首页> 外文期刊>Hippocampus >Chronic restraint stress in adolescence differentially influences hypothalamic-pituitary-adrenal axis function and adult hippocampal neurogenesis in male and female rats.
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Chronic restraint stress in adolescence differentially influences hypothalamic-pituitary-adrenal axis function and adult hippocampal neurogenesis in male and female rats.

机译:青春期的慢性束缚应激对雄性和雌性大鼠的下丘脑-垂体-肾上腺轴功能和成年海马神经发生有不同的影响。

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Previous studies have shown a relationship between adversity in adolescence and health outcomes in adulthood in a sex-specific manner. Adolescence is characterized by major changes in stress-responsive regions of the brain, including the hippocampus, the site of ongoing neurogenesis throughout the lifespan. Prepubertal male and female rats exhibit different acute reactions to chronic stress compared to adults, but less is known about whether these stress-induced changes persist into adulthood. Therefore, in this study, we investigated the effects of chronic, intermittent stress during adolescence on basal corticosterone levels, dentate gyrus (DG) volume, and neurogenesis in the hippocampus of adult male and female Sprague-Dawley rats. Adolescent male and female rats were either restrained for 1 h every other day for 3 weeks from postnatal days (PDs) 30-52 at unpredictable times or left undisturbed. All rats received a single injection of bromodeoxyuridine (BrdU; 200 mg/kg) in adulthood on PD70 and were perfused 3 weeks later. Brains were processed for Ki67 (endogenous marker of cell proliferation) and BrdU (to estimate effects on cell survival). In addition, blood samples were taken during the restraint stress period and in adulthood. Results show that males and females exhibit different corticosterone responses to chronic stress during adolescence and that only adult female rats exposed to stress during adolescence show higher basal corticosterone levels compared to nonstressed controls. Furthermore, stressed females showed a reduced number of proliferating and surviving cells in the DG in adulthood compared to nonstressed same-sex controls. The majority of BrdU-labeled cells were co-labeled with NeuN, an endogenous marker of mature neurons, indicating that neurogenesis was decreased in the DG of adult female rats that had undergone chronic restraint stress in adolescence. Although male rats were more responsive to the chronic stress as adolescents showing higher corticosterone levels and reduced body weight, as adults they showed a slight increase in cell survival and no effect of adolescent stress on basal corticosterone levels. These results suggest that stress during adolescence can have effects on hypothalamic-pituitary-adrenal axis function and hippocampus plasticity in adulthood, particularly in female rats.
机译:以前的研究表明,青春期的逆境与成年后的健康状况之间存在特定的性别关系。青春期的特征是大脑包括海马在内的应激反应区域发生了重大变化,海马是整个生命过程中不断发生神经发生的部位。与成年人相比,青春期前的雄性和雌性大鼠对慢性应激表现出不同的急性反应,但对于这些应激诱导的变化是否持续到成年期的了解还很少。因此,在这项研究中,我们调查了青春期慢性,间歇性应激对成年雄性和雌性Sprague-Dawley大鼠的基础皮质酮水平,齿状回(DG)体积和海马神经发生的影响。青春期的雄性和雌性大鼠从出生后的30-52天开始每隔一天束缚1 h,持续3周,时间不可预测,或者保持不受干扰。所有大鼠在成年期接受PD70单次注射溴脱氧尿苷(BrdU; 200 mg / kg),并于3周后灌注。对大脑进行Ki67(细胞增殖的内源标记)和BrdU(估计对细胞存活的影响)进行处理。另外,在约束压力期间和成年期采集血样。结果显示,雄性和雌性在青春期对慢性应激表现出不同的皮质酮反应,并且只有成年雌性大鼠在青春期暴露于应激下,其基础皮质酮水平高于非应激对照组。此外,与无压力的同性对照相比,有压力的女性在成年后的DG中显示出数量减少的增殖细胞和存活细胞。大多数BrdU标记的细胞与NeuN(成熟神经元的内源性标志物)共同标记,表明成年雌性大鼠DG在青春期受到慢性束缚应激后,其神经生成减少。尽管雄性大鼠对青少年的慢性应激反应更为敏感,因为青少年显示出较高的皮质酮水平并减轻了体重,但成年大鼠则显示出细胞存活率略有增加,并且青少年应激对基础皮质酮水平没有影响。这些结果表明,青春期期间的压力可能对成年期尤其是雌性大鼠的下丘脑-垂体-肾上腺轴功能和海马可塑性产生影响。

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