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首页> 外文期刊>Neuroscience Letters: An International Multidisciplinary Journal Devoted to the Rapid Publication of Basic Research in the Brain Sciences >Lipopolysaccharide stimulates norepinephrine efflux from the rat hypothalamus in vitro: blockade by soluble IL-1 receptor.
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Lipopolysaccharide stimulates norepinephrine efflux from the rat hypothalamus in vitro: blockade by soluble IL-1 receptor.

机译:脂多糖体外刺激大鼠下丘脑的去甲肾上腺素外排:被可溶性IL-1受体阻断。

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摘要

Lipopolysaccharide (LPS) has been shown to produce a number of central and neuroendocrine effects. While all mechanisms are not clear, it is believed that central catecholamines could be involved in this process. This study was done to investigate the direct effects of LPS on norepinephrine (NE) efflux from the medial basal hypothalamus in adult male rats using a combination of an in vitro incubation system and high performance liquid chromatography with electrochemical detection. Basal NE efflux was determined by incubating the hypothalami with Krebs Ringers Henseleit (KRH) alone for 60 min. Then, the hypothalami were incubated with KRH alone (control) or KRH containing 100 ng or 200 ng of LPS, 15 microg of soluble IL-1 receptor (sIL-1R) or a combination of 200 ng LPS and 5 or 15 microg of sIL-1R. In the third incubation period, the hypothalami were incubated with KRH alone to check for the residual effects of LPS if any. In the fourth incubation period, the hypothalami were incubated with high K+KRH to check for tissue viability. Incubation with LPS stimulated NE efflux in a dose-dependent manner. Incubation of hypothalami with 200 ng of LPS and 15 microg of sIL-1R completely blocked LPS-induced increase in NE efflux. These results indicate that LPS could act directly on the hypothalamus to stimulate the efflux of NE and this effect is probably mediated through IL-1.
机译:脂多糖(LPS)已显示产生许多中枢和神经内分泌作用。尽管所有机制尚不清楚,但据信中央儿茶酚胺可能参与了这一过程。这项研究的目的是结合体外孵育系统和高效液相色谱与电化学检测技术,研究LPS对成年雄性大鼠内侧基底下丘脑去甲肾上腺素(NE)流出的直接影响。通过将下丘脑单独与克雷布斯·林格·汉斯利特(KRH)孵育60分钟来确定基础NE外排。然后,将下丘脑与单独的KRH(对照)或含有100 ng或200 ng LPS,15微克可溶性IL-1受体(sIL-1R)或200 ng LPS和5或15微克sIL的组合的KRH一起孵育-1R。在第三潜伏期,将下丘脑单独与KRH一起孵育以检查LPS的残留效应(如果有)。在第四个潜伏期,将下丘脑与高K + KRH一起孵育以检查组织活力。用LPS孵育以剂量依赖性方式刺激NE流出。将下丘脑与200 ng LPS和15微克sIL-1R一起孵育,完全阻止LPS诱导的NE外流增加。这些结果表明,LPS可以直接作用于下丘脑,刺激NE的流出,这种作用可能是通过IL-1介导的。

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