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完全睡眠剥夺对大鼠棕色脂肪组织5'-脱碘酶活性的影响。

Effect of total sleep deprivation on 5'-deiodinase activity of rat brown adipose tissue.

作者信息

Balzano S, Bergmann B M, Gilliland M A, Silva J E, Rechtschaffen A, Refetoff S

机构信息

Department of Medicine, University of Chicago, Illinois 60637.

出版信息

Endocrinology. 1990 Aug;127(2):882-90. doi: 10.1210/endo-127-2-882.

Abstract

Prolonged sleep deprivation of the rat produces a progressive increase in energy expenditure and an eventual decrease in body temperature, which suggests a profound derangement in thermoregulation. Because increased thermogenic activity in brown adipose tissue (BAT) is a likely mechanism mediating the observed increase in energy expenditure, we focused our attention on the effect of total sleep deprivation on BAT type II 5'-deiodinase (5'D-II), since its activation indicates BAT stimulation and is essential for full BAT thermogenic response. Five euthyroid rats were subjected to total (92%) sleep deprivation (euD-rats). Sharing the sleep deprivation apparatus, yoked control rats (euC-rats) received the same degree of physical stimulation as the D-rats, but were only partially (25%) sleep deprived. Additional cage controls (euCC-rats) were housed in the same room. Since during sleep deprivation the animals undergo a reduction in plasma T4 concentration and inability to maintain body temperature heralds death, an identical study was performed in five trios of hyperthyroid rats (hyperD-, hyperC-, and hyper CC-rats) given daily ip injections of 15 micrograms T4/100 g BW, 10 days before and throughout the deprivation period. Experiments were carried out at an ambient temperature of 29 C, close to thermoneutrality for rats. Sleep deprivation in hyperD-rats was maintained until death seemed imminent (9-14 days), and in euD-rats for 12-15 days. Sleep deprivation induced a significant increase in BAT 5'D-II activity in both hyperD- and euD-rats compared with that in euCC-rats (P less than 0.01). BAT 5'D-II in euC-rats was also significantly higher than that in euCC-rats (P less than 0.05), probably because they were partially sleep deprived. BAT 5'D-II activity in hyperD-rats was increased compared to that in both hyperC- and hyperCC-rats (P less than 0.05), in which the activity was slightly but not significantly lower than that in euCC-rats. No significant differences were observed in liver and kidney type I 5'-D (5'D-I) and in pituitary 5'D-II among euD-rats, euC-rats, and euCC-rats. As expected, the hyperthyroid groups (hyperD-rats, hyperC-rats, and hyperCC-rats) had significantly higher kidney 5'D-I and lower pituitary 5'D-II than the euCC-rats. Liver 5'D-I was also significantly increased in the hyperC-rats and hyperCC-rats, but not in the hyperD-rats. These observations indicate that total sleep deprivation is associated with a marked increase in BAT 5'D-II activity in both euthyroid and hyperthyroid rats.(ABSTRACT TRUNCATED AT 400 WORDS)

摘要

对大鼠进行长期睡眠剥夺会使其能量消耗逐渐增加,最终体温下降,这表明体温调节出现了严重紊乱。由于棕色脂肪组织(BAT)中增加的产热活性可能是介导所观察到的能量消耗增加的机制,我们将注意力集中在完全睡眠剥夺对BAT II型5'-脱碘酶(5'D-II)的影响上,因为其激活表明BAT受到刺激,并且对于BAT的完全产热反应至关重要。五只甲状腺功能正常的大鼠接受完全(92%)睡眠剥夺(euD大鼠)。与睡眠剥夺装置共享,配对的对照大鼠(euC大鼠)受到与D大鼠相同程度的身体刺激,但仅部分(25%)睡眠剥夺。另外的笼养对照(euCC大鼠)饲养在同一房间。由于在睡眠剥夺期间动物的血浆T4浓度会降低,且无法维持体温预示着死亡,因此在五组甲状腺功能亢进的大鼠(hyperD、hyperC和hyperCC大鼠)中进行了相同的研究,在剥夺期前10天及整个剥夺期内,每天腹腔注射15微克T4/100克体重。实验在29℃的环境温度下进行,该温度接近大鼠的热中性温度。hyperD大鼠的睡眠剥夺持续到似乎即将死亡(9 - 14天),euD大鼠的睡眠剥夺持续12 - 15天。与euCC大鼠相比,睡眠剥夺使hyperD和euD大鼠的BAT 5'D-II活性显著增加(P < 0.01)。euC大鼠的BAT 5'D-II也显著高于euCC大鼠(P < 0.05),可能是因为它们部分睡眠剥夺。与hyperC和hyperCC大鼠相比,hyperD大鼠的BAT 5'D-II活性增加(P < 0.05),其中hyperC和hyperCC大鼠的活性略低于euCC大鼠,但差异不显著。在euD大鼠、euC大鼠和euCC大鼠之间,肝脏和肾脏的I型5'-D(5'D-I)以及垂体的5'D-II未观察到显著差异。正如预期的那样,甲状腺功能亢进组(hyperD大鼠、hyperC大鼠和hyperCC大鼠)的肾脏5'D-I显著高于euCC大鼠,垂体5'D-II则低于euCC大鼠。hyperC大鼠和hyperCC大鼠的肝脏5'D-I也显著增加,但hyperD大鼠未增加。这些观察结果表明,完全睡眠剥夺与甲状腺功能正常和甲状腺功能亢进大鼠的BAT 5'D-II活性显著增加有关。(摘要截断于400字)

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