进行分析。后代的饲养员来源与前脉冲抑制之间存在统计学相互作用;母体免疫激活模型中,聚肌胞苷酸挑战显著降低了来自饲养员 A 的孕鼠所生后代的前脉冲抑制水平,但对其他饲养员的后代没有影响。然而,在用所检查的老鼠数量进行检测时,我们未能发现 Poly(I:C)对惊跳反应和惊跳适应的影响在饲养员之间存在显著差异。鼠母的饲养环境对母体免疫激活模型中聚肌胞苷酸诱导的前脉冲抑制缺陷有显著影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8cb8/8411318/d97ec4126f9c/NPR2-41-416-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8cb8/8411318/bc51e12457e4/NPR2-41-416-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8cb8/8411318/d97ec4126f9c/NPR2-41-416-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8cb8/8411318/bc51e12457e4/NPR2-41-416-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8cb8/8411318/d97ec4126f9c/NPR2-41-416-g001.jpg

相似文献

1
Inter-breeder differences in prepulse inhibition deficits of C57BL/6J mice in a maternal immune activation model.母体免疫激活模型中 C57BL/6J 小鼠的前脉冲抑制缺陷的种间差异。
Neuropsychopharmacol Rep. 2021 Sep;41(3):416-421. doi: 10.1002/npr2.12178. Epub 2021 May 27.
2
Prenatal immune challenge in rats: effects of polyinosinic-polycytidylic acid on spatial learning, prepulse inhibition, conditioned fear, and responses to MK-801 and amphetamine.大鼠产前免疫刺激:聚肌苷酸-聚胞苷酸对空间学习、前脉冲抑制、条件性恐惧以及对MK-801和苯丙胺反应的影响
Neurotoxicol Teratol. 2015 Jan-Feb;47:54-65. doi: 10.1016/j.ntt.2014.10.007. Epub 2014 Nov 8.
3
Relationships between the acoustic startle response and prepulse inhibition in C57BL/6J mice: a large-scale meta-analytic study.C57BL/6J 小鼠的声惊反射与前脉冲抑制之间的关系:一项大规模的荟萃分析研究。
Mol Brain. 2018 Jul 13;11(1):42. doi: 10.1186/s13041-018-0382-7.
4
Sexually dimorphic effects of prenatal exposure to lipopolysaccharide, and prenatal and postnatal exposure to propionic acid, on acoustic startle response and prepulse inhibition in adolescent rats: relevance to autism spectrum disorders.产前暴露于脂多糖以及产前和产后暴露于丙酸对青春期大鼠听觉惊吓反应和前脉冲抑制的性别二态性影响:与自闭症谱系障碍的相关性。
Behav Brain Res. 2015 Feb 1;278:244-56. doi: 10.1016/j.bbr.2014.09.032. Epub 2014 Oct 7.
5
The risk for behavioural deficits is determined by the maternal immune response to prenatal immune challenge in a neurodevelopmental model.在神经发育模型中,行为缺陷的风险是由母体对产前免疫挑战的免疫反应决定的。
Brain Behav Immun. 2014 Nov;42:138-46. doi: 10.1016/j.bbi.2014.06.013. Epub 2014 Jun 26.
6
Effects of prenatal infection on prepulse inhibition in the rat depend on the nature of the infectious agent and the stage of pregnancy.产前感染对大鼠前脉冲抑制的影响取决于感染因子的性质和孕期阶段。
Behav Brain Res. 2007 Aug 6;181(2):270-7. doi: 10.1016/j.bbr.2007.04.016. Epub 2007 Apr 27.
7
Altered object-in-place recognition memory, prepulse inhibition, and locomotor activity in the offspring of rats exposed to a viral mimetic during pregnancy.孕期暴露于病毒类似物的大鼠后代的位置识别记忆、前脉冲抑制和运动活性改变。
Neuroscience. 2012 Jan 10;201:184-98. doi: 10.1016/j.neuroscience.2011.11.011. Epub 2011 Nov 11.
8
Prenatal immune challenge in rats: altered responses to dopaminergic and glutamatergic agents, prepulse inhibition of acoustic startle, and reduced route-based learning as a function of maternal body weight gain after prenatal exposure to poly IC.孕期免疫挑战对大鼠的影响:多巴胺能和谷氨酸能药物反应改变、声刺激前脉冲抑制、以及在孕期暴露于多聚肌苷酸后母体体重增加的情况下基于路径的学习减少。
Synapse. 2012 Aug;66(8):725-37. doi: 10.1002/syn.21561. Epub 2012 May 15.
9
Inbred strain differences in prepulse inhibition of the mouse startle response.小鼠惊吓反应的前脉冲抑制中的近交系差异。
Psychopharmacology (Berl). 1997 Jul;132(2):169-80. doi: 10.1007/s002130050333.
10
The effect of 17β-estradiol on maternal immune activation-induced changes in prepulse inhibition and dopamine receptor and transporter binding in female rats.17β-雌二醇对母体免疫激活诱导的雌性大鼠前脉冲抑制和多巴胺受体及转运体结合变化的影响。
Schizophr Res. 2020 Sep;223:249-257. doi: 10.1016/j.schres.2020.08.015. Epub 2020 Aug 31.

