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J W Jacklet

Publications and source records attributed to J W Jacklet.

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Protein synthesis requirement of the Aplysia circadian clock. Tested by active and inactive derivatives of the inhibitor anisomycin.

1. The circadian rhythm of compound action potential frequency recorded from the isolated eye of Aplysia in culture medium and darkness was subjected to 6 h pulse treatments with either anisomycin, a protein synthesis inhibitor, or inactive derivatives of anisomycin. 2. Anisomycin caused phase-dependent phase shifts of the rhythm as expected from previous experiments, but none of the derivative molecules caused phase shifts or perturbed the rhythm. 3. Anisomycin inhibited eye-protein synthesis by 75% at the concentrations (10(-6) M) used in the phase shifting experiments but none of the derivatives inhibited synthesis. 4. Only those molecules that actually inhibited protein synthesis caused phase shifts of the clock, although the inactive derivatives differed from anisomycin by only an acetyl group. 5. The results strengthen the conclusion that the inhibition of protein synthesis caused by anisomycin is important in perturbing the timing of the circadian clock and not some other characteristic effect of the inhibitor molecule. Together with the results from other systems, these findings imply that the daily synthesis of protein is a general requirement for circadian clocks.

Animals↗

Neuronal circadian rhythm: phase shifting by a protein synthesis inhibitor.

A potent inhibitor of protein synthesis, anisomycin, was applied (10(-6)M) in 6-hour pulses at specific phases in the circadian rhythm of endogenous compound action potential (CAP) activity recorded from the eye of Aplysia in vitro. The phase of the circadian rhythm was systematically advanced or delayed (up to 15 hours) depending on the specific phase at which the pulse was applied. The resultant phase response curve implicates protein synthesis on the eukaryotic ribosome as a fundamental part of the controlling processes that constitutes the circadian clock.

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Facilitation at neuromuscular junctions: contribution to habituation and dishabituation of the Aplysia gill withdrawal reflex.

The gill withdrawal reflex of Aplysia has been used as a model for studying the neuronal mechanisms of habituation, a behavioral plasticity. We have assessed the contribution of neuromuscular facilitation, an elementary synaptic plasticity, during habituation of the reflex by recording gill muscle potentials, which we show are caused by excitatory junctional potentials. These potentials show systematic frequency-dependent changes in amplitude. The gill withdrawal evoked by central motor neuron firing during each habituation trial is determined by facilitation of the excitatory junctional potentials during the trial and the facilitated state of the initial excitatory junctional potential in a trial, determined by neuron activity prior to the trial. The neuromuscular junctions, therefore, act like a frequency-dependent amplifier of central motor activity. They are fully responsive to the dynamic changes of motor neuron firing that occurs during habituation and especially after dishabituation.

Action Potentials↗

Habituation of reflexes in Aplysia: contribution of the peripheral and central nervous systems.

We studied the contribution of the Aplysia peripheral nervous system, in the siphon and gill, to habituation of the gill withdrawal reflex. After removal of one central ganglion, the parietovisceral, repeated stimulation of the siphon caused habituation of the reflex as it had with the ganglion intact, showing that there is a peripheral pathway between the siphon and gill with competence to mediate habituation. Repeated electrical stimulation of two efferent nerves to the gill, after removal of the parietovisceral ganglion, resulted in habituation of withdrawal movements, which shows that the terminals of the ganglion neurons in the gill are a site of habituation. Also, stimulation of one nerve dishabituates the withdrawal movements elicited by the other. These identify two sites of habituation in the gill in addition to sites in the parietovisceral ganglion.

Animals↗

Localization of catecholamines in the eyes and other tissues of Aplysia.

A green fluorescence indicative of catecholamines (CA) was localized in the secondary cells (nonreceptor neurons), neuropile and optic nerve of the eye and other tissues in Aplysia by using the formaldehyde-induced fluorescence method for the demonstration of biogenic amines. The specificity of the induced fluorescence was confirmed by its absence in tissue not exposed to formaldehyde vapor, relatively rapid decay upon exposure to UV light and its chemical reduction by sodium borohydride. The fluorescence was greatly reduced in eyes treated with reserpine (depletes serotonin and catecholamines). Furhter confirmation that the green fluorescence in the eye was due to a CA and not to serotonin was obtained by showing that it was decreased or eliminated by alpha-methyl-para-tyrosine (an inhibitor of catecholamine synthesis), increased by incubation in dopamine and exhibited a peak emission (470 nm) characteristic of CA fluroescence. CA fluorescence was also observed in the neuropiles of the cerebral, pedal, pleural and parieto-visceral ganglia and in cells in the pedal ganglion, statocyst, mantle, anterior tentacles and siphon. The finding of CA in secondary neurons of the eye was unusual since CA-containing cells have not been observed in other gastropod eyes. The distribution of CA in Aplysia, in tissue other than the eye, is similar to that of other gastropod molluscs.

Animals↗

Habituation and dishabituation: interactions between peripheral and central nervous systems in Aplysia.

