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食物剥夺对大鼠室旁核下丘脑一氧化氮合酶基因表达的抑制作用与血清素耗竭无关。

Inhibition of hypothalamic nitric oxide synthase gene expression in the rat paraventricular nucleus by food deprivation is independent of serotonin depletion.

作者信息

Ueta Y, Levy A, Chowdrey H S, Lightman S L

机构信息

Department of Medicine, University of Bristol, Bristol Royal Infirmary, UK.

出版信息

J Neuroendocrinol. 1995 Nov;7(11):861-5. doi: 10.1111/j.1365-2826.1995.tb00727.x.

DOI:10.1111/j.1365-2826.1995.tb00727.x
PMID:8748123
Abstract

We have investigated the effects of food deprivation on nitric oxide synthase (NOS) transcript levels in the rat paraventricular (PVN) and supraoptic nuclei (SON), using in situ hybridization histochemistry. Food deprivation for 48 h significantly and consistently reduced NOS transcript prevalence by approximately 50% in both sites. Since there is considerable evidence for an important role of 5-HT in feeding behaviour, we then examined the effect of food deprivation on NOS gene expression in the PVN following para-chlorophenylalanine (PCPA)-induced hypothalamic 5-HT depletion. As starvation causes central down-regulation of the thyroid axis, changes in thyrotropin-releasing hormone (TRH) and pituitary thyrotrophin (TSH) transcript prevalence were used as internal controls. PCPA pretreatment (200 mg/kg body weight as a single daily dose ip for 2 days) had no significant effect on basal levels of NOS, TRH or TSH transcripts, or on the effect of a subsequent 48 h fast, which significantly reduced all three. These results show for the first time, that food deprivation for 48 h significantly reduces NOS gene expression in the rat PVN and SON. Secondly, that basal levels and the fasting-induced reductions in the prevalence of NOS, TRH and TSH transcripts were not affected by PCPA-induced hypothalamic 5-HT depletion. Therefore, at least under the experimental conditions used here, 5-HT does not appear to be involved in setting baseline levels- or in the starvation-induced inhibition of NOS or thyroid axis gene expression in the PVN.

摘要

我们采用原位杂交组织化学技术,研究了食物剥夺对大鼠室旁核(PVN)和视上核(SON)中一氧化氮合酶(NOS)转录水平的影响。禁食48小时显著且持续地使两个部位的NOS转录本丰度降低了约50%。由于有大量证据表明5-羟色胺(5-HT)在摄食行为中起重要作用,我们随后研究了对氯苯丙氨酸(PCPA)诱导下丘脑5-HT耗竭后,食物剥夺对PVN中NOS基因表达的影响。由于饥饿会导致甲状腺轴的中枢下调,促甲状腺激素释放激素(TRH)和垂体促甲状腺激素(TSH)转录本丰度的变化被用作内部对照。PCPA预处理(200mg/kg体重,每日一次腹腔注射,共2天)对NOS、TRH或TSH转录本的基础水平,或随后48小时禁食的影响均无显著作用,禁食显著降低了所有这三种转录本的水平。这些结果首次表明,禁食48小时会显著降低大鼠PVN和SON中的NOS基因表达。其次,基础水平以及禁食诱导的NOS、TRH和TSH转录本丰度的降低不受PCPA诱导的下丘脑5-HT耗竭的影响。因此,至少在本文所采用的实验条件下,5-HT似乎不参与设定基础水平,也不参与饥饿诱导的PVN中NOS或甲状腺轴基因表达的抑制。

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