The opioid receptor-like 1 (ORL1) receptor shares a high degree of sequence homology with the classical mu-, delta- and kappa-opioid receptors and a functional mutual opposition between these receptors has been suggested. To further address this possible interaction we have used mu-, delta- and kappa-opioid receptor knockout mice to determine autoradiographically if there are any changes in the number or distribution of the ORL1 receptor, labelled with [(3)H]nociceptin, in the brains of mice deficient in each of the opioid receptors. An up-regulation of ORL1 expression was observed across all brain regions in delta-knockouts with cortical regions typically showing a 15-30% increase in binding that was most marked in heterozygous mice. In contrast, ORL1 receptor expression was down-regulated in virtually all brain structures in heterozygous kappa-knockouts although the magnitude of this change was not as great as for the delta-knockouts. No significant alterations in ORL1 receptor expression were observed across brain regions in mu-receptor knockout mice and there were no qualitative differences in ORL1 receptor expression in any groups. These data suggest there are interactions between the ORL1 system and the classical opioid receptors and that the interactions are receptor-specific. The greater differences observed in heterozygous mice suggest that these interactions might be most relevant when there is only partial loss of receptor function.

Autoradiographic mapping of the opioid receptor-like 1 (ORL1) receptor in the brains of the mu-, delta-, kappa- opioid receptor knockout mice / Slowe, S. J.; Clarke, S.; Lena, I.; Goody, R. J.; Lattanzi, Roberta; Negri, Lucia; Simonin, F.; Matthes, H. W. D.; Filliol, D.; Kieffer, B. L.; Kitchen, I.. - In: NEUROSCIENCE. - ISSN 0306-4522. - STAMPA. - 106:(2001), pp. 469-480. [10.1016/S0306-4522(01)00308-6]

Autoradiographic mapping of the opioid receptor-like 1 (ORL1) receptor in the brains of the mu-, delta-, kappa- opioid receptor knockout mice.

LATTANZI, Roberta;NEGRI, Lucia;
2001

Abstract

The opioid receptor-like 1 (ORL1) receptor shares a high degree of sequence homology with the classical mu-, delta- and kappa-opioid receptors and a functional mutual opposition between these receptors has been suggested. To further address this possible interaction we have used mu-, delta- and kappa-opioid receptor knockout mice to determine autoradiographically if there are any changes in the number or distribution of the ORL1 receptor, labelled with [(3)H]nociceptin, in the brains of mice deficient in each of the opioid receptors. An up-regulation of ORL1 expression was observed across all brain regions in delta-knockouts with cortical regions typically showing a 15-30% increase in binding that was most marked in heterozygous mice. In contrast, ORL1 receptor expression was down-regulated in virtually all brain structures in heterozygous kappa-knockouts although the magnitude of this change was not as great as for the delta-knockouts. No significant alterations in ORL1 receptor expression were observed across brain regions in mu-receptor knockout mice and there were no qualitative differences in ORL1 receptor expression in any groups. These data suggest there are interactions between the ORL1 system and the classical opioid receptors and that the interactions are receptor-specific. The greater differences observed in heterozygous mice suggest that these interactions might be most relevant when there is only partial loss of receptor function.
2001
ORL1 receptor,; opioid receptors,; knockout mice,; autoradiography,; transgenic
01 Pubblicazione su rivista::01a Articolo in rivista
Autoradiographic mapping of the opioid receptor-like 1 (ORL1) receptor in the brains of the mu-, delta-, kappa- opioid receptor knockout mice / Slowe, S. J.; Clarke, S.; Lena, I.; Goody, R. J.; Lattanzi, Roberta; Negri, Lucia; Simonin, F.; Matthes, H. W. D.; Filliol, D.; Kieffer, B. L.; Kitchen, I.. - In: NEUROSCIENCE. - ISSN 0306-4522. - STAMPA. - 106:(2001), pp. 469-480. [10.1016/S0306-4522(01)00308-6]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/131600
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