Endogenous opioid peptides contribute to associative LTP in the hippocampal CA3 region

Neurobiology of Learning and Memory

Volumn 96, Issue 2, 2011, Pages 207-217

  Martinez, Carlo O ^a,c   Do, Viet H ^b,c   Derrick, Brian E ^c  

^a UNIVERSITY OF TEXAS HEALTH SCIENCE CENTER AT SAN ANTONIO   (United States)

^b MICHIGAN STATE UNIVERSITY   (United States)

^c UNIVERSITY OF TEXAS AT SAN ANTONIO   (United States)

Author keywords

Associative LTP; CA3; Long term potentiation (LTP); Mu opioid receptor; NMDA receptor; Perforant path

Indexed keywords

DEXTRO PHENYLALANYLCYSTEINYLTYROSYL DEXTRO TRYPTOPHYLORNITHYLTHREONYLPENICILLAMINYLTHREONINAMIDE 2,7 DISULFIDE; N METHYL DEXTRO ASPARTIC ACID RECEPTOR; NALOXONE; OPIATE PEPTIDE; OPIATE RECEPTOR;

ANIMAL EXPERIMENT; ARTICLE; BRAIN FUNCTION; CONTROLLED STUDY; DENTATE GYRUS; EVOKED RESPONSE; HIPPOCAMPAL CA3 REGION; LATENT PERIOD; LONG TERM POTENTIATION; MALE; MOSSY FIBER; NERVE CELL PLASTICITY; NEUROTRANSMISSION; NONHUMAN; RAT; STATE DEPENDENT LEARNING; SYNAPSE; SYNAPTIC TRANSMISSION;

ANIMALS; CA3 REGION, HIPPOCAMPAL; LONG-TERM POTENTIATION; MALE; NALOXONE; NARCOTIC ANTAGONISTS; OPIOID PEPTIDES; PERFORANT PATHWAY; RATS; RATS, SPRAGUE-DAWLEY; RECEPTORS, OPIOID; SOMATOSTATIN;

EID: 79960843386     PISSN: 10747427     EISSN: 10959564     Source Type: Journal    
DOI: 10.1016/j.nlm.2011.04.014     Document Type: Article

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