Pauly J R, Ullman E A, Collins A C
Institute for Behavioral Genetics, University of Colorado, Boulder 80309.
Physiol Behav. 1988;44(1):109-16. doi: 10.1016/0031-9384(88)90353-8.
The possibility that nicotine-induced corticosterone (CCS) release regulates nicotine sensitivity was investigated in female mice of the C3H strain. Adrenalectomy (ADX) resulted in an increase in nicotine sensitivity as measured in a number of physiological and behavioral tests. In ADX animals, chronic CCS (100 micrograms/ml) administered in the drinking solution normalized nicotine sensitivity. Dexamethasone (DEX), a potent synthetic glucocorticoid which interacts with a distinct population of CNS steroid receptors, did not reverse the effects of ADX. Unoperated animals administered CCS (200 micrograms/ml) were protected from the effects of nicotine for several test battery parameters. ADX had no effect on the number of brain nicotinic cholinergic receptors and also did not alter nicotine metabolism. These data support the hypothesis that CCS secretion modulates nicotine sensitivity in the mouse; however, the mechanisms by which this regulation occurs are unknown.
在C3H品系雌性小鼠中研究了尼古丁诱导的皮质酮(CCS)释放调节尼古丁敏感性的可能性。肾上腺切除术(ADX)导致在多项生理和行为测试中测得的尼古丁敏感性增加。在ADX动物中,饮水中给予慢性CCS(100微克/毫升)可使尼古丁敏感性恢复正常。地塞米松(DEX)是一种强效合成糖皮质激素,可与不同的中枢神经系统类固醇受体相互作用,但并未逆转ADX的作用。给予CCS(200微克/毫升)的未手术动物在几个测试电池参数方面对尼古丁的作用具有抵抗力。ADX对脑烟碱胆碱能受体数量没有影响,也没有改变尼古丁代谢。这些数据支持了CCS分泌调节小鼠尼古丁敏感性的假设;然而,这种调节发生的机制尚不清楚。