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肿瘤坏死因子-α抑制大鼠肠肌间神经丛去甲肾上腺素释放的潜在机制。

Mechanism underlying tumor necrosis factor-alpha suppression of norepinephrine release from rat myenteric plexus.

作者信息

Hurst S M, Collins S M

机构信息

Intestinal Diseases Research Unit, McMaster University Medical Centre, Hamilton, Ontario, Canada.

出版信息

Am J Physiol. 1994 Jun;266(6 Pt 1):G1123-9. doi: 10.1152/ajpgi.1994.266.6.G1123.

Abstract

We studied the effect of tumor necrosis factor-alpha (TNF-alpha) on the release of [3H]norepinephrine ([3H]NE) from longitudinal muscle-myenteric plexus preparations of rat jejunum. TNF-alpha had no immediate effect on [3H]NE release. Preincubation of the tissue with TNF-alpha caused a suppression of [3H]NE release stimulated by KCl or electrical field stimulation. The action of TNF-alpha was time and concentration dependent (0.1-50 ng/ml) and was not due to endotoxin contamination. The effect of TNF-alpha was biphasic, occurring after 30 min and again after 120 min of preincubation. The early component was independent of protein synthesis but was inhibited by piroxicam or indomethacin, indicating the involvement of cyclooxygenase metabolites. The late component was dependent on protein synthesis, was blocked by an interleukin-1 receptor antagonist, and was inhibited by piroxicam or indomethacin. These results indicate that TNF-alpha suppresses NE release by two mechanisms, one of which is due to the synthesis and release of interleukin-1, each involving arachidonic acid metabolites.

摘要

我们研究了肿瘤坏死因子-α(TNF-α)对大鼠空肠纵行肌-肌间神经丛标本中[3H]去甲肾上腺素([3H]NE)释放的影响。TNF-α对[3H]NE的释放没有即时效应。用TNF-α对组织进行预孵育会抑制由氯化钾或电场刺激所引发的[3H]NE释放。TNF-α的作用具有时间和浓度依赖性(0.1 - 50 ng/ml),且并非由内毒素污染所致。TNF-α的效应呈双相性,在预孵育30分钟后出现,在120分钟后再次出现。早期成分不依赖蛋白质合成,但可被吡罗昔康或吲哚美辛抑制,这表明环氧化酶代谢产物参与其中。晚期成分依赖蛋白质合成,被白细胞介素-1受体拮抗剂阻断,且被吡罗昔康或吲哚美辛抑制。这些结果表明,TNF-α通过两种机制抑制NE释放,其中一种机制是由于白细胞介素-1的合成与释放,每种机制都涉及花生四烯酸代谢产物。

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