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神经肽Y可抵消睫状神经营养因子的厌食和减重作用。

Neuropeptide Y counteracts the anorectic and weight reducing effects of ciliary neurotropic factor.

作者信息

Pu S, Dhillon H, Moldawer L L, Kalra P S, Kalra S P

机构信息

Department of Neuroscience, University of Florida College of Medicine and University of Florida Brain Institute, Gainesville 32611, USA.

出版信息

J Neuroendocrinol. 2000 Sep;12(9):827-32. doi: 10.1046/j.1365-2826.2000.00526.x.

Abstract

Ciliary neurotrophic factor (CNTF), a cytokine of the interleukin-6 superfamily, has been shown to induce hypophagia and weight loss. Neuropeptide Y (NPY) and orexin are potent orexigenic signals in the hypothalamus. Anorexia, normally seen in response to infection, injury and inflammation, may result from diminished hypothalamic orexigenic signalling caused by persistently elevated cytokines, including CNTF. To test this hypothesis, we first examined the effects of chronic intracerebroventricular (i.c.v.) infusion of CNTF for 6-7 days on food intake and body weight as well as hypothalamic NPY and orexin gene expression in male rats. Subsequently, the effectiveness of NPY replacement to counteract the effects of CNTF by coinfusion of NPY and CNTF was evaluated. Chronic i.c.v. infusion of CNTF (2.5 microg/day) reduced body weight (14.3% vs control) at the end of 7 days. Food intake remained suppressed for 5 days postinfusion and subsequently gradually returned to the control range by day 7. Serum leptin concentrations in these rats were in the same range seen in control rats. Chronic i.c.v. infusion of higher doses of CNTF (5.0 microg/day) produced sustained anorexia and body weight loss (29% vs controls) through the entire duration of the experiment. This severe anorexia was accompanied by markedly suppressed serum leptin concentrations. Furthermore, CNTF infusion alone significantly reduced hypothalamic NPY gene expression (P < 0. 05) without affecting orexin gene expression. As expected, in fusion of NPY alone (18 microg/day) augmented food intake (191.6% over the initial control, P < 0.05) and produced a 25.1% weight gain in conjunction with a 10-fold increase in serum leptin concentrations at the end of the 7-day period. Interestingly, coinfusion of this regimen of NPY with the highly effective anorectic and body reducing effects of CNTF (5.0 microg/day) not only prevented the CNTF-induced anorexia and weight loss, but also normalized serum leptin concentrations and hypothalamic NPY gene expression. These results demonstrate that chronic central infusion to produce a persistent elevation of the cytokine at pathophysiological levels (a situation that may normally manifest during infection, injury and inflammation) produced severe anorexia and weight loss in conjunction with reduction in both serum leptin concentrations and hypothalamic NPY gene expression. Reinstatement of hypothalamic NPY signalling by coinfusion of NPY counteracted these CNTF-induced responses.

摘要

睫状神经营养因子(CNTF)是白细胞介素-6超家族的一种细胞因子,已被证明可诱导食欲减退和体重减轻。神经肽Y(NPY)和食欲素是下丘脑强效的促食欲信号。通常在感染、损伤和炎症反应中出现的厌食症,可能是由包括CNTF在内的细胞因子持续升高导致下丘脑促食欲信号减弱所致。为验证这一假设,我们首先检测了雄性大鼠慢性脑室内(i.c.v.)注射CNTF 6 - 7天对食物摄入量、体重以及下丘脑NPY和食欲素基因表达的影响。随后,评估了通过同时注射NPY来抵消CNTF作用的有效性。慢性i.c.v.注射CNTF(2.5微克/天)在7天结束时可使体重减轻(与对照组相比减轻14.3%)。注射后5天食物摄入量持续受到抑制,随后在第7天逐渐恢复到对照范围。这些大鼠的血清瘦素浓度与对照大鼠处于相同范围。慢性i.c.v.注射更高剂量的CNTF(5.0微克/天)在整个实验期间产生持续的厌食和体重减轻(与对照组相比减轻29%)。这种严重的厌食症伴随着血清瘦素浓度的显著降低。此外,单独注射CNTF可显著降低下丘脑NPY基因表达(P < 0.05),而不影响食欲素基因表达。正如预期的那样,单独注射NPY(18微克/天)可增加食物摄入量(比初始对照增加191.6%,P < 0.05),并在7天结束时使体重增加25.1%,同时血清瘦素浓度增加10倍。有趣的是,将这种NPY注射方案与具有高效厌食和减重作用的CNTF(5.0微克/天)同时注射,不仅可防止CNTF诱导的厌食和体重减轻,还可使血清瘦素浓度和下丘脑NPY基因表达恢复正常。这些结果表明,慢性中枢注射使细胞因子在病理生理水平持续升高(这种情况通常在感染、损伤和炎症期间可能出现)会导致严重的厌食和体重减轻,同时伴有血清瘦素浓度和下丘脑NPY基因表达降低。通过同时注射NPY恢复下丘脑NPY信号可抵消这些由CNTF诱导的反应。

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