• 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
Noradrenaline stimulation of the phosphoinositide system: evidence for a novel hydrophobic inositol-containing compound in resistance arterioles.去甲肾上腺素对磷酸肌醇系统的刺激作用:阻力小动脉中一种含新型疏水肌醇化合物的证据。
Br J Pharmacol. 1988 Jun;94(2):363-70. doi: 10.1111/j.1476-5381.1988.tb11538.x.
2
An unusual phosphatidylinositol turnover pathway in noradrenaline-perfused rat hearts.去甲肾上腺素灌注大鼠心脏中一条不寻常的磷脂酰肌醇代谢途径。
Clin Exp Pharmacol Physiol. 1988 Apr;15(4):251-5. doi: 10.1111/j.1440-1681.1988.tb01067.x.
3
Rapid formation of inositol 1,3,4,5-tetrakisphosphate and inositol 1,3,4-trisphosphate in rat parotid glands may both result indirectly from receptor-stimulated release of inositol 1,4,5-trisphosphate from phosphatidylinositol 4,5-bisphosphate.大鼠腮腺中肌醇1,3,4,5 - 四磷酸和肌醇1,3,4 - 三磷酸的快速形成可能均间接源于受体刺激下磷脂酰肌醇4,5 - 二磷酸释放出肌醇1,4,5 - 三磷酸。
Biochem J. 1986 Sep 1;238(2):507-16. doi: 10.1042/bj2380507.
4
Profile of phosphatidylinositol metabolism stimulated by carbachol and glutamate in primary cultures of rat cerebellar neurons.卡巴胆碱和谷氨酸刺激大鼠小脑神经元原代培养物中磷脂酰肌醇代谢的概况
Neuropharmacology. 1989 Dec;28(12):1309-15. doi: 10.1016/0028-3908(89)90004-x.
5
Resistance artery phosphoinositide metabolism in genetic hypertension.遗传性高血压中阻力动脉的磷酸肌醇代谢
J Hypertens. 1990 Jun;8(6):557-63. doi: 10.1097/00004872-199006000-00009.
6
Inositol 1,3,4,5-tetrakisphosphate and not phosphatidylinositol 3,4-bisphosphate is the probable precursor of inositol 1,3,4-trisphosphate in agonist-stimulated parotid gland.在激动剂刺激的腮腺中,肌醇1,3,4,5-四磷酸而非磷脂酰肌醇3,4-二磷酸可能是肌醇1,3,4-三磷酸的前体。
Biochem J. 1986 Sep 1;238(2):501-6. doi: 10.1042/bj2380501.
7
Comparison of norepinephrine- and veratrine-induced phosphoinositide hydrolysis in rat brain.去甲肾上腺素与藜芦碱诱导的大鼠脑磷酸肌醇水解的比较
J Pharmacol Exp Ther. 1987 Mar;240(3):729-36.
8
Inositol 1,2-cyclic 4,5-trisphosphate is not a product of muscarinic receptor-stimulated phosphatidylinositol 4,5-bisphosphate hydrolysis in rat parotid glands.肌醇1,2-环4,5-三磷酸不是毒蕈碱受体刺激大鼠腮腺中磷脂酰肌醇4,5-二磷酸水解的产物。
Biochem J. 1987 Apr 1;243(1):211-8. doi: 10.1042/bj2430211.
9
Carbachol causes rapid phosphodiesteratic cleavage of phosphatidylinositol 4,5-bisphosphate and accumulation of inositol phosphates in rabbit iris smooth muscle; prazosin inhibits noradrenaline- and ionophore A23187-stimulated accumulation of inositol phosphates.卡巴胆碱可导致兔虹膜平滑肌中磷脂酰肌醇4,5 -二磷酸的快速磷酸二酯酶裂解及肌醇磷酸的积累;哌唑嗪可抑制去甲肾上腺素和离子载体A23187刺激的肌醇磷酸积累。
Biochem J. 1984 Nov 15;224(1):291-300. doi: 10.1042/bj2240291.
10
Changes in the levels of inositol phosphates after agonist-dependent hydrolysis of membrane phosphoinositides.膜磷酸肌醇在激动剂依赖性水解后肌醇磷酸水平的变化。
Biochem J. 1983 May 15;212(2):473-82. doi: 10.1042/bj2120473.

