摘要
目的探讨双岐杆菌减轻盐酸环丙沙星所致小鼠血清睾酮下降。方法成年雄性昆明小鼠24只,随机分为灌胃0.9%Nacl溶液6 d(Sal6)组、灌胃抗生素6 d(A_6)组、灌胃抗生素6 d后灌胃0.9%Nacl溶液6 d(A_6+Sal_6)组和灌胃抗生素6 d后灌胃双岐杆菌6 d(A_6+P_6)组,每组6只。放免法检测血清睾酮含量;Western blot检测核转录相关因子2(Nrf2)、血红素氧化酶(HO-1)和4羟基壬烯醛(4-HNE)蛋白的表达;real-time PCR检测类固醇激素合成急性调控蛋白(St AR)、胆固醇侧链裂解酶(P450scc)和Nrf2 mRNA的表达;免疫组织化学检测4-HNE蛋白的表达。结果 A_6组血清睾酮水平明显低于Sal6组(P<0.001),A_6+P_6明显高于A_6(P<0.001)和A_6+Sal_6组(P<0.01);睾酮合成酶也表现为同样的变化趋势,A_6组St AR mRNA明显低于Sal6组(P<0.001),A_6+P_6组明显高于A_6组(P<0.01)和A_6+Sal_6组(P<0.01);P450scc mRNA明显低于Sal6组(P<0.001),A_6+P_6组明显高于A_6组(P<0.001)和A_6+Sal_6组(P<0.05);A_6组Nrf2表达明显低于Sal6组(P<0.01),A_6+P_6组明显高于A_6组(P<0.01)和A_6+Sal_6组(P<0.05);A_6组4-HNE的表达明显高于Sal6组(P<0.001),A_6+P_6组明显低于A_6组(P<0.01)和A_6+Sal_6组(P<0.05)。结论双岐杆菌可能是通过调节Nrf2通路,上调抗氧化酶蛋白水平并下调氧化损伤产物,进而减轻盐酸环丙沙星所致小鼠血清睾酮水平下调作用的。
Objective To explore if bacillus bifidus relieve CPFX-induced testosterone reduction in mouse testes. Methods Twenty-four male miees were divided into 4 groups, then administered saline for 6 days (Sal6 group) , CPFX for 6 days (A6 group), CPFX for 6 days followed by bifidobaeteria treatment for the next 6 days (A6+P6 group) , CPFX for 6 days and then saline for the next 6 days ( A6 +Sal6 group). We detected serum levels of testosterone by RIA, as well as levels of steroidogenic enzymes mRNA [ cholesterol side-chain cleavage enzyme (P450scc) and steroidogenic acute regulatory protein (STAR) ] and NF-E2-related factor2 (Nff2) mRNA in testes by real-time PCR, Nrf2, heine oxygenase-1 (HO-1), and 4-hydroxy-2-nonenal (4-HNE) by Western blot and 4-HNE by Immunohistochemistry. Results The A6 group had significantly lower serum testosterone levels compared with the Sal6 group (P〈0. 001), the A6+P6 group had significantly higher compared with the A6(P〈0. 001 ) and A6+Sal6 groups (P〈0. 01 ). The A6 group had significantly lower StAR mRNA compared with the Sal6 group (P〈 0. 001 ), the A6+P6 group had significantly higher level compared with the A6(P〈0. 01) and A6+Sal6 groups (P〈 0.01 ). The A6 group had significantly lower P450sec mRNA as compared with the Sal6 group ( P〈0. 001 ) , the A6 +P6 group had significantly higher compared with the A6(P〈0. 001) and A6+Sal6 groups (P〈0.05). The A6 group had significantly lower Nrf2 compared with the Sal6 group (P〈0. 001 ), the A6 +P6 group had significantly higher compared with the A6 (P〈0. 01 ) and A6+Sal6 groups (P〈0. 05).The A6 group higher 4-HNE expression compared with the Sal6 group, the A6+P6 group had significantly lower compared with the A6(P〈0.01 ) and A6+Sal6 groups (P〈 0. 05). Conclusions Bifidobaeteria the reduction of CPFX-indueed testosterone reduction, and these effects may potentially explained by Nrf2 inflammatory signaling pathway.
出处
《基础医学与临床》
CSCD
2017年第9期1270-1275,共6页
Basic and Clinical Medicine
基金
河北省教育厅高等学校科学技术研究项目(QN2014128)