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鬼臼毒素和芦丁联合使用通过负向调节致死性照射小鼠的NF-κB/p53信号通路减轻辐射诱导的胃肠道损伤。

A Combination of Podophyllotoxin and Rutin Attenuates Radiation Induced Gastrointestinal Injury by Negatively Regulating NF-κB/p53 Signaling in Lethally Irradiated Mice.

作者信息

Kalita Bhargab, Ranjan Rajiv, Singh Abhinav, Yashavarddhan M H, Bajaj Sania, Gupta Manju Lata

机构信息

Division of Radioprotective Drug Development and Research, Institute of Nuclear Medicine and Allied Sciences, Brig.S.K Mazumdar Marg, Delhi, INDIA.

出版信息

PLoS One. 2016 Dec 30;11(12):e0168525. doi: 10.1371/journal.pone.0168525. eCollection 2016.

Abstract

Development of an effective radio protector to minimise radiation-inflicted damages have largely failed owing to inherent toxicity of most of the agents examined so far. This study is centred towards delivering protection to lethally irradiated mice by pre-administration of a safe formulation G-003M (combination of podophyllotoxin and rutin) majorly through regulation of inflammatory and cell death pathways in mice. Single intramuscular dose of G-003M injected 60 min prior to 9 Gy exposure rescued 89% of whole body lethally irradiated C57BL/6J mice. Studies have revealed reduction in radiation induced reactive oxygen species (ROS), nitric oxide (NO) generation, prostaglandin E2 (PGE2) levels and intestinal apoptosis in G-003M pre-treated mice intestine. Restricted nuclear translocation of redox-sensitive Nuclear factor-κB (NF-κB) and subsequent downregulation of cyclo-oxygenase 2 (COX-2), inducible nitric oxide synthase (iNOS; EC 1.14.13.39) and tumor necrosis factor (TNF-α) levels demonstrated the anti-inflammatory effect that G-003M exerts. Support to early hematopoietic recovery was exhibited through G-003M mediated induction of granulocyte colony stimulating factor (G-CSF) and interleukin (IL-6) levels in lethally irradiated mice. Considerable attenuation in radiation induced morphological damage to the intestinal villi, crypts and mucosal layers was observed in G-003M pre-treated mice. Additionally, our formulation did not reduce the sensitivity of tumor tissue to radiation. Altogether, these results suggest that G-003M ameliorates the deleterious effects of radiation exposure by minimising ROS and NO generation and effectively regulating inflammatory and cell death pathways. Mechanism of protection elucidated in the current study demonstrates that G-003M can be used as a safe and effective radio protective agent in radiotherapy for human application.

摘要

由于目前所研究的大多数药物都具有内在毒性,开发一种有效的辐射防护剂以尽量减少辐射造成的损害在很大程度上已告失败。本研究的重点是通过预先给予一种安全制剂G-003M(鬼臼毒素和芦丁的组合),主要通过调节小鼠体内的炎症和细胞死亡途径,为受到致死性照射的小鼠提供保护。在9 Gy照射前60分钟单次肌肉注射G-003M,拯救了89%受到全身致死性照射的C57BL/6J小鼠。研究表明,在G-003M预处理的小鼠肠道中,辐射诱导的活性氧(ROS)、一氧化氮(NO)生成、前列腺素E2(PGE2)水平和肠道细胞凋亡均有所降低。氧化还原敏感的核因子-κB(NF-κB)的核转位受限,以及随后环氧化酶2(COX-2)、诱导型一氧化氮合酶(iNOS;EC 1.14.13.39)和肿瘤坏死因子(TNF-α)水平的下调,证明了G-003M发挥的抗炎作用。通过G-003M介导的致死性照射小鼠体内粒细胞集落刺激因子(G-CSF)和白细胞介素(IL-6)水平的诱导,显示出对早期造血恢复的支持。在G-003M预处理的小鼠中,观察到辐射诱导的肠道绒毛、隐窝和粘膜层形态损伤有显著减轻。此外,我们的制剂并未降低肿瘤组织对辐射的敏感性。总之,这些结果表明,G-003M通过减少ROS和NO的生成以及有效调节炎症和细胞死亡途径,减轻了辐射暴露的有害影响。本研究中阐明的保护机制表明,G-003M可作为一种安全有效的辐射防护剂用于人类放射治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c603/5201299/b3c711fcbfbd/pone.0168525.g001.jpg

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