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5-羟色胺诱导猪心动过速:一种新型5-羟色胺受体的可能参与

5-Hydroxytryptamine-induced tachycardia in the pig: possible involvement of a new type of 5-hydroxytryptamine receptor.

作者信息

Bom A H, Duncker D J, Saxena P R, Verdouw P D

机构信息

Department of Pharmacology, Erasmus University Rotterdam, The Netherlands.

出版信息

Br J Pharmacol. 1988 Mar;93(3):663-71. doi: 10.1111/j.1476-5381.1988.tb10324.x.

Abstract
  1. The mechanism of 5-hydroxytryptamine (5-HT)-induced tachycardia is species-dependent and is mediated directly or indirectly either by '5-HT1-like' (cat), 5-HT2 (rat, dog) or 5-HT3 (rabbit) receptors, or by an action similar to tyramine (guinea-pig). The present investigation is devoted to the analysis of the positive chronotropic effect of 5-HT in the pentobarbitone-anaesthetized pig. 2. Intravenous bolus injections of 5-HT (3, 10 and 30 micrograms kg-1) in pigs resulted in dose-dependent increases in heart rate of 24 +/- 2, 38 +/- 3 and 51 +/- 3 beats min-1, respectively (n = 39). Topical application of a high concentration of 5-HT (150 micrograms kg-1 in 5 ml) on the right atrium was also followed by tachycardia (38 +/- 6 beats min-1, n = 4). 3. A number of drugs which antagonize responses mediated by different 5-HT receptors--phenoxybenzamine, methiothepin, metergoline, methysergide and mesulergine ('5-HT1-like' and 5-HT2 receptors), ketanserin, cyproheptadine, pizotifen and mianserin (5-HT2 receptors), and MDL 72222 and ICS 205-930 (5-HT3 receptors)--did not attenuate the chronotropic responses to 5-HT. 4. The 5-HT-induced tachycardia was also not affected by antagonists at alpha- and beta-adrenoceptors, muscarinic, nicotinic, histamine and dopamine receptors, and calcium channels. 5. Selective inhibitors of 5-HT-uptake, indalpine and fluvoxamine, themselves increased porcine heart rate and facilitated 5-HT-induced tachycardia both in magnitude and in duration. 6. A number of putative selective agonists at '5-HT1-like' receptors or their possible subtypes (5- carboxamidotryptamine (5-CT), 8-hydroxy-24di-N,N-n-propylamino) tetralin (8-OH-DPAT), BEA 1654 and RU 24969), or at 5-HT3 receptors (2-methyl-5-HT), elicited no or only a weak tachycardiac response in the pig. RU 24969, but not 8-OH-DPAT, seemed to potentiate the responses to 5-HT, whereas 5-CT slightly inhibited these responses. 7. It was concluded that the tachycardia induced by 5-HT in the pig does not involve the receptors for some common neurotransmitter substances but may be mediated by a new 5-HT receptor type that is clearly different from '5-HT1-like', 5-HT2 or 5-HT3 receptors.
摘要
  1. 5-羟色胺(5-HT)诱发心动过速的机制因物种而异,直接或间接由“5-HT1样”受体(猫)、5-HT2受体(大鼠、狗)或5-HT3受体(兔)介导,或通过类似于酪胺的作用(豚鼠)介导。本研究致力于分析5-HT对戊巴比妥麻醉猪的正性变时作用。2. 给猪静脉推注5-HT(3、10和30微克/千克)导致心率分别呈剂量依赖性增加,增加幅度为24±2、38±3和51±3次/分钟(n = 39)。在右心房局部应用高浓度的5-HT(150微克/千克,溶于5毫升)也会导致心动过速(38±6次/分钟,n = 4)。3. 许多拮抗不同5-HT受体介导反应的药物——酚苄明、甲硫哒嗪、麦角新碱、甲基麦角新碱和美舒麦角(“5-HT1样”和5-HT2受体)、酮色林、赛庚啶、匹唑替芬和米安色林(5-HT2受体),以及MDL 72222和ICS 205-930(5-HT3受体)——并未减弱对5-HT的变时反应。4. 5-HT诱发的心动过速也不受α和β肾上腺素能受体、毒蕈碱、烟碱、组胺和多巴胺受体以及钙通道拮抗剂的影响。5. 5-HT摄取的选择性抑制剂吲哚哌啶和氟伏沙明本身可增加猪的心率,并在幅度和持续时间上促进5-HT诱发的心动过速。6. 一些推测的“5-HT1样”受体或其可能亚型(5-羧酰胺色胺(5-CT)、8-羟基-2,4-二-N,N-二正丙基氨基)四氢萘(8-OH-DPAT)、BEA 1654和RU 24969)或5-HT3受体(2-甲基-5-HT)的选择性激动剂在猪中未引起或仅引起微弱的心动过速反应。RU 24969似乎增强了对5-HT的反应,而8-OH-DPAT则无此作用,而5-CT则轻微抑制这些反应。7. 得出的结论是,5-HT在猪中诱发的心动过速不涉及某些常见神经递质物质的受体,可能由一种明显不同于“5-HT1样”、5-HT2或5-HT3受体的新型5-HT受体介导。

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Serotonin (5-hydroxytryptamine); the last four years.血清素(5-羟色胺);过去四年。
Physiol Rev. 1958 Apr;38(2):277-335. doi: 10.1152/physrev.1958.38.2.277.
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Two kinds of tryptamine receptor.两种色胺受体。
Br J Pharmacol Chemother. 1957 Sep;12(3):323-8. doi: 10.1111/j.1476-5381.1957.tb00142.x.

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