Cilostazol attenuates kainic acid-induced hippocampal cell death

نویسندگان

  • Young-Seop Park
  • Zhen Jin
  • Eun Ae Jeong
  • Chin-ok Yi
  • Jong Youl Lee
  • In Sung Park
  • Gu Seob Roh
چکیده

Cilostazol is a selective inhibitor of type 3 phosphodiesterase (PDE3) and has been widely used as an antiplatelet agent. Cilostazol mediates this activity through effects on the cyclic adenosine monophosphate (cAMP) signaling cascade. Recently, it has attracted attention as a neuroprotective agent. However, little is known about cilostazol's effect on excitotoxicity induced neuronal cell death. Therefore, this study evaluated the neuroprotective effect of cilostazol treatment against hippocampal neuronal damage in a mouse model of kainic acid (KA)-induced neuronal loss. Cilostazol pretreatment reduced KA-induced seizure scores and hippocampal neuron death. In addition, cilostazol pretreatment increased cAMP response element-binding protein (CREB) phosphorylation and decreased neuroinflammation. These observations suggest that cilostazol may have beneficial therapeutic effects on seizure activity and other neurological diseases associated with excitotoxicity.

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عنوان ژورنال:

دوره 22  شماره 

صفحات  -

تاریخ انتشار 2018