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引用本文的文献

1
5-hydroxytryptamine induced relaxation in the pig urinary bladder neck.5-羟色胺诱导猪膀胱颈松弛。
Br J Pharmacol. 2009 May;157(2):271-80. doi: 10.1111/j.1476-5381.2009.00144.x. Epub 2009 Mar 20.
2
Contribution of serotonin (5-HT) 5-HT2 receptor subtypes to the discriminative stimulus effects of cocaine in rats.血清素(5-羟色胺,5-HT)5-HT2受体亚型对可卡因在大鼠体内辨别刺激效应的作用。
Psychopharmacology (Berl). 2006 Jan;183(4):482-9. doi: 10.1007/s00213-005-0197-y. Epub 2005 Oct 28.
3
Heterogeneity of neuronal and smooth muscle receptors involved in the VIP- and PACAP-induced relaxations of the pig intravesical ureter.猪膀胱内输尿管中参与血管活性肠肽(VIP)和垂体腺苷酸环化酶激活肽(PACAP)诱导舒张的神经元和平滑肌受体的异质性
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本文引用的文献

1
The relationship between the penetration of tryptamine and 5-hydroxytryptamine into smooth muscle and the associated contractions.色胺和5-羟色胺进入平滑肌的渗透与相关收缩之间的关系。
Br J Pharmacol Chemother. 1967 Jan;29(1):105-18. doi: 10.1111/j.1476-5381.1967.tb01944.x.
2
Effects of ketanserin and DOI on spontaneous and 5-HT-evoked peristalsis of the pig ureter in vivo.酮色林和DOI对猪输尿管体内自发性及5-羟色胺诱发蠕动的影响。
Br J Pharmacol. 2002 Feb;135(4):1026-32. doi: 10.1038/sj.bjp.0704536.
3
5-Hydroxytryptamine(1A) receptor activation enhances norepinephrine release from nerves in the rabbit saphenous vein.5-羟色胺(1A)受体激活增强兔隐静脉神经去甲肾上腺素释放。
J Pharmacol Exp Ther. 1999 Sep;290(3):1195-201.
4
Pharmacological analysis of 5-hydroxytryptamine effects on human isolated ureter.5-羟色胺对人离体输尿管作用的药理学分析
Pharmacol Res. 1999 Jun;39(6):487-91. doi: 10.1006/phrs.1999.0469.
5
A2B adenosine receptors mediate relaxation of the pig intravesical ureter: adenosine modulation of non adrenergic non cholinergic excitatory neurotransmission.A2B 腺苷受体介导猪膀胱内输尿管舒张:腺苷对非肾上腺素能非胆碱能兴奋性神经传递的调节作用
Br J Pharmacol. 1999 Feb;126(4):969-78. doi: 10.1038/sj.bjp.0702386.
6
5-HT1-like receptors: a time to bid goodbye.5-羟色胺1样受体:是时候说再见了。
Trends Pharmacol Sci. 1998 Aug;19(8):311-6. doi: 10.1016/s0165-6147(98)01228-0.
7
Distribution and functional effects of neuropeptide Y on equine ureteral smooth muscle and resistance arteries.神经肽Y对马输尿管平滑肌和阻力动脉的分布及功能影响
Regul Pept. 1997 Apr 30;69(3):155-65. doi: 10.1016/s0167-0115(97)00003-7.
8
Influence of serotonin on the human ureter: an in vitro pharmacological study.血清素对人体输尿管的影响:一项体外药理学研究。
Urol Int. 1995;55(4):202-4. doi: 10.1159/000282786.
9
Pharmacological characterization of two novel and potent 5-HT4 receptor agonists, RS 67333 and RS 67506, in vitro and in vivo.新型强效5-HT4受体激动剂RS 67333和RS 67506的体内外药理学特性
Br J Pharmacol. 1995 Aug;115(8):1387-92. doi: 10.1111/j.1476-5381.1995.tb16628.x.
10
GR113808: a novel, selective antagonist with high affinity at the 5-HT4 receptor.GR113808:一种新型的、对5-羟色胺4受体具有高亲和力的选择性拮抗剂。
Br J Pharmacol. 1994 Jan;111(1):332-8. doi: 10.1111/j.1476-5381.1994.tb14064.x.

介导猪离体膀胱内输尿管收缩的5-羟色胺受体的特性研究

Characterization of the 5-hydroxytryptamine receptors mediating contraction in the pig isolated intravesical ureter.

作者信息

Hernández Medardo, Barahona María Victoria, Simonsen Ulf, Recio Paz, Rivera Luis, Martínez Ana Cristina, García-Sacristán Albino, Orensanz Luis M, Prieto Dolores

机构信息

Departamento de Fisiología, Facultad de Farmacia, Universidad Complutense de Madrid, 28040-Madrid, Spain.

