• 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

大鼠左心室实验性梗死灶周边缺血区的超微结构变化

Ultrastructural changes in the ischemic zone bordering experimental infarcts in rat left ventricles.

作者信息

Page E, Polimeni P I

出版信息

Am J Pathol. 1977 Apr;87(1):81-104.

PMID:851166
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2032068/
Abstract

Ultrastructural changes in myocardial cells from the ischemic border of infarcts (produced in rat left ventricles by ligating the anterior coronary artery in vivo) were examined 1 to 24 hours after ligation. Twenty-four hours after ligation, irreversibly injured cells showed a selective spreading of Z-band material over the I band; disappearance of M bands, prominent N bands, and disassembly of A bands were also noteworthy. Sixty minutes after ligation the cells of the ischemic border were ultrastructurally normal except for paradoxically relaxed sarcomeres, indicative of an inability to contract in response to the calcium influx produced by osmium tetroxide; progressive vacuolization of this zone was evident after 4 to 12 hours. Paradoxical relaxation may be an ultrastructural correlate of acute ischemic "pump failure".

摘要

对在体结扎大鼠左冠状动脉造成梗死灶缺血边缘区的心肌细胞进行超微结构变化检测,检测时间为结扎后1至24小时。结扎24小时后,不可逆损伤的细胞显示Z带物质选择性地扩展至I带;M带消失、N带突出以及A带解体也值得注意。结扎60分钟后,缺血边缘区的细胞超微结构正常,只是肌节出现反常松弛,这表明细胞无法对四氧化锇引发的钙内流做出收缩反应;4至12小时后,该区域逐渐出现空泡化。反常松弛可能是急性缺血性“泵衰竭”的超微结构相关表现。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a51a/2032068/e0fef2991de2/amjpathol00398-0108-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a51a/2032068/57aee540f186/amjpathol00398-0102-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a51a/2032068/f4b273ef8648/amjpathol00398-0102-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a51a/2032068/49801254976d/amjpathol00398-0102-c.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a51a/2032068/ed956a3ba94f/amjpathol00398-0110-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a51a/2032068/36482cb405cd/amjpathol00398-0110-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a51a/2032068/8ab3f2406ac6/amjpathol00398-0103-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a51a/2032068/33dc2123a55e/amjpathol00398-0111-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a51a/2032068/df5925c4ffa7/amjpathol00398-0111-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a51a/2032068/a18f2875a72e/amjpathol00398-0104-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a51a/2032068/203a2b84c0be/amjpathol00398-0112-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a51a/2032068/a2f416902e0d/amjpathol00398-0112-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a51a/2032068/bade6656de52/amjpathol00398-0105-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a51a/2032068/a755fbb6df22/amjpathol00398-0113-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a51a/2032068/476c76485733/amjpathol00398-0106-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a51a/2032068/e66fc31d65ac/amjpathol00398-0107-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a51a/2032068/8196080a552a/amjpathol00398-0107-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a51a/2032068/cef0ea831f27/amjpathol00398-0108-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a51a/2032068/e0fef2991de2/amjpathol00398-0108-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a51a/2032068/57aee540f186/amjpathol00398-0102-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a51a/2032068/f4b273ef8648/amjpathol00398-0102-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a51a/2032068/49801254976d/amjpathol00398-0102-c.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a51a/2032068/ed956a3ba94f/amjpathol00398-0110-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a51a/2032068/36482cb405cd/amjpathol00398-0110-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a51a/2032068/8ab3f2406ac6/amjpathol00398-0103-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a51a/2032068/33dc2123a55e/amjpathol00398-0111-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a51a/2032068/df5925c4ffa7/amjpathol00398-0111-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a51a/2032068/a18f2875a72e/amjpathol00398-0104-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a51a/2032068/203a2b84c0be/amjpathol00398-0112-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a51a/2032068/a2f416902e0d/amjpathol00398-0112-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a51a/2032068/bade6656de52/amjpathol00398-0105-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a51a/2032068/a755fbb6df22/amjpathol00398-0113-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a51a/2032068/476c76485733/amjpathol00398-0106-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a51a/2032068/e66fc31d65ac/amjpathol00398-0107-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a51a/2032068/8196080a552a/amjpathol00398-0107-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a51a/2032068/cef0ea831f27/amjpathol00398-0108-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a51a/2032068/e0fef2991de2/amjpathol00398-0108-b.jpg

