Gangbar S, Overall C M, McCulloch C A, Sodek J
Department of Periodontics, Faculty of Dentistry, University of Toronto, Ontario, Canada.
J Periodontal Res. 1990 Sep;25(5):257-67. doi: 10.1111/j.1600-0765.1990.tb00914.x.
In previous studies, elevations in the levels of active and latent collagenase in gingival crevicular fluid (GCF) have been correlated positively with periodontal disease activity. To provide a simple diagnostic approach for testing collagenolytic activity, the feasibility of using a 3.0 ml water mouthrinse to collect GCF simultaneously from all sites in the mouth was assessed. Patients with adult periodontitis (AP, n = 23) and local juvenile periodontitis (LJP, n = 7) were sampled before periodontal therapy and some (12 AP, 4 LJP) were also assessed longitudinally after scaling and root planing, administration of antibiotics, and following periodontal surgery. Healthy patients (n = 19) were used as controls. The levels of active collagenase, procollagenase, and collagenase inhibitor activity were determined by functional assays and quantitated after SDS-PAGE and fluorography. Gelatinase and progelatinase were assayed by enzymography on gelatin-substrate gels. Active collagenase levels were found to be significantly higher (14- to 20-fold) in AP and LJP patients compared to controls, whereas matrix metalloproteinase activity was not detected in mouthrinses from edentulous patients. Collagenase inhibitor levels were generally low in all groups of subjects tested. Following clinical treatment the levels of active collagenase and gelatinase were reduced; the reduction was significant for active collagenase after tetracycline treatment and scaling in LJP patients. Of the clinical indices recorded (gingival index, plaque index, and pocket depth) there were no significant correlations with enzyme activity but similar trends were observed between the changes in active collagenase and gingival index. In patients with untreated periodontal disease, collagenase occurred predominantly in the active form. N-ethylmaleimide (NEM) and p-aminophenylmercuric acetate (AMPA) were equally effective as activators of the latent collagenase, indicating that the collagenase was derived from PMNs, which were also the source of gelatinase. The results of these studies indicate that measurement of active collagenase and gelatinase in mouthrinse samples is potentially useful in the diagnosis and assessment of periodontal disease activity.
在以往的研究中,龈沟液(GCF)中活性和潜伏性胶原酶水平的升高与牙周疾病活动呈正相关。为了提供一种检测胶原溶解活性的简单诊断方法,评估了使用3.0毫升水含漱液同时从口腔所有部位收集GCF的可行性。在牙周治疗前对成人牙周炎(AP,n = 23)和局限性青少年牙周炎(LJP,n = 7)患者进行采样,部分患者(12例AP,4例LJP)在进行龈上洁治和根面平整、使用抗生素以及牙周手术后还进行了纵向评估。健康患者(n = 19)作为对照。通过功能测定法测定活性胶原酶、前胶原酶和胶原酶抑制剂活性水平,并在SDS - 聚丙烯酰胺凝胶电泳和荧光自显影后进行定量。发现AP和LJP患者的活性胶原酶水平比对照组显著更高(14至20倍),而无牙患者的含漱液中未检测到基质金属蛋白酶活性。在所有测试的受试者组中,胶原酶抑制剂水平通常较低。临床治疗后,活性胶原酶和明胶酶水平降低;LJP患者在四环素治疗和龈上洁治后,活性胶原酶水平的降低具有显著性。在所记录的临床指标(牙龈指数、菌斑指数和牙周袋深度)中,与酶活性无显著相关性,但在活性胶原酶变化和牙龈指数之间观察到相似趋势。在未经治疗的牙周疾病患者中,胶原酶主要以活性形式存在。N - 乙基马来酰亚胺(NEM)和对氨基苯基汞乙酸盐(AMPA)作为潜伏性胶原酶的激活剂效果相同,表明胶原酶源自中性粒细胞,中性粒细胞也是明胶酶的来源。这些研究结果表明,测量含漱液样本中的活性胶原酶和明胶酶可能有助于牙周疾病活动的诊断和评估。