• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

选择性环氧化酶-2抑制剂与ω-3脂肪酸对大鼠内毒素诱导性牙周炎的单独及联合作用

Individual and combined effects of selective cyclooxygenase-2 inhibitor and omega-3 fatty acid on endotoxin-induced periodontitis in rats.

作者信息

Vardar Saynur, Buduneli Eralp, Baylas Haluk, Berdeli Afig Hüseyinov, Buduneli Nurcan, Atilla Gül

机构信息

School of Dentistry, Department of Periodontology, Ege University, Izmir, Turkey.

出版信息

J Periodontol. 2005 Jan;76(1):99-106. doi: 10.1902/jop.2005.76.1.99.

DOI:10.1902/jop.2005.76.1.99
PMID:15830643
Abstract

BACKGROUND

The present study was planned to evaluate the individual and combined effects of selective cyclooxygenase-2 (COX-2) inhibitor, celecoxib, and omega-3 fatty acid on the gingival tissue levels of prostaglandin E2 (PGE2), prostaglandin F2alpha (PGF2alpha), leukotriene B4 (LTB4), and platelet activating factor (PAF) in endotoxin-induced periodontitis in rats.

METHODS

Experimental periodontitis was induced by repeated injection of Escherichia coli endotoxin (LPS). Forty-four adult male Sprague-Dawley rats were divided into five study groups: saline control, LPS, celecoxib, omega-3 fatty acid, and combination celecoxib and omega-3 fatty acid. Celecoxib and omega-3 fatty acid were given either as a single agent or as a combination therapy during 14 days of the study period. At the end of the 2-week protocol, the rats were sacrificed, the gingival tissues were dissected and extracted, and the extracts were analyzed for PGE2, PGF2alpha, and LTB4 levels by enzyme immunoassay and for PAF levels by radioimmunoassay. The defleshed jaws were analyzed morphometrically for alveolar bone loss. Data were evaluated statistically by using parametric tests.

RESULTS

LPS injection resulted in significantly more bone loss than the saline controls (P<0.05) and significant elevations in the gingival tissue levels of all the analyzed mediators except PGF2alpha. Individual administration of celecoxib revealed significant reductions in PGE2 and PAF levels (P <0.05), while omega-3 fatty acid provided significant reduction in PGE2, PGF2alpha, and LTB4 levels compared to the LPS group (P <0.05). Combined administration of celecoxib and omega-3 fatty acid exhibited significantly lower values than those of the LPS group in all the analyzed membrane phospholipid mediators (P <0.05), which approximated the levels in the saline control group (P>0.05).

CONCLUSIONS

The results of the present study indicate that celecoxib and omega-3 fatty acid, when used individually, show a rather partial effect on the control of the analyzed mediators, but when combined they show a synergic effect and provide significant reductions in the gingival tissue levels of PGE2, PGF2alpha, LTB4, and PAF in LPS-induced experimental periodontitis. These findings may pioneer further clinical human studies investigating the possible place of celecoxib and omega-3 fatty acid in periodontal treatment.

摘要

背景

本研究旨在评估选择性环氧化酶 -2(COX -2)抑制剂塞来昔布和ω-3脂肪酸对大鼠内毒素诱导的牙周炎中牙龈组织前列腺素E2(PGE2)、前列腺素F2α(PGF2α)、白三烯B4(LTB4)和血小板活化因子(PAF)水平的单独及联合作用。

方法

通过反复注射大肠杆菌内毒素(LPS)诱导实验性牙周炎。44只成年雄性Sprague-Dawley大鼠被分为五个研究组:生理盐水对照组、LPS组、塞来昔布组、ω-3脂肪酸组以及塞来昔布与ω-3脂肪酸联合组。在为期14天的研究期间,塞来昔布和ω-3脂肪酸分别作为单一药物或联合疗法给药。在为期2周的实验方案结束时,处死大鼠,解剖并提取牙龈组织,通过酶免疫测定法分析提取物中PGE2、PGF2α和LTB4的水平,通过放射免疫测定法分析PAF的水平。对去除软组织的颌骨进行形态计量分析以评估牙槽骨吸收情况。数据采用参数检验进行统计学评估。

