Cellular mechanisms for modulation of posture by octopamine and serotonin in the lobster.

Injection of the monoamines octopamine and serotonin into the hemolymph of lobsters causes them to assume opposing static postures: octopamine causes a tonic extension of all extremities, while serotonin induces a tonic flexion. These amines have been shown previously to act as circulating neurohormones and to cause contraction of isolated exoskeletal muscles. The opposing postures elicited by amine injection do not appear to arise from peripheral actions, however, since serotonin and octopamine have similar effects on both flexor and extensor muscles. Instead, the amines are present within the central nervous system where they are probably released synaptically to activate coordinated patterns of tonic motor activity generating the observed postures. These motor patterns have been recorded from abdominal ganglia and involve the synchronized activation and inhibition of multiple excitatory and inhibitory motoneurons innervating the postural flexor and extensor muscles. These effects can be observed in an isolated abdominal ganglion. To begin a search for the cellular targets of amine action within the central nervous system, we recorded from identified postural motoneurons in abdominal ganglia. In two motoneurons that act to produce postural extension, octopamine reduced and serotonin raised the apparent threshold for action potential generation recorded in the somata. The amines do not significantly affect the resting potential or input resistance of the motoneurons measured in the cell bodies. Although the amine effect on motoneuron excitability could be due to actions directly on the motoneurons, our evidence suggests that at least part of the effect results from activation or inhibition of premotor interneurons: (1) an increase in EPSP frequency is observed in the motoneurons during octopamine superfusion, while a small decrease is observed during serotonin superfusion; (2) the amine effects on action potential threshold are abolished by cobalt ion. These results suggest that octopamine and serotonin have dual effects on posture: within the central nervous system, they act specifically to generate coordinated motor patterns for flexion or extension; as circulating neurohormones, they act nonspecifically to enhance the responses of exoskeletal muscles to motoneuronal activation.