• 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

相似文献

1
Stimulation of alpha 1-adrenoceptors and protein kinase C-mediated activation of ecto-5'-nucleotidase in rat hearts in vivo.体内大鼠心脏中α1-肾上腺素能受体的刺激及蛋白激酶C介导的ecto-5'-核苷酸酶激活
J Physiol. 1997 Aug 15;503 ( Pt 1)(Pt 1):119-27. doi: 10.1111/j.1469-7793.1997.119bi.x.
2
Tyramine produces interstitial adenosine-mediated activation of ecto-5'-nucleotidase in rat heart in vivo.酪胺在体内可使大鼠心脏中的胞外5'-核苷酸酶由间质腺苷介导激活。
Eur J Pharmacol. 1999 Jun 11;374(1):25-31. doi: 10.1016/s0014-2999(99)00290-3.
3
Reserpine attenuates interstitial adenosine-mediated activation of ecto-5'-nucleotidase in rat hearts in vivo.利血平可减弱体内大鼠心脏间质腺苷介导的ecto-5'-核苷酸酶激活。
Arch Biochem Biophys. 2000 Mar 15;375(2):333-9. doi: 10.1006/abbi.1999.1647.
4
Norepinephrine evoked by potassium depolarization increases interstitial adenosine concentration via activation of ecto-5'-nucleotidase in rat hearts.钾离子去极化诱发的去甲肾上腺素通过激活大鼠心脏的外5'-核苷酸酶增加细胞间腺苷浓度。
J Pharmacol Exp Ther. 2003 May;305(2):719-24. doi: 10.1124/jpet.102.039917. Epub 2003 Feb 11.
5
Histamine increases interstitial adenosine concentration via activation of ecto-5'-nucleotidase in rat hearts in vivo.组胺通过激活大鼠体内心脏的胞外5'-核苷酸酶来增加间质腺苷浓度。
J Pharmacol Exp Ther. 2001 Jul;298(1):71-6.
6
The effect of glibenclamide on the production of interstitial adenosine by inhibiting ecto-5'-nucleotidase in rat hearts.格列本脲通过抑制大鼠心脏外5'-核苷酸酶对间质腺苷生成的影响。
Br J Pharmacol. 1997 Oct;122(4):611-8. doi: 10.1038/sj.bjp.0701424.
7
Fluvastatin, an HMG-CoA reductase inhibitor, facilitate adenosine production in the rat hearts via activation of ecto-5'-nucleotidase.氟伐他汀,一种HMG-CoA还原酶抑制剂,通过激活外切5'-核苷酸酶促进大鼠心脏中腺苷的生成。
Microvasc Res. 2016 Sep;107:1-5. doi: 10.1016/j.mvr.2016.04.006. Epub 2016 Apr 19.
8
Alpha 1-adrenoceptor activation increases ecto-5'-nucleotidase activity and adenosine release in rat cardiomyocytes by activating protein kinase C.α1-肾上腺素能受体激活通过激活蛋白激酶C增加大鼠心肌细胞外5'-核苷酸酶活性和腺苷释放。
Circulation. 1995 Apr 15;91(8):2226-34. doi: 10.1161/01.cir.91.8.2226.
9
NO and cGMP facilitate adenosine production in rat hearts via activation of ecto-5'-nucleotidase.一氧化氮(NO)和环磷酸鸟苷(cGMP)通过激活胞外5'-核苷酸酶促进大鼠心脏中腺苷的生成。
Pflugers Arch. 1998 Nov;436(6):984-90. doi: 10.1007/s004240050733.
10
An increase of the native interstitial adenosine concentration during histidine application.在应用组氨酸期间,内源性间质腺苷浓度增加。
Naunyn Schmiedebergs Arch Pharmacol. 2000 May;361(5):529-34. doi: 10.1007/s002109900194.

引用本文的文献

1
Adenosine A₂a receptors and O₂ sensing in development.腺苷 A₂a 受体与氧感应在发育中的作用。
Am J Physiol Regul Integr Comp Physiol. 2011 Sep;301(3):R601-22. doi: 10.1152/ajpregu.00664.2010. Epub 2011 Jun 15.
2
Stimulation of an alpha1-adrenergic receptor downregulates ecto-5' nucleotidase activity on the apical membrane of RPE cells.刺激α1-肾上腺素能受体可下调 RPE 细胞顶膜上的外核苷酸酶 5' 的活性。
Purinergic Signal. 2006 Sep;2(3):499-507. doi: 10.1007/s11302-005-3980-7. Epub 2006 Aug 11.

