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奥氮平对胃饥饿素分泌、CCK 敏感性、进餐量、运动活性和体温的急性影响。

The acute effects of olanzapine on ghrelin secretion, CCK sensitivity, meal size, locomotor activity and body temperature.

机构信息

Rudolf Magnus Institute of Neuroscience, Department of Neuroscience and Pharmacology, University Medical Center Utrecht, Utrecht, The Netherlands.

出版信息

Int J Obes (Lond). 2012 Feb;36(2):254-61. doi: 10.1038/ijo.2011.97. Epub 2011 May 10.

DOI:10.1038/ijo.2011.97
PMID:21556042
Abstract

OBJECTIVE

Significant weight gain is a problematic side effect of treatment with the antipsychotic drug olanzapine (OLA). Previous studies in rats suggest that one of the contributing factors is an impairment in satiation that results in increased food intake. However, the mechanisms underlying this impairment in satiation remain largely unclear.

METHODS AND RESULTS

In this study, we determined the effect of OLA on levels of leptin, insulin, ghrelin, cholecystokinin (CCK), glucagon-like peptide-1, peptide YY and amylin in male rats that had received a fixed amount of food. OLA did not affect the secretion of any of these hormones, except for ghrelin levels, which were increased compared with controls. Furthermore, when ghrelin levels were determined in rats just before they received their meal, OLA caused a significant increase in ghrelin levels compared with controls, whereas OLA failed to affect baseline ghrelin levels. Next, we investigated the effect of OLA on the efficacy of CCK to reduce meal size. With coadministration, OLA pretreatment counteracted the reduction in meal size by CCK, although there was no significant interaction between the treatments. Finally, telemetry measurements revealed that acute OLA treatment causes a temporary decrease in both locomotor activity and body core temperature.

CONCLUSION

Taken together, this study shows that acute injection of OLA selectively increases meal-related ghrelin secretion and this may partially underlie the impairment in satiation by OLA.

摘要

目的

抗精神病药奥氮平(OLA)治疗会导致显著的体重增加,这是一个有问题的副作用。先前在大鼠中的研究表明,导致饱食受损从而导致食物摄入量增加的一个促成因素是。然而,这种饱食受损的机制在很大程度上仍不清楚。

方法和结果

在这项研究中,我们确定了 OLA 对已摄入固定量食物的雄性大鼠中瘦素、胰岛素、胃饥饿素、胆囊收缩素(CCK)、胰高血糖素样肽-1、肽 YY 和胰淀素水平的影响。除了胃饥饿素水平增加外,OLA 对这些激素的分泌没有影响。此外,当在大鼠即将进食前测定胃饥饿素水平时,与对照组相比,OLA 导致胃饥饿素水平显著升高,而 OLA 未能影响基础胃饥饿素水平。接下来,我们研究了 OLA 对 CCK 降低进食量效果的影响。与共同给药时,OLA 预处理抵消了 CCK 对进食量的减少作用,尽管两种治疗方法之间没有显著的相互作用。最后,遥测测量显示急性 OLA 处理会导致运动活动和身体核心温度暂时下降。

结论

综上所述,这项研究表明,急性注射 OLA 会选择性地增加与进食相关的胃饥饿素分泌,这可能部分解释了 OLA 引起的饱食受损。

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