Blattner Margaret S, Mahoney Megan M
College of Medicine .
Chronobiol Int. 2014 Jun;31(5):637-44. doi: 10.3109/07420528.2014.885528. Epub 2014 Feb 14.
Estradiol influences the level and distribution of daily activity, the duration of the free-running period, and the behavioral phase response to light pulses. However, the mechanisms by which estradiol regulates daily and circadian rhythms are not fully understood. We tested the hypothesis that estrogens modulate daily activity patterns via both classical and "non-classical" actions at the estrogen receptor subtype 1 (ESR1). We used female transgenic mice with mutations in their estrogen response pathways; ESR1 knock-out (ERKO) mice and "non-classical" estrogen receptor knock-in (NERKI) mice. NERKI mice have an ESR1 receptor with a mutation in the estrogen-response-element binding domain, allowing only actions via "non-classical" genomic and second messenger pathways. Ovariectomized female NERKI, ERKO, and wildtype (WT) mice were given a subcutaneous capsule with low- or high-dose estradiol and compared with counterparts with no hormone replacement. We measured wheel-running activity in a light:dark cycle and constant darkness, and the behavioral phase response to light pulses given at different points during the subjective day and night. Estradiol increased average daily wheel-running, consolidated activity to the dark phase, and shortened the endogenous period in WT, but not NERKI and ERKO mice. The timing of activity onset during entrainment was advanced in all estradiol-treated animals regardless of genotype suggesting an ESR1-independent mechanism. We propose that estradiol modifies period, activity level, and distribution of activity via classical actions of ESR1 whereas an ESR1 independent mechanism regulates the phase of rhythms.
雌二醇会影响日常活动的水平和分布、自由运行周期的时长以及对光脉冲的行为相位反应。然而,雌二醇调节日常节律和昼夜节律的机制尚未完全明确。我们检验了这样一个假说:雌激素通过在雌激素受体亚型1(ESR1)上的经典和“非经典”作用来调节日常活动模式。我们使用了雌激素反应途径发生突变的雌性转基因小鼠;ESR1基因敲除(ERKO)小鼠和“非经典”雌激素受体基因敲入(NERKI)小鼠。NERKI小鼠的ESR1受体在雌激素反应元件结合域存在突变,仅允许通过“非经典”基因组和第二信使途径发挥作用。对卵巢切除的雌性NERKI、ERKO和野生型(WT)小鼠皮下植入低剂量或高剂量雌二醇胶囊,并与未进行激素替代的对照组进行比较。我们在明-暗周期和持续黑暗环境中测量转轮活动,并测量在主观昼夜的不同时间点给予光脉冲后的行为相位反应。雌二醇增加了WT小鼠的平均每日转轮活动,使活动巩固至暗期,并缩短了其内在周期,但NERKI和ERKO小鼠未出现此现象。在所有接受雌二醇治疗的动物中,无论基因型如何,夹带期间活动开始的时间都提前了,这表明存在一种不依赖ESR1的机制。我们提出,雌二醇通过ESR1的经典作用改变周期、活动水平和活动分布,而一种不依赖ESR1的机制则调节节律的相位。