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타액선(唾液腺) 적출(摘出)이 상아질(象牙質) 형성(形成)에 미치는 영향(影響)에 관(關)한 주사(走査) 전자현미경적(電子顯微鏡的) 연구(硏究)
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  • 타액선(唾液腺) 적출(摘出)이 상아질(象牙質) 형성(形成)에 미치는 영향(影響)에 관(關)한 주사(走査) 전자현미경적(電子顯微鏡的) 연구(硏究)
저자명
이영식,박상진,민병순,최호영,Lee. Young-Sik,Park. Sang-Jin,Min. Byung-Soon,Choi. Ho-Young
간행물명
大韓齒科保存學會誌
권/호정보
1989년|14권 1호|pp.57-70 (14 pages)
발행정보
대한치과보존학회
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이 논문은 한국과학기술정보연구원과 논문 연계를 통해 무료로 제공되는 원문입니다.
서지반출

기타언어초록

The purpose of this study was to investigate the effect of salivary gland on the calcification of dentin in rats. 80 Sprague-Dawley male rats that weighed approximately 120gm were used in this study. 5 rats among them were shared as controls. 75 rats received sialoadenectomy were divided into submaxillary adenectomy group, parotidectomy group, and submaxillary-parotid gland combined removal group. In experimental groups, 25 rats in each of the 3 groups were sacrificed at the following intervals; 3 days, 1, 2, 3 and 4 weeks. All animals were sacrificed by vascular perfusion with 10% formalin. The maxillary incisors including periapical tissues were removed and defatted in 20% KOH solution at $0^{circ}C$ for 24 hours, and dehydrated with acetone. Each tooth specimen was attached on the stab for scanning electron microscopic study. Gold was coated on the each specimen in the thickness of 300${AA}$ at D.C. 1400V, 6mA for 6 minutes with coating machine (Eiko IB-3). Inner dentinal surfaces of the specimens were observed with SEM (Hitachi S-450). The results were as follows, 1. Parotidectomy groups were found to be inhibited the formation of dentinal calcification compared to submaxillary adenectomy groups in the eady stages. 2. Combined removal of submaxillary and parotid gland was appeared to cause more severe inhibition effect on the dentinal calcification than that of each salivary gland separately. 3. Inhibition of the calcification and mineralization of dentin caused by sialoadenectomy was more extreme from 3 day to 2 weeks after beginning of the experiments. However it was tended to be normalized after that. 4. Salivary gland was responsible for alterations in calcification and mineralization of dentinal growth.