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孕期体重增加通过降低大脑黑皮质素活性影响大鼠后代的能量平衡。

Gestational weight gain by reduced brain melanocortin activity affects offspring energy balance in rats.

作者信息

Heinsbroek A C M, van Dijk G

机构信息

Unit Neuroendocrinology, Center for Behaviour and Neurosciences, University of Groningen, NN Haren, The Netherlands.

出版信息

Int J Obes (Lond). 2009 Jan;33(1):104-14. doi: 10.1038/ijo.2008.211. Epub 2008 Nov 11.

Abstract

INTRODUCTION

Excessive gestational body weight gain of mothers may predispose offspring towards obesity and metabolic derangements. It is difficult to discern the effects of maternal obesogenic factors-such as diet and/or thrifty genetic predisposition-from gestational weight gain per se.

METHODS

For this reason, genetically normal Wistar rats that were fed regular chow were rendered hypothalamically obese by chronic third-cerebral ventricular (i3vt) infusion during pregnancy and lactation with the melanocortin-3,4 receptor blocker SHU9119. This procedure caused significant increases in body weight gain during pregnancy and lactation compared with controls, and the effects thereof on offspring energy balance and fuel homeostasis were investigated.

RESULTS

At birth, litter weight and size, but not individual pup weight, of SHU9119-treated mothers were significantly smaller than controls. In litters culled to eight, pup weight gain during lactation was only transiently increased by treatment. After weaning, however, male offspring of SHU9119-treated mothers became increasingly heavier over time relative to controls until killing at 9 months. This effect was only transient in females. Increased body weights of males were not associated with disturbances in glucose homeostasis, but with increased energy expenditure instead. Multiple regression analysis revealed that gestational body weight gain, irrespective of the group, contributed positively to increased visceral fat deposition and carbohydrate oxidation in the male offspring. In contrast, the pre-pregnancy body weight of mothers contributed positively to male offspring daily energy expenditure, subcutaneous fat and eviscerated carcass as well as structural organ weights. In female offspring, gestational body weight gain, but not pre-gestational body weight, contributed both to aspects of weight gain as well as to the shift of fat oxidation toward carbohydrate oxidation.

CONCLUSION

Gestational weight gain induced by low brain melanocortin receptor activity can lead to increased body weight gain in the offspring (particularly in males) independent of obesogenic dietary and/or thrifty genetic predisposition.

摘要

引言

母亲孕期体重过度增加可能使后代易患肥胖症和代谢紊乱。很难区分母亲的致肥胖因素(如饮食和/或节俭基因易感性)与孕期体重增加本身的影响。

方法

因此,给喂食常规饲料的基因正常的Wistar大鼠在妊娠和哺乳期通过慢性第三脑室(i3vt)输注黑皮质素-3、4受体阻滞剂SHU9119使其下丘脑肥胖。与对照组相比,该操作导致妊娠和哺乳期体重显著增加,并研究了其对后代能量平衡和燃料稳态的影响。

结果

出生时,接受SHU9119治疗的母亲所产仔鼠的窝重和窝大小显著小于对照组,但个体幼崽体重无差异。在将窝仔数减至八只后,治疗仅使哺乳期幼崽体重增加短暂增加。然而,断奶后,接受SHU9119治疗的母亲的雄性后代相对于对照组随着时间的推移体重越来越重,直至9个月时处死。这种影响在雌性中只是短暂的。雄性体重增加与葡萄糖稳态紊乱无关,而是与能量消耗增加有关。多元回归分析显示,无论组别如何,孕期体重增加对雄性后代内脏脂肪沉积和碳水化合物氧化增加有正向贡献。相比之下,母亲的孕前体重对雄性后代的每日能量消耗、皮下脂肪、去内脏胴体以及器官结构重量有正向贡献。在雌性后代中,孕期体重增加而非孕前体重对体重增加以及脂肪氧化向碳水化合物氧化的转变均有贡献。

结论

低脑黑皮质素受体活性诱导的孕期体重增加可导致后代(尤其是雄性)体重增加,而与致肥胖饮食和/或节俭基因易感性无关。

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