Departamento de Química Biológica, Universidade Regional do Cariri, Crato, Ceará, Brasil.
Centro de Ciências Agrárias e da Biodiversidade, Universidade Federal do Cariri, Crato, Ceará, Brasil.
Fundam Clin Pharmacol. 2023 Feb;37(1):163-173. doi: 10.1111/fcp.12830. Epub 2022 Sep 16.
Chalcones are present in a wide variety of plants, having in their structure two aromatic rings that are linked together by a chain composed of three carbon atoms with α, β-unsaturated to carbonyl system. Bacteria have several drug resistance mechanisms, among them the efflux pump; this mechanism, when active, is able to expel different compounds from inside bacterial cells. Several efflux pumps have already been identified for Staphylococcus aureus bacteria, including MepA and NorA. Many chalcones have been isolated and identified with various activities, such as antimicrobial. In view of this, this article aimed to evaluate the antibiotic modifying effect of chalcone (E)-1-(2-hydroxyphenyl)-3-(3-nitrophenyl)prop-2-en-1-one against S. aureus carrier of NorA and MepA efflux pump. Regarding the antibiotic, there was a synergism when associated with ciprofloxacin in SA-K2068 strain, showing this chalcone as an alternative to reverse the resistance to this medicine. The physicochemical properties calculated were fundamental in the description of the predicted pharmacokinetic properties. Despite the mutagenic risk caused by the metabolic activation of nitrochalcone, it is possible to notice a pharmacological principle in a longer half-life for the performance of biological activities. The compound has a good bioavailability, as it is highly absorbed in the intestine and easily transported by plasma proteins, in addition to not presenting neurotoxic, hepatotoxic, and cardiotoxic damage.
查耳酮存在于广泛的植物中,其结构中包含两个芳环,通过由三个碳原子组成的链连接在一起,该链具有α、β-不饱和的羰基系统。细菌具有多种耐药机制,其中包括外排泵;当该机制活跃时,它能够将不同的化合物从细菌细胞内部排出。已经鉴定出许多金黄色葡萄球菌的外排泵,包括 MepA 和 NorA。已经分离和鉴定了许多查尔酮,具有各种活性,如抗菌。鉴于此,本文旨在评估查尔酮(E)-1-(2-羟基苯基)-3-(3-硝基苯基)-2-烯-1-酮对携带 NorA 和 MepA 外排泵的金黄色葡萄球菌的抗生素修饰作用。对于抗生素,当与环丙沙星在 SA-K2068 菌株中联合使用时,存在协同作用,表明这种查尔酮是逆转对这种药物的耐药性的一种替代方法。计算出的物理化学性质对于描述预测的药代动力学性质至关重要。尽管硝基查尔酮的代谢激活会带来致突变风险,但可以注意到在更长的半衰期下表现出药理作用的原则。该化合物具有良好的生物利用度,因为它在肠道中高度吸收,并且容易被血浆蛋白转运,此外,它不会引起神经毒性、肝毒性和心脏毒性损伤。