Sari Rima Parwati, Revianti Syamsulina, Andriani Dwi, Prananingrum Widyasri, Rahayu Retno Pudji, Sudjarwo Sri Agus
Department of Oral Biology, Faculty of Dentistry, Universitas Hang Tuah, Surabaya, Indonesia.
Department of Biomaterial, Faculty of Dentistry, Universitas Hang Tuah, Surabaya, Indonesia.
Eur J Dent. 2021 May;15(2):228-235. doi: 10.1055/s-0040-1719215. Epub 2021 Jan 28.
This article aimed to investigate the effect of (AG) shell's- scaffold on cluster of differentiation (CD)44 and interleukin-10 (IL-10) expression to decrease osteoclasts in socket healing.
Thirty male Wistar rats were divided into five groups. The lower left incisor was extracted, then given a placebo for group control (K), the treatment group was administered with scaffold from AG shells, and a treatment group with scaffold from blood cockle shell- with the concentration of 0.4, 0.8, and 1.6% (AGSH0.4; AGSH0.8; AGSH1.6). We made a bone graft from a combination of AGSH extract using the freeze-dried method. The socket was sutured by silk braid immediately. Third and Seventh days postextraction, animals are killed. CD44 and IL-10 expression were examined with immunohistochemistry, as well as osteoclast was examined with hematoxylin-eosin.
The data were analyzed using a one-way analysis of variance (for CD44 and osteoclast) and Kruskal-Wallis' test (for IL-10) followed by a post hoc test in which the result of < 0.05.
Scaffold from a combination of AGSH increased CD44 expression significantly, which enhanced IL-10 expression thereby decreased the number of osteoclasts in socket healing on days 3 and 7.
Scaffold of AG shell- with a concentration of 0.8% was effective to enhance CD44 and IL-10 expression to decrease osteoclast in socket healing after tooth extraction.
本文旨在研究(AG)贝壳支架对分化簇(CD)44和白细胞介素-10(IL-10)表达的影响,以减少拔牙窝愈合过程中的破骨细胞。
将30只雄性Wistar大鼠分为五组。拔除左下切牙,然后给对照组(K组)给予安慰剂,治疗组给予AG贝壳制成的支架,以及给予浓度为0.4%、0.8%和1.6%的血蚶贝壳制成的支架(AGSH0.4;AGSH0.8;AGSH1.6)。我们使用冻干法将AGSH提取物组合制成骨移植材料。拔牙窝立即用丝线缝合。拔牙后第3天和第7天,处死动物。采用免疫组织化学法检测CD44和IL-10的表达,并用苏木精-伊红染色法检测破骨细胞。
采用单因素方差分析(用于CD(44)和破骨细胞)和Kruskal-Wallis检验(用于IL-10)对数据进行分析,随后进行事后检验,结果(P\lt0.05)。
AGSH组合制成的支架显著增加了CD44的表达,从而增强了IL-10的表达,进而减少了拔牙后第3天和第7天拔牙窝愈合过程中破骨细胞的数量。
浓度为0.8%的AG贝壳支架可有效增强CD44和IL-10的表达,减少拔牙后拔牙窝愈合过程中的破骨细胞。