引用本文的文献

1
Phospholipase C-delta1 modulates sustained contraction of rat mesenteric small arteries in response to noradrenaline, but not endothelin-1.磷脂酶C-δ1调节大鼠肠系膜小动脉对去甲肾上腺素而非内皮素-1的持续收缩反应。
Am J Physiol Heart Circ Physiol. 2008 Aug;295(2):H826-34. doi: 10.1152/ajpheart.01396.2007. Epub 2008 Jun 20.
2
Diacylglycerol kinase theta is translocated and phosphoinositide 3-kinase-dependently activated by noradrenaline but not angiotensin II in intact small arteries.在完整的小动脉中,二酰甘油激酶θ会发生易位,并通过去甲肾上腺素而非血管紧张素II经磷脂酰肌醇3激酶依赖性方式被激活。
Biochem J. 2001 Jan 1;353(Pt 1):129-137.
3
Membrane-associated diacylglycerol kinase activity is increased by noradrenaline, but not by angiotensin II, in arterial smooth muscle.在动脉平滑肌中,膜相关二酰基甘油激酶活性可被去甲肾上腺素增强,但不能被血管紧张素II增强。
Biochem J. 1994 May 15;300 ( Pt 1)(Pt 1):51-6. doi: 10.1042/bj3000051.
4
Phospholipase D-induced phosphatidate production in intact small arteries during noradrenaline stimulation: involvement of both G-protein and tyrosine-phosphorylation-linked pathways.去甲肾上腺素刺激时完整小动脉中磷脂酶D诱导的磷脂酸生成:G蛋白和酪氨酸磷酸化相关途径的参与
Biochem J. 1995 Apr 15;307 ( Pt 2)(Pt 2):451-6. doi: 10.1042/bj3070451.
5
Alpha-adrenoceptor subtypes in dog saphenous vein that mediate contraction and inositol phosphate production.介导犬隐静脉收缩和肌醇磷酸生成的α-肾上腺素能受体亚型。
Br J Pharmacol. 1991 Jan;102(1):151-61. doi: 10.1111/j.1476-5381.1991.tb12146.x.

本文引用的文献

1
Phosphoinositides. 5. The inositol lipids of ox brain.磷酸肌醇。5. 牛脑的肌醇脂质
Biochem J. 1963 Jul;88(1):125-31. doi: 10.1042/bj0880125.
2
Protein measurement with the Folin phenol reagent.使用福林酚试剂进行蛋白质测定。
J Biol Chem. 1951 Nov;193(1):265-75.
3
An inositol phosphatide containing carbohydrate, isolated from human brain.一种从人脑中分离出的含碳水化合物的肌醇磷脂。
Biochim Biophys Acta. 1961 Jul 8;50:602-3. doi: 10.1016/0006-3002(61)90031-2.
4
Lithium amplifies agonist-dependent phosphatidylinositol responses in brain and salivary glands.锂可增强大脑和唾液腺中激动剂依赖性磷脂酰肌醇反应。
Biochem J. 1982 Sep 15;206(3):587-95. doi: 10.1042/bj2060587.
5
Breakdown of polyphosphoinositides and not phosphatidylinositol accounts for muscarinic agonist-stimulated inositol phospholipid metabolism in rat parotid glands.多磷酸肌醇而非磷脂酰肌醇的分解代谢是毒蕈碱激动剂刺激大鼠腮腺中肌醇磷脂代谢的原因。
Biochem J. 1983 Dec 15;216(3):633-40. doi: 10.1042/bj2160633.
6
Rapid changes in hepatocyte phosphoinositides induced by vasopressin.血管加压素诱导的肝细胞磷酸肌醇快速变化。
J Biol Chem. 1983 Nov 25;258(22):13727-32.
7
Inositol trisphosphate, a novel second messenger in cellular signal transduction.肌醇三磷酸,细胞信号转导中的一种新型第二信使。
Nature. 1984;312(5992):315-21. doi: 10.1038/312315a0.
8
Rapid formation of inositol 1,3,4,5-tetrakisphosphate following muscarinic receptor stimulation of rat cerebral cortical slices.毒蕈碱受体刺激大鼠大脑皮层切片后肌醇1,3,4,5-四磷酸的快速形成。
Biochem J. 1985 Nov 15;232(1):211-5. doi: 10.1042/bj2320211.
9
A second messenger function for inositol tetrakisphosphate.肌醇四磷酸的第二信使功能。
Nature. 1986;324(6098):613. doi: 10.1038/324613a0.
10
The fourth Sir George Pickering memorial lecture. The structure of the resistance vasculature in essential hypertension.第四届乔治·皮克林爵士纪念讲座。原发性高血压中阻力血管系统的结构
J Hypertens. 1987 Apr;5(2):129-36. doi: 10.1097/00004872-198704000-00001.

