Jia Fang, Sun Mei-Yang, Zhang Xiang-Jun, Zhou Xue-Zhang
Key Laboratory of Ministry of Education for Conservation and Utilization of Special Biological Resources of Western China, Yinchuan 750021, China.
Jilin Provincial Cancer Hospital, Changchun 130000, China.
Chin Herb Med. 2020 Sep 10;12(4):390-398. doi: 10.1016/j.chmed.2020.02.006. eCollection 2020 Oct.
To investigate the mechanism by which total alkaloids of (TASA) and matrine (MT) impair biofilm to increase the susceptibility of () to ciprofloxacin.
The minimum biofilm inhibitory concentration (mBIC) was determined using a 2-fold dilution method. Structure of biofilm of was examined by Confocal Laser Scanning Microscope (CLSM). The cellular reactive oxygen species (ROS) was determined using a DCFH-DA assay. The key factors related to the regulation of ROS were accessed using respective kits.
TASA and MT were more beneficial to impair biofilm of than ciprofloxacin (CIP) ( < 0.05). TASA and MT were not easily developed resistance to biofilm-producing . The mBIC of CIP decreased by 2-6-fold following the treatment of sub-biofilm inhibitory concentration (sub-BIC) TASA and MT, whereas the mBIC of CIP increased by 2-fold following a treatment of sub-BIC CIP from the first to sixth generations. TASA and MT can improve the production of ROS in biofilm-producing . The ROS content was decreased 23%-33% following the treatment of sub-mBIC CIP, whereas ROS content increased 7%-24% following treatment with TASA + CIP and MT + CIP combination from the first to sixth generations. Nitric oxide (NO) as a ROS, which was consistent with the previously confirmed relationship between ROS and drug resistance. Related regulatory factors-superoxide dismutase (SOD) and glutathione peroxidase (GSH) could synergistically maintain the redox balance .
TASA and MT enhanced reactive oxygen species to restore the susceptibility of to ciprofloxacin.
探讨[具体药物名称]总生物碱(TASA)和苦参碱(MT)破坏生物膜以增加[具体细菌名称]对环丙沙星敏感性的机制。
采用二倍稀释法测定最低生物膜抑制浓度(mBIC)。通过共聚焦激光扫描显微镜(CLSM)观察[具体细菌名称]生物膜的结构。使用DCFH-DA检测法测定细胞活性氧(ROS)。使用相应试剂盒检测与ROS调节相关的关键因素。
TASA和MT比环丙沙星(CIP)更有利于破坏[具体细菌名称]的生物膜(P<0.05)。TASA和MT不易对产生物膜的[具体细菌名称]产生耐药性。在亚生物膜抑制浓度(亚BIC)的TASA和MT处理后,CIP的mBIC降低了2至6倍,而在亚BIC的CIP处理第一代至第六代后,CIP的mBIC增加了2倍。TASA和MT可提高产生物膜的[具体细菌名称]中ROS的产生。在亚mBIC的CIP处理后,ROS含量降低了23%至33%,而在第一代至第六代用TASA+CIP和MT+CIP组合处理后,ROS含量增加了7%至24%。一氧化氮(NO)作为一种ROS,这与先前证实的ROS与耐药性之间的关系一致。相关调节因子——超氧化物歧化酶(SOD)和谷胱甘肽过氧化物酶(GSH)可协同维持氧化还原平衡。
TASA和MT增强活性氧以恢复[具体细菌名称]对环丙沙星的敏感性。