• 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

蛋白激酶C抑制剂和钠/氢交换抑制剂对大鼠左心室乳头肌α1-肾上腺素能受体介导的变力性反应的影响。

Effects of inhibitors of protein kinase C and Na+/H+ exchange on alpha 1-adrenoceptor-mediated inotropic responses in the rat left ventricular papillary muscle.

作者信息

Otani H, Otani H, Uriu T, Hara M, Inoue M, Omori K, Cragoe E J, Inagaki C

机构信息

Department of Pharmacology, Kansai Medical University, Osaka, Japan.

出版信息

Br J Pharmacol. 1990 Jun;100(2):207-10. doi: 10.1111/j.1476-5381.1990.tb15783.x.

DOI:10.1111/j.1476-5381.1990.tb15783.x
PMID:2165835
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1917418/
Abstract
  1. Alpha 1-adrenoceptor stimulation of rat left ventricular papillary muscle produced a triphasic inotropic response: an initial transient positive inotropic effect (PIE) followed by a transient negative inotropic effect (NIE) and a sustained PIE. 2. The protein kinase C inhibitor, staurosporine, at concentrations ranging from 30 nM to 100 nM inhibited the sustained PIE, but had no significant effect on the transient PIE and NIE. 3. H-7, 1-(5-isoquinoline sulphonyl)-2-methylpiperazine, a less specific inhibitor of protein kinase C than staurosporine, at a concentration of 100 microM inhibited both the transient NIE and the sustained PIE without affecting the transient PIE. 4. Amiloride, an inhibitor of Na+/H+ exchange, at concentrations ranging from 0.1 mM to 1 mM inhibited the sustained PIE and, at higher concentrations, also inhibited the transient NIE. 5. An amiloride analogue, 5-(N-methyl-N-isobutyl)amiloride (MIBA), inhibited only the sustained PIE with an IC50 of 0.3 microM which is approximately two orders of magnitude lower than amiloride. 6. The receptor-linked stimulation of Na+/H+ exchange through protein kinase C activation may be a mechanism for alpha 1-adrenoceptor-mediated sustained PIE.
摘要
  1. 刺激大鼠左心室乳头肌的α1 -肾上腺素能受体产生三相变力反应:初始短暂正性变力作用(PIE),随后是短暂负性变力作用(NIE)和持续的PIE。2. 蛋白激酶C抑制剂星形孢菌素,浓度范围为30 nM至100 nM时,抑制持续的PIE,但对短暂的PIE和NIE无显著影响。3. H - 7,1 -(5 -异喹啉磺酰基)- 2 -甲基哌嗪,一种比星形孢菌素特异性更低的蛋白激酶C抑制剂,浓度为100 μM时,抑制短暂的NIE和持续的PIE,而不影响短暂的PIE。4. 钠氢交换抑制剂阿米洛利,浓度范围为0.1 mM至1 mM时,抑制持续的PIE,在较高浓度时,也抑制短暂的NIE。5. 阿米洛利类似物5 -(N -甲基 - N -异丁基)阿米洛利(MIBA)仅抑制持续的PIE,IC50为0.3 μM,比阿米洛利低约两个数量级。6. 通过蛋白激酶C激活对钠氢交换的受体相关刺激可能是α1 -肾上腺素能受体介导的持续PIE的一种机制。

