RT Journal Article
SR Electronic
T1 The Expression of δ- and κ-Opioid Receptor Is Enhanced during Intestinal Inflammation in Mice
JF Journal of Pharmacology and Experimental Therapeutics
JO J Pharmacol Exp Ther
FD American Society for Pharmacology and Experimental Therapeutics
SP 455
OP 462
DO 10.1124/jpet.103.049346
VO 306
IS 2
A1 Pol, Olga
A1 Palacio, José R.
A1 Puig, Margarita M.
YR 2003
UL http://jpet.aspetjournals.org/content/306/2/455.abstract
AB In the gut, μ-, δ-, and κ-opioid receptors are present in the submucous and myenteric plexi and in enterocytes. Using pharmacological methods, our group has shown that intestinal inflammation enhances the antitransit and antisecretory effects of systemic opioids. The aim of the present study was to evaluate whether the enhanced antisecretory effects of δ and κ-agonists were associated with an increased transcription and/or expression of these receptors at central (brain and spinal cord) and/or peripheral sites (gut); we also evaluated the expression of δ- and κ-opioid receptors in dissected sections of the gut containing the myenteric (MP/LM) or submucous (SP/M) plexi. The mRNA and protein levels of both opioid receptors were determined using a reverse-transcriptase polymerase chain reaction and immunoprecipitation/Western blot, respectively. Intestinal inflammation significantly augmented the transcription of δ-opioid receptors in the spinal cord (34%) and in the whole gut (102%). Also increased mRNA and protein levels of δ-opioid receptors in the MP/LM and SP/M preparations. The κ-opioid receptors gene transcription was not altered by inflammation, whereas κ-opioid receptors protein levels were significantly enhanced in the SP/M preparation. No changes in gene transcription or protein levels for δ- and κ-opioid receptors could be demonstrated in the brain. These results suggest that local transcriptional and post-transcriptional changes of the δ- and κ-opioid receptors genes could be responsible for the enhanced antisecretory effects of δ- and κ-opioid agonists during intestinal inflammation. The American Society for Pharmacology and Experimental Therapeutics