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大鼠实验性根尖周病的酶组织化学研究 被引量:4

An Enzyme Histochemical Study of Rat Experimental Periapical Lesions
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摘要 目的 :本研究旨在通过石蜡包埋的酶组织化学染色法 ,观察大鼠实验性根尖周病病损区成骨细胞、破骨细胞的活动情况。方法 :将大鼠右下颌第一磨牙开髓后暴露口腔 2~ 2 8d ,诱导根尖周病损形成 ;对其进行心内固定后 ,将含牙和牙槽骨的标本经EDTA脱钙 ,采用石蜡包埋法制作切片 ,进行酸性磷酸酶和碱性磷酸酶酶组织化学染色。结果 :石蜡切片经酶组织化学染色后 ,可清晰辨别出酶阳性的成骨细胞和破骨细胞。随根尖周病的发展 ,成骨细胞和破骨细胞在数量上呈一定规律性变化。结论 :石蜡切片的酶组织化学法可用于研究根尖周病损区骨细胞的行为变化。 Objective:The behaviors of osteoblasts and osteoclasts in the rat experimental periapical lesions were examined by using enzyme histochemical methods of paraffin-embedded bone tissues.Methods:The right mandibular first molar was exposed to the oral environment for 2~28d to induce the formation of periapical lesions; Each animal was fixed by an intracardiac perfusion of 4% paraformoldehyde in a solution of 0.05M phosphate buffer;The first molar parts were then demineralized with 10% EDTA, and after being made into paraffin sections,the enzyme histochemical stainings were given.Results:Osteoblasts with strong alkaline phosphatase activity and osteoclasts with acid phosphatase activity have been identified in the periapical lesions by light microscopy,and the changes of behavior of osteoblasts and osteoclasts have been investigated too during the different developmental periods of periapical lesions.Conclusions:The results suggest that enzyme histochemical applications to paraffin sections are a useful means for clarifying the behavior of bone cells in periapical lesions.
作者 李福军 彭彬
出处 《口腔医学研究》 CAS CSCD 2003年第2期109-111,共3页 Journal of Oral Science Research
关键词 根尖周病 酶组织化学法 酸性磷酸酶 碱性磷酸酶 动物实验 大鼠 Periapical lesions Enyme histochemistry Acid phosphatase Alkaline phosphatase
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  • 1李琼英 仝毅 肖邦良.脱钙法在硬组织酶组织化学中的应用[J].华西口腔医学杂志,1998,6:68-69.
  • 2小川和郎 中根一穗主编 钟慈声主译.上海医科大学出版社[J].酶组织细胞化学技术,1987,:92-93.
  • 3龚志锦.詹镕洲[M].上海科学技术出版社,1993.316-317.
  • 4张壁,加藤征治,柳泽繁孝.大鼠牙周组织淋巴管的酶组织化学法研究[J].口腔医学纵横,2001,17(2):113-115. 被引量:1

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  • 1张琛,侯本祥.根尖周炎动物模型中CD14、TLR4的表达[J].中华口腔医学杂志,2007,42(3):148-149. 被引量:3
  • 2Sheela Rani CS, MacDougall M. Dental cells express factors that regulate bone resorption. Molecular Cell Biol Res Commun, 2000,3:145.
  • 3Kawamoto S, Ejiri S, Hoshi K, et al. Immunolocalization of osteoclast differentiation factor in rat periodontium. Arch Oral Biol, 2002,47: 55.
  • 4Teitelbaun SL. Bone resorption by osteoclasts. Science, 2000,289:1 504.
  • 5Anderson DM, Maraskovsky E, Billingsley WL, et al. A homologue of the TNF receptor and its ligand enhance T-cell growth and dendritic-cell function. Nature, 1997,390:175.
  • 6Wong BR, Rho J, Arron J, et al. TRANCE is a novel ligand of the tumor necrosis factor receptor family that activates c-Jun N-terminal kinase in T cells. J Biol Chem, 1997,272(40):25 190.
  • 7Lacey DL, Timms E, Tan HL, et al. Osteoprotegerin ligand is a cytokine that regulates osteoclast differentiation and activation. Cell, 1998,93: 165.
  • 8Yasuda H, Shima N, Nakagawa N, et al. Osteoclast differentiation factor is a ligand for osteoprotegerin/osteoclastogenesis-inhibitory factor and is identical to TRANCE/RANKL. Proc Natl Acad Sci USA, 1998,95:3 597.
  • 9Kong HH, Yoshida H, Sarosi I, et al. OPGL is a key regulator of osteoclastogenesis, lymphocyte development and lymph-node organogenesis. Nature, 1999, 397(28): 315.
  • 10Huang GTJ, Do M, Wingard M, et al. Effect of interleukin-6 deficiency on the format-ion of periapical lesions after pulp exposure in mice. Oral Surg Oral Med Oral Path-ol Oral Radiol Endod, 2001,92:83.

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