Hormones Department and Cell Biology Department, National Research Centre, Giza, Egypt.
Eur Rev Med Pharmacol Sci. 2012 Nov;16(12):1680-90.
A number of factors involved in the control of energy balance and metabolism act as modulators of gonadal axis. Ghrelin, a peptide secreted from the stomach and hypothalamus, has emerged as an orexigenic food intake controlling signal acting upon hypothalamus. Recently, the potential reproductive role of ghrelin has received great attention. This study was designed to investigate the influence of food restriction and consequent metabolic hormone (ghrelin) on the level and gene expression of female reproductive hormones in adult rats.
To study the effect of chronic food restriction on ghrelin level in adult female rats and its relation to female reproductive hormones, 32 adult female Sprague Dawley rats divided into 4 groups: Group I (control group) comprised 8 rats fed ad libitum for 30 days, Group II, III and IV (food-restricted groups for 10, 20 and 30 days respectively) each consisted of 8 rats fed 50% of ad libitum intake determined by the amount of food consumed by the control group.
Mean body weight of food restricted rats was observed to decrease during the period of the experiment. Food restriction produced significant increase of serum ghrelin with significant decrease of both gastric and hypothalamic ghrelin accompanied with significant increase in its gene expression in stomach and hypothalamus. Estradiol (E2), follicle-stimulating hormone (FSH) and luteinizing hormone (LH) levels showed significant decrease correlated with down-regulation of gonadotropins, cyclin-dependent kinase (cdc2), cyclin B and kisspeptin (Kiss1) genes in food restricted rats compared with control group.
Ghrelin could be one of the hormones responsible for the suppression of female reproductive axis in case of negative energy balance. Thus, ghrelin may operate as an autocrine/paracrine regulator of ovarian function. Overall, ghrelin may represent an additional link between body weight homeostasis and reproductive function.
许多参与能量平衡和代谢控制的因素都充当着性腺轴的调节剂。胃饥饿素是一种从胃和下丘脑分泌的肽,它作为一种促进食欲的食物摄入控制信号作用于下丘脑。最近,胃饥饿素的潜在生殖作用受到了广泛关注。本研究旨在探讨食物限制及随之而来的代谢激素(胃饥饿素)对成年雌性大鼠生殖激素水平和基因表达的影响。
为了研究慢性食物限制对成年雌性大鼠胃饥饿素水平的影响及其与雌性生殖激素的关系,将 32 只成年雌性 Sprague Dawley 大鼠分为 4 组:第 I 组(对照组)包括 8 只大鼠,自由进食 30 天;第 II 组、第 III 组和第 IV 组(分别限制进食 10、20 和 30 天)各包括 8 只大鼠,按对照组大鼠的进食量的 50%进食。
观察到限制进食大鼠的平均体重在实验期间下降。食物限制导致血清胃饥饿素显著增加,胃和下丘脑胃饥饿素显著减少,其基因表达在胃和下丘脑显著增加。与对照组相比,食物限制大鼠的雌二醇(E2)、促卵泡激素(FSH)和促黄体生成激素(LH)水平显著下降,与促性腺激素、周期蛋白依赖性激酶(cdc2)、周期蛋白 B 和 kisspeptin(Kiss1)基因下调相关。
在负能平衡的情况下,胃饥饿素可能是抑制雌性生殖轴的激素之一。因此,胃饥饿素可能作为卵巢功能的自分泌/旁分泌调节剂发挥作用。总的来说,胃饥饿素可能代表了体重平衡和生殖功能之间的另一个联系。