Ratka A, Veldhuis H D, De Kloet E R
Rudolf Magnus Institute for Pharmacology, Medical Faculty, University of Utrecht, The Netherlands.
Neuropharmacology. 1988 Jan;27(1):15-21. doi: 10.1016/0028-3908(88)90195-5.
The antinociceptive effect of parenterally and intracerebroventricularly injected morphine and beta-endorphin in adrenalectomized rats and in adrenalectomized rats treated with adrenal steroids was examined employing the hot-plate method. (1) Adrenalectomy sensitized the rats to an analgesic effect of morphine and beta-endorphin. (2) Replacement therapy (chronic and acute) with corticosterone, dexamethasone or RU 28362 (glucocorticoid receptor agonist) effectively reversed the increase in the sensitivity to the analgesic effect of peripherally injected morphine (5 mg/kg i.p.) induced by adrenalectomy to the level of sham-operated animals. Glucocorticosteroids administered to non-adrenalectomized rats did not change the sensitivity to morphine. (3) Corticosterone had a biphasic, dose-dependent effect; the most significant attenuation of the hypersensitivity to morphine-induced antinociception in adrenalectomized rats was achieved after 0.01 mg and after 10 mg (per kg b.w.). Doses of corticosterone of 0.005 mg/kg and in a range of 0.05-0.30 mg/kg were ineffective. (4) Corticosterone in a dose of 0.01 mg/kg (s.c.) had suppressant effects on the adrenalectomy-induced increase in the sensitivity to antinociception induced by morphine when given prior to morphine (60, 30 and 5 min) as well as after the injection of morphine (before the first and the second testing on the hot-plate, 15 and 5 min, respectively). (5) Intracerebroventricularly (i.c.v.) injected morphine and beta-endorphin also displayed the hypersensitivity to the analgesic effect in adrenalectomized rats which in both cases could be suppressed by 0.01 mg/kg of corticosterone given subcutaneously 5 min prior to administration of the opiate.(ABSTRACT TRUNCATED AT 250 WORDS)
采用热板法研究了经腹腔注射和脑室内注射吗啡及β-内啡肽对肾上腺切除大鼠以及用肾上腺皮质类固醇治疗的肾上腺切除大鼠的镇痛作用。(1)肾上腺切除术使大鼠对吗啡和β-内啡肽的镇痛作用敏感。(2)用皮质酮、地塞米松或RU 28362(糖皮质激素受体激动剂)进行替代疗法(慢性和急性)可有效将肾上腺切除术诱导的对腹腔注射5mg/kg吗啡镇痛作用的敏感性增加逆转至假手术动物水平。给予未肾上腺切除大鼠糖皮质激素不会改变其对吗啡的敏感性。(3)皮质酮具有双相剂量依赖性作用;肾上腺切除大鼠对吗啡诱导的镇痛作用超敏反应的最显著减弱在给予0.01mg和10mg(每千克体重)后出现。0.005mg/kg及0.05 - 0.30mg/kg范围内的皮质酮剂量无效。(4)0.01mg/kg(皮下注射)的皮质酮在吗啡给药前(60、30和5分钟)以及注射吗啡后(分别在热板上第一次和第二次测试前15分钟和5分钟)对肾上腺切除术诱导的对吗啡诱导的镇痛作用敏感性增加具有抑制作用。(5)脑室内注射吗啡和β-内啡肽在肾上腺切除大鼠中也表现出对镇痛作用的超敏反应,在两种情况下,在给予阿片类药物前5分钟皮下注射0.01mg/kg皮质酮均可抑制这种超敏反应。(摘要截断于250字)