Abstract:
:Although enterostatin (VPDPR) inhibited morphine-induced analgesia, it had no affinity for mu-opioid receptors. VPDPR administration was reported to elevate serum corticosterone levels. We found that corticosterone exhibited a similar anti-analgesic effect selective for mu-opioid. Furthermore, the anti-analgesic effect of VPDPR was inhibited by RU486, an antagonist for the glucocorticoid receptor. The anti-analgesic effect of VPDPR was not observed in adrenalectomized mice. These results suggest that the anti-analgesic activity of VPDPR is mediated by corticosterone released from the adrenal cortex.
journal_name
Peptidesjournal_title
Peptidesauthors
Takenaka Y,Nakamura F,Usui H,Lipkowski AW,Toth G,Yoshikawa Mdoi
10.1016/s0196-9781(03)00124-4subject
Has Abstractpub_date
2003-05-01 00:00:00pages
735-9issue
5eissn
0196-9781issn
1873-5169pii
S0196978103001244journal_volume
24pub_type
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