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再喂养诱导大鼠室旁核神经元型一氧化氮合酶的表达。

Refeeding-induced expression of neuronal nitric oxide synthase in the rat paraventricular nucleus.

作者信息

Jahng Jeong Won, Lee Joo Young, Yoo Sang Bae, Kim Yun Mi, Ryu Vitaly, Kang Dong Won, Lee Jong-Ho

机构信息

Department of Pharmacology, BK21 project for Medical Science, Yonsei University College of Medicine, Seoul 120-752, South Korea.

出版信息

Brain Res. 2005 Jun 28;1048(1-2):185-92. doi: 10.1016/j.brainres.2005.04.072.

DOI:10.1016/j.brainres.2005.04.072
PMID:15925328
Abstract

We have previously reported that food deprivation decreases the expression of neuronal nitric oxide synthase (nNOS) in the hypothalamic paraventricular nucleus (PVN) of rats, and this reduction is inhibited by blockade of glucocorticoid receptors. In this study, we examined whether the fasting-induced decrease in nNOS gene expression in the PVN is restored by refeeding. The number of nNOS immunopositive cells in the PVN, which was markedly decreased by 48 h of food deprivation, increased significantly after 6 h of refeeding and was fully restored by 24 h after refeeding. The plasma corticosterone level, which was markedly increased by food deprivation, decreased significantly within 30 min after refeeding and returned to the free fed control level by 6 h. Synthetic glucocorticoid dexamethasone blocked the refeeding-induced nNOS expression in the PVN without suppressing food intake. Refeeding with a non-caloric food mash for 5 h failed to restore the fasting-induced decrease in the PVN-nNOS but did, however, successfully restore the plasma corticosterone level. These results suggest that the refeeding-induced nNOS expression in the PVN is a nutrient-directed event and that plasma glucocorticoids may play an inhibitory role in the regulatory pathway. Additionally, glucocorticoid disinhibition alone does not appear to be sufficient to induce nNOS expression in the PVN; nNOS expression in the PVN upon refeeding may require both nutrient supplementation and glucocorticoid disinhibition.

摘要

我们之前曾报道,食物剥夺会降低大鼠下丘脑室旁核(PVN)中神经元型一氧化氮合酶(nNOS)的表达,而这种降低可被糖皮质激素受体阻断所抑制。在本研究中,我们检测了再喂养是否能恢复禁食诱导的PVN中nNOS基因表达的降低。PVN中nNOS免疫阳性细胞的数量在禁食48小时后显著减少,再喂养6小时后显著增加,并在再喂养24小时后完全恢复。血浆皮质酮水平在食物剥夺后显著升高,再喂养后30分钟内显著降低,并在6小时后恢复到自由进食对照组水平。合成糖皮质激素地塞米松阻断了再喂养诱导的PVN中nNOS的表达,而不抑制食物摄入。用无热量食物糊再喂养5小时未能恢复禁食诱导的PVN-nNOS降低,但成功恢复了血浆皮质酮水平。这些结果表明,再喂养诱导的PVN中nNOS表达是一个由营养物质导向的事件,血浆糖皮质激素可能在调节途径中起抑制作用。此外,单独的糖皮质激素去抑制似乎不足以诱导PVN中nNOS的表达;再喂养时PVN中nNOS的表达可能需要营养补充和糖皮质激素去抑制两者。

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