• 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
Carotid haemodynamics in pigs during infusions of 8-OH-DPAT: reduction in arteriovenous shunting is mediated by 5-HT1-like receptors.8-OH-DPAT输注期间猪的颈动脉血流动力学:动静脉分流的减少由5-HT1样受体介导。
Br J Pharmacol. 1989 Jan;96(1):125-32. doi: 10.1111/j.1476-5381.1989.tb11792.x.
2
Vascular 5-HT1-like receptors that mediate contraction of the dog isolated saphenous vein and carotid arterial vasoconstriction in anaesthetized dogs are not of the 5-HT1A or 5-HT1D subtype.介导犬离体隐静脉收缩及麻醉犬颈动脉血管收缩的血管5-羟色胺1样受体不属于5-羟色胺1A或5-羟色胺1D亚型。
Br J Pharmacol. 1991 Jan;102(1):191-7. doi: 10.1111/j.1476-5381.1991.tb12152.x.
3
The 5-HT1-like receptor mediating reduction of porcine carotid arteriovenous shunting by RU 24969 is not related to either the 5-HT1A or the 5-HT1B subtype.介导RU 24969降低猪颈动脉动静脉分流的5-羟色胺1样受体与5-羟色胺1A或5-羟色胺1B亚型均无关。
Eur J Pharmacol. 1989 Nov 14;171(1):87-96. doi: 10.1016/0014-2999(89)90432-9.
4
Constriction of porcine arteriovenous anastomoses by indorenate is unrelated to 5-HT1A, 5-HT1B, 5-HT1C or 5-HT1D receptor subtypes.吲哚拉明对猪动静脉吻合支的收缩作用与5-HT1A、5-HT1B、5-HT1C或5-HT1D受体亚型无关。
Eur J Pharmacol. 1990 Nov 6;190(1-2):167-76. doi: 10.1016/0014-2999(90)94123-f.
5
Reduction of cephalic arteriovenous shunting by ergotamine is not mediated by 5-HT1-like or 5-HT2 receptors.麦角胺对头部动静脉分流的减少作用并非由5-HT1样或5-HT2受体介导。
Br J Pharmacol. 1989 Jun;97(2):383-90. doi: 10.1111/j.1476-5381.1989.tb11965.x.
6
Acute administration of 8-hydroxy-2-(di-n-propylamino)tetralin (8-OH-DPAT), a selective 5-HT-receptor agonist, causes a biphasic blood pressure response and a bradycardia in the normotensive Sprague-Dawley rat and in the spontaneously hypertensive rat.急性给予8-羟基-2-(二正丙基氨基)四氢萘(8-OH-DPAT),一种选择性5-羟色胺受体激动剂,在正常血压的斯普拉格-道利大鼠和自发性高血压大鼠中会引起双相血压反应和心动过缓。
J Neural Transm. 1985;62(3-4):305-19. doi: 10.1007/BF01252244.
7
5-HT1A and alpha-2 adrenergic receptors mediate the hyperglycemic and hypoinsulinemic effects of 8-hydroxy-2-(di-n-propylamino)tetralin in the conscious rat.5-羟色胺1A受体和α-2肾上腺素能受体介导了8-羟基-2-(二正丙基氨基)四氢萘对清醒大鼠的高血糖和低胰岛素血症作用。
J Pharmacol Exp Ther. 1987 Dec;243(3):1159-66.
8
Cardiovascular response to 8-hydroxy-2-(di-n-propylamino) tetralin (8-OH-DPAT) in the rat: site of action and pharmacological analysis.大鼠对8-羟基-2-(二正丙基氨基)四氢萘(8-OH-DPAT)的心血管反应:作用部位及药理学分析
J Cardiovasc Pharmacol. 1987 Mar;9(3):328-47. doi: 10.1097/00005344-198703000-00010.
9
Involvement of 5-HT1A- and alpha 2-receptors in the decreased 5-hydroxytryptamine release and metabolism in rat suprachiasmatic nucleus after intravenous 8-hydroxy-2-(n-dipropylamino) tetralin.静脉注射8-羟基-2-(二丙基氨基)四氢萘后,5-羟色胺1A受体和α2受体参与大鼠视交叉上核中5-羟色胺释放和代谢的降低。
Br J Pharmacol. 1986 Oct;89(2):277-86. doi: 10.1111/j.1476-5381.1986.tb10257.x.
10
Comparison of the cardiovascular effects of the 5-HT1A receptor agonist flesinoxan with that of 8-OH-DPAT in the rat.5-羟色胺1A受体激动剂氟司必林与8-羟基二丙胺甲苯在大鼠体内心血管效应的比较。
Eur J Pharmacol. 1990 May 16;180(2-3):339-49. doi: 10.1016/0014-2999(90)90319-2.

