Authors: | Burdick, K.; Yu, W. Z.; Ragnauth, A.; Moroz, M.; Pan, Y. X.; Rossi, G. C.; Pasternak, G. W.; Bodnar, R. J. |
Article Title: | Antisense mapping of opioid receptor clones: Effects upon 2-deoxy-D-glucose-induced hyperphagia |
Abstract: | Antisense oligodeoxynucleotides (AS ODNs) directed against exons 1 and 2 of the MOR-1 clone significantly and markedly reduced (81-93%) hyperphagia induced by the anti-metabolic glucose analogue, 2-deoxy-D-glucose (2DG) across a 4 h time course. AS ODNs directed against exons 3 or 4 of the MOR-1 clone had a more limited (1-2 h) duration of action upon 2DG-induced hyperphagia. 2DG-induced hyperphagia was significantly reduced by AS ODNs directed against exon 2 (44-51%), but not exons 1 or 3 of the KOR-1 clone across a 4 h time course. Whereas an AS ODN probe directed against the KOR3/ORL-1 clone produced small (36%), but significant reductions in 2DG- induced hyperphagia, an AS ODN probe directed against the DOR-1 clone was ineffective. These data provide further converging evidence for the roles of primarily mu, but also kappa, and kappa3 opioid receptors in mediating the hyperphagic effects of glucoprivation. |
Keywords: | controlled study; exons; nonhuman; animals; animal experiment; weight reduction; feeding; food intake; cloning, molecular; rat; rats; rats, sprague-dawley; mu opiate receptor; opiate receptor; oligonucleotides, antisense; delta opiate receptor; kappa opiate receptor; antisense oligodeoxynucleotide; deoxyglucose; receptors, opioid; intracerebroventricular drug administration; male; priority journal; article; hyperphagia; glucoprivation; 2-deoxy-d-glucose; dor-1 clone; kor-1 clone; kor-3/orl-1 clone; mor-1 clone |
Journal Title: | Brain Research |
Volume: | 794 |
Issue: | 2 |
ISSN: | 0006-8993 |
Publisher: | Elsevier Science, Inc. |
Date Published: | 1998-06-01 |
Start Page: | 359 |
End Page: | 363 |
Language: | English |
DOI: | 10.1016/s0006-8993(98)00331-x |
PUBMED: | 9622675 |
PROVIDER: | scopus |
DOI/URL: | |
Notes: | Article -- Export Date: 12 December 2016 -- Source: Scopus |