Wadhwa Meetu, Chauhan Garima, Roy Koustav, Sahu Surajit, Deep Satyanarayan, Jain Vishal, Kishore Krishna, Ray Koushik, Thakur Lalan, Panjwani Usha
Defence Institute of Physiology & Allied Sciences (DIPAS), Defence Research and Development Organization (DRDO), New Delhi, India.
Front Cell Neurosci. 2018 Feb 28;12:49. doi: 10.3389/fncel.2018.00049. eCollection 2018.
: Sleep deprivation (SD) plagues modern society due to the professional demands. It prevails in patients with mood and neuroinflammatory disorders. Although growing evidence suggests the improvement in the cognitive performance by psychostimulants during sleep-deprived conditions, the impending involved mechanism is rarely studied. Thus, we hypothesized that mood and inflammatory changes might be due to the glial cells activation induced modulation of the inflammatory cytokines during SD, which could be improved by administering psychostimulants. The present study evaluated the role of caffeine/modafinil on SD-induced behavioral and inflammatory consequences. : Adult male Sprague-Dawley rats were sleep deprived for 48 h using automated SD apparatus. Caffeine (60 mg/kg/day) or modafinil (100 mg/kg/day) were administered orally to rats once every day during SD. Rats were subjected to anxious and depressive behavioral evaluation after SD. Subsequently, blood and brain were collected for biochemical, immunohistochemical and molecular studies. : Sleep deprived rats presented an increased number of entries and time spent in closed arms in elevated plus maze test and decreased total distance traveled in the open field (OF) test. Caffeine/modafinil treatment significantly improved these anxious consequences. However, we did not observe substantial changes in immobility and anhedonia in sleep-deprived rats. Caffeine/modafinil significantly down-regulated the pro- and up-regulated the anti-inflammatory cytokine mRNA and protein expression in the hippocampus during SD. Similar outcomes were observed in blood plasma cytokine levels. Caffeine/modafinil treatment significantly decreased the microglial immunoreactivity in DG, CA1 and CA3 regions of the hippocampus during SD, however, no significant increase in immunoreactivity of astrocytes was observed. Sholl analysis signified the improvement in the morphological alterations of astrocytes and microglia after caffeine/modafinil administration during SD. Stereological analysis demonstrated a significant improvement in the number of ionized calcium binding adapter molecule I (Iba-1) positive cells (different states) in different regions of the hippocampus after caffeine or modafinil treatment during SD without showing any significant change in total microglial cell number. Eventually, the correlation analysis displayed a positive relationship between anxiety, pro-inflammatory cytokines and activated microglial cell count during SD. : The present study suggests the role of caffeine or modafinil in the amelioration of SD-induced inflammatory response and anxious behavior in rats. - SD induced mood alterations in rats. - Glial cells activated in association with the changes in the inflammatory cytokines. - Caffeine or modafinil improved the mood and restored inflammatory changes during SD. - SD-induced anxious behavior correlated with the inflammatory consequences.
睡眠剥夺(SD)因职业需求而困扰着现代社会。它在患有情绪和神经炎症性疾病的患者中普遍存在。尽管越来越多的证据表明在睡眠剥夺状态下精神兴奋剂可改善认知表现,但相关的潜在机制鲜有研究。因此,我们推测情绪和炎症变化可能是由于睡眠剥夺期间神经胶质细胞激活诱导的炎症细胞因子调节所致,而给予精神兴奋剂可能会改善这种情况。本研究评估了咖啡因/莫达非尼对睡眠剥夺诱导的行为和炎症后果的作用。
成年雄性Sprague-Dawley大鼠使用自动睡眠剥夺装置进行48小时的睡眠剥夺。在睡眠剥夺期间,每天给大鼠口服一次咖啡因(60毫克/千克/天)或莫达非尼(100毫克/千克/天)。睡眠剥夺后对大鼠进行焦虑和抑郁行为评估。随后,采集血液和大脑进行生化、免疫组织化学和分子研究。
睡眠剥夺的大鼠在高架十字迷宫试验中进入封闭臂的次数和在封闭臂中停留的时间增加,在旷场试验中总行进距离减少。咖啡因/莫达非尼治疗显著改善了这些焦虑后果。然而,我们在睡眠剥夺的大鼠中未观察到不动和快感缺失的实质性变化。咖啡因/莫达非尼在睡眠剥夺期间显著下调海马中促炎细胞因子的表达并上调抗炎细胞因子的mRNA和蛋白质表达。血浆细胞因子水平也观察到类似结果。咖啡因/莫达非尼治疗在睡眠剥夺期间显著降低了海马DG、CA1和CA3区域的小胶质细胞免疫反应性,然而,未观察到星形胶质细胞免疫反应性的显著增加。Sholl分析表明,在睡眠剥夺期间给予咖啡因/莫达非尼后,星形胶质细胞和小胶质细胞的形态改变得到改善。立体学分析表明,在睡眠剥夺期间给予咖啡因或莫达非尼后,海马不同区域离子钙结合衔接分子I(Iba-1)阳性细胞(不同状态)的数量有显著改善,而小胶质细胞总数没有任何显著变化。最终,相关性分析显示睡眠剥夺期间焦虑、促炎细胞因子与激活的小胶质细胞计数之间呈正相关。
本研究表明咖啡因或莫达非尼在改善大鼠睡眠剥夺诱导的炎症反应和焦虑行为方面的作用。
睡眠剥夺诱导大鼠情绪改变。
神经胶质细胞的激活与炎症细胞因子的变化相关。
咖啡因或莫达非尼在睡眠剥夺期间改善情绪并恢复炎症变化。
睡眠剥夺诱导的焦虑行为与炎症后果相关。