OREXIN-1-RECEPTOR BLOCKER, SB-334867 MAY AFFECT BODY WEIGHT AND PROTECT AGAINST HYPOGLYCEMIA INDUCED BY PARADOXICAL SLEEP DEPRIVATION IN ADULT MALE RATS

Mohammad Ashraf Ahmad Ali, Hoda M. Moghazy, A. Mahmoud, K. Abdel-Sater
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Abstract

Background: Sleep deprivation (SD) can affect health through its effects on many systems. Orexin is involved in regulation of many physiological functions including sleep. This can give an explanation and a way of protection against some hazards of SD. Aim: To test the protective effect of orexin-1 receptor (OX1R) blocker, SB-334867 on changes in food intake, blood glucose level and insulin sensitivity caused by SD. Method: 72 adult male rats arranged in 4 equal groups: control group, SD group, SD-OX1R blocked group & SD-DMSO group. The 3 SD groups are subjected to 8 days of paradoxical SD using the modified multiple platform method. The SD-OX1R blocked group was injected intraperitoneally daily with single dose of SB-334867 dissolved in 2 ml DMSO and diluted 1:1000 in saline (3 mg/kg/day). The SD-DMSO group was injected by DMSO alone. Food intake, body weight, blood fasting glucose & insulin levels were assessed and insulin resistance was calculated using HOMA-IR formula. Results: The SD and SD-DMSO groups showed loss of weight inspite of increased food intake plus hypoglycemia with increased insulin sensitivity. The SD-OX1R blocked group showed no significant change in food intake but more drop in body weight plus delayed changes in fasting blood glucose and insulin sensitivity. Conclusion: SD can affect health through its effect on food intake and induction of hypoglycemia. OX1R blocker, SB-334867 protects against the increase in food intake and delays increased insulin sensitivity and subsequent hypoglycemia. So, orexin most probably is a mechanism by which SD causes these changes.
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食欲素-1受体阻滞剂sb-334867可能会影响成年雄性大鼠的体重,并防止睡眠剥夺引起的低血糖
背景:睡眠剥夺(SD)可以通过对许多系统的影响来影响健康。食欲素参与许多生理功能的调节,包括睡眠。这可以解释SD的一些危害,并提供一种保护方法。目的:探讨食欲素-1受体(OX1R)阻滞剂SB-334867对SD致食量、血糖水平及胰岛素敏感性变化的保护作用。方法:雄性成年大鼠72只,随机分为4组:对照组、SD组、SD- ox1r阻断组、SD- dmso组。采用改进的多平台方法对3组SD进行8天的矛盾SD。SD-OX1R阻断组每日腹腔注射单剂量SB-334867,溶解于2ml DMSO中,1:1000稀释生理盐水(3mg /kg/天)。SD-DMSO组单独注射DMSO。评估食物摄入量、体重、空腹血糖和胰岛素水平,并使用HOMA-IR公式计算胰岛素抵抗。结果:SD组和SD- dmso组体重减轻,尽管食物摄入量增加,血糖降低,胰岛素敏感性增加。SD-OX1R阻断组在食物摄入方面没有明显变化,但体重下降幅度更大,空腹血糖和胰岛素敏感性的变化延迟。结论:SD可通过影响摄食和诱导低血糖来影响健康。OX1R阻滞剂SB-334867防止食物摄入量增加,延缓胰岛素敏感性增加和随后的低血糖。所以,食欲素很可能是SD引起这些变化的一种机制。
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