断奶后的社会隔离可改变新生儿缺氧引起的大鼠能量代谢和生长变化。

IF 1.7 4区 医学 Q3 DEVELOPMENTAL BIOLOGY
Natalia Andrea Cruz-Ochoa, Lívia Clemente Motta-Teixeira, Pablo Felipe Cruz-Ochoa, Santiago Lopez-Paredes, Julieta Esperanza Ochoa-Amaya, Silvia Honda Takada, Gilberto Fernando Xavier, Maria Inês Nogueira
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引用次数: 0

摘要

大鼠新生儿缺氧可能会影响其生长和长期代谢平衡。为了便于进行代谢评估,实验对象通常单独饲养。然而,与单独饲养条件相关的社会隔离会改变动物的行为,从而可能影响实验结果。本研究调查了社会隔离对新生儿缺氧引起的生长和能量代谢变化的影响。雌雄 Wistar 大鼠在出生后第 2 天(P2)接受 25 分钟缺氧或对照组处理。从 P27 开始,每组的部分受试者被隔离在标准笼子中,其余受试者分组饲养。在P34或P95时,受试者禁食18小时,进食1小时,然后在30分钟后进行灌流。在这两个年龄段对受试者的血糖、瘦素、胰岛素和胰腺形态进行评估。对于在P95进行灌流的受试者,记录体重和摄食量直至P90,并收集大脑进行Fos和NeuN免疫组化。结果显示,暴露于新生儿缺氧和社会隔离的雄性大鼠体重增加,尽管食物摄入量没有变化。此外,社会隔离(1)减少了空腹后体重下降和空腹后食物摄入量,(2)增加了缺氧和对照组处理的雄性和雌性大鼠在P35和P95时的血糖、胰岛素和瘦素水平。此外,虽然缺氧会增加雄性大鼠的胰岛素水平,但会减少雌性大鼠胰腺中β阳性细胞的面积。在P95时,缺氧会增加雄性动物餐后体重下降、空腹后食物摄入量、胰岛素和瘦素,并减少雄性和雌性动物弓状核(ARC)中Fos的表达。食欲亢进可能与瘦素和胰岛素的抵抗有关,这两种激素的高循环水平和弓状核神经元的低活化水平可能与食欲亢进有关。这项研究表明,从断奶开始的持续社会隔离会以不同的方式改变暴露于新生儿缺氧甚至对照处理的雄性和雌性 Wistar 大鼠的长期能量代谢和生长。因此,应将社会隔离视为对实验结果和新生儿损伤结果产生负面影响的一个因素。在临床治疗过程中也应考虑到这些结果,因为所使用的模型模拟了早产儿的情况,而某些治疗方法需要隔离。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Post-weaning social isolation modifies neonatal anoxia-induced changes in energy metabolism and growth of rats

Post-weaning social isolation modifies neonatal anoxia-induced changes in energy metabolism and growth of rats

Neonatal oxygen deficiency in rats may disturb growth and long-term metabolic homeostasis. In order to facilitate metabolic evaluation, the subjects are usually housed individually. However, social isolation associated with individually housed conditions alters animal behavior, which may influence the experimental results. This study investigated the effects of social isolation on neonatal anoxia-induced changes in growth and energy metabolism. Male and female Wistar rats were exposed, on postnatal day 2 (P2), to either 25-min of anoxia or control treatment. From P27 onward, part of the subjects of each group was isolated in standard cages, and the remaining subjects were housed in groups. At P34 or P95, the subjects were fasted for 18 h, refeed for 1 h, and then perfused 30 min later. Glycemia, leptin, insulin, and morphology of the pancreas were evaluated at both ages. For subjects perfused at P95, body weight and food intake were recorded up to P90, and the brain was collected for Fos and NeuN immunohistochemistry. Results showed that male rats exposed to neonatal anoxia and social isolation exhibited increased body weight gain despite the lack of changes in food intake. In addition, social isolation (1) decreased post-fasting weight loss and post-fasting food intake and (2) increased glycemia, insulin, and leptin levels of male and female rats exposed to anoxia and control treatments, both at P35 and P95. Furthermore, although at P35, anoxia increased insulin levels of males, it decreased the area of the β-positive cells in the pancreas of females. At P95, anoxia increased post-prandial weight loss of males, post-fasting food intake, insulin, and leptin, and decreased Fos expression in the arcuate nucleus (ARC) of males and females. Hyperphagia was associated with possible resistance to leptin and insulin, suspected by the high circulating levels of these hormones and poor neuronal activation of ARC. This study demonstrated that continuous social isolation from weaning modifies, in a differentiated way, the long-term energy metabolism and growth of male and female Wistar rats exposed to neonatal anoxia or even control treatments. Therefore, social isolation should be considered as a factor that negatively influences experimental results and the outcomes of the neonatal injury. These results should also be taken into account in clinical procedures, since the used model simulates the preterm babies' conditions and some therapeutic approaches require isolation.

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来源期刊
CiteScore
3.30
自引率
5.60%
发文量
78
审稿时长
6-12 weeks
期刊介绍: International Journal of Developmental Neuroscience publishes original research articles and critical review papers on all fundamental and clinical aspects of nervous system development, renewal and regeneration, as well as on the effects of genetic and environmental perturbations of brain development and homeostasis leading to neurodevelopmental disorders and neurological conditions. Studies describing the involvement of stem cells in nervous system maintenance and disease (including brain tumours), stem cell-based approaches for the investigation of neurodegenerative diseases, roles of neuroinflammation in development and disease, and neuroevolution are also encouraged. Investigations using molecular, cellular, physiological, genetic and epigenetic approaches in model systems ranging from simple invertebrates to human iPSC-based 2D and 3D models are encouraged, as are studies using experimental models that provide behavioural or evolutionary insights. The journal also publishes Special Issues dealing with topics at the cutting edge of research edited by Guest Editors appointed by the Editor in Chief. A major aim of the journal is to facilitate the transfer of fundamental studies of nervous system development, maintenance, and disease to clinical applications. The journal thus intends to disseminate valuable information for both biologists and physicians. International Journal of Developmental Neuroscience is owned and supported by The International Society for Developmental Neuroscience (ISDN), an organization of scientists interested in advancing developmental neuroscience research in the broadest sense.
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