• 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

The influence of genetic background on the susceptibility of inbred mice to streptozotocin-induced diabetes.

作者信息

Wolf J, Lilly F, Shin S I

出版信息

Diabetes. 1984 Jun;33(6):567-71. doi: 10.2337/diab.33.6.567.

DOI:10.2337/diab.33.6.567
PMID:6233198
Abstract

Multiple low-dose injections of streptozotocin (STZ) induce a delayed but progressively increasing state of hyperglycemia in mice. Different inbred strains of mice show different susceptibility to this treatment. We examined whether genetic factors associated with the H-2 complex influence the susceptibility or resistance, using a selected group of 12 inbred and 5 congenic resistant strains of mice. We found that different congenic strains differed significantly in their susceptibility to STZ-induced diabetes, suggesting that H-2-associated genes do influence the susceptibility. However, at least some inbred strains sharing the same H-2 haplotype also differed in their susceptibility, indicating that genes outside the H-2 complex may also affect the susceptibility. Therefore, there appear to be at least two genes, one within and one or more outside the H-2 complex, that determine the susceptibility to multiple low doses of STZ.

摘要

相似文献

1
The influence of genetic background on the susceptibility of inbred mice to streptozotocin-induced diabetes.
Diabetes. 1984 Jun;33(6):567-71. doi: 10.2337/diab.33.6.567.
2
Genetic control of low-dose streptozotocin-induced autoimmune diabetes in mice.低剂量链脲佐菌素诱导的小鼠自身免疫性糖尿病的遗传控制
J Immunol. 1983 Apr;130(4):1719-22.
3
Genetic control by I-A subregion in H-2 complex of incidence of streptozocin-induced autoimmune diabetes in mice.
Diabetes. 1990 Oct;39(10):1298-304. doi: 10.2337/diab.39.10.1298.
4
Absence of H-2 genetic influence on streptozotocin-induced diabetes in mice.
Diabetologia. 1982 Aug;23(2):114-8. doi: 10.1007/BF01271171.
5
Genetic influence of the streptozotocin-induced insulitis and hyperglycemia.
Diabetes. 1977 Oct;26(10):916-20. doi: 10.2337/diab.26.10.916.
6
Murine streptozotocin diabetes: influences of the major histocompatibility complex, genetic background and blood transfusion.小鼠链脲佐菌素糖尿病:主要组织相容性复合体、遗传背景和输血的影响
Diabetologia. 1984 Jul;27 Suppl:160-2. doi: 10.1007/BF00275678.
7
Genetic control of pathogenesis of diabetes in C3H mice. Influence of the major histocompatibility complex.
Diabetes. 1984 Nov;33(11):1068-71. doi: 10.2337/diab.33.11.1068.
8
A single major gene controls most of the difference in susceptibility to streptozotocin-induced diabetes between C57BL/6J and C3H/HeJ mice.一个主要基因控制着C57BL/6J小鼠和C3H/HeJ小鼠对链脲佐菌素诱导糖尿病易感性的大部分差异。
Diabetologia. 1989 Oct;32(10):716-23. doi: 10.1007/BF00274530.
9
Low-dose streptozotocin-induced autoimmune diabetes is under the genetic control of the major histocompatibility complex in mice.
Diabetologia. 1982 Jul;23(1):69-71. doi: 10.1007/BF00257735.
10
Genetic control of susceptibility to streptozotocin diabetes in inbred mice: effect of testosterone and H-2 haplotype.近交系小鼠对链脲佐菌素诱导糖尿病易感性的遗传控制:睾酮和H-2单倍型的影响
Endocrinology. 1985 Jun;116(6):2450-5. doi: 10.1210/endo-116-6-2450.

引用本文的文献

1
Rodent models to study type 1 and type 2 diabetes induced human diabetic nephropathy.用于研究 1 型和 2 型糖尿病诱导的人类糖尿病肾病的啮齿动物模型。
Mol Biol Rep. 2023 Sep;50(9):7759-7782. doi: 10.1007/s11033-023-08621-z. Epub 2023 Jul 17.
2
Maternal hyperglycemia and fetal cardiac development: Clinical impact and underlying mechanisms.母体高血糖与胎儿心脏发育:临床影响及潜在机制。
Birth Defects Res. 2018 Dec 1;110(20):1504-1516. doi: 10.1002/bdr2.1435.
3
Induction of insulitis by glutamic acid decarboxylase peptide-specific and HLA-DQ8-restricted CD4(+) T cells from human DQ transgenic mice.
来自人DQ转基因小鼠的谷氨酸脱羧酶肽特异性且受HLA-DQ8限制的CD4(+) T细胞诱导胰岛炎
J Clin Invest. 1998 Sep 1;102(5):947-57. doi: 10.1172/JCI2723.
4
Susceptibility to db gene and streptozotocin-induced diabetes in C57BL mice: control by gender-associated, MHC-unlinked traits.C57BL小鼠对db基因和链脲佐菌素诱导糖尿病的易感性:由性别相关、与主要组织相容性复合体(MHC)无关的性状控制。
Immunogenetics. 1987;26(1-2):6-13. doi: 10.1007/BF00345448.
5
Essential fatty acid deficiency prevents multiple low-dose streptozotocin-induced diabetes in CD-1 mice.必需脂肪酸缺乏可预防CD-1小鼠中多次低剂量链脲佐菌素诱导的糖尿病。
Proc Natl Acad Sci U S A. 1988 Aug;85(16):6137-41. doi: 10.1073/pnas.85.16.6137.
6
Multiple low-dose streptozotocin-induced diabetes in the mouse: further evidence for involvement of an anti-B cell cytotoxic cellular auto-immune response.多次低剂量链脲佐菌素诱导的小鼠糖尿病:抗B细胞细胞毒性细胞自身免疫反应参与的进一步证据。
Diabetologia. 1987 Apr;30(4):232-8. doi: 10.1007/BF00270421.
7
A single major gene controls most of the difference in susceptibility to streptozotocin-induced diabetes between C57BL/6J and C3H/HeJ mice.一个主要基因控制着C57BL/6J小鼠和C3H/HeJ小鼠对链脲佐菌素诱导糖尿病易感性的大部分差异。
Diabetologia. 1989 Oct;32(10):716-23. doi: 10.1007/BF00274530.
8
The anti-diabetogenic effect of essential fatty acid deficiency in multiple low-dose streptozotocin-treated mice persists if essential fatty acid repletion occurs outside of a brief window of susceptibility.
Diabetologia. 1991 Oct;34(10):709-14. doi: 10.1007/BF00401515.