Anethole, a Medicinal Plant Compound, Decreases the Production of Pro-Inflammatory TNF-α and IL-1β in a Rat Model of LPS-Induced Periodontitis

被引:1
|
作者
Moradi, Janet [1 ]
Abbasipour, Fatemeh [1 ,2 ]
Zaringhalam, Jalal [3 ,4 ]
Maleki, Bita [1 ]
Ziaee, Narges [1 ]
Khodadoustan, Amin
Janahmadi, Mahyar [3 ,4 ]
机构
[1] Hamadan Univ Med Sci, Sch Dent, Dept Periodont, Hamadan, Iran
[2] Semnan Unvers Med Sci, Fac Dent, Senman, Iran
[3] Shahid Beheshti Univ Med Sci, Neurophysiol Res Ctr NPRC, Tehran, Iran
[4] Shahid Beheshti Univ Med Sci, Sch Med, Dept Physiol, Tehran, Iran
来源
关键词
Trans-anethole; LPS-induced periodontitis; Ketoprofen; Anti-inflammatory; IL-1; beta; TNF-alpha; FACTOR-KAPPA-B; INVOLVEMENT; DERIVATIVES; INHIBITION; RESPONSES; CHANNELS; DISEASES; EUGENOL; CA2+;
D O I
暂无
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Periodontitis (PD) is known to be one of most prevalent worldwide chronic inflammatory diseases. There are several treatments including antibiotics for PD; however, since drug resistance is an increasing problem, new drugs particularly derived from plants with fewer side effects are required. The effects of trans-anethole on IL-1 beta and TNF-alpha level in a rat model of PD were investigated and compared to ketoprofen. Eschericia coli lipopolysaccharide (LPS, 30 mu g) was injected bilaterally into the palatal gingiva (3 mu L/site) between the upper first and second molars every two days for 10 days in anesthetized rats. Administration of either trans-anethole (10 or 50 mg/Kg, i.p.) or ketoprofen (10 mg/Kg, i.p.) was started 20 minute before LPS injection and continued for 10 days. Then, IL-1 beta and TNF-alpha levels were measured in blood samples by ELISA at day 0 (control) and at day 10. Anethole at both concentrations significantly suppressed IL-1 beta and TNF-alpha production when compared to LPS-treated rats. The suppressive effects of anethole on LPS-induced proinflammatory cytokines were almost similar as seen with ketoprofen. In conclusion, the present results suggest that anethole may have a potent inhibitory effect on PD through suppression of pro-inflammatory molecules; therefore it could be a novel therapeutic strategy for PD.
引用
收藏
页码:1319 / 1325
页数:7
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