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原发性肾小球肾炎患者的血小板活化因子水平及PAF乙酰水解酶活性

Platelet-activating factor levels and PAF acetylhydrolase activities in patients with primary glomerulonephritis.

作者信息

Iatrou C, Moustakas G, Antonopoulou S, Demopoulos C A, Ziroyiannis P

机构信息

Department of Nephrology, General Hospital of Athens, Greece.

出版信息

Nephron. 1996;72(4):611-6. doi: 10.1159/000188948.

Abstract

Platelet-activating factor (PAF) belongs to a new class of lipid chemical inflammatory mediators described as acetyl glyceryl ether phosphorylcholine. Although PAF has been implicated in kidney injury, its role in renal immune injury has not been clearly defined yet. We studied the levels of PAF in the plasma and urine and acetylhydrolase (AH) activities in serum and in renal tissue (cortex, C and medulla, M) in patients with primary glomerulonephritis (PGN). PAF levels in the plasma and urine and AH activity in serum of normal volunteers as well as AH activities in normal renal parenchyma (C and M) from nephrectomized patients (served as control) were also measured. Our results demonstrate increased PAF levels in the plasma and urine as well as increased AH activity in serum in patients with PGN in comparison to normal volunteers. AH activity in cortex of those patients was diminished compared to normal kidney tissue. We propose that the enhanced AH activity in serum in patients with PGN could be due to hyperproduction and low degradation of PAF in nephritic tissue which on one hand results in enhanced PAF levels in the plasma and in urine and on the other hand results in enhanced serum AH activity by virtue of substrate (PAF) availability. These data provide new knowledge in the homeostasis of PAF and its degrative enzyme in the setting of PGN.

摘要

血小板活化因子(PAF)属于一类新型脂质化学炎症介质,被描述为乙酰甘油醚磷酸胆碱。尽管PAF与肾损伤有关,但其在肾脏免疫损伤中的作用尚未明确界定。我们研究了原发性肾小球肾炎(PGN)患者血浆和尿液中PAF的水平以及血清和肾组织(皮质,C和髓质,M)中乙酰水解酶(AH)的活性。还测量了正常志愿者血浆和尿液中的PAF水平、血清中的AH活性以及肾切除患者正常肾实质(C和M)中的AH活性(作为对照)。我们的结果表明,与正常志愿者相比,PGN患者血浆和尿液中的PAF水平升高,血清中的AH活性增加。与正常肾组织相比,这些患者皮质中的AH活性降低。我们认为,PGN患者血清中AH活性增强可能是由于肾病组织中PAF的过度产生和低降解,这一方面导致血浆和尿液中PAF水平升高,另一方面由于底物(PAF)的可用性导致血清AH活性增强。这些数据为PGN情况下PAF及其降解酶的稳态提供了新知识。

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