Ionizing irradiation protection and mitigation of murine cells by carbamazepine is p53 and autophagy independent

卡马西平对小鼠细胞的电离辐射保护和缓解作用不依赖于 p53 和自噬

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作者:Hyun Kim, Mark E Bernard, Amy Farkas, Julie Goff, Ronny Kalash, Frank Houghton, Donna Shields, Darcy Franicola, Tracy Dixon, Xichen Zhang, Michael Epperly, Hong Wang, Murat Can Cobanoglu, Joel S Greenberger

Background

Carbamazepine, a sodium channel blocker and pro-autophagy agent used in the treatment of epilepsy and trigeminal neuralgia, is also an ionizing radiation mitigator and protector. Materials and

Conclusion

Carbamazepine is a murine radiation protector and mitigator.

Methods

We measured the effect of carbamazepine, compared to other pro-autophagy drugs (i.e. lithium and valproic acid), on irradiation of autophagy incompetent (Atg5(-/-)) and competent (Atg5(+/+)) mouse embryonic fibroblasts, p53(-/-) and p53(+/+) bone marrow stromal cells, and human IB3, KM101, HeLa, and umbilical cord blood cell and in total body-irradiated or orthotopic tumor-bearing mice.

Results

Carbamazepine, but not other pro-autophagy drugs, was a radiation protector and mitigator for mouse cell lines, independent of apoptosis, autophagy, p53, antioxidant store depletion, and class I phosphatidylinositol 3-kinase, but was ineffective with human cells. Carbamazepine was effective when delivered 24 hours before or 12 hours after total body irradiation of C57BL/6HNsd mice and did not protect orthotopic Lewis lung tumors.

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