首页期刊介绍编委会投稿指南期刊订阅广告合作留言板联系我们English
包峰云,龙红,秦廷洋,霍春茂,唐克桐,张仕斌.自发矮小症突变大鼠家系的建立及其主要生物学特性测定[J].中国实验动物学报,2022,30(6):792~799.
自发矮小症突变大鼠家系的建立及其主要生物学特性测定
Establishment of a rat model family with spontaneous short stature and identification of its main biological characteristics
投稿时间:2022-05-16  
DOI:10. 3969 / j.issn.1005-4847. 2022. 06. 008
中文关键词:  矮小症  SD 大鼠  动物模型  表型鉴定
英文关键词:short stature  SD rat  animal model  phenotypic identification
基金项目:
作者单位
包峰云 贵州遵义医科大学实验动物中心,贵州 遵义 563006 
龙红 贵州遵义医科大学实验动物中心,贵州 遵义 563006 
秦廷洋 贵州遵义医科大学实验动物中心,贵州 遵义 563006 
霍春茂 贵州遵义医科大学实验动物中心,贵州 遵义 563006 
唐克桐 贵州遵义医科大学实验动物中心,贵州 遵义 563006 
张仕斌 贵州遵义医科大学实验动物中心,贵州 遵义 563006 
Author NameAffiliation
BAO Fengyun Laboratory Animal Center of Zunyi Medical University, Zunyi 563006, China 
LONG Hong Laboratory Animal Center of Zunyi Medical University, Zunyi 563006, China 
QIN Tingyang Laboratory Animal Center of Zunyi Medical University, Zunyi 563006, China 
HUO Chunmao Laboratory Animal Center of Zunyi Medical University, Zunyi 563006, China 
TANG Ketong Laboratory Animal Center of Zunyi Medical University, Zunyi 563006, China 
ZHANG Shibin Laboratory Animal Center of Zunyi Medical University, Zunyi 563006, China 
摘要点击次数: 88
全文下载次数: 22
中文摘要:
       目的 建立自发常染色体显性突变矮小症 SD 大鼠模型家系,测定其主要生物学特性数据。 方法 将封闭群 SD 大鼠生产群中出现的矮小症突变个体扩群繁殖建立家系,统计后代中矮小症与正常个体的性状分离比例,鉴定其遗传模式;测定家系个体的体重、体尺,主要脏器重量及指数,血液生理(18 项)生化(20 项)等指标以 及繁殖性能等数据,明确突变个体的表型特征及生物学特性。 结果 建立了自发常染色体显性突变的矮小症 SD 大鼠封闭群家系,家系暂时命名为 SSR;成年(12 周龄) SSR 体重分别为野生型的 57%(?)和 65%(♀),差异极具 显著(P< 0. 01);成年 SSR 体长、尾长、胫骨长、股骨长等体尺数据以及主要脏器(心、肝、脾、肺、肾、睾丸/ 卵巢)重量均显著低于野生型大鼠(P< 0. 01);成年 SSR 胫骨长、股骨长指数及主要脏器(心、肝、脾、肺、肾、睾丸/ 卵巢)指数与野生型之间无显著性差异(P> 0. 05);成年雌性 SSR 生殖器官发育正常,但不排卵。 结论 建立了能稳定遗传的自发常染色体显性突变的矮小症 SD 大鼠家系,可作为人类生长发育及生殖功能研究的动物模型。
英文摘要:
       Objective The aim of this study was to establish a rat model of spontaneous short stature associated with female infertility. The main biological characteristics of the rat model were then identified. Methods The pedigree of mutant individuals with a short stature in the production group of SD rats was established by expanding the population. The proportion of offspring of mutant individuals with a short stature and that of the normal individuals was calculated and the genetic model was identified. Weight, body size, weight and index of main organs, blood physiology ( 18 items), biochemistry ( 20 items ), and reproductive performance of the mutant individuals were determined to clarify their phenotypic characteristics and biological characteristics. Results A family of SD rats with idiopathic autosomal dominant mutations was established, which was named SSR. Adult (12 weeks old) SSR rat weights were 57% of wildtype (?) and 65% (♀),Very significant difference (P< 0. 01) . The body length, tail length, tibia length, femur length and other body size data of adult SSR and the weight of main organs ( heart, liver, spleen, lungs, kidneys, testes/ ovaries) were significantly lower than those of wild type rats (P< 0. 01); There were no significant differences in the adult SSR rat shinbone length, femoral bone length index, or major organ indexes, compared with the wildtype ( P> 0. 05 ). Reproductive organ development of adult female rats was normal, but ovulation was not observed. Conclusions Spontaneous autosomal dominant mutations in dwarfism lines that can be stably inherited were established, which can be used as an applied study for human growth and infertility models. Female individuals were found to be infertile during the study, but further studies are needed to determine whether infertile individuals can have children.
查看全文  查看/发表评论  下载PDF阅读器
关闭
您是第 3270074 位访问者
版权所有:中国实验动物学会 主管单位:中国科学技术协会 主办单位:中国实验动物学会    中国医学科学院医学实验动物研究所
地  址: 北京市朝阳区潘家园南里5号 邮编:100021 电话:010-67779337 E-mail:bjb2@cnilas.org
本系统由北京勤云科技发展有限公司设计
微信关注二维码