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新型益生菌储存介质中成纤维细胞的活力。

Viability of fibroblasts in a novel probiotic storage media.

机构信息

Department of Paediatric Dentistry, School of Dentistry, Yeditepe University, Istanbul, Turkey.

出版信息

Dent Traumatol. 2010 Oct;26(5):383-7. doi: 10.1111/j.1600-9657.2010.00914.x.

Abstract

A number of storage media have been investigated as to their ability to maintain the viability of the periodontal ligament (PDL) cells and thus to permit longer extra-alveolar periods prior to replantation of avulsed teeth. The aim of the present in vitro study was to evaluate the number of viable PDL cells of avulsed teeth treated by Hank's Balanced Salt Solutions (HBSS), saline, a novel probiotic solution and milk. Thirty-six freshly extracted single-rooted human teeth with closed apices were divided into one of the four experimental groups and two control groups (N = 6 each). The positive and negative controls corresponded to 0 min and an 8-h dry time respectively. Following extraction, the coronal 3 mm of PDL tissue was scraped with a #15 scalpel to remove cells that might have been damaged. The experimental teeth were dried for 30 min followed by a 45 min immersion in one of the four experimental media. Each experimental tooth, after drying and soaking, was incubated for 30 min with a 2.5 ml solution of 0.2 mg ml(-1) of collagenase CLS II and a 2.4 mg ml(-1) solution of dispase grade II in phosphate buffer saline (PBS). The cells were then labelled with 0.4% Trypan blue for determination of viability. The teeth stored in positive control demonstrated the highest number of viable PDL cells followed in rank order by HBSS, saline, Lactobacillus reuteri solution and milk. There was no significant difference in the number of viable PDL cells between HBSS, milk, L. reuteri solution and saline. Within the parameters of this study, it appears that probiotic may be able to maintain PDL cell viability as HBSS, milk, or saline.

摘要

已经研究了多种储存介质,以评估它们维持牙周膜(PDL)细胞活力的能力,从而可以在再植脱位牙之前延长牙槽外时间。本体外研究的目的是评估用 Hank's 平衡盐溶液(HBSS)、生理盐水、新型益生菌溶液和牛奶处理的脱位牙的活 PDL 细胞数量。将 36 颗刚提取的根尖闭合的单根人牙分为四个实验组和两个对照组(每组 N = 6)。阳性和阴性对照分别对应于 0 分钟和 8 小时干燥时间。提取后,用 #15 手术刀刮除 3 毫米的冠部 PDL 组织,以去除可能受损的细胞。实验牙干燥 30 分钟后,在四种实验介质之一中浸泡 45 分钟。每个实验牙在干燥和浸泡后,用 2.5 ml 浓度为 0.2 mg/ml 的 II 型胶原酶 CLS 和 2.4 mg/ml 的 II 型Dispase 溶液在磷酸盐缓冲盐水(PBS)中孵育 30 分钟。然后用 0.4%台盼蓝标记细胞以确定活力。阳性对照组储存的牙齿表现出最高数量的活 PDL 细胞,其次是 HBSS、生理盐水、鼠李糖乳杆菌溶液和牛奶。HBSS、牛奶、L. reuteri 溶液和生理盐水之间活 PDL 细胞数量无显着差异。在本研究的参数范围内,益生菌似乎能够像 HBSS、牛奶或生理盐水一样维持 PDL 细胞活力。

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