相似文献

1
Ultrastructural changes in the ischemic zone bordering experimental infarcts in rat left ventricles.大鼠左心室实验性梗死灶周边缺血区的超微结构变化
Am J Pathol. 1977 Apr;87(1):81-104.
2
Sites and mechanisms of localization of technetium-99m phosphorus radiopharmaceuticals in acute myocardial infarcts and other tissues.锝-99m磷放射性药物在急性心肌梗死及其他组织中的定位部位和机制。
J Clin Invest. 1977 Sep;60(3):724-40. doi: 10.1172/JCI108825.
3
Formation of leptofibrils is associated with remodelling of muscle cells and myofibrillogenesis in the border zone of myocardial infarction.细肌丝的形成与心肌梗死边缘区的肌肉细胞重塑和肌原纤维生成有关。
Micron. 2007;38(6):659-67. doi: 10.1016/j.micron.2006.08.006. Epub 2006 Sep 25.
4
[Size of myocardial sarcomeres and their potential use in the histological diagnosis of acute myocardial infarct].
Arkh Patol. 1981;43(1):24-9.
5
Ultrastructural influence of reperfusing dog myocardium with calcium-free blood after coronary artery occlusion.冠状动脉闭塞后用无钙血液再灌注犬心肌的超微结构影响
Am J Pathol. 1978 Feb;90(2):423-34.
6
The MRL mouse repairs both cryogenic and ischemic myocardial infarcts with scar.MRL小鼠能通过形成瘢痕修复低温和缺血性心肌梗死。
Cardiovasc Pathol. 2008 Jan-Feb;17(1):14-22. doi: 10.1016/j.carpath.2007.01.007. Epub 2007 Apr 2.
7
The effects of left coronary artery ligation on rat heart muscle angiographic, morphologic and chemical studies:左冠状动脉结扎对大鼠心肌血管造影、形态学及化学研究的影响:
Ann Acad Sci Fenn A. 1974(161):1-60.
8
High rate of right ventricular infarction after ligation of mid left anterior descending artery in rats.大鼠左前降支中段结扎后右心室梗死发生率高。
Cardiovasc Revasc Med. 2005 Jan-Mar;6(1):21-3. doi: 10.1016/j.carrev.2005.04.005.
9
Cytochemical localization of lysosomal enzyme activity in normal and ischemic dog myocardium.正常和缺血犬心肌中溶酶体酶活性的细胞化学定位
Am J Pathol. 1975 May;79(2):193-206.
10
Morphometric quantitation of early autolytic changes in rat myocardial cells.大鼠心肌细胞早期自溶变化的形态计量学定量分析。
Res Vet Sci. 1990 May;48(3):276-9.

引用本文的文献

1
Experimental acute myocardial infarction: telocytes involvement in neo-angiogenesis.实验性急性心肌梗死:telocytes 参与新生血管形成。
J Cell Mol Med. 2011 Nov;15(11):2284-96. doi: 10.1111/j.1582-4934.2011.01449.x.
2
Histoenzymological study of myocardial ATPase activity in experimental infarction in the rat.大鼠实验性梗死心肌ATP酶活性的组织酶学研究
Basic Res Cardiol. 1981 Nov-Dec;76(6):602-11. doi: 10.1007/BF01908050.
3
Response of the border zone to myocardial infarction in rats.大鼠心肌梗死边缘区的反应

本文引用的文献

1
Fatty change of the myocardium in early experimental infarction.
AMA Arch Pathol. 1956 Oct;62(4):318-23.
2
Ultrastructural changes in kidney, myocardium and skeletal muscle of the dog during excessive mobilization of free fatty acids.
J Ultrastruct Res. 1966 Sep;16(1):35-54. doi: 10.1016/s0022-5320(66)80021-7.
3
Inward spread of activation in vertebrate muscle fibres.脊椎动物肌纤维中激活的内向传播。
J Physiol. 1971 Feb;212(3):777-99. doi: 10.1113/jphysiol.1971.sp009356.
4
Am J Pathol. 1986 Dec;125(3):476-83.
4
The "border zone" in myocardial infarction. An ultrastructural study in the dog using an electron-dense blood flow marker.心肌梗死中的“边缘区”。使用电子致密血流标记物对犬进行的超微结构研究。
Am J Pathol. 1988 Jun;131(3):452-64.
5
Effects of verapamil and timolol on cellular morphometric changes in cat hearts with regional ischaemia.
Virchows Arch A Pathol Anat Histopathol. 1988;412(4):291-9. doi: 10.1007/BF00750254.
6
Ca overload and the action of calcium sensitive proteases, phospholipases and prostaglandin E2 in myocardial cell degradation.
Basic Res Cardiol. 1985 May-Jun;80(3):303-15. doi: 10.1007/BF01907906.
7
Ultrastructure of the myocardium after pulmonary embolism. A study in the rat.肺栓塞后心肌的超微结构。大鼠研究。
Am J Pathol. 1978 Aug;92(2):421-58.
8
The relaxation of sarcomeres in ischemic injury of myocardium.心肌缺血性损伤中肌节的舒张。
Virchows Arch A Pathol Anat Histol. 1978 Oct 26;380(2):149-54. doi: 10.1007/BF00430621.
Healing process in the marginal zone of an experimental myocardial infarct. Findings in the surviving cardiac muscle cells.实验性心肌梗死边缘区的愈合过程。存活心肌细胞的研究结果。
Am J Pathol. 1971 Mar;62(3):321-38.
5
Early phase of myocardial ischemic injury and infarction.心肌缺血性损伤和梗死的早期阶段。
Am J Cardiol. 1969 Dec;24(6):753-65. doi: 10.1016/0002-9149(69)90464-0.
6
On rate-controlling factors of long chain fatty acid oxidation.论长链脂肪酸氧化的速率控制因素。
J Biol Chem. 1971 Sep 10;246(17):5384-90.
7
Kinetics of calcium accumulation in acute myocardial ischemic injury.急性心肌缺血损伤中钙蓄积的动力学
Am J Pathol. 1972 Jun;67(3):441-52.
8
Myocardial calcium and magnesium in acute ischemic injury.急性缺血性损伤中的心肌钙和镁
Am J Pathol. 1972 Jun;67(3):417-40.
9
Ca 2+ -specific removal of Z lines from rabbit skeletal muscle.从兔骨骼肌中特异性去除Z线的钙离子作用。
J Cell Biol. 1972 Feb;52(2):367-81. doi: 10.1083/jcb.52.2.367.
10
Structural changes in myocardium during acute ischemia.急性缺血期间心肌的结构变化。
Circ Res. 1974 Sep;35 Suppl 3:156-72.