IBCN   20355
INSTITUTO DE BIOLOGIA CELULAR Y NEUROCIENCIA "PROFESOR EDUARDO DE ROBERTIS"
Unidad Ejecutora - UE
congresos y reuniones científicas
Título:
Muscarinic and adrenergic neurotransmission in the CA1 area of rat hippocampus.
Autor/es:
E N GONZALEZ; M V OBERHOLZER; E KORNISIUK; D A JERUSALINSKY
Lugar:
Huerta Grande
Reunión:
Congreso; XXVI Congreso Anual de SAN; 2011
Institución organizadora:
SAN-TAN
Resumen:
Muscarinic and adrenergic
neurotransmission in the CA1 area of rat hippocampus. González,
N.; Oberholzer, V.; Kornisiuk, E.; Cerveñansky, C.;
Jerusalinsky, D. XXVI Congreso Anual de la SAN, Córdoba, Argentina. Octubre de
2011.
Poster Number 234 | Session 3
"Muscarinic and adrenergic
neurotransmission in the CA1 area of rat hippocampus"
Nicolás González3, María Victoria
Oberholzer3, Edgar Kornisiuk3, Carlos Cerveñansky2, Diana Jerusalinsky 3,1
1CBC, UBA, Argentina, 2Insitut Pasteur, Uruguay, 3Instituto de Biología
Celular y Neurociencia, UBA-CONICET, Argentina
enicogon@gmail.com
Adrenergic
and muscarinic neurotransmission in rat hippocampus are involved in synaptic
plasticity. We have shown that muscarinic toxin 1 (MT1) from Mamba snake venom
(an M1 muscarinic receptor agonist and M4 antagonist) also binds to hippocampal
α-adrenergic (α-1) receptors. In radioligand binding assays in rat
hippocampal membranes, MT1 inhibited the binding of the muscarinic ligand
3H-N-methylscopolamine (3H-NMS, Ki=180±7 nM) and that of the α-1 antagonist 3H-prazosin (3H-PRZ, Ki=83±3
nM), with maximal inhibition of 49±5% and 34±4%, respectively. Furthermore, PRZ
inhibited 3H-NMS binding (Ki=5.1±1.2 µM). Further assays are carried out to
estimate inhibition parameters for the α-1 agonist phenylephrine (PE) on 3H-PRZ and 3H-NMS
binding. We registered field excitatory postsynaptic potentials (fEPSPs) in CA1
area of rat hippocampal fresh slices. Perfusion with MT1, PRZ and PE modified
fEPSPs. MT1 (1µM) and PRZ (10µM) significantly increased fEPSP (41.4±5.2%, n=5;
15.8±3.2%, n=6, respectively); while PE (10µM) decreased fEPSP (23.0±9.0%;
n=4). These indicate that activation of α-a receptors inhibits basal transmission at CA1
synapse. Co-perfusion of MT1+PRZ and MT1+PE would help to discriminate MT1
action on α-1 receptors.