• 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

糖酵解在豚鼠结肠带缺氧时张力发展中的作用。

Role of glycolysis in the tension development under anoxia in guinea pig taenia coli.

作者信息

Nasu T, Yui K, Nakagawa H, Ishida Y

出版信息

Jpn J Pharmacol. 1982 Feb;32(1):65-71. doi: 10.1254/jjp.32.65.

DOI:10.1254/jjp.32.65
PMID:7087264
Abstract

The role of glycolysis in the tension development under anoxic conditions in a high-K medium was studied in the intestinal smooth muscle of guinea pig taenia coli. After exposure to the high-K medium (isotonic, 60 mM) under normal oxygen for 30 min, the muscles were exposed to a high-K medium bubbled with N2 gas. The tonic contraction decreased gradually to about 10% of the original level. Glucose was then cumulatively added to the high-K medium under anoxia. The maximum tension was observed following the addition of the higher concentrations of glucose. The muscle tension which developed in the high-K medium with a high concentration of glucose under anoxia was dependent on the external Ca2+ and was inhibited by iodoacetic acid (IAA). The addition of glucose to a high-K medium under anoxia also increased lactate release from the muscle. Pretreatment with 1 mM IAA decreased the lactate release from the muscle. In a Ca2+-free medium under anoxia, the addition of glucose did not increase the muscle tension although there was a significant increase in the lactate release. In summary, it is considered that the smooth muscle of taenia coli develops tension utilizing energy produced by the glycolytic pathway under anoxia in a high-K medium.

摘要

在豚鼠结肠带肠平滑肌中,研究了糖酵解在高钾培养基缺氧条件下张力发展中的作用。在正常氧气条件下,将肌肉暴露于高钾培养基(等渗,60 mM)30分钟后,再将其暴露于用氮气鼓泡的高钾培养基中。强直收缩逐渐降至原始水平的约10%。然后在缺氧条件下向高钾培养基中累积添加葡萄糖。添加较高浓度葡萄糖后观察到最大张力。缺氧条件下在含高浓度葡萄糖的高钾培养基中产生的肌肉张力依赖于细胞外Ca2+,并被碘乙酸(IAA)抑制。在缺氧条件下向高钾培养基中添加葡萄糖也会增加肌肉中乳酸的释放。用1 mM IAA预处理可减少肌肉中乳酸的释放。在缺氧的无钙培养基中,添加葡萄糖虽会使乳酸释放显著增加,但不会增加肌肉张力。总之,认为结肠带平滑肌在高钾培养基缺氧条件下利用糖酵解途径产生的能量来发展张力。

相似文献

1
Role of glycolysis in the tension development under anoxia in guinea pig taenia coli.糖酵解在豚鼠结肠带缺氧时张力发展中的作用。
Jpn J Pharmacol. 1982 Feb;32(1):65-71. doi: 10.1254/jjp.32.65.
2
Tension maintenance, calcium content and energy production of the taenia of the guinea-pig caecum under hypoxia.缺氧状态下豚鼠盲肠带的张力维持、钙含量及能量产生
J Physiol. 1984 Feb;347:149-59. doi: 10.1113/jphysiol.1984.sp015058.
3
The recovery from the relaxant effect by ouabain and the metabolic dependency of K+ contractions in guinea-pig taenia coli.
Comp Biochem Physiol C Comp Pharmacol Toxicol. 1991;99(3):467-73. doi: 10.1016/0742-8413(91)90273-v.
4
Iodoacetic acid-induced rigor in ileal longitudinal smooth muscle of guinea-pig.
Comp Biochem Physiol C Comp Pharmacol Toxicol. 1990;97(2):269-74. doi: 10.1016/0742-8413(90)90140-5.
5
Effects of hypoxia on high-energy phosphagen content, energy metabolism and isometric force in guinea-pig taenia caeci.缺氧对豚鼠盲肠带高能磷酸原含量、能量代谢及等长力的影响。
J Physiol. 1990 May;424:41-56. doi: 10.1113/jphysiol.1990.sp018054.
6
Effects of ouabain on contractions induced by manganese ions in C2+a-free, isotonic solutions with varying concentrations of K+ in guinea-pig taenia coli.哇巴因对豚鼠结肠带无钙、等渗且含不同浓度钾离子的溶液中锰离子诱导的收缩的影响。
Fundam Clin Pharmacol. 2005 Jun;19(3):355-63. doi: 10.1111/j.1472-8206.2005.00334.x.
7
Selective utilization of L-isomer of lactate in the smooth muscle of the guinea pig taenia caeci.豚鼠盲肠带平滑肌中乳酸L-异构体的选择性利用
Can J Physiol Pharmacol. 1989 Dec;67(12):1540-3. doi: 10.1139/y89-248.
8
Dissociation of K+-induced tension and cellular Ca2+ retention in vascular and intestinal smooth muscle in normoxia and hypoxia.常氧和低氧条件下血管及肠道平滑肌中钾离子诱导的张力与细胞内钙离子潴留的解离
Pflugers Arch. 1982 Aug;394(2):118-23. doi: 10.1007/BF00582912.
9
Regulation of metabolism and contraction by cytoplasmic calcium in the intestinal smooth muscle.细胞质钙对肠道平滑肌代谢和收缩的调节作用。
J Biol Chem. 1988 Oct 5;263(28):14074-9.
10
Metabolic dependency of cadmium uptake and the relaxant effects of cadmium in smooth muscle of guinea pig tenia coli.豚鼠结肠带平滑肌中镉摄取的代谢依赖性及镉的舒张作用
Pharmacology. 1985;30(5):281-8. doi: 10.1159/000138079.

