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Neuroscience |
1 Institute of Neuroscience (CNR), 56100 Pisa, Italy
2 International School for Advanced Studies (SISSA), 34014 Trieste, Italy
3 Molecular Signaling Section, Laboratory of Bioorganic Chemistry, NIDDK, National Institutes of Health, Bethesda, MD 20892, USA
4 Dipartimento di Scienze e Tecnologie Biomediche, Università dell'Aquila, 67010, L'Aquila, Italy
In the present report, we focused our attention on the role played by the muscarinic acetylcholine receptors (mAChRs) in different forms of long-term synaptic plasticity. Specifically, we investigated long-term potentiation (LTP) and long-term depression (LTD) expression elicited by theta-burst stimulation (TBS) and low-frequency stimulation (LFS), respectively, in visual cortical slices obtained from different mAChR knockout (KO) mice. A normal LTP was evoked in M1/M3 double KO mice, while LTP was impaired in the M2/M4 double KO animals. On the other hand, LFS induced LTD in M2/M4 double KO mice, but failed to do so in M1/M3 KO mice. Interestingly, LFS produced LTP instead of LTD in M1/M3 KO mice. Analysis of mAChR single KO mice revealed that LTP was affected only by the simultaneous absence of both M2 and M4 receptors. A LFS-dependent shift from LTD to LTP was also observed in slices from M1 KO mice, while LTD was simply abolished in slices from M3 KO mice. Using pharmacological tools, we showed that LTP in control mice was blocked by pertussis toxin, an inhibitor of Gi/o proteins, but not by raising intracellular cAMP levels. In addition, the inhibition of phospholipase C by U73122 induced the same shift from LTD to LTP after LFS observed in M1 single KO and M1/M3 double KO mice. Our results indicate that different mAChR subtypes regulate different forms of long-term synaptic plasticity in the mouse visual cortex, activating specific G proteins and downstream intracellular mechanisms.
(Received 13 July 2006;
accepted after revision 4 October 2006;
first published online 5 October 2006)
Corresponding author L. Domenici: Dipartimento di Scienze e Tecnologie Biomediche, Università dell'Aquila, 67010, L'Aquila, Italy. Email: domenici{at}in.cnr.it
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