• 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

在年轻的DBA/2J mdx小鼠的骨骼肌和心肌中,肌(内)质网钙-ATP酶功能受损。

Sarco(endo)plasmic reticulum Ca-ATPase function is impaired in skeletal and cardiac muscles from young DBA/2J mdx mice.

作者信息

Cleverdon Riley E G, Braun Jessica L, Geromella Mia S, Whitley Kennedy C, Marko Daniel M, Hamstra Sophie I, Roy Brian D, MacPherson Rebecca E K, Fajardo Val A

机构信息

Department of Kinesiology, Brock University, 1812 Sir Isaac Brock Way, St. Catharines, ON, L2S 3A1, Canada.

Centre for Bone and Muscle Health, Brock University, St. Catharines, ON, Canada.

出版信息

iScience. 2022 Aug 18;25(9):104972. doi: 10.1016/j.isci.2022.104972. eCollection 2022 Sep 16.

DOI:10.1016/j.isci.2022.104972
PMID:36093052
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9459692/
Abstract

The DBA/2J (D2) mouse is a more severe model of Duchenne muscular dystrophy when compared to the traditional C57BL/10 (C57) mouse. Here, we questioned whether sarco(endo)plasmic reticulum Ca-ATPase (SERCA) function would differ in muscles from young D2 and C57 mice. Both D2 and C57 mice exhibited signs of impaired Ca uptake in the gastrocnemius, diaphragm, and left ventricle; however, the level of impairment was more severe in D2 mice. Reductions in maximal SERCA activity were also more prominent in the D2 gastrocnemius and diaphragm when compared to those from C57 mice; however, there were no differences detected in the left ventricle. Across all muscles, D2 mice had the highest levels of oxidative stress as indicated by protein nitrosylation and/or nitration. In conclusion, our study shows that SERCA function is more impaired in young D2 mice compared with age-matched C57 mice.

摘要

与传统的C57BL/10(C57)小鼠相比,DBA/2J(D2)小鼠是杜氏肌营养不良症更严重的模型。在此,我们质疑肌浆(内质)网Ca-ATP酶(SERCA)功能在年轻D2和C57小鼠的肌肉中是否会有所不同。D2和C57小鼠在腓肠肌、膈肌和左心室中均表现出钙摄取受损的迹象;然而,D2小鼠的受损程度更严重。与C57小鼠相比,D2腓肠肌和膈肌中SERCA最大活性的降低也更显著;然而,左心室中未检测到差异。在所有肌肉中,蛋白质亚硝化和/或硝化表明D2小鼠的氧化应激水平最高。总之,我们的研究表明,与年龄匹配的C57小鼠相比,年轻D2小鼠的SERCA功能受损更严重。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d12e/9459692/526e8518f75c/gr6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d12e/9459692/671d44384e9f/fx1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d12e/9459692/c5f12144e11d/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d12e/9459692/7ae31cc1b9ba/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d12e/9459692/b111ebcfeeb7/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d12e/9459692/1d46d91708ba/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d12e/9459692/3b7afd8ee45d/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d12e/9459692/526e8518f75c/gr6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d12e/9459692/671d44384e9f/fx1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d12e/9459692/c5f12144e11d/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d12e/9459692/7ae31cc1b9ba/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d12e/9459692/b111ebcfeeb7/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d12e/9459692/1d46d91708ba/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d12e/9459692/3b7afd8ee45d/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d12e/9459692/526e8518f75c/gr6.jpg

