首页> 外文期刊>Physiology & behavior >The orexigenic effect of peripheral ghrelin differs between rats of different age and with different baseline food intake, and it may in part be mediated by the area postrema.
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The orexigenic effect of peripheral ghrelin differs between rats of different age and with different baseline food intake, and it may in part be mediated by the area postrema.

机译:在不同年龄和不同基线食物摄入量的大鼠之间,外周生长激素释放肽的致食作用不同,并且可能部分由后区域引起。

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摘要

Ghrelin is mainly secreted during fasting. While an orexigenic effect of peripherally injected ghrelin has been reported, reproducing this effect has often proven difficult. Here, we hypothesized that ghrelin's effect to increase food intake may depend on the experimental conditions (e.g., age of animals). We therefore investigated the effect of an IP ghrelin injection (100 microg/kg) on food intake in rats of different age and at different times during the light-dark cycle, i.e. with different levels of baseline food intake. Ghrelin injected at dark onset in ad libitum fed young rats (body weight [BW] 92 g) slightly increased feeding while no such effect was observed in 12 h food deprived rats (BW 150 g). In the middle of the light phase, ghrelin significantly increased feeding up to 2 h after injection in ad libitum fed rats (BW 130 g; food intake 1 h after injection: NaCl 0.4 +/- 0.2 g versus ghrelin 1.2 +/- 0.3 g [p < 0.05]). In various subsequent experiments, older rats (BW 300-490 g) tested underthe same conditions did not respond to a single ghrelin injection. However repeated ghrelin injection (15 microg/kg/day once daily at light onset) over 10 days significantly increased food intake in rats (BW 400-460 g) starting from day 4 of the experiment (24 h food intake: NaCl approx. 19.5 g, ghrelin 22.5 g). Interestingly, the latter effect was completely abolished in rats lesioned in the area postrema (AP). Cumulative food intake was also increased in SHAM but not in AP-X animals (e.g., after 7 days: SHAM/NaCl 135.1 +/- 5.3 g versus SHAM/ghrelin 149.7 +/- 3.5 g [p < 0.05], AP-X/NaCl 127.2 +/- 16.4 versus AP-X/ghrelin 127.9 +/- 5.3). We conclude that ghrelin's effect to increase food intake can best be demonstrated when basal food intake is low. Ghrelin increases feeding mainly in young, fast growing animals. Ghrelin may therefore link the high energy needs to body growth in young individuals. In older animals, peripheral ghrelin increased feeding when injected repeatedly over several days. At least underthese conditions, ghrelin's effect was mediated by the AP/NTS region. Using repeated administration, ghrelin might be an interesting tool to increase feeding in patients suffering from wasting diseases such as cancer anorexia.
机译:Ghrelin主要在禁食期间分泌。尽管已经报道了外周注射生长激素释放肽的致癌作用,但事实证明再现这种作用是困难的。在这里,我们假设生长素释放肽对增加食物摄入的作用可能取决于实验条件(例如动物的年龄)。因此,我们研究了在黑暗-黑暗周期内,即不同基线食物摄取水平下,不同年龄和不同时间大鼠的IP ghrelin注射(100 microg / kg)对食物摄取的影响。在黑暗发作时,随意喂食幼年大鼠(体重[BW] 92 g)注射的Ghrelin略有增加进食量,而在12小时缺乏食物的大鼠(BW 150 g)中未观察到这种作用。在光照期的中间,注射任意剂量的大鼠中生长素释放肽显着增加了进食后2 h的体重(体重130 g;注射后1 h的食物摄入量:NaCl 0.4 +/- 0.2 g,而生长素释放肽1.2 +/- 0.3 g [p <0.05])。在随后的各种实验中,在相同条件下测试的老年大鼠(体重300-490克)对单次生长激素释放肽注射均无反应。但是,从实验的第4天开始(24小时进食:NaCl约19.5),在10天内重复注射ghrelin(轻度发作,每天一次,每天一次15微克/千克/天)会显着增加大鼠的进食量(体重400-460克)。 g,ghrelin 22.5 g)。有趣的是,后部区域的病变在后区域(AP)病变的大鼠中被完全消除。 SHAM的累积食物摄入量也增加了,但AP-X动物却没有增加(例如:7天后:SHAM / NaCl 135.1 +/- 5.3 g,而SHAM / ghrelin 149.7 +/- 3.5 g [p <0.05] / NaCl 127.2 +/- 16.4与AP-X / ghrelin 127.9 +/- 5.3)。我们得出的结论是,当基础食物摄入量较低时,ghrelin可以增加食物摄入量的效果最好。生长激素释放肽主要在幼小,快速生长的动物中增加喂养。因此,生长素释放肽可能将高能量需求与年轻人的身体生长联系起来。在年长的动物中,当连续几天注射时,外周生长素释放肽会增加摄食量。至少在这些条件下,ghrelin的作用是由AP / NTS区域介导的。通过重复施用,ghrelin可能是增加患有浪费性疾病(如癌症厌食症)的患者进食的有趣工具。

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