Activation of neuropeptide Y receptors is neuroprotective against excitotoxicity in organotypic hippocampal slice cultures

• Published in: The FASEB journal 2003-06, Vol.17 (9), p.1118-1120
• Main Authors: Silva, Ana P., Pinheiro, Paulo S., Carvalho, Arsélio P., Carvalho, Caetana M., Jakobsen, Birthe, Zimmer, Jens, Malva, João O.
• Format: Article
• Language: English
• Subjects: alpha-Amino-3-hydroxy-5-methyl-4-isoxazolepropionic Acid - toxicity; AMPA; Animals; Dentate Gyrus - drug effects; Dentate Gyrus - metabolism; Hippocampus - cytology; Hippocampus - drug effects; kainate; Kainic Acid - toxicity; Nerve Degeneration - chemically induced; Nerve Degeneration - prevention & control; neurodegeneration; neuroprotection; Neuroprotective Agents - metabolism; NPY; Organ Culture Techniques; Pyramidal Cells - drug effects; Pyramidal Cells - metabolism; Rats; Receptors, Neuropeptide - physiology; Receptors, Neuropeptide Y - agonists; Receptors, Neuropeptide Y - metabolism; Receptors, Neuropeptide Y - physiology
• ISSN: 0892-6638; 1530-6860
• DOI: 10.1096/fj.02-0885fje

ABSTRACT Glutamate and NPY have been implicated in hippocampal neuropathology in temporal lobe epilepsy. Thus, we investigated the involvement of NPY receptors in mediating neuroprotection against excitotoxic insults in organotypic cultures of rat hippocampal slices. Exposure of hippocampal slice cultures to 2 μM AMPA (α‐amino‐3‐hydroxy‐5‐methyl‐isoxazole‐4‐propionate) induced neuronal degeneration, monitored by propidium iodide uptake, of granule cells and CA1 pyramidal cells. For dentate granule cells, selective activation of Y1, Y2, or Y5 receptors with 1 μM [Leu31,Pro34]NPY, 300 nM NPY13–36 or 1 μM 500 nM NPY(19–23)‐(Gly1,Ser3,Gln4,Thr6,Ala31,Aib32,Gln34)‐PP, respectively, had a neuroprotective effect against AMPA, whereas only the activation of Y2 receptors was effective for CA1 pyramidal cells. When the slice cultures were exposed to 6 μM kainate, the CA3 pyramidal cells displayed significant degeneration, and in this case the activation of Y1, Y2, and Y5 receptors was neuroprotective. For the kainic acid‐induced degeneration of CA1 pyramidal cells, it was again found that only the Y2 receptor activation was effective. Based on the present findings, it was concluded that Y1, Y2, and Y5 receptors effectively can modify glutamate receptor‐mediated neurodegeneration in the hippocampus.