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未调理的大肠杆菌对用于培养牙龈炎和牙周炎患者白细胞的培养基中髓过氧化物酶活性的影响。

Effects of nonopsonized Escherichia coli on myeloperoxidase activity in medium used for incubation of leukocytes from patients with gingivitis and periodontitis.

作者信息

Zekonis J, Zekonis G, Sakalauskienè J

机构信息

Kaunas Medical Academy, Department of Prosthetic Stomatology.

出版信息

J Nihon Univ Sch Dent. 1997 Mar;39(1):12-6. doi: 10.2334/josnusd1959.39.12.

DOI:10.2334/josnusd1959.39.12
PMID:9198330
Abstract

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.

摘要

本研究旨在探究用于培养牙龈炎和牙周炎患者外周静脉血(PVB)白细胞的培养基中的髓过氧化物酶(MPO)活性,并将其与牙周健康受试者的进行比较。研究人群包括54名牙龈炎患者(G组)、52名牙周炎患者(P组)和52名对照受试者(C组)。所有这些组均通过临床、实验室和统计学方法进行评估。将白细胞与调理酵母聚糖、大肠埃希菌ATCC25922、未调理的大肠埃希菌或金黄色葡萄球菌256一起孵育。G组患者PVB白细胞孵育培养基中MPO活性的相应水平分别为598.0±29.2传统单位(c.u.)、640.0±26.3 c.u.、662.0±37.6 c.u.和750.0±40.8 c.u.(对照孵育培养基:564.0±25.1 c.u.);P组患者的分别为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:612.0±35.2 c.u.);C组受试者的分别为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:534.0±29.0 c.u.)。当将未调理的大肠埃希菌添加到牙周组织完整受试者的PVB白细胞孵育培养基中时,MPO活性增加最为显著。当白细胞取自牙周炎患者时,MPO活性未发生变化。

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