<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Walwyn W</submitter><funding>NIDA NIH HHS</funding><pagination>134-43</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC2701458</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>76(1)</volume><pubmed_abstract>Recombinant micro and delta opioid receptors expressed in cell lines can form heterodimers with distinctive properties and trafficking. However, a role for opioid receptor heterodimerization in neurons has yet to be identified. The inhibitory coupling of opioid receptors to voltage-dependent Ca(2+) channels (VDCCs) is a relatively inefficient process and therefore provides a sensitive assay of altered opioid receptor function and expression. We examined micro-receptor coupling to VDCCs in dorsal root ganglion neurons of delta(+/+), delta(+/-), and delta(-/-) mice. Neurons deficient in delta receptors exhibited reduced inhibition of VDCCs by morphine and [D-Ala(2),Phe(4),Gly(5)-ol]-enkephalin (DAMGO). An absence of delta receptors caused reduced efficacy of DAMGO without affecting potency. </pubmed_abstract><journal>Molecular pharmacology</journal><pubmed_title>Delta receptors are required for full inhibitory coupling of mu-receptors to voltage-dependent Ca(2+) channels in dorsal root ganglion neurons.</pubmed_title><pmcid>PMC2701458</pmcid><funding_grant_id>DA05010</funding_grant_id><funding_grant_id>P50 DA005010</funding_grant_id><funding_grant_id>DA00484</funding_grant_id><pubmed_authors>Walwyn W</pubmed_authors><pubmed_authors>Hales TG</pubmed_authors><pubmed_authors>Maga M</pubmed_authors><pubmed_authors>Evans CJ</pubmed_authors><pubmed_authors>John S</pubmed_authors></additional><is_claimable>false</is_claimable><name>Delta receptors are required for full inhibitory coupling of mu-receptors to voltage-dependent Ca(2+) channels in dorsal root ganglion neurons.</name><description>Recombinant micro and delta opioid receptors expressed in cell lines can form heterodimers with distinctive properties and trafficking. However, a role for opioid receptor heterodimerization in neurons has yet to be identified. The inhibitory coupling of opioid receptors to voltage-dependent Ca(2+) channels (VDCCs) is a relatively inefficient process and therefore provides a sensitive assay of altered opioid receptor function and expression. We examined micro-receptor coupling to VDCCs in dorsal root ganglion neurons of delta(+/+), delta(+/-), and delta(-/-) mice. Neurons deficient in delta receptors exhibited reduced inhibition of VDCCs by morphine and [D-Ala(2),Phe(4),Gly(5)-ol]-enkephalin (DAMGO). An absence of delta receptors caused reduced efficacy of DAMGO without affecting potency. </description><dates><release>2009-01-01T00:00:00Z</release><publication>2009 Jul</publication><modification>2026-05-03T14:51:34.303Z</modification><creation>2019-03-27T00:23:10Z</creation></dates><accession>S-EPMC2701458</accession><cross_references><pubmed>19357247</pubmed><doi>10.1124/mol.109.055913</doi></cross_references></HashMap>