Levetiracetam mitigates doxorubicin-induced DNA and synaptic damage in neurons

被引:44
|
作者
Manchon, Jose Felix Moruno [1 ]
Dabaghian, Yuri [2 ,3 ]
Uzor, Ndidi-Ese [1 ,4 ]
Kesler, Shelli R. [5 ]
Wefel, Jeffrey S. [5 ]
Tsvetkov, Andrey S. [1 ,4 ]
机构
[1] Univ Texas Houston, Sch Med, Dept Neurobiol & Anat, Houston, TX 77225 USA
[2] Baylor Coll Med, Jan & Dan Duncan Neurol Res Inst, Houston, TX 77030 USA
[3] Rice Univ, Dept Computat & Appl Math, Houston, TX USA
[4] Univ Texas Grad Sch Biomed Sci, Houston, TX USA
[5] Univ Texas MD Anderson Canc Ctr, Dept Neurooncol, Houston, TX 77030 USA
来源
SCIENTIFIC REPORTS | 2016年 / 6卷
关键词
BLOOD-BRAIN-BARRIER; INTRATHECAL METHOTREXATE; PERIPHERAL NEUROPATHY; COGNITIVE DEFICITS; BREAST-CANCER; STRAND BREAKS; CHEMOTHERAPY; PLASTICITY; RECEPTORS; GENE;
D O I
10.1038/srep25705
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Neurotoxicity may occur in cancer patients and survivors during or after chemotherapy. Cognitive deficits associated with neurotoxicity can be subtle or disabling and frequently include disturbances in memory, attention, executive function and processing speed. Searching for pathways altered by anticancer treatments in cultured primary neurons, we discovered that doxorubicin, a commonly used antineoplastic drug, significantly decreased neuronal survival. The drug promoted the formation of DNA double-strand breaks in primary neurons and reduced synaptic and neurite density. Pretreatment of neurons with levetiracetam, an FDA-approved anti-epileptic drug, enhanced survival of chemotherapy drug-treated neurons, reduced doxorubicin-induced formation of DNA double-strand breaks, and mitigated synaptic and neurite loss. Thus, levetiracetam might be part of a valuable new approach for mitigating synaptic damage and, perhaps, for treating cognitive disturbances in cancer patients and survivors.
引用
收藏
页数:12
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