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Agmatine attenuates hyperactivity and weight loss associated with activity-based anorexia in female rats

机译:胍丁胺减轻雌性大鼠活动性厌食症引起的过度活跃和体重减轻

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Anorexia nervosa is a debilitating eating disorder characterized by hypophagia, body weight loss, amenorrhea and intense fear of weight gain. In present study, the effect of subchronic agmatine treatment on development of activity based anorexia (ABA) in female rats has been investigated. Animals were injected with saline or agmatine (10-40 mg/kg, ip) just before the onset of dark phase and shifted to experimental cage with wheel for ABA test for 10 days. A pre-weighed quantity of food pellets (10 g) was placed daily for a restricted period of only 2 h (1700-1900 h) and food intake was monitored (g) manually by weighing the leftover food. Rats restricted to ABA paradigm, showed greater wheel running, suppressed food consumption, disrupted estrous cycle and weight loss. On the other hand, subchronic agmatine (10-40 mg/kg, ip, for 10 days) treatment decreased wheel running activity, pronounced increased in food intake and restored body weights as compared to saline treated animals. Further, agmatine treatment decreased corticosterone levels in ABA rats, thereby stabilizing HPA axis in ABA rats. Subchronic agmatine treatment also prevented the disruptions of estrous cycle. Considering the common resistance of anorexia nervosa to current pharmacotherapy, the preliminary data on reduction of physical activity by agmatine, may have potential therapeutic importance. Thus, the role of agmatine in feeding behavior is likely to provide insight into the circumstances that facilitate treatment in eating disorders like anorexia nervosa. (C) 2015 Elsevier Inc. All rights reserved.
机译:神经性厌食症是一种虚弱的饮​​食失调症,特征在于吞咽不足,体重减轻,闭经和强烈担心体重增加。在本研究中,已研究了亚慢性胍丁胺治疗对雌性大鼠活动性厌食症(ABA)发育的影响。在黑暗阶段即将来临之前,向动物注射生理盐水或胍丁胺(10-40 mg / kg,腹膜内),并转移至带有轮子的实验笼中进行ABA测试10天。每天放置预先称重的食物颗粒(10 g),限制时间仅为2 h(1700-1900 h),并通过称量剩余的食物来手动监控食物摄入(g)。局限在ABA范式下的大鼠表现出更大的转轮运动,抑制了食物消耗,破坏了发情周期并减轻了体重。另一方面,与盐水处理的动物相比,亚慢性胍丁胺(10-40 mg / kg,腹膜内注射,持续10天)治疗降低了轮转活动,显着增加了食物摄入并恢复了体重。此外,胍丁胺治疗降低了ABA大鼠中的皮质酮水平,从而稳定了ABA大鼠中的HPA轴。亚慢性胍丁胺治疗也防止了发情周期的中断。考虑到神经性厌食症对当前药物治疗的普遍耐药性,胍丁胺降低身体活动的初步数据可能具有潜在的治疗重要性。因此,胍丁胺在进食行为中的作用很可能提供对促进进食障碍(如神经性厌食症)治疗的情况的见解。 (C)2015 Elsevier Inc.保留所有权利。

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