Everson C A, Reed H L
Clinical Psychobiology Branch, National Institute of Mental Health, National Institutes of Health, Bethesda, Maryland 20892.
Endocrinology. 1995 Apr;136(4):1426-34. doi: 10.1210/endo.136.4.7895653.
Sleep deprivation is associated with poor cognitive ability and impaired physical health, but the ways in which the brain and body become compromised are not understood. In sleep-deprived rats, plasma total T4 and T3 concentrations decline progressively to 78% and 47% below baseline values, respectively, brown adipose tissue 5'-deiodinase type II activity increases 100-fold, and serum TSH values are unknown. The progressive decline in plasma thyroid hormones is associated with a deep negative energy balance despite normal or increased food intake and malnutrition-like symptoms that eventuate in hypothermia and lethal systemic infections. The purpose of the present experiment was to evaluate the probable causes of the low plasma total T4 during sleep deprivation by measuring the free hormone concentration to minimize binding irregularities and by challenging the pituitary-thyroid axis with iv TRH to determine both 1) the pituitary release of TSH and 2) the thyroidal response of free T4 (FT4) and free T3 (FT3) release to the TSH increment. Sleep-deprived rats were awake 91% of the total time compared with 63% of the total time in yoked control rats and 50% of the total time during the baseline period. Cage control comparison rats were permitted to sleep normally. Sustained sleep deprivation resulted in a decline from baseline in plasma FT4 of 73 +/- 6% and FT3 of 45 +/- 12%, which were similar to the declines in total hormone concentrations observed previously; nonstimulated TSH was unchanged. In the yoked and cage control groups, FT4 also declined, but much less than that of the sleep-deprived group. The relative changes in free compared with total hormone concentrations over the study were also less parallel than those in the sleep-deprived group. The plasma TSH response to TRH was similar in all groups across experimental days. The plasma FT4 and FT3 concentrations in sleep-deprived rats increased after TRH-stimulated TSH release to an extent comparable to control values. Taken together, low basal FT4 and FT3 hormone concentrations and unchanged TSH and thyroidal responses to TRH suggest a pituitary or hypothalamic contribution to the hypothyroxinemia during sleep deprivation.
睡眠剥夺与认知能力差和身体健康受损有关,但大脑和身体受损的方式尚不清楚。在睡眠剥夺的大鼠中,血浆总T4和T3浓度分别逐渐下降至低于基线值的78%和47%,棕色脂肪组织II型5'-脱碘酶活性增加100倍,血清TSH值未知。尽管食物摄入量正常或增加,但血浆甲状腺激素的逐渐下降与深度负能量平衡以及最终导致体温过低和致命性全身感染的营养不良样症状有关。本实验的目的是通过测量游离激素浓度以尽量减少结合异常,并通过静脉注射TRH刺激垂体-甲状腺轴,来评估睡眠剥夺期间血浆总T4降低的可能原因,从而确定1)垂体释放TSH以及2)游离T4(FT4)和游离T3(FT3)释放对TSH增加的甲状腺反应。与配对对照大鼠总时间的63%以及基线期总时间的50%相比,睡眠剥夺的大鼠清醒时间占总时间的91%。笼养对照大鼠可正常睡眠。持续睡眠剥夺导致血浆FT4较基线下降73±6%,FT3下降45±12%,这与之前观察到的总激素浓度下降情况相似;未刺激的TSH未发生变化。在配对和笼养对照组中,FT4也有所下降,但远低于睡眠剥夺组。在整个研究过程中,游离激素与总激素浓度的相对变化也不如睡眠剥夺组那样平行。在实验的各个天数中,所有组对TRH的血浆TSH反应相似。TRH刺激TSH释放后,睡眠剥夺大鼠的血浆FT4和FT3浓度增加到与对照值相当的程度。综上所述,基础FT4和FT3激素浓度较低以及TSH和甲状腺对TRH的反应未发生变化,提示在睡眠剥夺期间,垂体或下丘脑对甲状腺素血症有影响。