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Effects of adrenoceptor blocking agents on body temperature

机译:肾上腺素受体阻断剂对体温的影响

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摘要

1. The effect on rectal temperature of adrenoceptor blocking agents, injected through a cannula chronically implanted into a lateral cerebral ventricle, was examined in unanaesthetized rabbits, cats and rats, kept at room temperature (19-22° C).2. In rabbits, the α-adrenoceptor blocking agent phenoxybenzamine (50 or 100 μg) produced marked hypothermia when injected intraventricularly but not when injected intravenously. In some rabbits as little as 1 μg was effective on intraventricular injection. Phentolamine and ergotamine, the other α-adrenoceptor blocking agents examined, had a much weaker hypothermic action when injected intraventricularly, whereas the β-adrenoceptor blocking agents propranolol, pronethalol and Trasicor had no effect.3. In rabbits in which the noradrenaline stores of the hypothalamus were depleted by intraventricular injections of reserpine, the hypothermic effect of phenoxybenzamine was abolished and remained abolished for a few days.4. In cats, an intraventricular injection of phenoxybenzamine (200 μg) produced long-lasting hyperthermia, but not in all cats, and only with the first, or the first two or three injections. Injected intraperitoneally, this dose had no effect on temperature. Phentolamine (100 or 200 μg) had a very weak hyperthermic effect and phentolamine (500 μg), a hypothermic effect, but only on intraventricular injection, whereas ergotamine (100 and 200 μg) had a weak hyperthermic effect both on intraventricular and intraperitoneal injection. Propranolol and Trasicor had no effect on temperature when injected intraventricularly.5. In rats, phenoxybenzamine (5 or 20 μg) produced long-lasting hypothermia on intraventricular injection.6. Some of the temperature effects produced by intraventricular injections of the α-adrenoceptor blocking agents are explained on the assumption that they prevent the effect on temperature produced by a continuous release of noradrenaline from adrenergic neurones innervating the anterior hypothalamus.
机译:1.在保持在室温(19-22°C)的未麻醉的兔子,猫和大鼠中,研究了通过长期植入脑侧脑室的套管注射的肾上腺素受体阻断剂对直肠温度的影响。2。在兔中,当进行心室内注射时,α-肾上腺素受体阻断剂苯氧基苯甲胺(50或100μg)产生明显的体温过低,而静脉注射时则没有。在一些兔子中,脑室内注射仅1μg有效。脑室内注射时,其他被检查的α-肾上腺素受体阻断剂苯酚和麦角胺对体温的作用要弱得多,而β-肾上腺素受体阻断剂普萘洛尔,普萘太洛和Trasicor没有作用。3。脑室注射利血平耗尽下丘脑去甲肾上腺素的去甲肾上腺素的兔子,苯氧基苯扎明的降温作用消失,并保持了几天。4。在猫中,脑室内注射苯氧基苯扎明(200μg)会产生持久的体温过高,但并非在所有猫中都产生,并且仅在第一次或前两次或前三次注射中产生。腹膜内注射,该剂量对温度没有影响。酚妥拉明(100或200μg)的体温过高,苯妥拉明(500μg)的体温过低,但仅对脑室内注射有效,而麦角胺(100和200μg)的脑室内和腹膜内均具有较弱的高热作用。脑室内注射普萘洛尔和曲沙可对温度无影响。5。在大鼠中,苯氧苯扎明(5或20μg)在脑室内注射后会产生持久的体温过低6。脑室内注射α-肾上腺素受体阻断剂产生的一些温度效应是在以下假设的基础上进行解释的:它们阻止了神经支配肾上腺素神经元持续释放去甲肾上腺素对去甲肾上腺素产生的温度影响。

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