引用本文的文献

1
Volumetric changes in subcortical structures following repeated ketamine treatment in patients with major depressive disorder: a longitudinal analysis.重复使用氯胺酮治疗抑郁症患者后皮质下结构的体积变化:一项纵向分析。
Transl Psychiatry. 2020 Aug 3;10(1):264. doi: 10.1038/s41398-020-00945-9.
2
Serotonin and blood pressure regulation.血清素与血压调节。
Pharmacol Rev. 2012 Apr;64(2):359-88. doi: 10.1124/pr.111.004697. Epub 2012 Mar 8.
3
Inhibitory 5-hydroxytryptamine receptors involved in pressor effects obtained by stimulation of sympathetic outflow from spinal cord in pithed rats.抑制性5-羟色胺受体参与在脊髓横断大鼠中通过刺激脊髓交感神经传出而获得的升压效应。
Br J Pharmacol. 1994 Dec;113(4):1358-62. doi: 10.1111/j.1476-5381.1994.tb17147.x.
4
Proceedings of the British Pharmacological Society. University of Manchester, 13-15 September 1989.英国药理学会会议记录。曼彻斯特大学,1989年9月13日至15日。
Br J Pharmacol. 1989 Dec;98 Suppl(Suppl):775P-952P.
5
An examination of the putative sigma-receptor in the mouse isolated vas deferens.对小鼠离体输精管中假定的σ受体的研究。
Br J Pharmacol. 1989 Oct;98(2):429-36. doi: 10.1111/j.1476-5381.1989.tb12614.x.
6
Role of 5-HT1-like receptors in the reduction of porcine cranial arteriovenous anastomotic shunting by sumatriptan.5-羟色胺1样受体在舒马曲坦减少猪颅部动静脉吻合分流中的作用。
Br J Pharmacol. 1991 Feb;102(2):323-30. doi: 10.1111/j.1476-5381.1991.tb12173.x.
7
Vascular 5-HT1-like receptors that mediate contraction of the dog isolated saphenous vein and carotid arterial vasoconstriction in anaesthetized dogs are not of the 5-HT1A or 5-HT1D subtype.介导犬离体隐静脉收缩及麻醉犬颈动脉血管收缩的血管5-羟色胺1样受体不属于5-羟色胺1A或5-羟色胺1D亚型。
Br J Pharmacol. 1991 Jan;102(1):191-7. doi: 10.1111/j.1476-5381.1991.tb12152.x.
8
Carotid vascular effects of ergotamine and dihydroergotamine in the pig: no exclusive mediation via 5-HT1-like receptors.麦角胺和双氢麦角胺对猪颈动脉血管的作用:并非仅通过5-HT1样受体介导。
Br J Pharmacol. 1991 Sep;104(1):183-9. doi: 10.1111/j.1476-5381.1991.tb12405.x.
9
Further characterization of the putative 5-HT receptor which mediates blockade of neurogenic plasma extravasation in rat dura mater.对介导大鼠硬脑膜神经源性血浆外渗阻断作用的假定5-羟色胺受体的进一步表征。
Br J Pharmacol. 1991 Jun;103(2):1421-8. doi: 10.1111/j.1476-5381.1991.tb09805.x.
10
5-HT1-like receptor mediated changes in porcine carotid haemodynamics: are 5-HT1D receptors involved?5-羟色胺1样受体介导的猪颈动脉血流动力学变化:5-羟色胺1D受体是否参与其中?
Naunyn Schmiedebergs Arch Pharmacol. 1992 May;345(5):509-15. doi: 10.1007/BF00168941.

本文引用的文献

1
Discrimination of multiple [3H]5-hydroxytryptamine binding sites by the neuroleptic spiperone in rat brain.抗精神病药螺哌隆对大鼠脑中多个[3H]5-羟色胺结合位点的鉴别
J Neurochem. 1981 Jan;36(1):220-6. doi: 10.1111/j.1471-4159.1981.tb02397.x.
2
Effect of isometheptene on the distribution and shunting of 15 microM microspheres throughout the cephalic circulation of the cat.
Headache. 1980 Mar;20(2):103-6. doi: 10.1111/j.1526-4610.1980.hed2002103.x.
3
Computer programs for the radioactive microsphere technique. Determination of regional blood flows and other haemodynamic variables in different experimental circumstances.用于放射性微球技术的计算机程序。在不同实验条件下测定局部血流量及其他血流动力学变量。
Comput Programs Biomed. 1980 Dec;12(2-3):63-84. doi: 10.1016/0010-468x(80)90053-7.
4
Antimigraine drugs and cranial arteriovenous shunting in the cat.猫的抗偏头痛药物与颅动静脉分流
Neurology. 1980 Jul;30(7 Pt 1):696-701. doi: 10.1212/wnl.30.7.696.
5
Redistribution by 5-hydroxytryptamine of carotid arterial blood at the expense of arteriovenous anastomotic blood flow.5-羟色胺以动静脉吻合血流为代价对颈动脉血液进行再分配。
J Physiol. 1982 Nov;332:501-20. doi: 10.1113/jphysiol.1982.sp014427.
6
Redistribution of carotid artery blood flow by 5-HT: effects of the 5-HT2 receptor antagonists ketanserin and Wal 1307.5-羟色胺对颈动脉血流的重新分配作用:5-羟色胺2受体拮抗剂酮色林和Wal 1307的影响
Eur J Pharmacol. 1984 Jul 20;102(3-4):499-509. doi: 10.1016/0014-2999(84)90571-5.
7
Effects of methysergide and 5-hydroxytryptamine on carotid blood flow distribution in pigs: further evidence for the presence of atypical 5-HT receptors.甲基麦角新碱和5-羟色胺对猪颈动脉血流分布的影响:存在非典型5-羟色胺受体的进一步证据。
Br J Pharmacol. 1984 Aug;82(4):817-26. doi: 10.1111/j.1476-5381.1984.tb16478.x.
8
8-Hydroxy-2-(di-n-propylamino)-tetralin discriminates between subtypes of the 5-HT1 recognition site.8-羟基-2-(二正丙基氨基)四氢萘可区分5-HT1识别位点的亚型。
Eur J Pharmacol. 1983 May 20;90(1):151-3. doi: 10.1016/0014-2999(83)90230-3.
9
Cardiovascular effects of 40 percent nitrous oxide in man.
Anesth Analg. 1972 Nov-Dec;51(6):956-63.
10
Quantitative autoradiographic mapping of serotonin receptors in the rat brain. I. Serotonin-1 receptors.大鼠脑中5-羟色胺受体的定量放射自显影图谱。I. 5-羟色胺-1受体。
Brain Res. 1985 Nov 4;346(2):205-30. doi: 10.1016/0006-8993(85)90856-x.