相似文献

1
Sarco(endo)plasmic reticulum Ca-ATPase function is impaired in skeletal and cardiac muscles from young DBA/2J mdx mice.在年轻的DBA/2J mdx小鼠的骨骼肌和心肌中,肌(内)质网钙-ATP酶功能受损。
iScience. 2022 Aug 18;25(9):104972. doi: 10.1016/j.isci.2022.104972. eCollection 2022 Sep 16.
2
Kynurenine metabolism is altered in mdx mice: a potential muscle to brain connection.肌营养不良症模型小鼠色氨酸代谢改变:肌肉与大脑关联的潜在机制。
Exp Physiol. 2022 Sep;107(9):1029-1036. doi: 10.1113/EP090381. Epub 2022 Aug 15.
3
Characterization of Alzheimer's disease-like neuropathology in Duchenne's muscular dystrophy using the DBA/2J mdx mouse model.利用 DBA/2J mdx 小鼠模型对杜氏肌营养不良症中的阿尔茨海默病样神经病理学进行特征描述。
FEBS Open Bio. 2022 Jan;12(1):154-162. doi: 10.1002/2211-5463.13317. Epub 2021 Nov 11.
4
Increased sarcolipin expression and decreased sarco(endo)plasmic reticulum Ca2+ uptake in skeletal muscles of mouse models of Duchenne muscular dystrophy.在杜氏肌营养不良症的小鼠模型的骨骼肌中,肌浆球蛋白表达增加,肌浆(内质)网 Ca2+摄取减少。
J Muscle Res Cell Motil. 2013 Dec;34(5-6):349-56. doi: 10.1007/s10974-013-9350-0. Epub 2013 Jun 8.
5
Effect of genetic background on the dystrophic phenotype in mdx mice.遗传背景对mdx小鼠营养不良表型的影响。
Hum Mol Genet. 2016 Jan 1;25(1):130-45. doi: 10.1093/hmg/ddv460. Epub 2015 Nov 12.
6
Indices of Defective Autophagy in Whole Muscle and Lysosome Enriched Fractions From Aged D2-mdx Mice.衰老的D2-mdx小鼠全肌肉和富含溶酶体组分中自噬缺陷的指标
Front Physiol. 2021 Jul 9;12:691245. doi: 10.3389/fphys.2021.691245. eCollection 2021.
7
The D2.mdx mouse as a preclinical model of the skeletal muscle pathology associated with Duchenne muscular dystrophy.D2.mdx 小鼠作为与杜氏肌营养不良症相关的骨骼肌病理的临床前模型。
Sci Rep. 2020 Aug 21;10(1):14070. doi: 10.1038/s41598-020-70987-y.
8
Lipogenesis mitigates dysregulated sarcoplasmic reticulum calcium uptake in muscular dystrophy.脂肪生成减轻了肌肉营养不良中肌浆网钙摄取的失调。
Biochim Biophys Acta. 2015 Dec;1851(12):1530-8. doi: 10.1016/j.bbalip.2015.09.001. Epub 2015 Sep 8.
9
Blunted cardiac beta-adrenergic response as an early indication of cardiac dysfunction in Duchenne muscular dystrophy.心脏β-肾上腺素能反应迟钝是杜氏肌营养不良症心脏功能障碍的早期迹象。
Cardiovasc Res. 2014 Jul 1;103(1):60-71. doi: 10.1093/cvr/cvu119. Epub 2014 May 8.
10
Alteration of skeletal and cardiac muscles function in mice background: a focus on high intensity interval training.小鼠背景下骨骼肌和心肌功能的改变:聚焦于高强度间歇训练
Intractable Rare Dis Res. 2021 Nov;10(4):269-275. doi: 10.5582/irdr.2021.01097.

引用本文的文献

1
Inhibition of mitochondrial fission protein Drp1 ameliorates skeletal myopathy in the D2-mdx model of Duchenne muscular dystrophy.抑制线粒体分裂蛋白Drp1可改善杜氏肌营养不良症D2-mdx模型中的骨骼肌病。
Am J Physiol Cell Physiol. 2025 Jul 1;329(1):C307-C324. doi: 10.1152/ajpcell.01009.2024. Epub 2025 Jun 16.
2
GSK3 inhibition improves skeletal muscle function and whole-body metabolism in male mouse models of Duchenne muscular dystrophy.GSK3 抑制可改善杜氏肌营养不良症雄性小鼠模型的骨骼肌功能和整体代谢。
Nat Commun. 2024 Nov 25;15(1):10210. doi: 10.1038/s41467-024-53886-y.
3
Spaceflight increases sarcoplasmic reticulum Ca leak and this cannot be counteracted with BuOE treatment.

