• 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

小鼠的生长和存活特征

Growth and survival characteristics of mice.

作者信息

Brandenburg Joline E, Fogarty Matthew J, Sieck Gary C

机构信息

Department of Physical Medicine and Rehabilitation Mayo Clinic College of Medicine Rochester MN USA.

Department of Pediatric and Adolescent Medicine Mayo Clinic College of Medicine Rochester MN USA.

出版信息

Animal Model Exp Med. 2020 Oct 10;3(4):319-324. doi: 10.1002/ame2.12137. eCollection 2020 Dec.

DOI:10.1002/ame2.12137
PMID:33532707
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7824963/
Abstract

Characterization of growth and survival of mice displaying early onset hypertonic symptoms is critical as these animals are important for research investigating mechanisms and treatments of pediatric conditions associated with hypertonia, such as cerebral palsy. Currently, most animal models of cerebral palsy reproduce risk factors for developing this condition, with most failing to develop the physical symptoms or failing to survive in the postnatal period. The B6.Cg- /J (Gly receptor mutation) transgenic mouse ( mouse), displays symptoms of early onset hypertonia, though little has been reported on growth and survival, with no reports of growth and survival since genotyping became available. We found that the majority of mice display symptoms by P14-P16. Of mice surviving to weaning, only ~9% were mice. By weaning age, mice had significantly lower weights than their heterozygote and wild-type littermates. Of mice that died after weaning and prior to use in experiments or being culled, 48% were mice. The poor growth and decreased survival of mice across multiple developmental and adult ages resembled the varied survival rates observed in humans with mild or severe cerebral palsy. The understanding of the expected survival of these mice is helpful for planning breeding and animal numbers for experiments. Due to the symptoms and timing of symptom onset, mice will be valuable in uncovering mechanisms and long-term effects of early onset hypertonia in order to move toward interventions for these conditions.

摘要

对表现出早期高渗症状的小鼠的生长和存活情况进行表征至关重要,因为这些动物对于研究与张力亢进相关的儿科疾病(如脑瘫)的机制和治疗方法具有重要意义。目前,大多数脑瘫动物模型再现了引发这种疾病的风险因素,但大多数模型未能出现身体症状或在出生后无法存活。B6.Cg- /J(甘氨酸受体突变)转基因小鼠表现出早期高渗症状,不过关于其生长和存活情况的报道很少,自基因分型可用以来尚无生长和存活情况的报告。我们发现,大多数转基因小鼠在出生后14至16天出现症状。存活至断奶的小鼠中,只有约9%是转基因小鼠。到断奶时,转基因小鼠的体重明显低于其杂合子和野生型同窝小鼠。在断奶后至用于实验或被淘汰前死亡的小鼠中,48%是转基因小鼠。转基因小鼠在多个发育阶段和成年期的生长不良和存活率降低,类似于在患有轻度或重度脑瘫的人类中观察到的不同存活率。了解这些小鼠的预期存活率有助于规划繁殖和实验所需的动物数量。由于症状和症状出现的时间,转基因小鼠对于揭示早期高渗的机制和长期影响以便针对这些病症采取干预措施将具有重要价值。

相似文献

1
Growth and survival characteristics of mice.小鼠的生长和存活特征
Animal Model Exp Med. 2020 Oct 10;3(4):319-324. doi: 10.1002/ame2.12137. eCollection 2020 Dec.
2
Phrenic motor neuron loss in an animal model of early onset hypertonia.在早发性张力亢进动物模型中膈神经运动神经元丢失。
J Neurophysiol. 2020 May 1;123(5):1682-1690. doi: 10.1152/jn.00026.2020. Epub 2020 Apr 1.
3
Differences in lumbar motor neuron pruning in an animal model of early onset spasticity.早发性痉挛动物模型中腰段运动神经元修剪的差异。
J Neurophysiol. 2018 Aug 1;120(2):601-609. doi: 10.1152/jn.00186.2018. Epub 2018 May 2.
4
Diaphragm neuromuscular transmission failure in a mouse model of an early-onset neuromotor disorder.早期运动神经障碍小鼠模型中膈肌神经肌肉传递失败。
J Appl Physiol (1985). 2021 Mar 1;130(3):708-720. doi: 10.1152/japplphysiol.00864.2020. Epub 2020 Dec 31.
5
Impaired neuromuscular transmission of the tibialis anterior in a rodent model of hypertonia.痉挛型脑性瘫痪动物模型中胫骨前肌神经肌肉传递功能障碍。
J Neurophysiol. 2020 May 1;123(5):1864-1869. doi: 10.1152/jn.00095.2020. Epub 2020 Apr 15.
6
Erratum: Eyestalk Ablation to Increase Ovarian Maturation in Mud Crabs.勘误:切除眼柄以增加泥蟹的卵巢成熟度。
J Vis Exp. 2023 May 26(195). doi: 10.3791/6561.
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
Glycine receptor subunit-β-deficiency in a mouse model of spasticity results in attenuated physical performance, growth, and muscle strength.痉挛模型中小鼠甘氨酸受体亚基-β 缺乏导致运动能力、生长和肌肉力量减弱。
Am J Physiol Regul Integr Comp Physiol. 2022 May 1;322(5):R368-R388. doi: 10.1152/ajpregu.00242.2020. Epub 2022 Feb 2.
9
Toxicology and Carcinogenesis Studies of 5,5-Diphenylhydantoin (CAS No. 57-41-0) (Phenytoin) in F344/N Rats and B6C3F1 Mice (Feed Studies).5,5-二苯基乙内酰脲(CAS编号:57-41-0)(苯妥英)在F344/N大鼠和B6C3F1小鼠中的毒理学和致癌性研究(饲料研究)
Natl Toxicol Program Tech Rep Ser. 1993 Nov;404:1-303.
10
Early (< 8 days) systemic postnatal corticosteroids for prevention of bronchopulmonary dysplasia in preterm infants.早期(<8天)全身性产后使用皮质类固醇预防早产儿支气管肺发育不良
Cochrane Database Syst Rev. 2017 Oct 24;10(10):CD001146. doi: 10.1002/14651858.CD001146.pub5.