The withdrawal response of the isolated siphon of Aplysia habituates to a light stimulus and dishabituates to a tactile stimulus, and vice versa, with or without connections to the central nervous system. The peripheral nervous system can dishabituate or enhance the response mediated by the central nervous system and vice versa. Normally the adaptive siphon withdrawal response of the intact animal must be mediated by the integrated activity of the peripheral and central nervous systems.

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Circadian rhythm: population of interacting neurons.

The circadian rhythm in the requency of compound action potentials recorded from the isolated eye of Aplysia is a consequence of interactions among the cells of the retinal population. As the population number is reduced to a critical 20 percent, progressively shorter circadian periods and ranges are expressed. Below the critical number, the population oscillates at ultradian frequencies.

Action Potentials↗

Circadian rhythm of optic nerve impulses recorded in darkness from isolated eye of Aplysia.

The isolated eye of the sea hare Aplysia califomica shows a circadian rhythm of optic nerve impulses when kept in total darkness. Peak activity on the first day of isolation occurs during the projected " dawn" of the light-dark cycle to which the whole animal had previously been entrained. Eyes from animals previously exposed to constant light show a free-running rhythm. This simple photoreceptor provides a quantized output with an ideal control (the other eye) for studies on rhythms.

Action Potentials↗

Electrophysiological organization of the eye of Aplysia.

The eye of Aplysia californica was studied by electrophysiological and histological methods. It has a central spheroidal lens which is surrounded by a retina composed of several thousand receptor cells which are replete with clear vesicles, pigmented support cells, neurons which contain secretory granules, and glial cells. The thin optic nerve that connects the eye to the cerebral ganglion gives a simple "on" response of synchronized action potentials. Tonic activity occurs in the optic nerve in the dark and is dependent on previous dark adaptation. Micropipette recordings indicate that the ERG is positive (relative to a bathelectrode) on the outer surface of the eye and negative in the region of the distal segments of the receptors. Intracellular recordings show that receptor cells have resting potentials of 40-50 mv and respond to illumination with graded potentials of up to 55 mv. Dark-adapted receptors exhibit discrete bumps on the graded response to brief light flashes. Other elements in the retina that do not give large graded responses fall into two classes. One class responds to illumination with action potentials that are in synchrony with the extracellularly recorded compound optic nerve potentials. The other class is tonically active and is depolarized or hyperpolarized and inhibited upon illumination. It is apparent that complex excitatory and lateral inhibitory interactions occur among the elements of the retina.

Action Potentials↗

Synaptic connections between a transplanted insect ganglion and muscles of the host.

When a metathoracic ganglion from one cockroach (Periplaneta americana) is transplanted into the coxa of another cockroach, it innervates only those leg muscles that have been previously denervated. The transplanted ganglion evokes hyperpolarizing synaptic potentials in the host muscles that it innervates. These potentials are correlated with twitching of the host limb.

Animals↗

Nerve regeneration: correlation of electrical, histological, and behavioral events.

Wihtin 5 days after the leg nerves of a cockroach are injured, miniature end-plate potentials have disappeared. and the muscle is unresponsive to electrical stimulation. The soma of the injured neutron has a dense perinuclear ring of RNA. By 40 days after the injury, locomotor activity has returned, and the miniature end-plate potentials and evoked electrical responses have reappeared in the muscle. The RNA ring has disappeared, and the nucleus of the regenerating neuron has shifted to an eccentric position.

Evoked Potentials↗

Circadian pacemaker neurons: membranes and molecules.

1. A circadian pacemaker is located in the eyes of a variety of marine gastropods, including Aplysia and Bulla. It produces a circadian rhythm in the frequency of spontaneously occurring optic nerve (ON) compound action potentials (CAPs). The circadian pacemaker in Bulla includes a population of 100 retinal pacemaker neurons, that produce the rhythmic CAP output. Intracellular recording from the Bulla pacemaker neurons has yielded new insight into their time-keeping ability. 2. Intracellular injection of Lucifer yellow dye into a single pacemaker neuron results in the spread of dye to several neurons. This dye coupling is presumably mediated by the gap junctions among neurons that are responsible for the synchronous firing of the population of pacemaker neurons and the generation of ON CAPs. 3. The circadian pacemaker in each eye interacts with the paired pacemaker in the contralateral eye. The interaction results in the coordinating firing of CAPs from each eye and in the coordinated phasing of the circadian rhythms of CAP activity generated in each eye. This interaction occurs by reciprocal excitatory chemical synapses. These synaptic receptors occur in the ON as well as in the retinal neuropil and CAP synchrony occurs in the ON as well as in the basal retina. 4. Pacemaker neurons are depolarized by 5-HT and membrane permeable cAMP analogues. The membrane resistance increases during the depolarization suggesting a background potassium current is decreased. 5. The tetrapeptide FMRF-HN2 hyperpolarizes the pacemaker neurons. It reverses the effect of 5-HT and cAMP, suggesting 5-HT and FMRF-NH2 may be acting on the same membrane channel, the S channel.(ABSTRACT TRUNCATED AT 250 WORDS)

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