相似文献

1
Effects of inhibitors of protein kinase C and Na+/H+ exchange on alpha 1-adrenoceptor-mediated inotropic responses in the rat left ventricular papillary muscle.蛋白激酶C抑制剂和钠/氢交换抑制剂对大鼠左心室乳头肌α1-肾上腺素能受体介导的变力性反应的影响。
Br J Pharmacol. 1990 Jun;100(2):207-10. doi: 10.1111/j.1476-5381.1990.tb15783.x.
2
Inotropic effects of staurosporine, NA 0345 and H-7, protein kinase C inhibitors, on rabbit ventricular myocardium: selective inhibition of the positive inotropic effect mediated by alpha 1-adrenoceptors.
Jpn J Pharmacol. 1993 Sep;63(1):17-26. doi: 10.1254/jjp.63.17.
3
Protein kinase C is not involved in alpha 1-adrenoceptor-mediated positive inotropic effect.
Am J Physiol. 1991 Jan;260(1 Pt 2):H27-36. doi: 10.1152/ajpheart.1991.260.1.H27.
4
Alpha 1-adrenoceptor stimulation increases intracellular pH and Ca2+ in cardiomyocytes through Na+/H+ and Na+/Ca2+ exchange.
Eur J Pharmacol. 1990 Sep 4;186(1):29-40. doi: 10.1016/0014-2999(90)94057-5.
5
WS-1 human fibroblasts contain distinct calcium and protein kinase C-mediated pathways for activation of Na+/H+ exchange: contrasting effects of thrombin and PMA.WS-1人成纤维细胞含有用于激活Na+/H+交换的不同钙和蛋白激酶C介导的途径:凝血酶和佛波酯的对比作用。
J Cell Physiol. 1991 Feb;146(2):290-7. doi: 10.1002/jcp.1041460214.
6
Alpha1-adrenoceptor-mediated negative inotropic effect caused by intracellular ionic activities in guinea-pig papillary muscle.豚鼠乳头肌细胞内离子活动引起的α1肾上腺素能受体介导的负性肌力作用。
J Vet Med A Physiol Pathol Clin Med. 2005 Dec;52(10):498-505. doi: 10.1111/j.1439-0442.2005.00772.x.
7
Phorbol ester potentiates alpha 1-adrenoceptor-mediated positive inotropic effect in rat papillary muscle.佛波酯增强大鼠乳头肌中α1-肾上腺素能受体介导的正性肌力作用。
Jpn J Pharmacol. 1987 Nov;45(3):425-8. doi: 10.1254/jjp.45.425.
8
[Analysis of membrane current system involved in the inotropic effects mediated by alpha-adrenoceptors in the heart].[心脏中α-肾上腺素能受体介导的变力作用所涉及的膜电流系统分析]
Hokkaido Igaku Zasshi. 1988 Sep;63(5):754-71.
9
The positive inotropic effect of alpha 1A-adrenoceptor stimulation is inhibited by 4-aminopyridine.α1A -肾上腺素能受体刺激的正性肌力作用被4-氨基吡啶抑制。
Eur J Pharmacol. 1996 May 23;304(1-3):73-80. doi: 10.1016/0014-2999(96)00132-x.
10
Pharmacological differentiation of synergistic contribution of L-type Ca2+ channels and Na+/H+ exchange to the positive inotropic effect of phenylephrine, endothelin-3 and angiotensin II in rabbit ventricular myocardium.L型钙通道和钠/氢交换对去氧肾上腺素、内皮素-3和血管紧张素II在兔心室肌中产生正性肌力作用的协同贡献的药理学区分
Naunyn Schmiedebergs Arch Pharmacol. 1997 Jan;355(1):87-96. doi: 10.1007/pl00004923.

引用本文的文献

1
Rapid acid extrusion response triggered by alpha(1) adrenoceptor in CHO cells.α1肾上腺素能受体在CHO细胞中引发的快速酸外排反应。
J Physiol. 2001 Aug 15;535(Pt 1):107-13. doi: 10.1111/j.1469-7793.2001.00107.x.
2
Cardiac alpha(1)-adrenoceptors that regulate contractile function: subtypes and subcellular signal transduction mechanisms.调节收缩功能的心脏α₁肾上腺素能受体:亚型与亚细胞信号转导机制
Neurochem Res. 1996 Feb;21(2):217-29. doi: 10.1007/BF02529138.
3
Response of cardiac myocytes to a ramp increase of diacylglycerol generated by photolysis of a novel caged diacylglycerol.心肌细胞对新型笼状二酰甘油光解产生的二酰甘油浓度斜坡式增加的反应。
Biophys J. 1996 May;70(5):2448-57. doi: 10.1016/S0006-3495(96)79816-8.
4
Inositol-1,4,5-trisphosphate mass content in isolated perfused rat heart during alpha-1-adrenoceptor stimulation.α-1肾上腺素能受体刺激期间分离灌注大鼠心脏中肌醇-1,4,5-三磷酸的质量含量
Mol Cell Biochem. 1996 Oct-Nov;163-164:167-72. doi: 10.1007/BF00408654.
5
Adenosine-sensitive alpha 1-adrenoceptor effects on reperfused ischaemic hearts: comparison with phorbol ester.腺苷敏感的α1肾上腺素能受体对再灌注缺血心脏的作用:与佛波酯的比较。
Br J Pharmacol. 1994 Aug;112(4):1007-16. doi: 10.1111/j.1476-5381.1994.tb13183.x.
6
On the mechanism of action of phenylephrine in rat atrial heart muscle.去氧肾上腺素对大鼠心房肌的作用机制
Naunyn Schmiedebergs Arch Pharmacol. 1994 Apr;349(4):408-15. doi: 10.1007/BF00170888.
7
Coupling of dual acid extrusion in the guinea-pig isolated ventricular myocyte to alpha 1- and beta-adrenoceptors.豚鼠离体心室肌细胞中双酸排出与α1和β肾上腺素能受体的偶联
J Physiol. 1993 May;464:49-73. doi: 10.1113/jphysiol.1993.sp019624.
8
Differential electrophysiologic and inotropic effects of phenylephrine in atrial and ventricular heart muscle preparations from rats.去氧肾上腺素对大鼠心房和心室心肌标本的电生理及变力作用差异
Naunyn Schmiedebergs Arch Pharmacol. 1991 Nov;344(5):574-81. doi: 10.1007/BF00170655.
9
A single myocardial stretch or decreased systolic fiber shortening stimulates the expression of heat shock protein 70 in the isolated, erythrocyte-perfused rabbit heart.
J Clin Invest. 1991 Dec;88(6):2018-25. doi: 10.1172/JCI115529.
10
Different patterns of protein kinase C redistribution mediated by alpha 1-adrenoceptor stimulation and phorbol ester in rat isolated left ventricular papillary muscle.α1-肾上腺素能受体刺激和佛波酯介导的大鼠离体左心室乳头肌中蛋白激酶C再分布的不同模式
Br J Pharmacol. 1992 Sep;107(1):22-6. doi: 10.1111/j.1476-5381.1992.tb14458.x.

