非调理大肠杆菌对牙龈炎和牙周炎患者白细胞培养培养基中髓过氧化物酶活性的影响。

J Zekonis, G Zekonis, J Sakalauskienè
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引用次数: 0

摘要

目的探讨牙龈炎和牙周炎患者外周血静脉血(PVB)白细胞培养培养基中髓过氧化物酶(MPO)的活性,并与牙周健康人进行比较。研究人群为牙龈炎患者(G) 54例,牙周炎患者(P) 52例,对照组(C) 52例。采用临床、实验室和统计学方法对各组进行评估。白细胞与调理酶、大肠杆菌ATCC25922、非调理大肠杆菌或金黄色葡萄球菌256孵育。G组患者PVB白细胞培养液中MPO活性水平分别为598.0 +/- 29.2常规单位(c.u)、640.0 +/- 26.3 c.u、662.0 +/- 37.6 c.u和750.0 +/- 40.8 c.u(对照培养液:564.0 +/- 25.1 c.u);P组患者为672.0 +/- 34.3 c.u、678.0 +/- 43.1 c.u、692.0 +/- 47.9 c.u和762.0 +/- 34.7 c.u(对照组:612.0 +/- 35.2 c.u);C组为556.0 +/- 30.2 c.u., 714.0 +/- 28.2 c.u., 1276.0 +/- 69.0 c.u.和794.0 +/- 47.1 c.u.(对照组:534.0 +/- 29.0 c.u.)。当将非调理的大肠杆菌加入到完整牙周组织的PVB白细胞培养液中时,MPO活性显著增加。从牙周炎患者身上提取白细胞后,MPO活性没有变化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effects of nonopsonized Escherichia coli on myeloperoxidase activity in medium used for incubation of leukocytes from patients with gingivitis and periodontitis.

An attempt was made to explore the myeloperoxidase (MPO) activity in medium used for incubation of peripheral venous blood (PVB) leukocytes from patients with gingivitis and periodontitis and to compare it with that of periodontally healthy subjects. The study population included 54 gingivitis patients (G), 52 periodontitis patients (P) and 52 control subjects (C). All these groups were assessed by clinical, laboratory and statistical methods. The leukocytes were incubated with opsonized zymosan, Escherichia coli ATCC25922, nonopsonized E.coli or Staphylococcus aureus 256. The respective levels of MPO activity in incubation media of PVB leukocytes taken from group G patients were 598.0 +/- 29.2 conventional units (c.u.), 640.0 +/- 26.3 c.u., 662.0 +/- 37.6 c.u. and 750.0 +/- 40.8 c.u. (control incubation medium: 564.0 +/- 25.1 c.u.); those for group P patients were 672.0 +/- 34.3 c.u., 678.0 +/- 43.1 c.u., 692.0 +/- 47.9 c.u. and 762.0 +/- 34.7 c.u. (control: 612.0 +/- 35.2 c.u.); those for group C subjects were 556.0 +/- 30.2 c. u., 714.0 +/- 28.2 c.u., 1276.0 +/- 69.0 c.u. and 794.0 +/- 47.1 c.u. (control: 534.0 +/- 29.0 c.u.). MPO activity was increased most significantly when nonopsonized E.coli was added to the incubation medium of PVB leukocytes taken from subjects with intact periodontium. MPO activity was unchanged when the leukocytes were taken from periodontitis patients.

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