TY - JOUR
T1 - Multiple opioid receptors mediate feeding elicited by mu and delta opioid receptor subtype agonists in the nucleus accumbens shell in rats
AU - Ragnauth, André
AU - Moroz, Malgorzata
AU - Bodnar, Richard J.
N1 - Funding Information:
This research was supported by National Science Foundation Grant IBN 98-16699 to RJB. MM was a CUNY Project ASCEND Fellow.
PY - 2000/9/8
Y1 - 2000/9/8
N2 - The nucleus accumbens, and particularly its shell region, is a critical site at which feeding responses can be elicited following direct administration of opiate drugs as well as μ-selective and δ-selective, but not κ-selective opioid receptor subtype agonists. In contrast to observations of selective and receptor-specific opioid antagonist effects upon corresponding agonist-induced actions in analgesic studies, ventricular administration of opioid receptor subtype antagonists blocks feeding induced by multiple opioid receptor subtype agonists. The present study examined whether feeding responses elicited by either putative μ ([D-Ala2, NMe- Phe4, Gly-ol5]-enkephalin (DAMGO)), δ1 ([D-Pen2, D-Pen5]-enkephalin (DPDPE)) or δ2 ([D-Ala2, Glu4]-deltorphin (Deltorphin)) opioid receptor subtype agonists administered into the nucleus accumbens shell were altered by accumbens pretreatment with either selective μ (β-funaltrexamine), μ1 (naloxonazine), δ1 ([D-Ala2, Leu5, Cys6]-enkephalin (DALCE)), δ2 (naltrindole isothiocyanate) or κ1 (nor-binaltorphamine) opioid receptor subtype antagonists. Similar magnitudes and durations of feeding responses were elicited by bilateral accumbens administration of either DAMGO (2.5 μg), DPDPE (5 μg) or Deltorphin (5 μg). DAMGO-induced feeding in the nucleus accumbens shell was significantly reduced by accumbens pretreatment of μ, δ1, δ2 and κ1, but not μ1 opioid receptor subtype antagonists. DPDPE-induced feeding in the accumbens was significantly reduced by accumbens pretreatment of μ, δ1, δ2 and κ1, but not μ1 opioid receptor subtype antagonists. Deltorphin-induced feeding in the accumbens was largely unaffected by accumbens δ2 antagonist pretreatment, and was significantly enhanced by accumbens μ or κ1 antagonist pretreatment. These data indicate different opioid pharmacological profiles for feeding induced by putative μ, δ1 and δ2 opioid agonists in the nucleus accumbens shell, as well as the participation of multiple opioid receptor subtypes in the elicitation and maintenance of feeding by these agonists in the nucleus accumbens shell. (C) 2000 Elsevier Science B.V.
AB - The nucleus accumbens, and particularly its shell region, is a critical site at which feeding responses can be elicited following direct administration of opiate drugs as well as μ-selective and δ-selective, but not κ-selective opioid receptor subtype agonists. In contrast to observations of selective and receptor-specific opioid antagonist effects upon corresponding agonist-induced actions in analgesic studies, ventricular administration of opioid receptor subtype antagonists blocks feeding induced by multiple opioid receptor subtype agonists. The present study examined whether feeding responses elicited by either putative μ ([D-Ala2, NMe- Phe4, Gly-ol5]-enkephalin (DAMGO)), δ1 ([D-Pen2, D-Pen5]-enkephalin (DPDPE)) or δ2 ([D-Ala2, Glu4]-deltorphin (Deltorphin)) opioid receptor subtype agonists administered into the nucleus accumbens shell were altered by accumbens pretreatment with either selective μ (β-funaltrexamine), μ1 (naloxonazine), δ1 ([D-Ala2, Leu5, Cys6]-enkephalin (DALCE)), δ2 (naltrindole isothiocyanate) or κ1 (nor-binaltorphamine) opioid receptor subtype antagonists. Similar magnitudes and durations of feeding responses were elicited by bilateral accumbens administration of either DAMGO (2.5 μg), DPDPE (5 μg) or Deltorphin (5 μg). DAMGO-induced feeding in the nucleus accumbens shell was significantly reduced by accumbens pretreatment of μ, δ1, δ2 and κ1, but not μ1 opioid receptor subtype antagonists. DPDPE-induced feeding in the accumbens was significantly reduced by accumbens pretreatment of μ, δ1, δ2 and κ1, but not μ1 opioid receptor subtype antagonists. Deltorphin-induced feeding in the accumbens was largely unaffected by accumbens δ2 antagonist pretreatment, and was significantly enhanced by accumbens μ or κ1 antagonist pretreatment. These data indicate different opioid pharmacological profiles for feeding induced by putative μ, δ1 and δ2 opioid agonists in the nucleus accumbens shell, as well as the participation of multiple opioid receptor subtypes in the elicitation and maintenance of feeding by these agonists in the nucleus accumbens shell. (C) 2000 Elsevier Science B.V.
KW - Feeding
KW - Nucleus accumbens shell
KW - δ Opioid receptor
KW - δ Opioid receptor
KW - κ Opioid receptor
KW - μ Opioid receptor
KW - μ Opioid receptor
UR - http://www.scopus.com/inward/record.url?scp=0034623269&partnerID=8YFLogxK
U2 - 10.1016/S0006-8993(00)02631-7
DO - 10.1016/S0006-8993(00)02631-7
M3 - Article
C2 - 10973595
AN - SCOPUS:0034623269
SN - 0006-8993
VL - 876
SP - 76
EP - 87
JO - Brain Research
JF - Brain Research
IS - 1-2
ER -