本文引用的文献

1
Inhibition of Na+/Ca2+ exchange in membrane vesicle and papillary muscle preparations from guinea pig heart by analogs of amiloride.氨氯地平类似物对豚鼠心脏膜囊泡和乳头肌制剂中Na+/Ca2+交换的抑制作用。
Proc Natl Acad Sci U S A. 1984 May;81(10):3238-42. doi: 10.1073/pnas.81.10.3238.
2
alpha-Adrenoceptors mediating the positive inotropic effect of phenylephrine in the right ventricular muscle of the monkey (Macaca fuscata).介导去氧肾上腺素对猕猴(食蟹猴)右心室肌正性肌力作用的α-肾上腺素能受体。
Naunyn Schmiedebergs Arch Pharmacol. 1982 Mar;318(4):370-3. doi: 10.1007/BF00501181.
3
Inositol trisphosphate and diacylglycerol as second messengers.肌醇三磷酸和二酰甘油作为第二信使。
Biochem J. 1984 Jun 1;220(2):345-60. doi: 10.1042/bj2200345.
4
The role of the Na+/H+ exchange system in cardiac cells in relation to the control of the internal Na+ concentration. A molecular basis for the antagonistic effect of ouabain and amiloride on the heart.钠/氢交换系统在心肌细胞中对细胞内钠浓度控制的作用。哇巴因和阿米洛利对心脏拮抗作用的分子基础。
J Biol Chem. 1984 Jul 25;259(14):8880-5.
5
Pyrazine diuretics. II. N-amidino-3-amino-5-substituted 6-halopyrazinecarboxamides.吡嗪类利尿剂。II. N-脒基-3-氨基-5-取代的6-卤代吡嗪甲酰胺。
J Med Chem. 1967 Jan;10(1):66-75. doi: 10.1021/jm00313a014.
6
Comparison of protein kinase C functional assays to clarify mechanisms of inhibitor action.比较蛋白激酶C功能测定以阐明抑制剂作用机制。
Biochem Pharmacol. 1988 Apr 15;37(8):1541-5. doi: 10.1016/0006-2952(88)90016-0.
7
Correlative studies on the effect of carbachol on myo-inositol trisphosphate accumulation, myosin light chain phosphorylation and contraction in sphincter smooth muscle of rabbit iris.卡巴胆碱对兔虹膜括约肌平滑肌中肌醇三磷酸积累、肌球蛋白轻链磷酸化及收缩作用的相关性研究
J Pharmacol Exp Ther. 1986 Nov;239(2):574-83.
8
Evidence that phosphoinositide response is mediated by alpha 1-adrenoceptor stimulation, but not linked with excitation-contraction coupling in cardiac muscle.
Biochem Biophys Res Commun. 1986 May 14;136(3):863-9. doi: 10.1016/0006-291x(86)90412-2.
9
The Na+/H+ antiport is activated by serum and phorbol esters in proliferating myoblasts but not in differentiated myotubes. Properties of the activation process.在增殖的成肌细胞中,钠氢逆向转运体可被血清和佛波酯激活,但在分化的肌管中则不会。激活过程的特性。
J Biol Chem. 1985 Jul 5;260(13):8008-13.
10
Alpha-adrenoceptor antagonistic action of amiloride.
Biochem Pharmacol. 1987 Oct 15;36(20):3509-15. doi: 10.1016/0006-2952(87)90333-9.