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本文引用的文献

1
Activation of central, but not peripheral, estrogen receptors is necessary for estradiol's anorexigenic effect in ovariectomized rats.中枢而非外周雌激素受体的激活对于去卵巢大鼠中雌二醇的厌食作用是必要的。
Endocrinology. 2010 Dec;151(12):5680-8. doi: 10.1210/en.2010-0731. Epub 2010 Nov 10.
2
Activation of ERα is necessary for estradiol's anorexigenic effect in female rats.雌激素受体α的激活是雌二醇在雌性大鼠中产生厌食作用所必需的。
Horm Behav. 2010 Nov;58(5):872-7. doi: 10.1016/j.yhbeh.2010.08.012. Epub 2010 Aug 31.
3
Divergent effects of estradiol and the estrogen receptor-alpha agonist PPT on eating and activation of PVN CRH neurons in ovariectomized rats and mice.雌二醇和雌激素受体α激动剂PPT对去卵巢大鼠和小鼠进食及室旁核促肾上腺皮质激素释放激素神经元激活的不同影响。
Brain Res. 2009 May 1;1268:88-96. doi: 10.1016/j.brainres.2009.02.067. Epub 2009 Mar 10.
4
Estradiol increases Pet-1 and serotonin transporter mRNA in the midbrain raphe nuclei of ovariectomized rats.雌二醇可增加去卵巢大鼠中脑缝核中的Pet-1和5-羟色胺转运体信使核糖核酸。
Brain Res. 2009 Mar 9;1259:51-8. doi: 10.1016/j.brainres.2008.12.067. Epub 2009 Jan 10.
5
Estradiol decreases the orexigenic effect of neuropeptide Y, but not agouti-related protein, in ovariectomized rats.在去卵巢大鼠中,雌二醇可降低神经肽Y的促食欲作用,但对刺鼠相关蛋白无此作用。
Behav Brain Res. 2008 Aug 22;191(2):173-7. doi: 10.1016/j.bbr.2008.03.019. Epub 2008 Mar 25.
6
The orexigenic effect of melanin-concentrating hormone (MCH) is influenced by sex and stage of the estrous cycle.促黑素细胞激素(MCH)的促食欲作用受性别和发情周期阶段的影响。
Physiol Behav. 2008 Mar 18;93(4-5):842-50. doi: 10.1016/j.physbeh.2007.11.050. Epub 2007 Dec 5.
7
Hindbrain administration of estradiol inhibits feeding and activates estrogen receptor-alpha-expressing cells in the nucleus tractus solitarius of ovariectomized rats.对去卵巢大鼠孤束核中表达雌激素受体α的细胞,经后脑给予雌二醇可抑制进食并激活这些细胞。
Endocrinology. 2008 Apr;149(4):1609-17. doi: 10.1210/en.2007-0340. Epub 2007 Dec 20.
8
Acute activation of ER alpha decreases food intake, meal size, and body weight in ovariectomized rats.雌激素受体α的急性激活可降低去卵巢大鼠的食物摄入量、进食量和体重。
Am J Physiol Regul Integr Comp Physiol. 2007 Dec;293(6):R2194-201. doi: 10.1152/ajpregu.00385.2007. Epub 2007 Oct 17.
9
Melanin concentrating hormone and estrogen receptor-alpha are coexstensive but not coexpressed in cells of male rat hypothalamus.黑色素聚集激素和雌激素受体α在雄性大鼠下丘脑细胞中共存但不共表达。
Neurosci Lett. 2007 Nov 12;427(3):123-6. doi: 10.1016/j.neulet.2007.09.031. Epub 2007 Sep 22.
10
Oestrogenic regulation of pro-opiomelanocortin, neuropeptide Y and corticotrophin-releasing hormone mRNAs in mouse hypothalamus.雌激素对小鼠下丘脑阿黑皮素原、神经肽Y和促肾上腺皮质激素释放激素信使核糖核酸的调节作用
J Neuroendocrinol. 2007 Jun;19(6):426-31. doi: 10.1111/j.1365-2826.2007.01548.x.

雌激素在大鼠的视前内侧区、弓状核和中缝背核发挥作用,减少去卵巢大鼠的食物摄入。

Estradiol acts in the medial preoptic area, arcuate nucleus, and dorsal raphe nucleus to reduce food intake in ovariectomized rats.

机构信息

Program in Neuroscience, Florida State University, Tallahassee, FL 32306, USA.

出版信息

Horm Behav. 2011 Jun;60(1):86-93. doi: 10.1016/j.yhbeh.2011.03.009. Epub 2011 Apr 1.

DOI:10.1016/j.yhbeh.2011.03.009
PMID:21439964
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3112293/
Abstract

Estradiol (E2) exerts an inhibitory effect on food intake in a variety of species. While compelling evidence indicates that central, rather than peripheral, estrogen receptors (ERs) mediate this effect, the exact brain regions involved have yet to be conclusively identified. In order to identify brain regions that are sufficient for E2's anorectic effect, food intake was monitored for 48 h following acute, unilateral, microinfusions of vehicle and two doses (0.25 and 2.5 μg) of a water-soluble form of E2 in multiple brain regions within the hypothalamus and midbrain of ovariectomized rats. Dose-related decreases in 24-h food intake were observed following E2 administration in the medial preoptic area (MPOA), arcuate nucleus (ARC), and dorsal raphe nucleus (DRN). Within the former two brain areas, the larger dose of E2 also decreased 4-h food intake. Food intake was not influenced, however, by similar E2 administration in the paraventricular nucleus, lateral hypothalamus, or ventromedial nucleus. These data suggest that E2-responsive neurons within the MPOA, ARC, and DRN participate in the estrogenic control of food intake and provide specific brain areas for future investigations of the cellular mechanism underlying estradiol's anorexigenic effect.

摘要

雌二醇(E2)在多种物种中对摄食具有抑制作用。虽然有强有力的证据表明,中枢而非外周雌激素受体(ER)介导了这种作用,但确切的涉及脑区尚未得到明确鉴定。为了确定大脑区域是 E2 产生厌食作用所必需的,在去卵巢大鼠下丘脑和中脑的多个脑区中,急性单侧微注射载体和两种剂量(0.25 和 2.5μg)水溶性 E2 后,监测 48 小时的食物摄入量。在中脑导水管周围灰质(MPOA)、弓状核(ARC)和中缝背核(DRN)中,E2 给药后观察到 24 小时食物摄入量呈剂量相关性下降。然而,在这两个前脑区域,较大剂量的 E2 也降低了 4 小时的食物摄入量。然而,类似的 E2 给药对室旁核、下丘脑外侧区或腹内侧核的食物摄入量没有影响。这些数据表明,MPOA、ARC 和 DRN 内的 E2 反应神经元参与了雌激素对食物摄入的控制,并为进一步研究雌激素的厌食作用的细胞机制提供了特定的脑区。