本文引用的文献

1
Time course and fibre type-dependent nature of calcium-handling protein responses to sprint interval exercise in human skeletal muscle.人类骨骼肌中钙处理蛋白对短跑间歇运动反应的时间进程及纤维类型依赖性特征
J Physiol. 2022 Jun;600(12):2897-2917. doi: 10.1113/JP282739. Epub 2022 May 29.
2
Role of SERCA and sarcolipin in adaptive muscle remodeling.肌浆网钙 ATP 酶和肌浆网钙结合蛋白在适应性肌肉重塑中的作用。
Am J Physiol Cell Physiol. 2022 Mar 1;322(3):C382-C394. doi: 10.1152/ajpcell.00198.2021. Epub 2022 Jan 19.
3
Reducing sarcolipin expression improves muscle metabolism in mice.
太空飞行会增加肌浆网钙泄漏,而这种情况无法通过丁基氧化偶氮醇(BuOE)治疗来抵消。
NPJ Microgravity. 2024 Jul 19;10(1):78. doi: 10.1038/s41526-024-00419-y.
4
Perimenopause Decreases SERCA2a Activity in the Hearts of a Mouse Model of Ovarian Failure.围绝经期降低卵巢衰竭小鼠模型心脏中的 SERCA2a 活性。
Biomolecules. 2024 Jun 9;14(6):675. doi: 10.3390/biom14060675.
5
Ion Channels of the Sarcolemma and Intracellular Organelles in Duchenne Muscular Dystrophy: A Role in the Dysregulation of Ion Homeostasis and a Possible Target for Therapy.肌细胞膜的离子通道和细胞内细胞器在杜氏肌营养不良症中的作用:在离子动态平衡失调中的作用及可能的治疗靶点。
Int J Mol Sci. 2023 Jan 23;24(3):2229. doi: 10.3390/ijms24032229.
6
Histological Methods to Assess Skeletal Muscle Degeneration and Regeneration in Duchenne Muscular Dystrophy.评估杜氏肌营养不良症骨骼肌退化和再生的组织学方法。
Int J Mol Sci. 2022 Dec 16;23(24):16080. doi: 10.3390/ijms232416080.
降低肌浆球蛋白表达可改善小鼠的肌肉代谢。
Am J Physiol Cell Physiol. 2022 Feb 1;322(2):C260-C274. doi: 10.1152/ajpcell.00125.2021. Epub 2022 Jan 5.
4
Murine models of Duchenne muscular dystrophy: is there a best model?杜氏肌营养不良症的小鼠模型:是否存在最佳模型?
Am J Physiol Cell Physiol. 2021 Aug 1;321(2):C409-C412. doi: 10.1152/ajpcell.00212.2021. Epub 2021 Jul 14.
5
Sarcolipin haploinsufficiency prevents dystrophic cardiomyopathy in mice.肌联蛋白单倍不足可预防小鼠的营养不良性心肌病。
Am J Physiol Heart Circ Physiol. 2021 Jan 1;320(1):H200-H210. doi: 10.1152/ajpheart.00601.2020. Epub 2020 Nov 20.
6
The D2.mdx mouse as a preclinical model of the skeletal muscle pathology associated with Duchenne muscular dystrophy.D2.mdx 小鼠作为与杜氏肌营养不良症相关的骨骼肌病理的临床前模型。
Sci Rep. 2020 Aug 21;10(1):14070. doi: 10.1038/s41598-020-70987-y.
7
TGF-β-driven muscle degeneration and failed regeneration underlie disease onset in a DMD mouse model.TGF-β 驱动的肌肉退化和再生失败是 DMD 小鼠模型疾病发作的基础。
JCI Insight. 2020 Mar 26;5(6):135703. doi: 10.1172/jci.insight.135703.
8
Single SERCA2a Therapy Ameliorated Dilated Cardiomyopathy for 18 Months in a Mouse Model of Duchenne Muscular Dystrophy.单一 SERCA2a 治疗可改善杜氏肌营养不良症小鼠模型的扩张型心肌病 18 个月。
Mol Ther. 2020 Mar 4;28(3):845-854. doi: 10.1016/j.ymthe.2019.12.011. Epub 2020 Jan 10.
9
Three weeks of sprint interval training improved high-intensity cycling performance and limited ryanodine receptor modifications in recreationally active human subjects.三周的冲刺间歇训练提高了业余活跃人群的高强度自行车运动表现,并限制了兰尼碱受体的改变。
Eur J Appl Physiol. 2019 Sep;119(9):1951-1958. doi: 10.1007/s00421-019-04183-w. Epub 2019 Jun 27.
10
Natural disease history of the D2 mouse model for Duchenne muscular dystrophy.Duchenne 型肌营养不良症 D2 小鼠模型的自然病史。
FASEB J. 2019 Jul;33(7):8110-8124. doi: 10.1096/fj.201802488R. Epub 2019 Apr 1.