Abstract：
:The stimulatory effect of insulin-like growth factor I (IGF-I) on myelin basic protein (MBP) expression, a parameter for oligodendrocyte development, is mediated by the MAPK and PI3K signaling pathways. We have previously shown that the second messenger cAMP inhibits IGF-I-induced MAPK activation as well as MBP expression. We also showed that the PKA inhibitor Rp-cAMPS reverted the cAMP effect on IGF-I-induced MBP without affecting the cAMP effect on IGF-I-induced MAPK activation. Here we report that, in contrast to Rp-cAMPS, H89 (a PKA inhibitor structurally non-related to Rp-cAMPS) enhances both the inhibitory effect of cAMP on IGF-I-induced MBP expression and the inhibitory effect of cAMP on IGF-I-induced MAPK activation. Likewise, H89 is capable of inhibiting the IGF-I-induced MAPK activation in the absence of PKA stimulation. Thus, we hypothesize that an unspecific action of H89 on a target located upstream MAPK could account for the discrepancies between the effects elicited by Rp-cAMPS and H89.
journal_name
Brain Resjournal_title
Brain researchauthors
Palacios N,Sánchez-Franco F,Fernández M,Sánchez I,Villuendas G,Cacicedo Ldoi
10.1016/j.brainres.2007.07.018subject
Has Abstractpub_date
2007-10-31 00:00:00pages
1-11eissn
0006-8993issn
1872-6240pii
S0006-8993(07)01595-8journal_volume
1178pub_type
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