结果

注射LPS导致的骨吸收明显多于生理盐水对照组(P<0.05),并且除PGF2α外,所有分析的介质在牙龈组织中的水平均显著升高。单独给予塞来昔布可使PGE2和PAF水平显著降低(P<0.05),而与LPS组相比,ω-3脂肪酸可使PGE2、PGF2α和LTB4水平显著降低(P<0.05)。塞来昔布与ω-3脂肪酸联合给药后,所有分析的膜磷脂介质水平均显著低于LPS组(P<0.05),接近生理盐水对照组水平(P>0.05)。

结论

本研究结果表明,塞来昔布和ω-3脂肪酸单独使用时,对所分析介质的控制作用较为有限,但联合使用时具有协同作用,可使LPS诱导的实验性牙周炎中牙龈组织的PGE2、PGF2α、LTB4和PAF水平显著降低。这些发现可能为进一步开展临床人体研究以探究塞来昔布和ω-3脂肪酸在牙周治疗中的潜在作用奠定基础。

相似文献

1
Individual and combined effects of selective cyclooxygenase-2 inhibitor and omega-3 fatty acid on endotoxin-induced periodontitis in rats.选择性环氧化酶-2抑制剂与ω-3脂肪酸对大鼠内毒素诱导性牙周炎的单独及联合作用
J Periodontol. 2005 Jan;76(1):99-106. doi: 10.1902/jop.2005.76.1.99.
2
Therapeutic versus prophylactic plus therapeutic administration of omega-3 fatty acid on endotoxin-induced periodontitis in rats.ω-3脂肪酸治疗性给药与预防性加治疗性给药对大鼠内毒素诱导的牙周炎的影响
J Periodontol. 2004 Dec;75(12):1640-6. doi: 10.1902/jop.2004.75.12.1640.
3
Effects of combined systemic administration of low-dose doxycycline and alendronate on endotoxin-induced periodontitis in rats.低剂量强力霉素与阿仑膦酸钠联合全身给药对大鼠内毒素诱导性牙周炎的影响。
J Periodontol. 2004 Nov;75(11):1516-23. doi: 10.1902/jop.2004.75.11.1516.
4
Effects of selective cyclooxygenase-2 inhibitor and omega-3 fatty acid on serum interleukin-1beta, osteocalcin, and C-reactive protein levels in rats.选择性环氧化酶-2抑制剂和ω-3脂肪酸对大鼠血清白细胞介素-1β、骨钙素和C反应蛋白水平的影响
J Periodontol. 2006 Apr;77(4):657-63. doi: 10.1902/jop.2006.050164.
5
The effects of selective COX-2 inhibitor/celecoxib and omega-3 fatty acid on matrix metalloproteinases, TIMP-1, and laminin-5gamma2-chain immunolocalization in experimental periodontitis.选择性环氧化酶-2抑制剂/塞来昔布和ω-3脂肪酸对实验性牙周炎中基质金属蛋白酶、基质金属蛋白酶组织抑制因子-1及层粘连蛋白-5γ2链免疫定位的影响
J Periodontol. 2008 Oct;79(10):1934-41. doi: 10.1902/jop.2008.080001.
6
Effects of selective cyclooxygenase-2 inhibition on gingival tissue levels of prostaglandin E2 and prostaglandin F2alpha and clinical parameters of chronic periodontitis.选择性环氧化酶-2抑制对慢性牙周炎患者牙龈组织中前列腺素E2和前列腺素F2α水平及临床参数的影响
J Periodontol. 2003 Jan;74(1):57-63. doi: 10.1902/jop.2003.74.1.57.
7
Dietary supplementation of omega-3 fatty acid and circulating levels of interleukin-1beta, osteocalcin, and C-reactive protein in rats.大鼠中ω-3脂肪酸的膳食补充与白细胞介素-1β、骨钙素和C反应蛋白的循环水平
J Periodontol. 2006 May;77(5):814-20. doi: 10.1902/jop.2006.050214.
8
Matrix metalloproteinases, tissue inhibitor of matrix metalloproteinase-1, and laminin-5 gamma2 chain immunolocalization in gingival tissue of endotoxin-induced periodontitis in rats: effects of low-dose doxycycline and alendronate.基质金属蛋白酶、基质金属蛋白酶组织抑制剂-1和层粘连蛋白-5γ2链在大鼠内毒素诱导的牙周炎牙龈组织中的免疫定位:低剂量强力霉素和阿仑膦酸盐的作用
J Periodontol. 2007 Jan;78(1):127-34. doi: 10.1902/jop.2007.050451.
9
Effects of Selective Cyclooxygenase-2 Inhibitor and Omega-3 Fatty Acid on Serum Interleukin-1β, Osteocalcin, and C-Reactive Protein Levels in Rats.
J Periodontol. 2006 Apr;77(4):657-663. doi: 10.1902/jop.2006.050164.
10
Systemic low-dose doxycycline and alendronate administration and serum interleukin-1beta, osteocalcin, and C-reactive protein levels in rats.大鼠全身低剂量强力霉素和阿仑膦酸盐给药与血清白细胞介素-1β、骨钙素及C反应蛋白水平
J Periodontol. 2005 Nov;76(11):1927-33. doi: 10.1902/jop.2005.76.11.1927.

