Skip to main content
. Author manuscript; available in PMC: 2007 May 24.
Published in final edited form as: J Biol Chem. 2006 Apr 18;281(26):17870–17881. doi: 10.1074/jbc.M602632200

FIGURE 2. cAMP reverses 6-OHDA-induced CRE repression and cell death.

FIGURE 2

A, cells were transfected with pCRE-luc plasmid and then stimulated with vehicle, Bt2cAMP, 6-OHDA, or 6-OHDA following a 10-min pretreatment with Bt2cAMP. After 3 h, cells were lysed, and luciferase activity was measured. Data are the mean ± S.D. and are representative of five independent experiments. *, p < 0.05 by ANOVA followed by Student’s t test with Bonferroni correction. B, B65 cells were treated for 10 min with medium (None) or Bt2cAMP before exposure to vehicle or 6-OHDA for 18 h. Cell injury was assayed using the LDH release assay, and data are representative of at least three independent experiments. *, p < 0.05 versus 6-OHDA with no pretreatment (Student’s t test). C, cells were photographed immediately prior to performing the LDH assay, showing that Bt2cAMP pretreatment results in greater numbers of viable neuronal cells (right) compared with the shrunken, dead morphology observed with 6-OHDA alone (left).