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A comparison of the cardiovascular and sedative actions of the α-adrenoceptor agonists FLA-136 and clonidine in the rat

机译:α-肾上腺素受体激动剂FLA-136和可乐定在大鼠中的心血管和镇静作用的比较

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摘要

>1 The cardiovascular and sedative effects of FLA-136 have been compared with those of clonidine after intracerebroventricular (i.c.v.) administration in the rat. The effects of both drugs on pre- and postsynaptic α-adrenoceptors in the periphery have been investigated after intravenous (i.v.) administration in the pithed rat.>2 In the anaesthetized rat, i.c.v. FLA-136 and clonidine produced dose-related hypotension, FLA-136 having three to 30 times less activity than clonidine; both drugs caused concomitant bradycardia. In the conscious rat i.c.v. FLA-136 had less sedative potential than clonidine, in terms of overt sedation assessed visually.>3 Yohimbine reduced the hypotension and bradycardia produced by i.c.v. FLA-136 and clonidine; prazosin and mianserin also antagonized the cardiovascular responses to clonidine, but not those to FLA-136.>4 Chemical sympathectomy by 6-hydroxydopamine (6-OHDA) markedly reduced the cardiovascular effects of FLA-136 but only slightly reduced those of clonidine.>5 Naloxone antagonized the cardiovascular responses to clonidine, but not FLA-136, suggesting a direct or indirect involvement of central opiate receptors in the responses induced by clonidine.>6 Metiamide attenuated the cardiovascular responses to FLA-136 and clonidine, implying a direct or indirect involvement of central histamine (H2)-receptors in such responses.>7 FLA-136, unlike clonidine, did not stimulate peripheral pre- or postsynaptic α-adrenoceptors in the pithed rat.>8 FLA-136 is a novel centrally-acting hypotensive compound which, unlike clonidine, selectively stimulates central α-autoreceptors (yohimbine-sensitive) in the rat; these autoreceptors may be different from peripheral pre- and postsynaptic α-adrenoceptors. The results suggest that clonidine lowers blood pressure by stimulation of two types of central postsynaptic α-adrenoceptors in the rat, one type being sensitive to yohimbine and the other to prazosin.
机译:> 1 已比较了大鼠脑室内(i.c.v.)施用后FLA-136与可乐定的心血管和镇静作用。 > 2 在麻醉大鼠中,静脉注射i.v.后,已研究了这两种药物对外周突触前和突触后α-肾上腺素受体的影响。> 2 FLA-136和可乐定产生与剂量有关的低血压,FLA-136的活性比可乐定低三至三十倍;两种药物均引起心动过缓。在有意识的老鼠中就视觉评估的明显镇静而言,FLA-136的镇静潜力低于可乐定。> 3 育亨宾可降低i.c.v.引起的低血压和心动过缓。 FLA-136和可乐定;哌唑嗪和棉桃素也拮抗可乐定的心血管反应,但对FLA-136无效。> 4 6-羟基多巴胺(6-OHDA)的化学交感神经切除术显着降低了FLA-136的心血管作用,但仅轻微降低降低了可乐定的含量。> 5 。纳洛酮拮抗可乐定的心血管反应,但不拮抗FLA-136,表明中枢阿片受体直接或间接参与了可乐定诱导的反应。> 6 甲氨酰胺减弱了对FLA-136和可乐定的心血管反应,表明中央组胺(H2)受体直接或间接参与了这种反应。> 7 与可乐定不同,FLA-136并未刺激> 8 FLA-136是一种新型的中枢性降压化合物,与可乐定不同,它可选择性刺激中枢神经系统的α-自身受体(育亨宾敏感)。鼠;这些自身受体可能与突触前后的α-肾上腺素受体不同。结果表明可乐定通过刺激大鼠中的两种类型的突触后中央α-肾上腺素能受体来降低血压,一种对育亨宾敏感,另一种对哌唑嗪敏感。

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