Marotta S F, Hiles L G, Lanuza D M, Boonayathap U
Horm Metab Res. 1975 Jul;7(4):334-7. doi: 10.1055/s-0028-1093725.
Plasma corticosterone levels and the in vitro capacity of the liver to reduce the delta(4)3-ketone group of corticosterone were ascertained at 4 hr intervals in male rats maintained on a normal lighting schedule (12L:12D). The rates of delta(4)3-ketone reduction, as well as wet liver weight, were highest during the early portion (08.00 hr) of the light period when liver protein and plasma corticosterone concentrations were low. Shortly (2000 hr) after the beginning of the dark period plasma corticosterone reached peak levels, while hepatic inactivation of corticosterone was markedly depressed. This inverse relationship suggests that the rhythmicity in the capacity of the liver to inactivate corticosterone may contribute to the circadian periodicity of plasma corticosterone.
在按照正常光照时间表(12小时光照:12小时黑暗)饲养的雄性大鼠中,每隔4小时测定一次血浆皮质酮水平以及肝脏在体外还原皮质酮Δ⁴-3-酮基团的能力。在光照期的早期(08:00时),当肝脏蛋白质和血浆皮质酮浓度较低时,Δ⁴-3-酮还原率以及肝脏湿重最高。黑暗期开始后不久(20:00时),血浆皮质酮达到峰值水平,而肝脏对皮质酮的失活作用则明显受到抑制。这种反比关系表明,肝脏使皮质酮失活能力的节律性可能有助于血浆皮质酮的昼夜周期性变化。