SDZ ENS 163, a selective muscarinic M 1 receptor agonist, facilitates the induction of long-term potentiation in rat hippocampal slices

Abstract

The effect of SDZ ENS 163; (+)-(3S,cis)-3-ethyldihydro-4-[(1-methyl-lH-imidazol-5-yl)methyl-2(3H)-thiphenonedihydrogenphosphate], a selective muscarinic M1 agonist, on long-term potentiation (LTP) was studied in a rat hippocampal slice preparation. LTP was induced by theta-burst stimulation (TBS) delivered to the Schaffer/commissural fibers. In untreated slices delivery of 8 or 10 trains at 100 Hz induced a 27 ± 8.3 and 54 ± 7.2% potentiation of the amplitude of the excitatory postsynaptic potential (epsp), respectively (calculated as percentage of the pre-LTP amplitude). In slices pretreated with SDZ ENS 163 (2 × 10 −6 M, -30 min) delivery of 8 or 10 trains at 100 Hz induced a 62 ± 8.4 and 54 t 7.1% potentiation of the epsp amplitude, respectively. In addition, treatment with SDZ ENS 163 (2 x 10 −6 M) increased the N-methyl-D-aspartate receptor-induced component of the epsp response to TBS from 21 ± 3 (control) to 33 ± 2%. Pretreatment with the muscarinic antagonist, scopolamine (6 × 10 −8 M), or with the M1 selective muscarinic receptor antagonist, pirenzepine (6 × 10 −8 M), did not affect LTP in untreated slices but inhibited the enhancement of UP by SDZ ENS 163 (2 x 10 −6 M) completely. AF-DX 116 10 −6 M, −60 min), a selective muscarinic M 2 receptor antagonist did not affect UP in control slices nor in slices treated with SDZ ENS 163 (2 x 10 −6 M). These data suggest that activation of muscarinic M1 receptors by SDZ ENS 163 facilitates the induction of LTP.