The possible role of prolactin in the circadian rhythm of leptin secretion in male rats.

C. Mastronardi, A. Walczewska, W. H. Yu, S. Karanth, A. Parlow, S. Mccann
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引用次数: 34

Abstract

In humans there is a circadian rhythm of leptin concentrations in plasma with a minimum in the early morning and a maximum in the middle of the night. By taking blood samples from adult male rats every 3 hr for 24 hr, we determined that a circadian rhythm of plasma leptin concentrations also occurs in the rat with a peak at 0130h and a minimum at 0730h. To determine if this rhythm is controlled by nocturnally released hormones, we evaluated the effect of hormones known to be released at night in humans, some of which are also known to be released at night in rats. In humans, prolactin (PRL), growth hormone (GH), and melatonin are known to be released at night, and adrenocorticotropic hormone (ACTH) release is inhibited. In these experiments, conscious rats were injected intravenously with 0.5 ml diluent or the substance to be evaluated just after removal of the first blood sample (0.3 ml), and additional blood samples (0.3 ml) were drawn every 10 min thereafter for 2 hr. The injection of highly purified sheep PRL (500 microg) produced a rapid increase in plasma leptin that persisted for the duration of the experiment. Lower doses were ineffective. To determine the effect of blockade of PRL secretion on leptin secretion, alpha bromoergocryptine (1.5 mg), a dopamine-2-receptor agonist that rapidly inhibits PRL release, was injected. It produced a rapid decline in plasma leptin within 10 min, and the decline persisted for 120 min. The minimal effective dose of GH to lower plasma leptin was 1 mg/rat. Insulin-like growth factor (IGF-1) (10 microg), but not IGF-2 (10 microg), also significantly decreased plasma leptin. Melatonin, known to be nocturnally released in humans and rats, was injected at a dose of 1 mg/rat during daytime (1100h) or nighttime (2300h). It did not alter leptin release significantly. Dexamethasone (DEX), a potent glucocorticoid, was ineffective at a 0. 1-mg dose but produced a delayed, significant increase in leptin, manifest 100-120 min after injection of a 1 mg dose. Since glucocorticoids decrease at night in humans at the time of the maximum plasma concentrations of leptin, we hypothesize that this increase in leptin from a relatively high dose of DEX would mimic the response to the release of corticosterone following stress in the rat and that glucocorticoids are not responsible for the circadian rhythm of leptin concentration. Therefore, we conclude that an increase in PRL secretion during the night may be responsible, at least in part, for the nocturnal elevation of leptin concentrations observed in rats and humans.
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催乳素在雄性大鼠瘦素分泌昼夜节律中的可能作用。
人体血浆中瘦素浓度有昼夜节律,清晨最低,午夜最高。通过在24小时内每3小时采集一次成年雄性大鼠的血液样本,我们确定大鼠的血浆瘦素浓度也存在昼夜节律,在0130h达到峰值,在0730h达到最低。为了确定这种节律是否受夜间释放的激素控制,我们评估了人类在夜间释放的激素的影响,其中一些激素在夜间也会在老鼠身上释放。在人类中,泌乳素(PRL)、生长激素(GH)和褪黑激素在夜间被释放,促肾上腺皮质激素(ACTH)的释放被抑制。在这些实验中,清醒的大鼠在取出第一个血样(0.3 ml)后立即静脉注射0.5 ml稀释剂或待评估物质,此后每10分钟再抽取0.3 ml血样,持续2小时。高纯度绵羊PRL(500微克)的注射使血浆瘦素迅速增加,并在实验期间持续增加。较低剂量无效。为了确定阻断PRL分泌对瘦素分泌的影响,注射可快速抑制PRL释放的多巴胺-2受体激动剂α -溴代隐碱(1.5 mg)。在10分钟内使血浆瘦素迅速下降,并持续下降120分钟。生长激素降低血浆瘦素的最小有效剂量为1 mg/大鼠。胰岛素样生长因子(IGF-1)(10微克),而不是IGF-2(10微克),也显著降低血浆瘦素。褪黑素是人类和大鼠在夜间释放的,在白天(1100小时)或夜间(2300小时)注射剂量为1mg /大鼠。它没有显著改变瘦素的释放。地塞米松(Dexamethasone, DEX)是一种强效糖皮质激素,在0时无效。1毫克剂量,但产生延迟,显著增加瘦素,表现在注射1毫克剂量后100-120分钟。由于人体内的糖皮质激素在夜间会减少,而此时正是血中瘦素浓度最高的时候,因此我们假设,相对高剂量的DEX导致的瘦素增加可能与大鼠应激后皮质酮释放的反应类似,而糖皮质激素并不是导致瘦素浓度昼夜节律的原因。因此,我们得出结论,夜间PRL分泌的增加可能是夜间瘦素浓度升高的原因,至少部分原因是在大鼠和人类中观察到的。
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