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槟榔提取物可抑制培养的人牙龈成纤维细胞的生长、黏附及基质蛋白合成。

Areca nut extract inhibits the growth, attachment, and matrix protein synthesis of cultured human gingival fibroblasts.

作者信息

Chang M C, Kuo M Y, Hahn L J, Hsieh C C, Lin S K, Jeng J H

机构信息

Team of Biomedical Science, Chang-Gung Institute of Nursing, Taoyuan, Taiwan.

出版信息

J Periodontol. 1998 Oct;69(10):1092-7. doi: 10.1902/jop.1998.69.10.1092.

Abstract

Betel quid chewing is a popular oral habit in India, South Africa, and many Southeast Asian countries. The effects of areca nut (AN) extract on the growth, attachment, and protein synthesis of healthy human gingival fibroblasts (GF) were investigated to determine why betel quid (BQ) chewers have higher prevalence of periodontal disease than non-chewers. Twenty-four hour exposure of human GF to AN extract (> 200 microg/ml) in culture led to the formation of numerous intracellular vacuoles. As analyzed by modified MTT [3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl-tetrazolium bromide] assay, AN extract significantly suppressed the growth of GF over 5 days of incubation in a dose-dependent manner. At concentrations of 50 and 300 microg/ml, AN extract suppressed the growth of GF with 30% and 57% (P < 0.05), respectively. AN extract also significantly suppressed the synthesis of [3H]proline incorporation into trichloroacetic acid (TCA) precipitated proteins. At concentrations of 200, 400, and 600 microg/ml, AN extract suppressed the protein synthesis with 33%, 58%, and 63% of inhibition (P < 0.05), respectively. Preincubation of cells in a medium containing AN extract for 2 hours inhibits the subsequent attachment of cultured GF to type I collagen at the 50% inhibitory concentration (IC50) which is about 720 to 798 microg/ml. Considering the frequent consumption of BQ throughout the day, impairment of sequential fibroblast functions by BQ ingredients is a potential mechanism through which BQ chewing exert a deleterious effect to the gingival tissues.

摘要

嚼食槟榔是印度、南非和许多东南亚国家常见的口腔习惯。为了确定为何嚼食槟榔者比不嚼食者患牙周病的几率更高,研究了槟榔提取物对健康人牙龈成纤维细胞(GF)生长、黏附及蛋白质合成的影响。在培养过程中,将人GF暴露于槟榔提取物(>200微克/毫升)24小时会导致大量细胞内空泡形成。通过改良的MTT[3-(4,5-二甲基噻唑-2-基)-2,5-二苯基溴化四氮唑]分析,槟榔提取物在5天的孵育期内以剂量依赖方式显著抑制GF的生长。在50和300微克/毫升浓度下,槟榔提取物分别抑制GF生长30%和57%(P<0.05)。槟榔提取物还显著抑制[3H]脯氨酸掺入三氯乙酸(TCA)沉淀蛋白的合成。在200、400和600微克/毫升浓度下,槟榔提取物分别抑制蛋白质合成33%、58%和63%(P<0.05)。在含槟榔提取物的培养基中预孵育细胞2小时,在50%抑制浓度(IC50)约为720至798微克/毫升时,会抑制培养的GF随后与I型胶原的黏附。考虑到全天频繁嚼食槟榔,槟榔成分对成纤维细胞连续功能的损害是嚼食槟榔对牙龈组织产生有害影响的潜在机制。

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