QUANTITATIVE AUTORADIOGRAPHY OF PERIPHERAL OPIOID BINDING-SITES IN RAT LUNG

Citation
Pj. Cabot et al., QUANTITATIVE AUTORADIOGRAPHY OF PERIPHERAL OPIOID BINDING-SITES IN RAT LUNG, European journal of pharmacology, 310(1), 1996, pp. 47-53
Citations number
19
Categorie Soggetti
Pharmacology & Pharmacy
ISSN journal
00142999
Volume
310
Issue
1
Year of publication
1996
Pages
47 - 53
Database
ISI
SICI code
0014-2999(1996)310:1<47:QAOPOB>2.0.ZU;2-V
Abstract
Previous studies in our laboratory have characterized non-conventional opioid binding sites in membrane preparations from both rat and human lung. The studies described in this paper utilized autoradiography to investigate the regional distribution of these [H-3]morphine binding sites within rat lungs. Specific binding of [H-3]morphine was saturabl e and Rosenthal analysis of tissue section wipes revealed the presence of both high-affinity and low-affinity opioid binding sites. The mean +/- S.E.M. binding affinity and the mean +/- S.E.M. density values fo r the low-affinity binding site (K-d = 217 +/- 160 nM, B-max = 12 +/- 8 pmol/mg protein) were similar to the values obtained in our previous whole-rat lung membrane binding assays (K-d = 187 +/- 36 nM, B-max = 13.5 +/- 2 pmol/mg protein) (Cabot, P.J., P.R. Dodd, T. Cramond and M. T. Smith, 1994, Eur. J. Pharmacol. 265, 247). Quantitative autoradiogr aphy showed that the highest density of opioid binding sites appeared to be present within the alveolar wall (13.2 +/- 0.8 pmol/mg protein). A significantly lower (P < 0.05) density of binding was also observed in the smooth muscle of the trachea and main bronchi (5.5 +/- 2.1 pmo l/mg protein). However, no morphine binding sites were evident in the smooth muscle surrounding the smaller airways and pulmonary vasculatur e within the lobes of the rat lung. It remains to be investigated whet her the opioid binding sites located within the trachea and main bronc hi of the rat airways are the prejunctional opioid receptors on C-affe rent nerve fibres which modulate the release of potent inflammatory ne uropeptides.