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预防性给予鬼臼毒素和芦丁联合治疗可促进致死剂量辐射诱导的造血抑制小鼠造血功能的恢复。

Prophylactic administration of podophyllotoxin and rutin combination assists the revival of radiation-induced hematopoietic suppression in lethally irradiated mice.

机构信息

Division of Radioprotective Drug Development and Research, Institute of Nuclear Medicine and Allied Sciences, Brig. S.K. Mazumdar Marg, Delhi, 110054, India.

Institute of Virology and Immunology, Amity University Campus, Sector -125, Noida, 201313, India.

出版信息

Biochem Biophys Res Commun. 2021 Apr 16;549:214-220. doi: 10.1016/j.bbrc.2021.02.085. Epub 2021 Mar 8.

Abstract

Hematopoietic syndrome contributes to mortality after exposure to high doses of low LET radiation. In this context, we have earlier demonstrated the potential of G-003 M (a combination of podophyllotoxin and rutin) in alleviating radiation-induced bone marrow suppression. Similarly, we here demonstrate that G-003 M protected mice from death (>83% protection) and increased the populations of CD 34 (Cluster of differentiation 34) as well as CD 117 (Cluster of differentiation 117) positive cell population and their colony forming capacity. This was accompanied with increase in the serum titre of granulocyte colony stimulating factor (G-CSF), granulocyte-macrophage colony stimulating factor (GM-CSF). Interestingly, G-003 M lowered down the titre of fms-like tyrosine kinase (Flt-3) ligands. Our results furthermore demonstrates that G-003 M facilitated the nuclear translocation of β-catenin and upregulated the expression of Wnt 10b. Conditioning of animal with G-003 M activated the expression of survivin, inhibited the activation of Caspase-3 in CD 34/117 progenitor stem cells and protected the bone marrow vascularity and splenic colonies in lethally irradiated animals, which collectively promoted hemopoietic recovery in lethally irradiated mice.

摘要

造血综合征是导致高剂量低 LET 辐射暴露后死亡的原因之一。在此背景下,我们之前已经证明了 G-003M(鬼臼毒素和芦丁的组合)在缓解辐射引起的骨髓抑制方面的潜力。同样,我们在这里证明 G-003M 可以保护小鼠免受死亡(>83%的保护),增加 CD34(分化群 34)和 CD117(分化群 117)阳性细胞群体及其集落形成能力。这伴随着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)的血清滴度增加。有趣的是,G-003M 降低了 fms 样酪氨酸激酶(Flt-3)配体的滴度。我们的研究结果进一步表明,G-003M 促进了 β-连环蛋白的核易位,并上调了 Wnt10b 的表达。用 G-003M 对动物进行预处理激活了生存素的表达,抑制了 CD34/117 祖细胞干细胞中 Caspase-3 的激活,并保护了致死性照射动物的骨髓血管和脾脏集落,这些共同促进了致死性照射小鼠的造血恢复。

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