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本文引用的文献

1
Characterization of adenosine receptors on rat ileum, ileal longitudinal muscle and muscularis mucosae.大鼠回肠、回肠纵行肌和黏膜肌层上腺苷受体的特性研究
Eur J Pharmacol. 1997 Nov 5;338(2):143-50. doi: 10.1016/s0014-2999(97)81942-5.
2
Species differences in brain adenosine A1 receptor pharmacology revealed by use of xanthine and pyrazolopyridine based antagonists.基于黄嘌呤和吡唑并吡啶的拮抗剂揭示的脑腺苷A1受体药理学中的物种差异。
Br J Pharmacol. 1997 Nov;122(6):1202-8. doi: 10.1038/sj.bjp.0701465.
3
Characterization of adenosine receptors mediating spinal sensory transmission related to nociceptive information in the rat.介导大鼠脊髓中与伤害性信息相关的感觉传递的腺苷受体的特性研究。
Anesthesiology. 1997 Sep;87(3):577-84. doi: 10.1097/00000542-199709000-00018.
4
Characterisation of pre- and post-synaptic alpha-adrenoceptors in modulation of the rat ileum longitudinal and circular muscle activities.突触前和突触后α-肾上腺素能受体对大鼠回肠纵行和环行肌活动调节的特征分析
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Functional classification of P1-purinoceptors in guinea-pig left and right atria: anomalous characteristics of antagonism by cyclopentyltheophylline.豚鼠左右心房中P1嘌呤受体的功能分类:环戊基茶碱拮抗作用的异常特征
Naunyn Schmiedebergs Arch Pharmacol. 1997 Jun;355(6):759-66. doi: 10.1007/pl00005010.
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Response to prejunctional adenosine receptors is dependent on stimulus frequency.对突触前腺苷受体的反应取决于刺激频率。
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A simple method for measuring the effects of drugs on intestinal longitudinal and circular muscle.一种测量药物对肠道纵肌和环肌作用的简单方法。
J Pharmacol Toxicol Methods. 1996 Nov;36(3):147-54. doi: 10.1016/s1056-8719(96)00110-4.
8
Characterization of P1-purinoceptors on rat isolated duodenum longitudinal muscle and muscularis mucosae.大鼠离体十二指肠纵肌和黏膜肌层上P1嘌呤受体的特性研究
Br J Pharmacol. 1996 Jan;117(1):170-4. doi: 10.1111/j.1476-5381.1996.tb15170.x.
9
Excitation and inhibition via adenosine receptors of the twitch response to electrical stimulation in isolated guinea pig ileum.通过腺苷受体对豚鼠离体回肠电刺激引发的抽搐反应的兴奋与抑制作用
Jpn J Pharmacol. 1995 Dec;69(4):429-33. doi: 10.1254/jjp.69.429.
10
Extended concentration-response curves used to reflect full agonist efficacies and receptor occupancy-response coupling ranges.用于反映完全激动剂效力和受体占有率-反应偶联范围的延长浓度-反应曲线。
Br J Pharmacol. 1995 Jul;115(5):745-52. doi: 10.1111/j.1476-5381.1995.tb14996.x.

大鼠回肠中神经腺苷受体的表征及组织定位

Characterization and tissue location of the neural adenosine receptor in the rat ileum.

作者信息

Coupar I M

机构信息

Department of Pharmaceutical Biology and Pharmacology, Victorian College of Pharmacy, Monash University, Parkville, Australia.

出版信息

Br J Pharmacol. 1999 Mar;126(5):1269-75. doi: 10.1038/sj.bjp.0702411.

DOI:10.1038/sj.bjp.0702411
PMID:10205018
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1565885/
Abstract
  1. The aim of the present investigation was to characterize and determine the tissue location of the adenosine receptors present in the rat ileum using a method that detects drug action on the cholinergic nerves innervating the longitudinal and circular muscles. 2. The non-selective adenosine agonist, NECA (10 and 100 nM) caused significant concentration-related reductions in the circular muscle responses to transmural stimulation over the frequency range of 2.5-40 Hz, but did not affect the responses of the longitudinal muscle, nor did it reduce the muscle responses of the guinea-pig ileum. 3. The affinity order of antagonists at inhibiting the effect of NECA on the circular muscle was: CPDPX>8-PT>DMPX with apparent pA2 values of 9.31, 7.54 and 5.63 respectively. CPDPX (10-100 nM) caused parallel displacements of the concentration-effect curves to CPA with a pKb value of 9.15 and Schild slope of 1.03. 4. The agonists previously tested in the rat jejunum peristaltic reflex preparation were also shown to inhibit responses of the rat ileum in the following decreasing order of potency: CPA>NECA>2-CADO>R-PIA>S-PIA>>PAA. In addition, CHA and CCPA were also potent agonists. NECA (100 nM) and CPA (32 nM) did not inhibit carbachol (1 microM)-induced tone of tissues pre-treated with TTX (1 microM). 5. In conclusion, the rat ileum contains inhibitory A1 adenosine receptors situated on cholinergic nerve endings innervating the circular muscle.
摘要
  1. 本研究的目的是使用一种检测药物对支配纵行肌和环行肌的胆碱能神经作用的方法,来表征和确定大鼠回肠中存在的腺苷受体的组织定位。2. 非选择性腺苷激动剂NECA(10和100 nM)在2.5 - 40 Hz频率范围内,可引起环行肌对跨壁刺激的反应出现与浓度相关的显著降低,但不影响纵行肌的反应,也不降低豚鼠回肠的肌肉反应。3. 拮抗剂抑制NECA对环行肌作用的亲和力顺序为:CPDPX > 8 - PT > DMPX,其表观 pA2值分别为9.31、7.54和5.63。CPDPX(10 - 100 nM)使浓度 - 效应曲线平行右移至CPA,pKb值为9.15,Schild斜率为1.03。4. 先前在大鼠空肠蠕动反射制备中测试过的激动剂,也显示出以以下效力递减顺序抑制大鼠回肠的反应:CPA > NECA > 2 - CADO > R - PIA > S - PIA >> PAA。此外,CHA和CCPA也是强效激动剂。NECA(100 nM)和CPA(32 nM)不抑制用TTX(1 microM)预处理的组织对卡巴胆碱(1 microM)诱导的张力。5. 总之,大鼠回肠在支配环行肌的胆碱能神经末梢上含有抑制性A1腺苷受体。