本文引用的文献

1
Preconditioning against myocardial dysfunction after ischemia and reperfusion by an alpha 1-adrenergic mechanism.通过α1-肾上腺素能机制对缺血再灌注后心肌功能障碍进行预处理。
Circ Res. 1993 Oct;73(4):656-70. doi: 10.1161/01.res.73.4.656.
2
Alpha 1-adrenoceptors in myocardium: functional aspects and transmembrane signaling mechanisms.心肌中的α1肾上腺素能受体:功能方面及跨膜信号转导机制
Physiol Rev. 1993 Apr;73(2):469-87. doi: 10.1152/physrev.1993.73.2.469.
3
Role of adenosine and its interaction with alpha adrenoceptor activity in ischaemic and reperfusion injury of the myocardium.腺苷在心肌缺血及再灌注损伤中的作用及其与α肾上腺素能受体活性的相互作用
Cardiovasc Res. 1993 Jan;27(1):18-27. doi: 10.1093/cvr/27.1.18.
4
Alpha 1-adrenoceptor activation mediates the infarct size-limiting effect of ischemic preconditioning through augmentation of 5'-nucleotidase activity.α1-肾上腺素能受体激活通过增强5'-核苷酸酶活性介导缺血预处理的梗死面积限制效应。
J Clin Invest. 1994 May;93(5):2197-205. doi: 10.1172/JCI117216.
5
In vivo monitoring of norepinephrine and .OH generation on myocardial ischemic injury by dialysis technique.采用透析技术对心肌缺血损伤时去甲肾上腺素和·OH生成进行体内监测。
Am J Physiol. 1994 Mar;266(3 Pt 2):H903-8. doi: 10.1152/ajpheart.1994.266.3.H903.
6
Evidence that translocation of protein kinase C is a key event during ischemic preconditioning of rabbit myocardium.蛋白激酶C易位是兔心肌缺血预处理期间关键事件的证据。
J Mol Cell Cardiol. 1994 May;26(5):661-8. doi: 10.1006/jmcc.1994.1078.
7
Protein kinase C. Its role in ischemic preconditioning in the rat.蛋白激酶C。其在大鼠缺血预处理中的作用。
Circ Res. 1994 Sep;75(3):586-90. doi: 10.1161/01.res.75.3.586.
8
Alpha 1-adrenoceptor activation increases ecto-5'-nucleotidase activity and adenosine release in rat cardiomyocytes by activating protein kinase C.α1-肾上腺素能受体激活通过激活蛋白激酶C增加大鼠心肌细胞外5'-核苷酸酶活性和腺苷释放。
Circulation. 1995 Apr 15;91(8):2226-34. doi: 10.1161/01.cir.91.8.2226.
9
Involvement of endogenous adenosine in ischaemic preconditioning in swine.内源性腺苷在猪缺血预处理中的作用。
Pflugers Arch. 1995 Jun;430(2):273-82. doi: 10.1007/BF00374659.
10
In vitro regulation of rat heart 5'-nucleotidase by adenine nucleotides and magnesium.腺嘌呤核苷酸和镁对大鼠心脏5'-核苷酸酶的体外调节作用
J Biol Chem. 1971 May 10;246(9):3057-63.

体内大鼠心脏中α1-肾上腺素能受体的刺激及蛋白激酶C介导的ecto-5'-核苷酸酶激活

Stimulation of alpha 1-adrenoceptors and protein kinase C-mediated activation of ecto-5'-nucleotidase in rat hearts in vivo.

作者信息

Sato T, Obata T, Yamanaka Y, Arita M

机构信息

Department of Physiology, Oita Medical University, Japan.

出版信息

J Physiol. 1997 Aug 15;503 ( Pt 1)(Pt 1):119-27. doi: 10.1111/j.1469-7793.1997.119bi.x.

