P7C3-A20 treatments

AL Anni S. Lee
HJ Héctor De Jesús-Cortés
ZK Zeeba D. Kabir
WK Whitney Knobbe
MO Madeline Orr
CB Caitlin Burgdorf
PH Paula Huntington
LM Latisha McDaniel
JB Jeremiah K. Britt
FH Franz Hoffmann
DB Daniel J. Brat
AR Anjali M. Rajadhyaksha
AP Andrew A. Pieper
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All mice were single-housed for the duration of treatment. Forebrain-Cav1.2 cKO and wild-type littermate mice received 10 mg/kg P7C3-A20 or vehicle (5% DMSO, 20% cremaphor in 5% dextrose), intraperitoneally, twice a day for 30 d, starting at P21. This dose of P7C3-A20 was chosen based on efficacy in multiple animal models of neuroprotection (De Jesus-Cortés et al., 2012; Tesla et al., 2012; Yin et al., 2014). Mice were transcardially perfused with 4% PFA 24 h after the last BrdU injection. In separate experiments, brains were flash frozen and processed for BDNF ELISA.

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