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在脊髓横断大鼠心脏中,介导心脏加速节前抑制的α2-肾上腺素能受体亚型的研究。

Investigation of the subtype of alpha 2-adrenoceptor mediating prejunctional inhibition of cardioacceleration in the pithed rat heart.

作者信息

Smith K, Gavin K, Docherty J R

机构信息

Department of Physiology, Royal College of Surgeons in Ireland, Dublin.

出版信息

Br J Pharmacol. 1995 May;115(2):316-20. doi: 10.1111/j.1476-5381.1995.tb15879.x.

Abstract
  1. We have investigated the subtype of alpha 2-adrenoceptor mediating prejunctional inhibition of cardioacceleration in the pithed rat heart in comparison with alpha 2-adrenoceptor ligand binding sites. 2. In pithed rats, prejunctional alpha 2-adrenoceptors were investigated in terms of the ability of alpha 2-adrenoceptor antagonists to shift the inhibitory potency of the alpha 2-adrenoceptor agonist, xylazine, against the tachycardia to a single electrical stimulus given via the pithing rod. 3. Antagonist potency at prejunctional alpha 2-adrenoceptors in pithed rat heart was correlated with antagonist affinity at alpha 2-adrenoceptor ligand binding sites in membranes of rat kidney and submandibular gland labelled with [3H]-yohimbine. 4. The correlation with the prejunctional alpha 2-adrenoceptor in pithed rat heart was best for the alpha 2D-adrenoceptor ligand binding site of rat submandibular gland (r = 0.98, n = 10, P < 0.0001), as compared to correlations with the alpha 2A-adrenoceptor ligand binding site of human platelet (r = 0.90, n = 9, P < 0.001), the alpha 2B-adrenoceptor ligand binding site of rat kidney (r = 0.82, n = 10, P < 0.01) and with published results for the alpha 2C-adrenoceptor ligand binding site (r = 0.48, n = 6, NS). 5. It is concluded that the functional prejunctional alpha 2-adrenoceptor of pithed rat heart closely resembles the alpha 2D-adrenoceptor ligand binding site of rat submandibular gland.
摘要
  1. 我们研究了介导脊髓麻醉大鼠心脏心动加速节前抑制的α₂-肾上腺素能受体亚型,并与α₂-肾上腺素能受体配体结合位点进行了比较。2. 在脊髓麻醉大鼠中,通过α₂-肾上腺素能受体拮抗剂将α₂-肾上腺素能受体激动剂赛拉嗪对经脊髓穿刺棒给予单次电刺激所致心动过速的抑制效力进行移位,以此研究节前α₂-肾上腺素能受体。3. 脊髓麻醉大鼠心脏节前α₂-肾上腺素能受体的拮抗剂效力与用[³H]-育亨宾标记的大鼠肾脏和下颌下腺膜中α₂-肾上腺素能受体配体结合位点的拮抗剂亲和力相关。4. 与人类血小板的α₂A-肾上腺素能受体配体结合位点(r = 0.90,n = 9,P < 0.001)、大鼠肾脏的α₂B-肾上腺素能受体配体结合位点(r = 0.82,n = 10,P < 0.01)以及已发表的α₂C-肾上腺素能受体配体结合位点结果(r = 0.48,n = 6,无显著性差异)相比,脊髓麻醉大鼠心脏节前α₂-肾上腺素能受体与大鼠下颌下腺的α₂D-肾上腺素能受体配体结合位点的相关性最佳(r = 0.98,n = 10,P < 0.0001)。5. 得出的结论是,脊髓麻醉大鼠心脏功能性节前α₂-肾上腺素能受体与大鼠下颌下腺的α₂D-肾上腺素能受体配体结合位点极为相似。

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Molecular characterization of alpha 1- and alpha 2-adrenoceptors.
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