To characterize the transfer of graded potentials and the properties of the associated noise in the photoreceptor-interneuron synapse of the blowfly (CaUiphora vicina) compound eye, we recorded voltage responses of photoreceptors (R1-6) and large monopolar cells (LMC) evoked by: (a) steps of light presented in the dark; (b) contrast steps; and (c) pseudorandomly modulated contrast stimuli at backgrounds covering 6 log intensity units. Additionally, we made recordings from photoreceptor axon terminals. Increased light adaptation gradually changed the synaptic signal transfer from low-pass to band-pass filtering. This was accompanied by decreased synaptic delay and increased contrast gain, but the overall synaptic gain and the intrinsic noise (i.e., transmission noise) were reduced. Based on these results, we describe a descriptive synaptic model, in which the kinetics of the tonic transmitter (histamine) release from the photoreceptor axon terminals change with mean photoreceptor depolarization. During signal transmission, tonic transmitter release is augmented by voltage-dependent contrast-enhancing mechanisms in the photoreceptor axons that produce fast transients from the rising phases of the photoreceptor responses and add these enhanced voltages to the original photoreceptor responses. The model can predict the experimental findings and it agrees with the recently proposed theory of maximizing sensory information.
1. We studied the graded and spiking properties of the "non-spiking" first-order visual interneurons of the fly compound eye in situ with the use of intracellular recordings. Iontophoretical QX-314 injections, Lucifer yellow marking, and (discontinuous) current-clamp method together with transfer function analysis were used to characterize the neural signal processing mechanisms in these neurons. 2. A light-OFF spike was seen in one identified anatomic subtype (L3, n = 6) of the three first-order visual interneurons (L1, L2, and L3, or LMCs) when recorded from synaptic region (i.e., in the 1st visual ganglion, lamina ganglionaris) in dark-adapted conditions. Hyperpolarization of the membrane potential by current caused the identified L1 (n = 4), as well as L3 (n = 6), to produce an OFF spike, a number of action potentials, and some subthreshold depolarizations after the light-ON response. In L2 the OFF spike or action potentials could not be elicited. 3. To produce action potentials in L1 and L3, it was found to be necessary to hyperpolarize the cells approximately 35-45 mV (n = 43) below the resting potential (RP) in the synaptic zone. Recordings from the axons of these cells revealed that near the second neuropil (chiasma) the threshold of these spikes was near to (approximately 10 mV below, n = 16) or even at the RP when an ON spike was also produced (n = 4). 4. The recorded spikes were up to 54 mV in amplitude, appeared with a maximum frequency of up to 120 impulses/s, and had a duration of approximately 8 ms. In L1 and L3 the spikes were elicited either after a light pulse (L3) or after a negative current step that was superimposed on a hyperpolarizing steady-state current (L3 and L1). A positive current step (similarly superimposed on a hyperpolarizing steady-state current) also triggered the spikes during the step. 5. Iontophoretic injection of a potent intracellularly effective blocker of voltage-gated sodium channels, QX-314, irreversibly eradicated the spikes and subthreshold depolarizations (n = 5). In addition, further injections elongated the light-ON responses and decreased or even abolished the light-OFF response. 6. Negative prepulses followed by positive current steps were applied from the RP, to test the activation-inactivation properties of the channels responsible for the OFF spike.(ABSTRACT TRUNCATED AT 400 WORDS)
1. We studied graded synaptic transmission in the fly photoreceptor-interneuron synapse by using intracellular in situ recordings from pre- and postsynaptic cells. 2. A large presynaptic hyperpolarization after light adaptation, caused by the activation of the electrogenic Na+/K+ pump, drastically reduced the conspicuous postsynaptic dark noise. At the same time, the postsynaptic neurons depolarized, with an increase of input resistance of 5-10 M omega. 3. The spectral characteristics of the postsynaptic membrane noise in dark and during noise reduction, together with the other results, suggested that the transmitter release decreased dramatically approximately 12 mV below the resting potential of the presynaptic photoreceptors. 4. During the postsynaptic noise reduction, the saturated and subsaturated first-order visual interneuron responses were increased up to 9 mV with a time constant of recovery of approximately 10 s. This increase was shown to be caused by the negative shift of the reversal potential of the transmitter-gated (mainly Cl-) conductance, caused apparently by the reduced transmitter input. 5. The results strongly suggest that the photoreceptor transmitter release in fly is tonic, even in dark, and further support the modulation of the synaptic voltage transfer by postsynaptic Cl- extrusion.
1. Randomly modulated light stimuli were used to characterize the nonlinear dynamic properties of the synapse between photoreceptors and large monopolar neurons (LMC) in the fly retina. Membrane potential fluctuations produced by constant variance contrast stimuli were recorded at eight different levels of background light intensity. 2. Representation of the photoreceptor-LMC input-output data in the form of traditional characteristic curves indicated that synaptic gain was reduced by light adaptation. However, this representation did not include the time-dependent properties of the synaptic function, which are known to be nonlinear. Therefore nonlinear systems analysis was used to characterize the synapse. 3. The responses of photoreceptors and LMCs to random light fluctuations were characterized by second-order Volterra series, with kernel estimation by the parallel cascade method. Photoreceptor responses were approximately linear, but LMC responses were clearly nonlinear. 4. Synaptic input-output relationships were measured by passing the light stimuli to LMCs through the measured photoreceptor characteristics to obtain an estimate of the synaptic input. The resulting nonlinear synaptic functions were well characterized by second-order Volterra series. They could not be modeled by a linear-nonlinear-linear cascade but were better approximated by a nonlinear-linear-nonlinear cascade. 5. These results support two possible structural models of the synapse, the first having two parallel paths for signal flow between the photoreceptor and LMC, and the second having two distinct nonlinear operations, occurring before and after chemical transmission. 6. The two models were cach used to calculate the synaptic gain to a brief change in photoreceptor membrane potential. Both models predicted that synaptic gain is reduced by light adaptation.
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