McArthur A J, Hunt A E, Gillette M U
Department of Physiology and Biophysics, University of Illinois-Urbana-Champaign 61801, USA.
Endocrinology. 1997 Feb;138(2):627-34. doi: 10.1210/endo.138.2.4925.
Nocturnal synthesis of the pineal hormone melatonin (MEL) is regulated by the circadian clock in the suprachiasmatic nucleus (SCN) of the hypothalamus. We examined the hypothesis that MEL can feed back to regulate the SCN using a brain slice preparation from rat. We monitored the SCN ensemble firing rate and found that MEL advanced the time of peak firing rate by more than 3 h at restricted circadian times (CTs) near subjective dusk [CT 10-14 (10-14 h after lights on)] and dawn (CT 23-0) on days 2 and 3 after treatment. The effect of MEL at CT 10 was blocked by pertussis toxin. The protein kinase C (PKC) activator, 12-O-tetradecanoylphorbol 13-acetate, reset the SCN firing rate rhythm with a profile of temporal sensitivity congruent with that of MEL. Two specific PKC inhibitors, calphostin C and chelerythrine chloride, independently blocked MEL-induced phase advances at each sensitive period. Furthermore, MEL administration increased PKC phosphotransferase activity transiently to 200% at CT 10 and CT 23, but not at CT 6. These data demonstrate that 1) MEL can directly modulate the circadian timing of the SCN within two windows of sensitivity corresponding to dusk and dawn; and 2) MEL alters SCN cellular function via a pertussis toxin-sensitive G protein pathway that activates PKC.
松果体激素褪黑素(MEL)的夜间合成受下丘脑视交叉上核(SCN)中的昼夜节律时钟调节。我们使用大鼠脑片制备物检验了MEL可反馈调节SCN的假说。我们监测了SCN整体放电频率,发现在处理后第2天和第3天,在接近主观黄昏[昼夜时间(CT)10 - 14(开灯后10 - 14小时)]和黎明(CT 23 - 0)的受限昼夜时间,MEL使放电频率峰值时间提前了3小时以上。百日咳毒素可阻断MEL在CT 10时的作用。蛋白激酶C(PKC)激活剂12 - O - 十四酰佛波醇13 - 乙酸酯重置了SCN放电频率节律,其时间敏感性特征与MEL的特征一致。两种特异性PKC抑制剂,钙泊三醇C和氯化白屈菜红碱,在每个敏感时期均独立阻断了MEL诱导的相位提前。此外,在CT 10和CT 23时,给予MEL可使PKC磷酸转移酶活性瞬时增加至200%,但在CT 6时则无此作用。这些数据表明:1)MEL可在对应黄昏和黎明的两个敏感窗口内直接调节SCN的昼夜节律时间;2)MEL通过激活PKC的百日咳毒素敏感G蛋白途径改变SCN细胞功能。