Metabotropic Glutamate Receptor Antagonist AIDA Blocks Induction of Mossy Fiber-CA3 LTP In Vivo

• Published in: Journal of neurophysiology 2005-05, Vol.93 (5), p.2668-2673
• Main Authors: Thompson, Kenira J, Mata, Mario L, Orfila, James E, Barea-Rodriguez, Edwin J, Martinez, Joe L., Jr
• Format: Article
• Language: English
• Subjects: Animals; Electric Stimulation - methods; Excitatory Amino Acid Antagonists - pharmacology; Excitatory Postsynaptic Potentials - drug effects; Excitatory Postsynaptic Potentials - physiology; Excitatory Postsynaptic Potentials - radiation effects; Indans - pharmacology; Long-Term Potentiation - drug effects; Long-Term Potentiation - radiation effects; Male; Mossy Fibers, Hippocampal - drug effects; Mossy Fibers, Hippocampal - physiology; Naloxone - pharmacology; Narcotic Antagonists - pharmacology; Piperazines - pharmacology; Rats; Rats, Long-Evans; Rats, Sprague-Dawley
• ISSN: 0022-3077; 1522-1598
• DOI: 10.1152/jn.00901.2004

University of Texas at San Antonio, Department of Biology, San Antonio, Texas Submitted 30 August 2004; accepted in final form 12 November 2004 Metabotropic glutamate receptors (mGluR) are implicated in long-term memory storage. mGluR-I and mGluR-II antagonists impede various forms of learning and long-term potentiation (LTP) in animals. Despite the evidence linking mGluR to learning mechanisms, their role in mossy fiber-CA3 long-term potentiation (LTP) is not yet clear. To explain the involvement of mGluR-I in memory mechanisms, we examined the function of the mGluR-I antagonist 1-aminoindan-1, 5-dicarboxylic acid (AIDA) on the induction of mossy fiber-CA3 LTP in vivo in male Sprague Dawley and Fischer 344 (F344) rats. Acute extracellular mossy fiber (MF) responses were evoked by stimulation of the MF bundle and recorded in the stratum lucidum of CA3. The excitatory postsynaptic potential (EPSP) magnitude was measured by using the initial slope of the field EPSP slope measured 2–3 ms after response onset. After collection of baseline MF-CA3 responses at 0.05 Hz, animals received either ((±))-3-(2-carboxypiperazin-4-yl)-propyl-1-phosphonic acid ( N -methyl- D -aspartate-R antagonist, 10 mg/kg ip), naloxone (opioid-R antagonist, 10 mg/kg ip), or AIDA (mGluR antagonist, 1 mg/kg ip or 37.5 nmol ic). LTP was induced by two 100-Hz trains at the intensity sufficient to evoke 50% of the maximal response. Responses were collected for an additional 1 h. AIDA blocked induction of LTP in the mossy fiber pathway ( P < 0.05) in both strains of rats after systemic and in Sprague Dawley rats after intrahippocampal injection. Address for reprint requests and other correspondence: K. Thompson, University of Texas at San Antonio, Dept. of Biology, 6900 N. Loop 1604 West, San Antonio, TX 78249 (E-mail: kthompson{at}utsa.edu )