Department of Pharmacology and Therapeutics, College of Medicine and Health Sciences, United Arab Emirates University, Al Ain P.O. Box 15551, United Arab Emirates.
Department of Biotechnology, School of Engineering and Technology (SET), Sharda University, Greater Noida 201310, UP, India.
Int J Mol Sci. 2022 Sep 10;23(18):10528. doi: 10.3390/ijms231810528.
Doxorubicin (DOX) is a well-known and effective antineoplastic agent of the anthracycline family. But, multiple organ toxicities compromise its invaluable therapeutic usage. Among many toxicity types, nephrotoxicity is one of the major concerns. In recent years many approaches, including bioactive agents of natural origin, have been explored to provide protective effects against chemotherapy-related complications. α-Bisabolol is a naturally occurring monocyclic sesquiterpene alcohol identified in the essential oils of various aromatic plants and possesses a wide range of pharmacological properties such as antioxidant, anti-inflammatory, analgesic, cardioprotective, antibiotic, anti-irritant, and anticancer activities. The present study aimed to evaluate the effects of α-Bisabolol on DOX-induced nephrotoxicity in Wistar male albino rats. Nephrotoxicity was induced in rats by injecting a single dose of DOX (12.5 mg/kg, i.p.), and the test compound, α-Bisabolol (25 mg/kg) was administered intraperitoneally along with DOX as a co-treatment daily for 5 days. DOX-injected rats showed reduction in body weight along with a concomitant fall in antioxidants and increased lipid peroxidation in the kidney. DOX-injection also increased levels/expressions of proinflammatory cytokines namely tumor necrosis factor-α (TNF-α), interleukin-6 (IL-6), and interleukin-1β (IL-1β) and inflammatory mediators like inducible nitric oxide synthase (iNOS) and cyclooxygenase-2 (COX-2) and activated nuclear factor kappa-B (NF-κB)/mitogen-activated protein kinases (MAPK) signaling in the kidney tissues. DOX also triggered apoptotic cell death, evidenced by the increased expression of pro-apoptotic markers like BCL2-Associated X Protein (Bax), cleaved caspase-3, caspase- 9, and cytochrome-C) and a decrease in the expressions of anti-apoptotic markers namely B-cell lymphoma 2 (Bcl2) and B-cell lymphoma-extra large (Bcl-xL) in the kidney. These biochemical alterations were additionally supported by light microscopic findings, which revealed structural alterations in the kidney. However, treatment with α-Bisabolol prevented body weight loss, restored antioxidants, mitigated lipid peroxidation, and inhibited the rise in proinflammatory cytokines, as well as favorably modulated the expressions of NF-κB/MAPK signaling and apoptosis markers in DOX-induced nephrotoxicity. Based on the results observed, it can be concluded that α-Bisabolol has potential to attenuate DOX-induced nephrotoxicity by inhibiting oxidative stress and inflammation mediated activation of NF-κB/MAPK signaling alongwith intrinsic pathway of apoptosis in rats. The study findings are suggestive of protective potential of α-Bisabolol in DOX associated nephrotoxicity and this could be potentially useful in minimizing the adverse effects of DOX and may be a potential agent or adjuvant for renal protection.
阿魏醇是一种天然存在的单环倍半萜醇,存在于各种芳香植物的精油中,具有广泛的药理活性,如抗氧化、抗炎、镇痛、心脏保护、抗生素、抗刺激和抗癌活性。本研究旨在评估阿魏醇对 DOX 诱导的 Wistar 雄性白化大鼠肾毒性的影响。通过单次注射 DOX(12.5mg/kg,ip)诱导大鼠肾毒性,并用 DOX 作为共处理,每天腹膜内给予测试化合物阿魏醇(25mg/kg)共 5 天。DOX 注射大鼠体重减轻,同时抗氧化剂降低,肾脏脂质过氧化增加。DOX 注射还增加了促炎细胞因子如肿瘤坏死因子-α(TNF-α)、白细胞介素-6(IL-6)和白细胞介素-1β(IL-1β)以及炎症介质如诱导型一氧化氮合酶(iNOS)和环氧化酶-2(COX-2)和激活核因子 kappa-B(NF-κB)/丝裂原激活蛋白激酶(MAPK)信号在肾脏组织中的水平/表达。DOX 还触发了细胞凋亡死亡,证据是促凋亡标志物如 BCL2 相关 X 蛋白(Bax)、裂解的 caspase-3、caspase-9 和细胞色素-C 的表达增加,以及抗凋亡标志物如 B 细胞淋巴瘤 2(Bcl2)和 B 细胞淋巴瘤-extra large(Bcl-xL)在肾脏中的表达减少。这些生化变化还得到了光镜发现的支持,这些发现揭示了肾脏的结构改变。然而,阿魏醇的治疗可防止体重减轻,恢复抗氧化剂,减轻脂质过氧化,并抑制 DOX 诱导的肾毒性中促炎细胞因子的升高,同时有利地调节 NF-κB/MAPK 信号和凋亡标志物的表达。根据观察到的结果,可以得出结论,阿魏醇通过抑制氧化应激和炎症介导的 NF-κB/MAPK 信号激活以及大鼠内在凋亡途径,具有减轻 DOX 诱导的肾毒性的潜力。研究结果表明,阿魏醇在 DOX 相关肾毒性中具有保护潜力,这可能有助于最小化 DOX 的不良反应,并可能成为肾脏保护的潜在药物或佐剂。