Institute of Chinese Medicine, The Chinese University of Hong Kong, Shatin, New Territories, Hong Kong.
J Ethnopharmacol. 2011 Sep 1;137(1):767-73. doi: 10.1016/j.jep.2011.06.039. Epub 2011 Jul 1.
Baicalein, the active constituent derived from Scutellaria baicalensis Georgi., has previously been shown to significantly restore the effectiveness of β-lactam antibiotics and tetracycline against methicillin-resistant Staphylococcus aureus (MRSA). With multiple therapeutic benefits, the antibacterial actions of baicalein may also be involved in overcoming other bacterial resistance mechanisms. The aim of the present study was to further investigate antibacterial activities of baicalein in association with various antibiotics against selected Staphylococcus aureus strains with known specific drug resistance mechanisms.
A panel of clinical MRSA strains was used for further confirmation of the antibacterial activities of baicalein. The effect of baicalein on inhibiting the enzymatic activity of a newly discovered MRSA-specific pyruvate kinase (PK), which is essential for Staphylococcus aureus growth and survival was also examined.
In the checkerboard dilution test and time-kill assay, baicalein at 16 μg/ml could synergistically restore the antibacterial actions of ciprofloxacin against the NorA efflux pump overexpressed SA-1199B, but not with the poor NorA substrate, pefloxacin. Moreover, synergistic effects were observed when baicalein was combined with ciprofloxacin against 12 out of 20 clinical ciprofloxacin resistant strains. For MRSA PK studies, baicalein alone could inhibit the enzymatic activity of MRSA PK in a dose-dependent manner.
Our results demonstrated that baicalein could significantly reverse the ciprofloxacin resistance of MRSA possibly by inhibiting the NorA efflux pump in vitro. The inhibition of MRSA PK by baicalein could lead to a deficiency of ATP which might further contribute to the antibacterial actions of baicalein against MRSA.
黄芩素是从黄芩中提取的活性成分,先前已被证明可显著恢复β-内酰胺类抗生素和四环素对耐甲氧西林金黄色葡萄球菌(MRSA)的疗效。具有多种治疗益处,黄芩素的抗菌作用也可能涉及克服其他细菌耐药机制。本研究的目的是进一步研究黄芩素与各种抗生素联合使用对具有已知特定药物耐药机制的选定金黄色葡萄球菌菌株的抗菌活性。
使用一组临床 MRSA 菌株进一步确认黄芩素的抗菌活性。还研究了黄芩素对新发现的 MRSA 特异性丙酮酸激酶(PK)的酶活性的抑制作用,该酶对金黄色葡萄球菌的生长和存活至关重要。
在棋盘稀释试验和时间杀伤试验中,黄芩素在 16μg/ml 时可协同增强环丙沙星对过表达 NorA 外排泵的 SA-1199B 的抗菌作用,但对差的 NorA 底物培氟沙星则不行。此外,当黄芩素与环丙沙星联合使用时,对 20 株临床环丙沙星耐药株中的 12 株表现出协同作用。对于 MRSA PK 研究,黄芩素本身可以以剂量依赖性方式抑制 MRSA PK 的酶活性。
我们的结果表明,黄芩素可以通过体外抑制 NorA 外排泵显著逆转 MRSA 对环丙沙星的耐药性。黄芩素对 MRSA PK 的抑制作用可能导致 ATP 缺乏,这可能进一步有助于黄芩素对 MRSA 的抗菌作用。