Department of Epidemic Disease Research, Institute for Research and Medical Consultations (IRMC), Imam Abdulrahman Bin Faisal University, 31441 Dammam, Saudi Arabia.
Department Biochemistry, Faculty of Medicine, Aligarh Muslim University, Aligarh, Uttar Pradesh 202002, India.
J Infect Public Health. 2023 Sep;16(9):1443-1459. doi: 10.1016/j.jiph.2023.07.016. Epub 2023 Jul 26.
Tuberculosis is a disease of poverty, discrimination, and socioeconomic burden. Epidemiological studies suggest that the mortality and incidence of tuberculosis are unacceptably higher worldwide. Genomic mutations in embCAB, embR, katG, inhA, ahpC, rpoB, pncA, rrs, rpsL, gyrA, gyrB, and ethR contribute to drug resistance reducing the susceptibility of Mycobacterium tuberculosis to many antibiotics. Additionally, treating tuberculosis with antibiotics also poses a serious risk of hepatotoxicity in the patient's body. Emerging data on drug-induced liver injury showed that anti-tuberculosis drugs remarkably altered levels of hepatotoxicity biomarkers. The review is an attempt to explore the anti-mycobacterial potential of selected, commonly available, and well-known phytocompounds and extracts of medicinal plants against strains of Mycobacterium tuberculosis. Many studies have demonstrated that phytocompounds such as flavonoids, alkaloids, terpenoids, and phenolic compounds have antibacterial action against Mycobacterium species, inhibiting the bacteria's growth and replication, and sometimes, causing cell death. Phytocompounds act by disrupting bacterial cell walls and membranes, reducing enzyme activity, and interfering with essential metabolic processes. The combination of these processes reduces the overall survivability of the bacteria. Moreover, several phytochemicals have synergistic effects with antibiotics routinely used to treat TB, improving their efficacy and decreasing the risk of resistance development. Interestingly, phytocompounds have been presented to reduce isoniazid- and ethambutol-induced hepatotoxicity by reversing serum levels of AST, ALP, ALT, bilirubin, MDA, urea, creatinine, and albumin to their normal range, leading to attenuation of inflammation and hepatic necrosis. As a result, phytochemicals represent a promising field of research for the development of new TB medicines.
结核病是一种与贫困、歧视和社会经济负担有关的疾病。流行病学研究表明,结核病的死亡率和发病率在全球范围内高得令人无法接受。embCAB、embR、katG、inhA、ahpC、rpoB、pncA、rrs、rpsL、gyrA、gyrB 和 ethR 中的基因突变导致结核分枝杆菌对许多抗生素的耐药性降低。此外,用抗生素治疗结核病也会使患者身体面临严重的肝毒性风险。关于药物性肝损伤的新数据表明,抗结核药物显著改变了肝毒性生物标志物的水平。本综述试图探讨选定的、常见的、众所周知的植物化合物和药用植物提取物对结核分枝杆菌菌株的抗分枝杆菌潜力。许多研究表明,植物化合物如类黄酮、生物碱、萜类化合物和酚类化合物对分枝杆菌属具有抗菌作用,抑制细菌的生长和复制,有时甚至导致细胞死亡。植物化合物通过破坏细菌细胞壁和细胞膜、降低酶活性以及干扰重要代谢过程来发挥作用。这些过程的综合作用降低了细菌的整体存活率。此外,一些植物化学物质与常规用于治疗结核病的抗生素具有协同作用,提高了它们的疗效,降低了耐药性发展的风险。有趣的是,植物化合物已被证明可以通过将 AST、ALP、ALT、胆红素、MDA、尿素、肌酐和白蛋白的血清水平逆转到正常范围来减少异烟肼和乙胺丁醇引起的肝毒性,从而减轻炎症和肝坏死。因此,植物化学物质代表了开发新的结核病药物的一个有前途的研究领域。