Differential modulation of synaptic strength and timing regulate synaptic efficacy in a motor network

• Published in: Journal of neurophysiology 2011-01, Vol.105 (1), p.293-304
• Main Authors: Johnson, Bruce R, Brown, Jessica M, Kvarta, Mark D, Lu, Jay Y J, Schneider, Lauren R, Nadim, Farzan, Harris-Warrick, Ronald M
• Format: Article
• Language: English
• Subjects: Animals; Dopamine - pharmacology; Homarus americanus; Marine; Models, Animal; Motor Neurons - drug effects; Motor Neurons - physiology; Nerve Net - drug effects; Nerve Net - physiology; Octopamine - pharmacology; Palinuridae - physiology; Pylorus - innervation; Serotonin - pharmacology; Synapses - drug effects; Synapses - physiology; Time Factors
• ISSN: 0022-3077; 1522-1598
• DOI: 10.1152/jn.00809.2010

Neuromodulators modify network output by altering neuronal firing properties and synaptic strength at multiple sites; however, the functional importance of each site is often unclear. We determined the importance of monoamine modulation of a single synapse for regulation of network cycle frequency in the oscillatory pyloric network of the lobster. The pacemaker kernel of the pyloric network receives only one chemical synaptic feedback, an inhibitory synapse from the lateral pyloric (LP) neuron to the pyloric dilator (PD) neurons, which can limit cycle frequency. We measured the effects of dopamine (DA), octopamine (Oct), and serotonin (5HT) on the strength of the LP→PD synapse and the ability of the modified synapse to regulate pyloric cycle frequency. DA and Oct strengthened, whereas 5HT weakened, LP→PD inhibition. Surprisingly, the DA-strengthened LP→PD synapse lost its ability to slow the pyloric oscillations, whereas the 5HT-weakened LP→PD synapse gained a greater influence on the oscillations. These results are explained by monoamine modulation of factors that determine the firing phase of the LP neuron in each cycle. DA acts via multiple mechanisms to phase-advance the LP neuron into the pacemaker's refractory period, where the strengthened synapse has little effect. In contrast, 5HT phase-delays LP activity into a region of greater pacemaker sensitivity to LP synaptic input. Only Oct enhanced LP regulation of cycle period simply by enhancing LP→PD synaptic strength. These results show that modulation of the strength and timing of a synaptic input can differentially affect the synapse's efficacy in the network.