Division of Radiation Biosciences, Institute of Nuclear Medicine and Allied Sciences (INMAS), DRDO, Delhi, India.
Division of Radioprotective Drug Development Research, Institute of Nuclear Medicine and Allied Sciences (INMAS), DRDO, Delhi, India.
Free Radic Res. 2020 Jul;54(7):497-516. doi: 10.1080/10715762.2020.1805447. Epub 2020 Aug 11.
The present study was conceptualized to delineate radioprotective efficacy of a formulation G-003M (a combination of podophyllotoxin and rutin) against radiation-induced damage to the lymphohematopoietic system of mice. C57BL/6J mice, treated with G-003M 1 h prior to 9 Gy lethal dose, were assessed for reactive oxygen species (ROS)/nitric oxide (NO) generation, antioxidant alterations, Annexin V/PI and TUNEL staining for apoptosis, modulation of apoptotic proteins, cell proliferation, histological alterations in thymus and cell cycle arrest in bone marrow cells. Induction of granulocyte colony-stimulating factor (G-CSF), granulocytes macrophage colony-stimulating factor (GM-CSF), interleukin-IL-6, IL-10, IL-1α, and IL-1β in response to G-003M was also evaluated in different groups of mice. Haematopoietic reconstitution with G-003M was explored by examining endogenous spleen colony-forming units (CFU-S) in irradiated animals. G-003M significantly inhibited ROS/NO, malondialdehyde (MDA) and restored cellular antioxidant glutathione in the thymus of irradiated animals. G-003M pre-treatment significantly ( < 0.001) restrained apoptosis in thymocytes via upregulation of Bcl2 and down-regulation of Bax, p53 and caspase-3. Stimulation of cell proliferation and inhibition of apoptosis by G-003M, restored architecture of thymus in irradiated animals within 30 days as evaluated by histological analysis. G-003M arrested cells at the G2/M phase by inducing reversible cell cycle arrest. Peak expression of G-CSF (45-fold) and IL-6 (60-fold) as well as moderate induction of GM-CSF, IL-10, IL-1α by G-003M helped in haematopoietic recovery of irradiated mice. A higher number of endogenous CFU-S in G-003M pre-treated irradiated mice suggested haematopoietic recovery. Data obtained from the current study affirms that G-003M can be proved as a potential radioprotective agent against radiation damage.
本研究旨在探讨 G-003M(鬼臼毒素和芦丁的组合)对小鼠淋巴血液系统辐射损伤的防护作用。将 C57BL/6J 小鼠用 G-003M 处理 1 小时,然后用 9Gy 致死剂量照射,评估其活性氧(ROS)/一氧化氮(NO)生成、抗氧化改变、凋亡的 Annexin V/PI 和 TUNEL 染色、凋亡蛋白的调节、细胞增殖、胸腺组织学改变和骨髓细胞周期阻滞。还评估了 G-003M 对不同组小鼠粒细胞集落刺激因子(G-CSF)、粒细胞巨噬细胞集落刺激因子(GM-CSF)、白细胞介素-6(IL-6)、IL-10、IL-1α 和 IL-1β 的诱导作用。通过检测照射动物的内源性脾集落形成单位(CFU-S),探讨了 G-003M 对造血重建的影响。G-003M 显著抑制 ROS/NO、丙二醛(MDA)并恢复照射动物胸腺中的细胞抗氧化谷胱甘肽。G-003M 预处理通过上调 Bcl2 和下调 Bax、p53 和 caspase-3 显著(<0.001)抑制胸腺细胞凋亡。G-003M 通过刺激细胞增殖和抑制凋亡,在 30 天内恢复照射动物的胸腺结构,通过组织学分析进行评估。G-003M 通过诱导可逆的细胞周期阻滞将细胞阻滞在 G2/M 期。G-003M 诱导 G-CSF(45 倍)和 IL-6(60 倍)的峰值表达以及 GM-CSF、IL-10 和 IL-1α 的适度诱导有助于照射小鼠的造血恢复。G-003M 预处理照射小鼠的内源性 CFU-S 数量较多,提示造血恢复。本研究获得的数据证实,G-003M 可被证明是一种对抗辐射损伤的潜在放射防护剂。