Novak M J, Polson A M
Department of Periodontology, Eastman Dental Center, Rochester, NY.
J Periodontol. 1989 Mar;60(3):137-44. doi: 10.1902/jop.1989.60.3.137.
Although the chemotaxis and efflux of functionally normal polymorphonuclear leukocytes (PMN) into the periodontal sulcus may have a protective role in periodontitis, these cells are also associated with periodontal tissue destruction. The immunomodulating agent, levamisole hydrochloride, is known to enhance PMN chemotaxis. The present study was designed to evaluate the effects of enhanced PMN chemotaxis on the tissue destruction associated with an experimental periodontitis. Levamisole was administered by oro-gastric intubation to 4 squirrel monkeys (experimental) at 3 mg/kg/bw every 2 days for 18 days. After 2 doses of levamisole, marginal periodontitis was induced around maxillary and mandibular bicuspids and the maxillary first molars by tying plaque-retentive ligatures at the gingival margins. Periodontitis was induced around corresponding teeth in 4 animals (control) which had not received levamisole. All animals were killed 2 weeks after induction of periodontitis. Clinically, gingival inflammation was more pronounced in experimental animals at both 7 and 14 days after periodontitis induction. The progression of periodontitis was evaluated histometrically and alterations in the cell populations characterized using step serial sections. The results were analyzed statistically. No significant differences were observed between the groups with respect to areas of infiltrated supracrestal connective tissue and total numbers of cells present, loss of connective tissue attachment and loss of coronal alveolar bone. However, in experimental specimens, a much denser band of inflammatory cells was evident between the apical extent of the bacterial plaque and the gingival sulcular tissues the connective tissue of which contained significantly fewer inflammatory cells and demonstrated more pronounced fibrogenesis.(ABSTRACT TRUNCATED AT 250 WORDS)
尽管功能正常的多形核白细胞(PMN)向牙周袋的趋化作用和流出可能在牙周炎中具有保护作用,但这些细胞也与牙周组织破坏有关。免疫调节剂盐酸左旋咪唑已知可增强PMN趋化作用。本研究旨在评估增强的PMN趋化作用对实验性牙周炎相关组织破坏的影响。通过经口胃插管,以3mg/kg体重的剂量每2天给4只松鼠猴(实验组)施用盐酸左旋咪唑,共18天。在给予2剂盐酸左旋咪唑后,通过在牙龈边缘系上菌斑滞留结扎线,在上颌和下颌双尖牙以及上颌第一磨牙周围诱导边缘性牙周炎。在未接受盐酸左旋咪唑的4只动物(对照组)的相应牙齿周围诱导牙周炎。在诱导牙周炎2周后处死所有动物。临床上,在诱导牙周炎后7天和14天,实验组动物的牙龈炎症更明显。通过组织计量学评估牙周炎的进展,并使用连续切片对细胞群体的变化进行表征。对结果进行统计学分析。在浸润的龈上结缔组织面积、存在的细胞总数、结缔组织附着丧失和牙槽嵴顶骨丧失方面,两组之间未观察到显著差异。然而,在实验标本中,在细菌菌斑的根尖范围与牙龈沟组织之间可见一条更密集的炎症细胞带,其中牙龈沟组织的结缔组织中炎症细胞明显较少,且纤维化更明显。(摘要截断于250字)