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停用脱氢表雄酮补充剂对 Zucker 大鼠食物摄入量和下丘脑神经递质的影响。

The effect of discontinuing dehydroepiandrosterone supplementation on Zucker rat food intake and hypothalamic neurotransmitters.

作者信息

Porter J R, Abadie J M, Wright B E, Browne E S, Svec F

机构信息

Department of Medicine, LSU Medical Center, New Orleans 70112, USA.

出版信息

Int J Obes Relat Metab Disord. 1995 Jul;19(7):480-8.

PMID:8520638
Abstract

OBJECTIVE

Dehydroepiandrosterone (DHEA) decreases body weight and food intake of the obese Zucker rat, a model of youth-onset obesity associated with hyperphagia. The effects of discontinuing DHEA treatment on these parameters, however, has not been investigated. This question was studied in rats that had been maintained on DHEA-supplemented (0.0%, 0.06%, 0.15%, 0.3% or 0.6%) diets for 7 days.

METHOD

The results were correlated with regional levels of hypothalamic neurotransmitters in rats treated with 0.6% DHEA for 7 days in a separate experiment. Neurotransmitter changes were evaluated after Day 0 (7 days of treatment), and Day +1 and Day+2 post-DHEA.

RESULTS

Upon removing dietary DHEA, rats immediately (+1 day) consumed significantly more food than while on the DHEA-supplemented diet. Indeed, they consumed even more food than the group that had always been on the DHEA-free diet. This intake above control lasted for as long as +9 days post-DHEA treatment. After 7 days of DHEA treatment, lateral hypothalamic (LH) serotonin (5-HT) and dopamine (Dpm) were elevated significantly (P < 0.05) immediate changes in 5-HT and Dpm returned to baseline by day 2 of post-DHEA treatment. No significant changes occurred in either the ventromedial hypothalamus (VMH) or the paraventricular nucleus (PVN).

CONCLUSIONS

These observations suggest that there is a possible relationship between increases of LH 5-HT and Dpm with 0.6% DHEA treatment. Both are inhibitory to food intake and DHEA at the 0.6% dose causes hypophagia after 7 days of treatment (i.e. 0 days). Subsequent decreases of these monoamines occurred during the post-DHEA period at both +1 and +2 days. Return of these inhibitory monoamines to baseline could be responsible for reversal of the hypophagia, however, they do not rule out the production of a separate stimulator of food intake.

摘要

目的

脱氢表雄酮(DHEA)可降低肥胖 Zucker 大鼠的体重和食物摄入量,该大鼠是一种与食欲亢进相关的青少年肥胖模型。然而,停用 DHEA 治疗对这些参数的影响尚未得到研究。在补充了 DHEA(0.0%、0.06%、0.15%、0.3%或 0.6%)的饮食中维持 7 天的大鼠中研究了这个问题。

方法

在另一个实验中,将结果与用 0.6% DHEA 治疗 7 天的大鼠下丘脑神经递质的区域水平相关联。在第 0 天(治疗 7 天)以及 DHEA 治疗后的第 +1 天和第 +2 天评估神经递质变化。

结果

去除饮食中的 DHEA 后,大鼠立即(+1 天)比在补充 DHEA 的饮食时消耗更多的食物。实际上,它们消耗的食物甚至比一直食用不含 DHEA 饮食的组还要多。这种高于对照组的摄入量在 DHEA 治疗后持续长达 +9 天。DHEA 治疗 7 天后,下丘脑外侧(LH)的 5-羟色胺(5-HT)和多巴胺(Dpm)显著升高(P < 0.05),5-HT 和 Dpm 的即时变化在 DHEA 治疗后第 2 天恢复到基线水平。腹内侧下丘脑(VMH)或室旁核(PVN)均未发生显著变化。

结论

这些观察结果表明,0.6% DHEA 治疗导致 LH 中 5-HT 和 Dpm 的增加之间可能存在关联。两者均抑制食物摄入,0.6%剂量的 DHEA 在治疗 7 天后(即 0 天)导致食欲减退。在 DHEA 治疗后的 +1 天和 +2 天期间,这些单胺类物质随后减少。这些抑制性单胺类物质恢复到基线水平可能是食欲减退逆转的原因,然而,它们并不排除产生一种单独的食物摄入刺激物。

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