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豚鼠结肠中腺苷受体的分子鉴定与药理学特性研究

Molecular identification and pharmacological characterization of adenosine receptors in the guinea-pig colon.

作者信息

Kadowaki M, Takeda M, Tokita K, Hanaoka K, Tomoi M

机构信息

Pharmacological Research Laboratory, Fujisawa Pharmaceutical Co. Ltd., Osaka 532-0031, Japan.

出版信息

Br J Pharmacol. 2000 Mar;129(5):871-6. doi: 10.1038/sj.bjp.0703123.

Abstract

The aim of this study is to elucidate the role of adenosine in the motor function of the guinea-pig distal colon.2 To determine whether adenosine A(1) receptors and A(2B) receptors are expressed in the guinea-pig colon, we employed the reverse transcription-polymerase chain reaction (RT - PCR). The gene expression of A(1) receptor and A(2B) receptor was found for the first time in the guinea-pig proximal and distal colon.3 Adenosine A(1) agonist N(6)-cyclopentyladenosine (CPA), and A(1)/A(2) agonist 5'-N-ethylcarboxamidoadenosine (NECA) concentration-dependently inhibited neurogenic responses to electrical field stimulation (EC(50)=1.07x10(-8) and 2.12x10(-8) M) in the longitudinal muscle, but A(2A) agonist 2-p-(2-carboxyethyl)phenylethylamino-5'-N-ethycarboxamido-ad enosine (CGS21680) had only a slight inhibitory effect (25.9%, 1 microM). A(1) antagonist 8-cyclopentyl-1,3-dipropylxanthine (DPCPX, 10 nM: A(1) selective concentration) antagonized responses to CPA and NECA. Furthermore, the affinity order of antagonists at inhibiting the effect NECA was: DPCPX>8-phenyltheophylline (8-PT: A(1)/A(2) antagonist).3 In the presence of tetrodotoxin (TTX, 0.3 microM), CPA and NECA relaxed myogenic precontraction induced by KCl (50 mM) (EC(50)=1.26x10(-5) and 1.04x10(-5) M, respectively), but CGS21680 (1 microM) did not cause any relaxation. DPCPX did not affect responses to CPA and NECA at a concentration of 10 nM, but a higher concentration (1 microM) of DPCPX and 10 microM of 8-PT antagonized those responses.5 These data lead us to the hypothesis that adenosine may mediate relaxation through two different inhibitory receptor subtypes; A(1) receptors on the enteric neuron and A(2B) receptor on the smooth muscle in the guinea-pig distal colon.

摘要

本研究的目的是阐明腺苷在豚鼠远端结肠运动功能中的作用。2为了确定腺苷A(1)受体和A(2B)受体是否在豚鼠结肠中表达,我们采用了逆转录-聚合酶链反应(RT-PCR)。首次在豚鼠近端和远端结肠中发现了A(1)受体和A(2B)受体的基因表达。3腺苷A(1)激动剂N(6)-环戊基腺苷(CPA)和A(1)/A(2)激动剂5'-N-乙基羧酰胺腺苷(NECA)在纵行肌中浓度依赖性地抑制对电场刺激的神经源性反应(EC(50)=1.07x10(-8)和2.12x10(-8)M),但A(2A)激动剂2-p-(2-羧乙基)苯乙氨基-5'-N-乙基羧酰胺腺苷(CGS21680)只有轻微的抑制作用(25.9%,1μM)。A(1)拮抗剂8-环戊基-1,3-二丙基黄嘌呤(DPCPX,10 nM:A(1)选择性浓度)拮抗对CPA和NECA的反应。此外,拮抗剂抑制NECA作用的亲和力顺序为:DPCPX>8-苯基茶碱(8-PT:A(1)/A(2)拮抗剂)。3在存在河豚毒素(TTX,0.3μM)的情况下,CPA和NECA使由氯化钾(50 mM)诱导的肌源性预收缩松弛(EC(50)分别为1.26x10(-5)和1.04x10(-5)M),但CGS21680(1μM)未引起任何松弛。DPCPX在10 nM浓度时不影响对CPA和NECA的反应,但更高浓度(1μM)的DPCPX和10μM的8-PT拮抗这些反应。5这些数据使我们提出这样的假设,即腺苷可能通过两种不同的抑制性受体亚型介导松弛;豚鼠远端结肠中肠神经元上的A(1)受体和平滑肌上的A(2B)受体。

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