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1
Hypotensive effects of 8-hydroxy-2-(di-n-propylamino)tetralin and 5-methylurapidil following stereotaxic microinjection into the ventral medulla of the rat.8-羟基-2-(二正丙基氨基)四氢萘和5-甲基乌拉地尔立体定向微量注射到大鼠延髓腹侧后的降压作用
Br J Pharmacol. 1990 Apr;99(4):713-6. doi: 10.1111/j.1476-5381.1990.tb12994.x.
2
Influence of urapidil and 8-OH-DPAT on brain 5-HT turnover and blood pressure in rats.乌拉地尔和8-羟基二丙胺对大鼠脑5-羟色胺代谢及血压的影响。
J Cardiovasc Pharmacol. 1990;15 Suppl 7:S68-74.
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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.
4
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。
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Differential cardiovascular effects of 8-hydroxy-2-(di-n-propylamino) tetralin (8-OH-DPAT), flesinoxan, 5-methyl-urapidil and MDL 75,608A in conscious spontaneously hypertensive rats.8-羟基-2-(二正丙基氨基)四氢萘(8-OH-DPAT)、氟司立哌、5-甲基乌拉地尔和MDL 75,608A对清醒自发性高血压大鼠的心血管差异作用。
Fundam Clin Pharmacol. 1993;7(9):499-511. doi: 10.1111/j.1472-8206.1993.tb00254.x.
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Ventrolateral medulla: an important site of action for the hypotensive effect of drugs that activate serotonin-1A receptors.
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Involvement of brain 5-HT1A receptors in the hypotensive response to urapidil.脑5-羟色胺1A受体参与乌拉地尔的降压反应。
Am J Cardiol. 1989 Aug 15;64(7):7D-10D. doi: 10.1016/0002-9149(89)90688-7.
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Ventrolateral medullary pressor area: site of hypotensive and sympatho-inhibitory effects of (+/-)8-OH-DPAT in anaesthetized dogs.延髓腹外侧加压区:麻醉犬中(±)8-羟基二丙胺基四氢萘产生降压和交感神经抑制作用的部位。
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Cardiovascular effects of the 5-HT1A receptor ligand, MDL 73005EF, in conscious spontaneously hypertensive rats.5-HT1A受体配体MDL 73005EF对清醒自发性高血压大鼠的心血管效应
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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。
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Pressor effects following microinjection of 5-HT1A receptor agonists into the raphe obscurus of the anaesthetized rat.将5-羟色胺1A受体激动剂微量注射到麻醉大鼠的中缝隐核后产生的升压效应。
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本文引用的文献

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Functional roles of monoaminergic pathways to sympathetic preganglionic neurons.单胺能通路对交感神经节前神经元的功能作用。
Clin Exp Hypertens A. 1982;4(4-5):543-62. doi: 10.3109/10641968209061598.
2
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.
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Serotonergic projections from the ventral medulla to the intermediolateral cell column in the rat.大鼠延髓腹侧至中间外侧细胞柱的5-羟色胺能投射
Brain Res. 1981 Apr 27;211(1):146-52. doi: 10.1016/0006-8993(81)90074-3.
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Comparative effects of urapidil, prazosin, and clonidine on ligand binding to central nervous system receptors, arterial pressure, and heart rate in experimental animals.乌拉地尔、哌唑嗪和可乐定对实验动物中枢神经系统受体配体结合、动脉血压及心率的比较作用。
Am J Med. 1984 Oct 5;77(4A):87-95. doi: 10.1016/s0002-9343(84)80042-x.
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Spinal cord serotonin release and raised blood pressure after brainstem kainic acid injection.脑干注射海藻酸后脊髓5-羟色胺释放与血压升高
Brain Res. 1986 Feb 26;366(1-2):354-7. doi: 10.1016/0006-8993(86)91318-1.
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Hypotensive action of 8-hydroxy-2-(di-N-propylamino)tetralin (8-OH-DPAT) in spontaneously hypertensive rats.8-羟基-2-(二-N-丙基氨基)四氢萘(8-OH-DPAT)对自发性高血压大鼠的降压作用
Arch Int Pharmacodyn Ther. 1985 Feb;273(2):251-61.
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Effects of serotonin1 and serotonin2 receptor agonists and antagonists on blood pressure, heart rate and sympathetic nerve activity.
J Pharmacol Exp Ther. 1987 Sep;242(3):1152-9.
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Presynaptic 5-HT autoreceptors on serotonergic cell bodies and/or dendrites but not terminals are of the 5-HT1A subtype.
Eur J Pharmacol. 1985 Jul 31;113(3):463-4. doi: 10.1016/0014-2999(85)90099-8.
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5-Methyl-urapidil discriminates between subtypes of the alpha 1-adrenoceptor.5-甲基-乌拉地尔可区分α1-肾上腺素能受体的亚型。
Eur J Pharmacol. 1988 Jul 7;151(2):333-5. doi: 10.1016/0014-2999(88)90819-9.
10
Urapidil and some analogues with hypotensive properties show high affinities for 5-hydroxytryptamine (5-HT) binding sites of the 5-HT1A subtype and for alpha 1-adrenoceptor binding sites.乌拉地尔及一些具有降压特性的类似物对5-HT1A亚型的5-羟色胺(5-HT)结合位点和α1-肾上腺素能受体结合位点表现出高亲和力。
Naunyn Schmiedebergs Arch Pharmacol. 1987 Dec;336(6):597-601. doi: 10.1007/BF00165749.

