Wright B E, Svec F, Porter J R
Department of Physiology, Louisiana State University Medical Center, New Orleans 70119, USA.
Int J Obes Relat Metab Disord. 1995 Dec;19(12):887-92.
To investigate whether dehydroepiandrosterone (DHEA), an adrenal/gonadal androgen, can act centrally to reduce energy intake in a model of genetic obesity, the Zucker fatty rat. To investigate a possible mechanism of action.
Two experiments were performed in lean and obese female Zucker rats. In the first experiment, 24 h following administration of i.p. DHEA (200 mg/kg), three hypothalamic regions [lateral hypothalamus (LH), ventromedial nucleus (VMH), and paraventricular nucleus (PVN)] were analyzed for monoamine neurotransmitter concentrations. In the second experiment, DHEA (50 micrograms) was administered by i.c.v. injection. Energy intake for the following day was measured.
In the first experiment, concentrations of norepinephrine (NE), epinephrine (EPI), dopamine (DA), serotonin (5HT), the serotonin metabolite 5-hydroxyindoleacetic acid (5-HIAA) were measured. Ratios of 5HT/5HIAA were calculated. In the second experiment, kilojoules consumed per 24 h were calculated.
All LH monoamines, and PVN DA, displayed lower concentrations in obese than lean control rats. DHEA treatment reversed these reductions in obese rats without affecting lean rats. DHEA increased VMH EPI in obese rats only. DHEA increased PVN NE in both lean and obese rats. I.C.V. DHEA decreased energy intake in obese but not lean rats.
The i.c.v. results suggest that DHEA exerts a phenotype specific, centrally mediated inhibitory effect on food intake. In addition, in doses previously shown to reduce energy intake in obese but not lean rats, i.p. DHEA reversed reduced concentrations of many monoamines, particularly in the LH, in obese animals only. These latter changes provide indirect evidence to suggest that these central neurotransmitters may play an important role in the antiobesity effect of DHEA in the Zucker fatty rat.
研究脱氢表雄酮(DHEA),一种肾上腺/性腺雄激素,是否能在遗传性肥胖模型——Zucker肥胖大鼠中发挥中枢作用以减少能量摄入。研究其可能的作用机制。
对瘦型和肥胖型雌性Zucker大鼠进行了两项实验。在第一个实验中,腹腔注射DHEA(200mg/kg)24小时后,分析三个下丘脑区域[下丘脑外侧区(LH)、腹内侧核(VMH)和室旁核(PVN)]的单胺神经递质浓度。在第二个实验中,通过脑室内注射给予DHEA(50微克)。测量次日的能量摄入量。
在第一个实验中,测量去甲肾上腺素(NE)、肾上腺素(EPI)、多巴胺(DA)、5-羟色胺(5HT)、5-羟色胺代谢产物5-羟吲哚乙酸(5-HIAA)的浓度。计算5HT/5HIAA的比值。在第二个实验中,计算每24小时消耗的千焦数。
与瘦型对照大鼠相比,肥胖大鼠的所有LH单胺以及PVN DA浓度均较低。DHEA治疗逆转了肥胖大鼠的这些降低情况,而对瘦型大鼠无影响。DHEA仅增加了肥胖大鼠VMH中的EPI。DHEA增加了瘦型和肥胖大鼠PVN中的NE。脑室内注射DHEA降低了肥胖大鼠而非瘦型大鼠的能量摄入。
脑室内注射的结果表明,DHEA对食物摄入具有表型特异性的、中枢介导的抑制作用。此外,腹腔注射DHEA在先前已证明能降低肥胖大鼠而非瘦型大鼠能量摄入的剂量下,仅逆转了肥胖动物中许多单胺浓度的降低,尤其是在LH中。这些变化提供了间接证据,表明这些中枢神经递质可能在DHEA对Zucker肥胖大鼠的抗肥胖作用中发挥重要作用。