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白三烯B4在大鼠肾毒性血清肾炎中的作用

LTB4 in nephrotoxic serum nephritis in rats.

作者信息

Fauler J, Wiemeyer A, Marx K H, Kühn K, Koch K M, Frölich J C

机构信息

Department of Clinical Pharmacology, Hannover Medical School, Federal Republic of Germany.

出版信息

Kidney Int. 1989 Jul;36(1):46-50. doi: 10.1038/ki.1989.159.

Abstract

We studied leukotriene B4 (LTB4) synthesis in isolated glomeruli of rats with nephrotoxic serum nephritis. This nephritis was induced in male Sprague Dawley rats by injecting one proteinuric dose of nephrotoxic serum (rabbit anti-rat-GBM serum) after prior immunization of the rats with rabbit IgG. Histological and analytical examinations were performed in kidneys perfused until free of blood 6, 12, 24, 48 and 72 hours after induction of the disease. To investigate LTB4 production, glomeruli were isolated and incubated for one hour in the presence of Ca++-ionophore A23187. The supernatants were analyzed for LTB4. The peak comigrating on reverse-phase high performance liquid chromatography (RP-HPLC) with reference LTB4 was isolated. The ethyl ester trimethylsilyl ether derivative of this peak was analyzed by gaschromatography-mass spectrometry (GC/MS). Identical spectra of the glomerular samples and of reference LTB4 in the positive and in the negative ion chemical ionization mode provided unequivocal evidence that the substance released from the nephritic glomeruli was indeed LTB4. Six hours after injection of nephrotoxic serum, glomerular LTB4 release was highest with 5.52 +/- 0.50, then declining to 2.20 +/- 0.10 ng/mg glomerular protein at 12 hours. At 24, 48 and 72 hours no statistically significant difference from control animals was found. No metabolism of LTB4 to 20-hydroxy- or 20-carboxy-LTB4 was detected during the incubation period. Albuminuria developed during the first 24 hours after nephrotoxic serum challenge and rose steadily throughout the observation period up to 277 +/- 25 mg/24 hr after 72 hours.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

我们研究了肾毒性血清性肾炎大鼠分离肾小球中白三烯B4(LTB4)的合成情况。在雄性斯普拉格-道利大鼠先用兔IgG免疫后,注射一剂蛋白尿剂量的肾毒性血清(兔抗大鼠肾小球基底膜血清)诱导产生这种肾炎。在疾病诱导后6、12、24、48和72小时,对灌注直至无血的肾脏进行组织学和分析检查。为了研究LTB4的产生,分离肾小球并在钙离子载体A23187存在下孵育1小时。分析上清液中的LTB4。分离出在反相高效液相色谱(RP-HPLC)上与参考LTB4共迁移的峰。通过气相色谱-质谱联用(GC/MS)分析该峰的乙酯三甲基硅醚衍生物。肾小球样品和参考LTB4在正离子和负离子化学电离模式下的相同光谱明确证明,从肾炎性肾小球释放的物质确实是LTB4。注射肾毒性血清6小时后,肾小球LTB4释放最高,为5.52±0.50,然后在12小时时降至2.20±0.10 ng/mg肾小球蛋白。在24、48和72小时,与对照动物相比未发现统计学上的显著差异。在孵育期间未检测到LTB4代谢为20-羟基-LTB4或20-羧基-LTB4。肾毒性血清攻击后最初24小时内出现蛋白尿,并在整个观察期内稳步上升,72小时后达到277±25 mg/24小时。(摘要截短于250字)

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