Anti-analgesic activity of enterostatin (VPDPR) is mediated by corticosterone.

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

Peptides

journal_title

Peptides

authors

Takenaka Y,Nakamura F,Usui H,Lipkowski AW,Toth G,Yoshikawa M

doi

10.1016/s0196-9781(03)00124-4

subject

Has Abstract

pub_date

2003-05-01 00:00:00

pages

735-9

issue

5

eissn

0196-9781

issn

1873-5169

pii

S0196978103001244

journal_volume

24

pub_type

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