华西口腔医学杂志
華西口腔醫學雜誌
화서구강의학잡지
WEST CHINA JOURNAL OF STOMATOLOGY
2015年
4期
357-360
,共4页
代晓明%刘华%左志斌%秦少华%阮永华%李逸松
代曉明%劉華%左誌斌%秦少華%阮永華%李逸鬆
대효명%류화%좌지빈%진소화%원영화%리일송
4-硝基喹啉-1-氧化物%C57BL/6小鼠%舌黏膜%癌变%动物模型
4-硝基喹啉-1-氧化物%C57BL/6小鼠%舌黏膜%癌變%動物模型
4-초기규람-1-양화물%C57BL/6소서%설점막%암변%동물모형
4-nitroquinoline 1-oxide%C57BL/6 mice%lingual mucosa%carcinogenesis%animal model
目的:用4-硝基喹啉-1-氧化物(4NQO)诱导C57BL/6小鼠舌黏膜癌变。方法将85只小鼠随机分为蒸馏水对照组(n=5)、1,2丙二醇对照组(n=5)、实验组(n=75),分别给予蒸馏水、1,2丙二醇及4NQO溶液饮用。实验组小鼠再分为15笼,每2周处死一笼,对照组小鼠于28周处死。对小鼠进行称质量和大体观察及组织病理学检查。结果实验组死亡1只。实验组小鼠体质量在24周后体质量较对照组明显降低(P<0.05)。实验动物的舌、口底、上颚、颊部共出现79处肉眼可见的病变,其中舌部病变70处(88.6%)。实验组动物在不同时间点黏膜病变不同,28周时均发生高分化鳞状细胞癌。对照组未见病变。结论舌癌动物模型被成功建立。实验12~16周及20~28周可作为研究舌黏膜癌变早期和中晚期阶段的时间点。
目的:用4-硝基喹啉-1-氧化物(4NQO)誘導C57BL/6小鼠舌黏膜癌變。方法將85隻小鼠隨機分為蒸餾水對照組(n=5)、1,2丙二醇對照組(n=5)、實驗組(n=75),分彆給予蒸餾水、1,2丙二醇及4NQO溶液飲用。實驗組小鼠再分為15籠,每2週處死一籠,對照組小鼠于28週處死。對小鼠進行稱質量和大體觀察及組織病理學檢查。結果實驗組死亡1隻。實驗組小鼠體質量在24週後體質量較對照組明顯降低(P<0.05)。實驗動物的舌、口底、上顎、頰部共齣現79處肉眼可見的病變,其中舌部病變70處(88.6%)。實驗組動物在不同時間點黏膜病變不同,28週時均髮生高分化鱗狀細胞癌。對照組未見病變。結論舌癌動物模型被成功建立。實驗12~16週及20~28週可作為研究舌黏膜癌變早期和中晚期階段的時間點。
목적:용4-초기규람-1-양화물(4NQO)유도C57BL/6소서설점막암변。방법장85지소서수궤분위증류수대조조(n=5)、1,2병이순대조조(n=5)、실험조(n=75),분별급여증류수、1,2병이순급4NQO용액음용。실험조소서재분위15롱,매2주처사일롱,대조조소서우28주처사。대소서진행칭질량화대체관찰급조직병이학검사。결과실험조사망1지。실험조소서체질량재24주후체질량교대조조명현강저(P<0.05)。실험동물적설、구저、상악、협부공출현79처육안가견적병변,기중설부병변70처(88.6%)。실험조동물재불동시간점점막병변불동,28주시균발생고분화린상세포암。대조조미견병변。결론설암동물모형피성공건립。실험12~16주급20~28주가작위연구설점막암변조기화중만기계단적시간점。
Objective This?study?aimed?to?induce?carcinogenesis?of?lingual?mucosa?in?C57BL/6?mice?by?feeding?them?4-nitroquinoline?1-oxide?(4NQO)?solution.?Methods???A?total?of?85?C57BL/6?mice?were?randomly?divided?into?distilled?water?control?group?(DD?group,?n=5),?1,2-propylene?glycol?control?group?(PG?group,?n=5),?and?experimental?group?(EP?group,?n=75).?The?mice?in?the?experimental?group?were?medially?fed?in?15?cages.?By?contrast,?the?mice?in?DD,?EP,?and?PG?groups?were?watered with distilled water, 50 mg·L-1?4NQO?solution,?and?1,2-propylene?glycol?solution.?The?mice?in?EP?group?were?executed?every?two?weeks?from?week?0,?and?the?mice?in?the?control?groups?were?sacrificed?at?the?28th?week.?The?mice?were?weighed.?Mucosal?lesions?were?measured?by?macroscopic?observation?and?histopathologic?detection.?Results???One?mouse?in?EP?group?died?of?unknown?reason.?The?weight?of?the?mice?in?EP?group?presented?weight?loss?compared?with?the?mice?in?DD?and?PG?groups?after?the?24th?week.?Seventy-nine?macroscopic?lesions?were?observed?in?the?lingual?mucosa,?oral?floor,?and?upper?palatal?and?buccal?mucosa.?A?total?of?70?macroscopic?lesions?(88.6%)?were?located?in?the?lingual?mucosa.?Mucosal?lesions?changed?from?simple?hyperplasia?to?squamous?cell?carcinomas.?Well-differentiated?squamous?cell?carcinomas?were?observed?in?all?mice?of?EP?group?by?pathological?section?at?the?28th?week.?No?lesion?was?found?in?the?mice?of?DD?and?PG?groups.?Conclusion?The?animal?model?of?lingual?squamous?cell?carcinomas?was?successfully?established.?The?periods?from?12th?to?16th?week?and?20th?to?28th?week?were?the?ideal?times?for?the?research?on?pathogenesis?of?early?and?medial-advanced?stage?during?carcinogenesis?of?squamous?cell?carcinomas.