引用本文的文献

1
Diaphragm Muscle: A Pump That Can Not Fail.膈肌:一个不会失灵的泵。
Physiol Rev. 2025 Jul 11. doi: 10.1152/physrev.00043.2024.
2
Inhibitory Synaptic Influences on Developmental Motor Disorders.抑制性突触对发育性运动障碍的影响。
Int J Mol Sci. 2023 Apr 9;24(8):6962. doi: 10.3390/ijms24086962.
3
Diaphragm muscle function in a mouse model of early-onset spasticity.早期痉挛性瘫痪小鼠模型中的膈肌功能。

本文引用的文献

1
Impaired neuromuscular transmission of the tibialis anterior in a rodent model of hypertonia.痉挛型脑性瘫痪动物模型中胫骨前肌神经肌肉传递功能障碍。
J Neurophysiol. 2020 May 1;123(5):1864-1869. doi: 10.1152/jn.00095.2020. Epub 2020 Apr 15.
2
Phrenic motor neuron loss in an animal model of early onset hypertonia.在早发性张力亢进动物模型中膈神经运动神经元丢失。
J Neurophysiol. 2020 May 1;123(5):1682-1690. doi: 10.1152/jn.00026.2020. Epub 2020 Apr 1.
3
Defining body-weight reduction as a humane endpoint: a critical appraisal.定义体重减轻为一个人道终点:批判性评价。
J Appl Physiol (1985). 2022 Jul 1;133(1):60-68. doi: 10.1152/japplphysiol.00157.2022. Epub 2022 May 19.
4
Diaphragm neuromuscular transmission failure in a mouse model of an early-onset neuromotor disorder.早期运动神经障碍小鼠模型中膈肌神经肌肉传递失败。
J Appl Physiol (1985). 2021 Mar 1;130(3):708-720. doi: 10.1152/japplphysiol.00864.2020. Epub 2020 Dec 31.
Lab Anim. 2020 Feb;54(1):99-110. doi: 10.1177/0023677219883319. Epub 2019 Oct 30.
4
A Critical Evaluation of Current Concepts in Cerebral Palsy.脑性瘫痪当前概念的批判性评价。
Physiology (Bethesda). 2019 May 1;34(3):216-229. doi: 10.1152/physiol.00054.2018.
5
Environmental enrichment prevents pup mortality in laboratory mice.环境富集可预防实验室小鼠幼崽死亡。
Lab Anim. 2019 Feb;53(1):53-62. doi: 10.1177/0023677218777536. Epub 2018 May 22.
6
Differences in lumbar motor neuron pruning in an animal model of early onset spasticity.早发性痉挛动物模型中腰段运动神经元修剪的差异。
J Neurophysiol. 2018 Aug 1;120(2):601-609. doi: 10.1152/jn.00186.2018. Epub 2018 May 2.
7
Intrinsic and synaptic homeostatic plasticity in motoneurons from mice with glycine receptor mutations.甘氨酸受体突变小鼠运动神经元的内在和突触稳态可塑性
J Neurophysiol. 2014 Apr;111(7):1487-98. doi: 10.1152/jn.00728.2013. Epub 2014 Jan 8.
8
Analysis of the medical causes of death in cerebral palsy.脑瘫患者死亡原因的医学分析。
Ann Phys Rehabil Med. 2014 Feb;57(1):24-37. doi: 10.1016/j.rehab.2013.11.002. Epub 2013 Dec 2.
9
Social enrichment during postnatal development induces transgenerational effects on emotional and reproductive behavior in mice.产后发育期间的社会丰富化对小鼠的情绪和生殖行为产生跨代影响。
Front Behav Neurosci. 2009 Sep 15;3:25. doi: 10.3389/neuro.08.025.2009. eCollection 2009.
10
Maternal care affects the development of maternal behavior in inbred mice.母性关怀会影响近交系小鼠母性行为的发育。
Dev Psychobiol. 2009 May;51(4):345-57. doi: 10.1002/dev.20375.