去甲肾上腺素对磷酸肌醇系统的刺激作用:阻力小动脉中一种含新型疏水肌醇化合物的证据。

Noradrenaline stimulation of the phosphoinositide system: evidence for a novel hydrophobic inositol-containing compound in resistance arterioles.

作者信息

Ollerenshaw J D, Heagerty A M, Swales J D

机构信息

Department of Medicine, Leicester Royal Infirmary.

出版信息

Br J Pharmacol. 1988 Jun;94(2):363-70. doi: 10.1111/j.1476-5381.1988.tb11538.x.

DOI:10.1111/j.1476-5381.1988.tb11538.x
PMID:2840158
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1853973/
Abstract
  1. Five inositol phosphates were extracted from adult rat resistance arterioles and separated by ion-exchange high performance liquid chromatography. 2. By use of this technique, inositol phosphates liberated were identified as inositol 1-phosphate, inositol 1,4-bisphosphate, inositol 1,3,4-trisphosphate, inositol 1,4,5-trisphosphate and inositol 1,3,4,5-tetrakisphosphate. Stimulation of phosphoinositide hydrolysis with noradrenaline produced increases in inositol phosphate production. 3. Three inositol-containing phospholipids extracted from resistance arterioles were measured as their glycerol esters following deacylation, thereby permitting an analysis of both membrane and cytosolic components of the phosphoinositide signalling system. 4. A substantial agonist-sensitive pool of a previously undescribed inositol but not glycerol-containing lipid extract component was also identified in this tissue. 5. These experiments for the first time allow a precise description of phosphoinositide metabolism in resting and agonist-stimulated resistance arterioles and provide data on a novel compound possibly similar to that recently described in other tissues.
摘要
  1. 从成年大鼠阻力微动脉中提取了五种肌醇磷酸,并通过离子交换高效液相色谱法进行分离。2. 利用该技术,所释放的肌醇磷酸被鉴定为肌醇-1-磷酸、肌醇-1,4-二磷酸、肌醇-1,3,4-三磷酸、肌醇-1,4,5-三磷酸和肌醇-1,3,4,5-四磷酸。用去甲肾上腺素刺激磷脂酰肌醇水解会使肌醇磷酸生成增加。3. 从阻力微动脉中提取的三种含肌醇磷脂在脱酰基后作为其甘油酯进行测量,从而能够分析磷脂酰肌醇信号系统的膜成分和胞质成分。4. 在该组织中还鉴定出了一个大量的、对激动剂敏感的、先前未描述的含肌醇但不含甘油的脂质提取物成分库。5. 这些实验首次精确描述了静息和激动剂刺激的阻力微动脉中的磷脂酰肌醇代谢,并提供了一种可能与最近在其他组织中描述的化合物类似的新化合物的数据。