引用本文的文献

1
GABA system as the cause and effect in early development.GABA 系统作为早期发育的因果关系。
Neurosci Biobehav Rev. 2024 Jun;161:105651. doi: 10.1016/j.neubiorev.2024.105651. Epub 2024 Apr 4.
2
Maternal immune activation and role of placenta in the prenatal programming of neurodevelopmental disorders.母体免疫激活与胎盘在神经发育障碍产前编程中的作用。
Neuronal Signal. 2023 May 31;7(2):NS20220064. doi: 10.1042/NS20220064. eCollection 2023 Jul.
3
Beadchip technology to detect DNA methylation in mouse faithfully recapitulates whole-genome bisulfite sequencing.

本文引用的文献

1
Maternal Immune Activation Affects Hippocampal Excitatory and Inhibitory Synaptic Transmission in Offspring From an Early Developmental Period to Adulthood.母体免疫激活会影响子代从早期发育阶段到成年期的海马兴奋性和抑制性突触传递。
Front Cell Neurosci. 2020 Aug 4;14:241. doi: 10.3389/fncel.2020.00241. eCollection 2020.
2
Influence of poly(I:C) variability on thermoregulation, immune responses and pregnancy outcomes in mouse models of maternal immune activation.聚肌苷酸胞苷酸(poly(I:C))变异性对母体免疫激活小鼠模型体温调节、免疫反应和妊娠结局的影响。
Brain Behav Immun. 2019 Aug;80:406-418. doi: 10.1016/j.bbi.2019.04.019. Epub 2019 Apr 10.
3
芯片技术检测 DNA 甲基化在老鼠身上忠实地再现了全基因组亚硫酸氢盐测序。
Epigenomics. 2023 Feb;15(3):115-129. doi: 10.2217/epi-2023-0034. Epub 2023 Apr 5.
4
Assessment of the effects of sex, age, and rearing condition on ultrasonic vocalizations elicited by pups during the maternal potentiation paradigm in C57BL/6J mice.评估性别、年龄和饲养条件对 C57BL/6J 小鼠母性增强范式中幼崽诱发的超声发声的影响。
Dev Psychobiol. 2022 Dec;64(8):e22341. doi: 10.1002/dev.22341.
5
Behavioral features and disorganization of oscillatory activity in C57BL/6J mice after acute low dose MK-801 administration.急性低剂量给予MK-801后C57BL/6J小鼠的行为特征及振荡活动紊乱
Front Neurosci. 2022 Sep 14;16:1001869. doi: 10.3389/fnins.2022.1001869. eCollection 2022.
6
Adolescent THC Treatment Does Not Potentiate the Behavioral Effects in Adulthood of Maternal Immune Activation.青少年大麻素治疗不会增强母体免疫激活对成年后行为的影响。
Cells. 2021 Dec 11;10(12):3503. doi: 10.3390/cells10123503.
7
Effects of Importin α1/KPNA1 deletion and adolescent social isolation stress on psychiatric disorder-associated behaviors in mice.Importin α1/KPNA1 缺失和青少年社交隔离应激对小鼠精神障碍相关行为的影响。
PLoS One. 2021 Nov 12;16(11):e0258364. doi: 10.1371/journal.pone.0258364. eCollection 2021.
Taxonomic classification for microbiome analysis, which correlates well with the metabolite milieu of the gut.
用于微生物组分析的分类学分类与肠道代谢环境密切相关。
BMC Microbiol. 2018 Nov 16;18(1):188. doi: 10.1186/s12866-018-1311-8.
4
Maternal immune activation: reporting guidelines to improve the rigor, reproducibility, and transparency of the model.母体免疫激活:报告指南以提高模型的严谨性、可重复性和透明度。
Neuropsychopharmacology. 2019 Jan;44(2):245-258. doi: 10.1038/s41386-018-0185-7. Epub 2018 Aug 21.
5
Mouse models of maternal immune activation: Mind your caging system!母体免疫激活的小鼠模型:注意你的饲养系统!
Brain Behav Immun. 2018 Oct;73:643-660. doi: 10.1016/j.bbi.2018.07.014. Epub 2018 Jul 17.
6
GABAergic malfunction in the anterior cingulate cortex underlying maternal immune activation-induced social deficits.母体免疫激活引起的社会缺陷的前扣带皮层中 GABA 能功能障碍。
J Neuroimmunol. 2018 Aug 15;321:92-96. doi: 10.1016/j.jneuroim.2018.06.006. Epub 2018 Jun 7.
7
Maternal gut bacteria promote neurodevelopmental abnormalities in mouse offspring.母体肠道细菌会导致小鼠后代出现神经发育异常。
Nature. 2017 Sep 28;549(7673):528-532. doi: 10.1038/nature23910. Epub 2017 Sep 13.
8
Reversing behavioural abnormalities in mice exposed to maternal inflammation.逆转暴露于母体炎症的小鼠的行为异常。
Nature. 2017 Sep 28;549(7673):482-487. doi: 10.1038/nature23909. Epub 2017 Sep 13.
9
Microbiota differences between commercial breeders impacts the post-stroke immune response.商业养殖者之间的微生物组差异会影响中风后的免疫反应。
Brain Behav Immun. 2017 Nov;66:23-30. doi: 10.1016/j.bbi.2017.03.011. Epub 2017 Mar 24.
10
Composition of fecal microbiota of laboratory mice derived from Japanese commercial breeders using 16S rRNA gene clone libraries.利用16S rRNA基因克隆文库分析源自日本商业饲养者的实验小鼠粪便微生物群的组成。
J Vet Med Sci. 2016 Jul 1;78(6):1045-50. doi: 10.1292/jvms.15-0454. Epub 2016 Feb 20.