Born J, Steinbach D, Dodt C, Fehm H L
Department of Internal Medicine, University of Lübeck, Germany.
J Clin Endocrinol Metab. 1997 Apr;82(4):1106-10. doi: 10.1210/jcem.82.4.3856.
Pituitary-adrenal activity has been found to be inhibited during early nocturnal sleep in humans. This inhibition was supposed to reflect a regulatory influence of hippocampal cells characterized by the expression of mineralocorticoid receptors (MR). Pituitary adrenal responsiveness to bolus injections of CRH (50 micrograms) was examined in each of nine healthy men on four occasions: CRH was injected either during early nocturnal sleep or at the same time of night while the subject was kept awake. Both of these conditions were run after pretreatment with the selective MR antagonist, canrenoate (2 x 200 mg, 0800 and 1700 h, preceding the experimental night) and after placebo administration. After placebo, sleep reduced ACTH and cortisol secretory responses to CRH to about 65% of the size observed during wakefulness (P < 0.05). After canrenoate, ACTH and cortisol secretory responses during sleep and wakefulness did not differ and were comparable with those obtained in placebo-treated subjects during wakefulness. Compared with placebo, canrenoate also distinctly reduced the time spent in slow-wave sleep (P < 0.005). The findings confirm an inhibition of pituitary-adrenal responsiveness during early sleep. The inhibition disappearance after blockage of MR suggests that sleep exerts this influence via central nervous MR-expressing cells. These cells seem to be simultaneously involved in the generation of slow-wave sleep.
研究发现,人类在夜间早期睡眠期间垂体 - 肾上腺活动受到抑制。这种抑制作用被认为反映了以盐皮质激素受体(MR)表达为特征的海马细胞的调节影响。对9名健康男性在四种情况下分别进行了垂体肾上腺对静脉注射促肾上腺皮质激素释放激素(CRH,50微克)的反应性检查:CRH要么在夜间早期睡眠期间注射,要么在受试者保持清醒的同一夜间时段注射。这两种情况均在选择性MR拮抗剂坎利酸盐(2×200毫克,实验前一晚的08:00和17:00)预处理后以及给予安慰剂后进行。给予安慰剂后,睡眠使促肾上腺皮质激素(ACTH)和皮质醇对CRH的分泌反应降低至清醒时观察到的约65%(P<0.05)。给予坎利酸盐后,睡眠和清醒期间的ACTH和皮质醇分泌反应没有差异,且与安慰剂治疗的受试者在清醒时获得的反应相当。与安慰剂相比,坎利酸盐还明显减少了慢波睡眠的时长(P<0.005)。这些发现证实了早期睡眠期间垂体 - 肾上腺反应性受到抑制。MR被阻断后抑制作用消失,这表明睡眠通过表达MR的中枢神经细胞发挥这种影响。这些细胞似乎同时参与了慢波睡眠的产生。