摘要
目的:研究盐酸小檗碱(Ber)作用于体外培养的人牙周膜细胞(PDLCs),在脂多糖(LPS)刺激下,合成和分泌前列腺素E2(PGE2)、白细胞介素-1β(IL-1β)和白细胞介素-6(IL-6)的变化,初步推断Ber对牙周炎的治疗作用。方法:将体外培养的PDLCs根据加入LPS与否设定为NLPS和LPS两大组,再根据培养液中Ber终浓度0μg/mL、5μg/mL、10μg/mL和20μg/mL将其分为NLPS0、NLPS1、NLPS2、NLPS3以及LPS0、LPS1、LPS2和LPS3共八个组,用ELISA法检测上清液中PGE2、IL-1β和IL-6的浓度。结果:培养48h后,各组PGE2、IL-6和IL-1β有一定的表达量,NLPS各组该三者表达的差异无统计学意义(P>0.05);加入LPS后,LPS0组上清液中PGE2、IL-1β和IL-6表达明显升高,与NLPS各组之间差异具有统计学意义(P<0.05);在加入LPS的同时加入Ber后与LPS0组比较PGE2、IL-1β和IL-6表达明显下降(P<0.05);PGE2表达,LPS各组差异具有统计学意义(P<0.05),其中除LPS3以外,其他LPS组与NLPS各对应组差异具有统计学意义(P<0.05);IL-1β表达,LPS0与其他LPS组差异有统计学意义(P<0.05),而LPS1、LPS2和LPS3之间差异无统计学意义(P>0.05),且该三组与NLPS对应组之间差异无统计学意义(P>0.05);IL-6表达,随着Ber浓度升高,各LPS组表达逐渐降低(P<0.05),且与对应NLPS组差异有统计学意义(P<0.05)。结论:Ber可以抑制LPS刺激体外培养的PDLCs产生的炎性反应。
Objective:To evaluate the effect of Berberine hydrochloride (Ber) on periodontitis by detecting the changes in concentration of postaglandin E2 ( PGE2 ), interleukin - 113 ( IL - 1β ) and interleukin - 6 ( IL - 6 ), which were expressed by homan periodontal ligament cells ( PDLCs ) in vitro after simulated by lipepolysaceharide (LPS). Methods:The PDLCs cultured in vitro were Divided into NLPS groups and LPS groups, then each group were further divided into four subgroups (NLPS0, NLPS1, NLPS2 and NLPS3; LPS0, LPS1, LPS2 and LPS3), according to their different concentration (O/μg/rnL, 5μg/mL, 10/μg/mL and 20/μg/mL) of Ber added. And then detected the concentrations of PGE2, IL - 1β and IL - 6 in the subgroups by ELISA. Results:l:GE2, IL - 1β and 1L - 6 were detected in every subgroup after 48h. There was no statistically difference about the expressions of PGE2, IL- 1βand IL-6 among each NLPS greups(P 〉 0. 05 ). Compared with NLPS groups, the expressions in LPSO increased ( P 〈 0. 05 ). However, after adding Ber, the expressions reduced in LPS groups ( P 〈 0.05 ). There were statistically differences in expressing PGE2 among each TPS groups{ P 〈 O. 05 ). Except LPS3 , no significant differences were recorded among each corresponding LPS and NLPS groupslP 〈 0.05 ). in expressing 1L - 1β, there were statistically difference between the I2cA) and the other LPS groups( P 〈 0.05 ). However, there was no statistically difference among LPS1, LPS2 and LPS3 groups( P 〉 0.05) ; and no statistically difference were found among these three groups and corresponding NLPS groups, too(P 〉 0.05 ). The expressions of IL- 6 in each LPS groups were reduced along with adding Ber (P 〈 0.05 )and there were statistically difference among each corresponding LPS and NLPS groups( P 〈 0.05 ). Conclusions : Ber can inhibit the LPS - stimulated imflammatory responses generated by PDLCs in vitro.
出处
《激光杂志》
CAS
CSCD
北大核心
2013年第1期83-85,共3页
Laser Journal
基金
重庆市自然科学基金(2011BA5013)