8-羟基-2-(二正丙基氨基)四氢萘和5-甲基乌拉地尔立体定向微量注射到大鼠延髓腹侧后的降压作用

Hypotensive effects of 8-hydroxy-2-(di-n-propylamino)tetralin and 5-methylurapidil following stereotaxic microinjection into the ventral medulla of the rat.

作者信息

Valenta B, Singer E A

机构信息

Institute of Pharmacology, University of Vienna, Austria.

出版信息

Br J Pharmacol. 1990 Apr;99(4):713-6. doi: 10.1111/j.1476-5381.1990.tb12994.x.

DOI:10.1111/j.1476-5381.1990.tb12994.x
PMID:1972893
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1917564/
Abstract
  1. The effects of the 5-HT1a receptor agonists 8-hydroxy-2-(di-n-propylamino)tetralin (8-OH-DPAT) and 5-methylurapidil (5-MU) on blood pressure and heart rate were investigated in the anaesthetized normotensive rat after local injection into the ventral medulla (medial part of the area of the B1/B3 cell group). 2. Both 8-OH-DPAT and 5-MU, decreased arterial blood pressure and heart rate. Local injection of the alpha 1-adrenoceptor antagonist prazosin did not affect cardiovascular parameters. 3. Subcutaneous injection of the 5-HT1a receptor antagonists spiroxatrine or spiperone inhibited the cardiovascular response to 8-OH-DPAT and 5-MU. 4. Histological examination showed the injection sites which were associated with cardiovascular responses to the agonists to be contained within the medial part of the area of the B1/B3 cell group, corresponding to the region of the nucleus raphe magnus and pallidus. Injections of agonists into adjacent areas had no effect on blood pressure or heart rate. 5. The results support the hypothesis that activation of somatodendritic 5-HT1a autoreceptors located on 5-hydroxytryptaminergic neurones in the ventral medulla of the rat results in a decrease in blood pressure and heart rate. The region of the B1/B3 cell group is suggested as a possible site for the hypotensive action of 5-HT1a receptor agonists.
摘要
  1. 研究了5-羟色胺1a受体激动剂8-羟基-2-(二正丙基氨基)四氢萘(8-OH-DPAT)和5-甲基乌拉地尔(5-MU)在麻醉的正常血压大鼠中局部注射到延髓腹侧(B1/B3细胞群区域的内侧部分)后对血压和心率的影响。2. 8-OH-DPAT和5-MU均降低动脉血压和心率。局部注射α1-肾上腺素能受体拮抗剂哌唑嗪不影响心血管参数。3. 皮下注射5-羟色胺1a受体拮抗剂螺沙群或螺哌隆可抑制对8-OH-DPAT和5-MU的心血管反应。4. 组织学检查显示,与激动剂心血管反应相关的注射部位位于B1/B3细胞群区域的内侧部分,对应于中缝大核和中缝苍白核区域。向相邻区域注射激动剂对血压或心率无影响。5. 结果支持以下假说:位于大鼠延髓腹侧5-羟色胺能神经元上的树突体5-羟色胺1a自身受体的激活导致血压和心率降低。B1/B3细胞群区域被认为是5-羟色胺1a受体激动剂降压作用的可能部位。