8-OH-DPAT输注期间猪的颈动脉血流动力学:动静脉分流的减少由5-HT1样受体介导。

Carotid haemodynamics in pigs during infusions of 8-OH-DPAT: reduction in arteriovenous shunting is mediated by 5-HT1-like receptors.

作者信息

Bom A H, Verdouw P D, Saxena P R

机构信息

Department of Pharmocology, Erasmus University Rotterdam, The Netherlands.

出版信息

Br J Pharmacol. 1989 Jan;96(1):125-32. doi: 10.1111/j.1476-5381.1989.tb11792.x.

DOI:10.1111/j.1476-5381.1989.tb11792.x
PMID:2522333
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1854297/
Abstract
  1. The effects of intracarotid infusions of 8-hydroxy-2-[di-n-propyl-amino]-tetralin (8-OH-DPAT) on heart rate, blood pressure and carotid blood flow and its distribution were studied in anaesthetized pigs by use of radioactive microspheres of 15 microns diameter. 2. Control experiments with physiological saline showed that systemic and carotid haemodynamics remain essentially unchanged during the experimental period. In contrast to results obtained in rat, cat and dog experiments, 8-OH-DPAT did not decrease arterial blood pressure. 3. 8-OH-DPAT, which has a high affinity and is selective for the 5-HT1A recognition site, caused a dose-related decrease in arteriovenous anastomotic (non-nutrient) blood flow, resulting in a decrease in carotid blood flow. At the highest dose used, a small increase in arteriolar (nutrient) blood flow was observed. 4. The decrease in arteriovenous anastomotic and carotid blood flow induced by 8-OH-DPAT was not significantly modified by pretreatment with the 5-HT2 receptor antagonist ketanserin (0.5 mg kg-1), but was markedly reduced by pretreatment with methiothepin (1 mg kg-1), which blocks both the 5-HT1-like and 5-HT2 receptors. 5. It is concluded that the effects of 8-OH-DPAT on arteriovenous anastomotic blood flow are mediated by 5-HT1-like receptors. These receptors, however, cannot yet be classified as belonging to 5-HT1A receptor subtype. Since a number of antimigraine drugs reduce arteriovenous shunting, it is tempting to suggest that 8-OH-DPAT may have similar clinical efficacy.
摘要
  1. 利用直径为15微米的放射性微球,研究了颈内注射8-羟基-2-[二正丙基氨基]四氢萘(8-OH-DPAT)对麻醉猪心率、血压、颈动脉血流量及其分布的影响。2. 生理盐水对照实验表明,实验期间全身和颈动脉血流动力学基本保持不变。与大鼠、猫和狗实验结果不同,8-OH-DPAT并未降低动脉血压。3. 8-OH-DPAT对5-HT1A识别位点具有高亲和力且具有选择性,可引起动静脉吻合(非营养性)血流量呈剂量依赖性减少,导致颈动脉血流量下降。在使用的最高剂量下,观察到小动脉(营养性)血流量略有增加。4. 8-OH-DPAT诱导的动静脉吻合和颈动脉血流量减少,用5-HT2受体拮抗剂酮色林(0.5毫克/千克)预处理后无明显改变,但用甲硫噻平(1毫克/千克)预处理后显著降低,甲硫噻平可阻断5-HT1样和5-HT-2受体。5. 得出结论,8-OH-DPAT对动静脉吻合血流量的影响是由5-HT1样受体介导的。然而,这些受体尚未归类为5-HT1A受体亚型。由于一些抗偏头痛药物可减少动静脉分流,因此很容易推测8-OH-DPAT可能具有类似的临床疗效。