出版信息

Br J Pharmacol. 2003 Jan;138(1):137-44. doi: 10.1038/sj.bjp.0705019.

DOI:10.1038/sj.bjp.0705019
PMID:12522083
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1573645/
Abstract

1 This study was designed to investigate the effect of 5-hydroxytryptamine (5-HT) and to characterize the 5-HT receptors involved in 5-HT responses in the pig intravesical ureter. 2 5-HT (0.01-10 microM) concentration-dependently increased the tone of intravesical ureteral strips, whereas the increases in phasic contractions were concentration-independent. The 5-HT(2) receptor agonist alpha-methyl 5-HT, mimicked the effect on tone whereas weak or no response was obtained with 5-CT, 8-OH-DPAT, m-chlorophenylbiguanide and RS 67333, 5-HT(1), 5-HT(1A), 5-HT(3) and 5-HT(4) receptor agonists, respectively. 5-HT did not induce relaxation of U46619-contracted ureteral preparations. Pargyline (100 microM), a monoaminooxidase A/B activity inhibitor, produced leftward displacements of the concentration-response curves for 5-HT. 3 5-HT-induced tone was reduced by the 5-HT(2) and 5-HT(2A) receptor antagonists ritanserine (0.1 microM) and spiperone (0.2 microM), respectively. However, 5-HT contraction was not antagonized by cyanopindolol (2 microM), SDZ-SER 082 (1 microM), Y-25130 (1 microM) and GR 113808 (0.1 microM), which are respectively, 5-HT(1A/1B), 5-HT(2B/2C), 5-HT(3), and 5-HT(4) selective receptor antagonists. 4 Removal of the urothelium did not modify 5-HT-induced contractions. Blockade of neuronal voltage-activated sodium channels, alpha-adrenergic receptors and adrenergic neurotransmission with tetrodotoxin (1 microM), phentolamine (0.3 microM) and guanethidine (10 microM), respectively, reduced the contractions to 5-HT. However, physostigmine (1 microM), atropine (0.1 microM) and suramin (30 microM), inhibitors of cholinesterase activity, muscarinic- and purinergic P(2)-receptors, respectively, failed to modify the contractions to 5-HT. 5 These results suggest that 5-HT increases the tone of the pig intravesical ureter through 5-HT(2A) receptors located at the smooth muscle. Part of the 5-HT contraction is indirectly mediated via noradrenaline release from sympathetic nerves.

摘要
  1. 本研究旨在探讨5-羟色胺(5-HT)的作用,并鉴定猪膀胱内输尿管中参与5-HT反应的5-HT受体。2. 5-HT(0.01 - 10微摩尔)浓度依赖性地增加膀胱内输尿管条的张力,而相性收缩的增加与浓度无关。5-HT(2)受体激动剂α-甲基5-HT模拟了对张力的作用,而5-CT、8-OH-DPAT、间氯苯双胍和RS 67333分别作为5-HT(1)、5-HT(1A)、5-HT(3)和5-HT(4)受体激动剂,作用微弱或无反应。5-HT未诱导U46619收缩的输尿管制剂舒张。单胺氧化酶A/B活性抑制剂帕吉林(100微摩尔)使5-HT的浓度-反应曲线向左移位。3. 5-HT(2)和5-HT(2A)受体拮抗剂利坦色林(0.1微摩尔)和螺哌隆(0.2微摩尔)分别降低了5-HT诱导的张力。然而,5-HT收缩未被氰吲哚洛尔(2微摩尔)、SDZ-SER 082(1微摩尔)、Y-25130(1微摩尔)和GR 113808(0.1微摩尔)拮抗,它们分别是5-HT(1A/1B)、5-HT(2B/2C)、5-HT(3)和5-HT(4)选择性受体拮抗剂。4. 去除尿路上皮并未改变5-HT诱导的收缩。用河豚毒素(1微摩尔)、酚妥拉明(0.3微摩尔)和胍乙啶(10微摩尔)分别阻断神经元电压激活钠通道、α-肾上腺素能受体和肾上腺素能神经传递,可降低对5-HT的收缩反应。然而,胆碱酯酶活性抑制剂毒扁豆碱(1微摩尔)、毒蕈碱和嘌呤能P(2)受体抑制剂阿托品(0.1微摩尔)和苏拉明(30微摩尔)未能改变对5-HT的收缩反应。5. 这些结果表明,5-HT通过位于平滑肌的5-HT(2A)受体增加猪膀胱内输尿管的张力。5-HT收缩的一部分是通过交感神经释放去甲肾上腺素间接介导的。