引用本文的文献

1
Phloridzin inhibits high K-induced contraction via the inhibition of sodium: glucose cotransporter 1 in rat ileum.根皮苷通过抑制大鼠回肠中的钠-葡萄糖协同转运蛋白1来抑制高钾诱导的收缩。
J Vet Med Sci. 2017 Mar 23;79(3):593-601. doi: 10.1292/jvms.16-0560. Epub 2017 Feb 11.
2
Hypoxia-induced inhibition of calcium channels in guinea-pig taenia caeci smooth muscle cells.缺氧对豚鼠盲肠平滑肌细胞钙通道的抑制作用。
J Physiol. 1997 Nov 15;505 ( Pt 1)(Pt 1):107-19. doi: 10.1111/j.1469-7793.1997.107bc.x.
3
Dissociation of K+-induced tension and cellular Ca2+ retention in vascular and intestinal smooth muscle in normoxia and hypoxia.
常氧和低氧条件下血管及肠道平滑肌中钾离子诱导的张力与细胞内钙离子潴留的解离
Pflugers Arch. 1982 Aug;394(2):118-23. doi: 10.1007/BF00582912.
4
The inhibitory effect of X537A on vascular and intestinal smooth muscle contraction.X537A对血管和平滑肌收缩的抑制作用。 (注:原文中intestinal应为intestinal,你提供的原文可能有误,这里按照正确的词汇进行翻译)
Naunyn Schmiedebergs Arch Pharmacol. 1984 Jan;325(1):80-4. doi: 10.1007/BF00507058.
5
Tension maintenance, calcium content and energy production of the taenia of the guinea-pig caecum under hypoxia.缺氧状态下豚鼠盲肠带的张力维持、钙含量及能量产生
J Physiol. 1984 Feb;347:149-59. doi: 10.1113/jphysiol.1984.sp015058.
6
The inhibitory effects of N2-dansyl-L-arginine-4-t-butylpiperidine amide (TI233) on contraction of vascular and intestinal smooth muscle.N2-丹磺酰-L-精氨酸-4-叔丁基哌啶酰胺(TI233)对血管和平滑肌收缩的抑制作用。
Br J Pharmacol. 1983 Nov;80(3):519-25. doi: 10.1111/j.1476-5381.1983.tb10724.x.
7
Possibility of metabolic control of membrane excitation.膜兴奋代谢控制的可能性。
Experientia. 1985 Aug 15;41(8):963-70. doi: 10.1007/BF01952115.
8
Effects of hypoxia on high-energy phosphagen content, energy metabolism and isometric force in guinea-pig taenia caeci.缺氧对豚鼠盲肠带高能磷酸原含量、能量代谢及等长力的影响。
J Physiol. 1990 May;424:41-56. doi: 10.1113/jphysiol.1990.sp018054.