引用本文的文献

1
Impact of health and lifestyle food supplements on periodontal tissues and health.健康与生活方式类食品补充剂对牙周组织和健康的影响。
Periodontol 2000. 2022 Oct;90(1):146-175. doi: 10.1111/prd.12455. Epub 2022 Aug 2.
2
Establishing an osteoimmunomodulatory coating loaded with aspirin on the surface of titanium primed with phase-transited lysozyme.在经相转变溶菌酶预处理的钛表面上构建载阿司匹林的骨免疫调节涂层。
Int J Nanomedicine. 2019 Feb 5;14:977-991. doi: 10.2147/IJN.S190766. eCollection 2019.
3
The efficacy and prophylactic characteristics of omega-3 fatty acids in experimental gingivitis in rats.
ω-3 脂肪酸在大鼠实验性牙龈炎中的功效和预防特性。
Iran J Basic Med Sci. 2014 Feb;17(2):87-92.
4
Resolvin D1 protects periodontal ligament.解析度蛋白 D1 可保护牙周韧带。
Am J Physiol Cell Physiol. 2013 Sep 15;305(6):C673-9. doi: 10.1152/ajpcell.00242.2012. Epub 2013 Jul 17.
5
Dental tissue repair: novel models for tissue regeneration strategies.牙齿组织修复:组织再生策略的新型模型
Open Dent J. 2012;6:214-9. doi: 10.2174/1874210601206010214. Epub 2012 Dec 28.
6
Host modulation by therapeutic agents.治疗药物对宿主的调节作用。
J Pharm Bioallied Sci. 2012 Aug;4(Suppl 2):S256-9. doi: 10.4103/0975-7406.100244.
7
Levels of gingival tissue platelet activating factor after conventional and regenerative periodontal surgery.传统牙周手术和再生性牙周手术后牙龈组织血小板活化因子的水平
Clin Oral Investig. 2007 Dec;11(4):369-76. doi: 10.1007/s00784-007-0123-2. Epub 2007 May 24.
8
Novel host response therapeutic approaches to treat periodontal diseases.治疗牙周疾病的新型宿主反应治疗方法。
Periodontol 2000. 2007;43:294-315. doi: 10.1111/j.1600-0757.2006.00166.x.