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. 2014 Feb;32(1):23-6.
doi: 10.7518/hxkq.2014.01.006.

[Effect of carbon monoxide releasing molecule on experimental periodontitis in rats]

[Article in Chinese]

[Effect of carbon monoxide releasing molecule on experimental periodontitis in rats]

[Article in Chinese]
Lingling Wei et al. Hua Xi Kou Qiang Yi Xue Za Zhi. 2014 Feb.

Abstract

Objective: To evaluate the effects of carbon monoxide releasing molecule-2 (CORM-2) on experimental periodontitis in rats.

Methods: Forty-two Wistar rats were divided into three groups. Rats in the normal group (NL group) did not undergo any procedure, whereas the other rats were ligatured and treated with saline solution (NaCl 0.9%) (LO group) or treated with CORM-2 (10 mg kg(-1) per day) (CO group). A 3-0 silk suture was placed around the mandibular first molars. Rats were sacrificed after 3, 7, and 10 d. Blood samples were collected from all animals for tumor necrosis factor-alpha (TNF-alpha) and interleukin-1beta (IL-1beta) analysis. Changes in alveolar bone levels were measured clinically, and periodontal tissues were histopathologically examined to assess the infiltration of inflammatory cells.

Results: Ligature placement increased alveolar bone loss and inflammatory cell infiltration in periodontal tissue. Alveolar bone loss in CO group was significantly higher than that in NL group, but was lower than that in LO group (P<0.05). The ratio of inflammatory cell infiltration in LO group was significantly higher than that in CO and NL groups, and that in CO group was lower than in LO group (P<0.05). Serum levels of TNF-alpha and IL-1beta in the LO group were significantly higher than those in the CO and NL groups, and those in CO group were lower than in LO group (P<0.05).

Conclusion: Systemic administration of CORM-2 reduced periodontal inflammation and alveolar bone loss in experimental periodontitis in rats.

目的: 研究一氧化碳释放分子(CORM)对大鼠实验性牙周炎的影响。

方法: 将42只健康雄性Wistar大鼠分为正常组(NL组)、牙周炎组(LO组)和一氧化碳干预组(CO组)。NL组不作任何处理;CO及LO组采用牙周丝线结扎法建立牙周炎实验模型;建模当天起CO组经腹腔注射CORM-2,每天10 mg·kg−1,连续10 d,LO组注射等体积生理盐水。分别于结扎3、7、10 d后自心脏抽取静脉血,用酶联免疫吸附测定法检测血清中肿瘤坏死因子-α(TNF-α)和白细胞介素-1β(IL-1β)的质量浓度。10 d后在体视显微镜下测量牙槽骨的吸收高度,并于光镜下观察牙周组织炎症细胞的浸润情况。

结果: 丝线结扎10 d后,LO、CO组牙槽骨的吸收高度均明显大于NL组,而CO组明显小于LO组(P<0.05);LO、CO组炎症细胞浸润指数明显高于NL组,而CO组明显低于LO组(P<0.05)。在同一观察时期内,LO组TNF-α及IL-1β质量浓度均明显高于其他两组,而CO组虽高于NL组,但明显低于LO组(P<0.05)。

结论: CORM-2能有效抑制大鼠实验性牙周炎的炎症细胞浸润和牙槽骨吸收。

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Figures

图 1
图 1. 各组牙槽骨的吸收情况
Fig 1 The alveolar bone loss in different groups 左:NL组;中:LO组;右:CO组;a:釉牙骨质界;b:牙槽嵴顶。
图 2
图 2. 牙周组织炎症细胞的浸润情况 HE
Fig 2 The periodontal inflammatory cell infiltration HE 左:× 10;右:× 20;上:NL组;中:LO组;下:CO组。

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