DOI:10.1111/j.1469-7793.1997.119bi.x
PMID:9288680
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1159892/
Abstract
  1. To determine whether protein kinase C (PKC)-mediated activation of ecto-5'-nucleotidase would increase interstitial adenosine concentrations in the rat heart in vivo, we made use of the microdialysis technique and a flexibly mounted probe, which was implanted in the left ventricular myocardium and perfused with Tyrode solution. 2. The baseline level of dialysate adenosine was 0.51 +/- 0.09 microM (n = 16). Perfusion of adenosine 5'-monophosphate (AMP, 100 microM) through the probe increased the dialysate adenosine concentration markedly to 9.25 +/- 0.46 microM (n = 15). alpha, beta-Methyleneadenosine 5'-diphosphate (AOPCP, 100 microM), an inhibitor of ecto-5'-nucleotidase, abolished the AMP-induced increase in dialysate adenosine, but did not affect the baseline level of adenosine. These observations suggest that the dialysate adenosine obtained during the perfusion with AMP, but not the baseline levels of adenosine, originated from the dephosphorylation of AMP by ecto-5'-nucleotidase. Thus, the level of adenosine measured during AMP perfusion gives an index of the activity of ecto-5'-nucleotidase in the tissue. 3. Noradrenaline (10 microM) increased the adenosine concentration measured in the presence of 100 microM AMP (i.e. the activity of ecto-5'-nucleotidase) by 38.7 +/- 9.6% (n = 5, P < 0.05), an increase which was inhibited by an antagonist of the alpha 1-adrenoceptor (prazosin, 50 microM) or of PKC (chelerythrine, 10 microM). Further application of either the alpha 1-adrenoceptor agonist methoxamine (100 microM) or the diacylglycerol analogue 1,2-dioctanoyl-sn-glycerol (DOG, 100 microM) also increased the adenosine concentration by 35.1 +/- 10.0% (n = 6, P < 0.05) or 40.6 +/- 8.3% (n = 5, P < 0.05), respectively. 4. The presence of okadaic acid (50 microM), an inhibitor of protein phosphatase, enhanced the noradrenaline-induced increase in adenosine concentration by 112.4 +/- 35.9% (n = 4, P < 0.05), to a level significantly (P < 0.05) greater than the increase caused by noradrenaline alone (38.7 +/- 9.6%). 5. These data provide the first evidence that alpha 1-adrenoceptor stimulation and the subsequent activation of PKC can increase adenosine concentrations in interstitial spaces of ventricular muscle in vivo, through activation of endogenous ecto-5'-nucleotidase.
摘要
  1. 为了确定蛋白激酶C(PKC)介导的ecto - 5'-核苷酸酶激活是否会增加大鼠心脏体内间质腺苷浓度,我们采用了微透析技术和一个灵活安装的探针,将其植入左心室心肌并用台氏液灌注。2. 透析液腺苷的基线水平为0.51±0.09微摩尔/升(n = 16)。通过探针灌注5'-单磷酸腺苷(AMP,100微摩尔/升)可使透析液腺苷浓度显著增加至9.25±0.46微摩尔/升(n = 15)。ecto - 5'-核苷酸酶抑制剂α,β-亚甲基腺苷5'-二磷酸(AOPCP,100微摩尔/升)可消除AMP诱导的透析液腺苷增加,但不影响腺苷的基线水平。这些观察结果表明,在灌注AMP期间获得的透析液腺苷,而非腺苷的基线水平,源自ecto - 5'-核苷酸酶对AMP的去磷酸化。因此,在AMP灌注期间测量的腺苷水平给出了组织中ecto - 5'-核苷酸酶活性的指标。3. 去甲肾上腺素(10微摩尔/升)使在100微摩尔/升AMP存在下测量的腺苷浓度(即ecto - 5'-核苷酸酶的活性)增加了38.7±9.6%(n = 5,P < 0.05),α1 -肾上腺素能受体拮抗剂(哌唑嗪,50微摩尔/升)或PKC拮抗剂(白屈菜红碱,10微摩尔/升)可抑制这种增加。进一步应用α1 -肾上腺素能受体激动剂甲氧明(100微摩尔/升)或二酰基甘油类似物1,2 -二辛酰基 - sn -甘油(DOG,100微摩尔/升)也分别使腺苷浓度增加了35.1±10.0%(n = 6,P < 0.05)或40.6±8.3%(n = 5,P < 0.05)。4. 蛋白磷酸酶抑制剂冈田酸(50微摩尔/升)的存在使去甲肾上腺素诱导的腺苷浓度增加增强了112.4±35.9%(n = 4,P < 0.05),达到显著高于单独由去甲肾上腺素引起的增加水平(38.7±9.6%,P < 0.05)。5. 这些数据提供了首个证据,即α1 -肾上腺素能受体刺激以及随后PKC的激活可通过激活内源性ecto - 5'-核苷酸酶增加体内心室肌间质空间中的腺苷浓度。