Journal of neurophysiology · 2008
Serotonin transduction cascades mediate variable changes in pyloric network cycle frequency in response to the same modulatory challenge.
СтатьяПоддержка NIH: внешняя программаПоддержка исследования: вне правительства СШАПоддержка правительства СШАНазвание и аннотация: Перевод в очереди
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Spitzer Nadja, Cymbalyuk Gennady, Zhang Hongmei, Edwards Donald H, Baro Deborah J
Аннотация
A fundamental question in systems biology addresses the issue of how flexibility is built into modulatory networks such that they can produce context-dependent responses. Here we examine flexibility in the serotonin (5-HT) response system that modulates the cycle frequency (cf) of a rhythmic motor output. We found that depending on the preparation, the same 5-min bath application of 5-HT to the pyloric network of the California spiny lobster, Panulirus interruptus, could produce a significant increase, decrease, or no change in steady-state cf relative to baseline. Interestingly, the mean circuit output was not significantly different among preparations prior to 5-HT application. We developed pharmacological tools to examine the preparation-to-preparation variability in the components of the 5-HT response system. We found that the 5-HT response system consisted of at least three separable components: a 5-HT(2betaPan)-like component mediated a rapid decrease followed by a sustained increase in cf; a 5-HT(1alphaPan)-like component produced a small and usually gradual increase in cf; at least one other component associated with an unknown receptor mediated a sustained decrease in cf. The magnitude of the change in cf produced by each component was highly variable, so that when summed they could produce either a net increase, decrease, or no change in cf depending on the preparation. Overall, our research demonstrates that the balance of opposing components of the 5-HT response system determines the direction and magnitude of 5-HT-induced change in steady-state cf relative to baseline.
Предметные рубрики MeSH
Action PotentialsAnimalsButaclamolCell Line, TransformedDopamine AntagonistsDrug InteractionsGanglia, InvertebrateHumansIn Vitro TechniquesInositol PhosphatesNerve NetNeuronsPalinuridaePiperazinesReceptor, Serotonin, 5-HT1AReceptors, Serotonin, 5-HT2SerotoninSerotonin Receptor AgonistsSignal TransductionTime FactorsTransfection