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Biomedical subjects

L Tauc

Publications and source records attributed to L Tauc.

At least 91 records · Page 5Linked to original sources
PubMed1977

Membrane properties of Aplysia neurones intracellularly injected with phospholipases A and C.

1. The effects of phospholipases A from bee venom and from porcine pancreas and of phospholipases C from Clostridium welchii and Bacillus cereus on active and passive membrane properties of Aplysia neurones have been studied. Consistent alterations in electrical membrane properties were found following intracellular application of three of these enzymes.2. Bee venom phospholipase A produced a rapid decrease of membrane potential and resistance. Voltage clamping revealed a marked depression of peak transient current with little or no effect in the late outward current.3. Mammalian phospholipase A was found ineffective in changing either the resting or active membrane properties.4. Phospholipase C from Bacillus cereus led to a strong hyperpolarization and a fall in membrane resistance. Voltage clamping revealed a marked increase in the late outward current.5. Neurones injected with Clostridium welchii phospholipase C manifested a several-fold rise in resting membrane resistance as well as a tendency to slight hyperpolarization.6. All enzymes were ineffective when externally applied.7. It is tentatively concluded that the internally applied phospholipases affect specific ionic permeabilities both in the resting and active excitable membrane. Various mechanisms by which the differing actions of enzymes of the same type could be explained are discussed.

Animals↗
PubMed1975

Multiple interneuronal afferents to the giant cells in Aplysia.

1. Several different types of presynaptic neurones to the giant cells of Aplysia have been found in the pleural ganglion. Some of these presynaptic neurones are common to the left giant cell in the pleural ganglion and to the right giant cell in the abdominal ganglion but others make contact only with one. 2. Interneurones of the left giant cell were studied in detail. They can be identified not only physiologically from the type of post-synapitc potential (p.s.p.) which they produce in the left giant cell, but also by their localization in the ganglion. 3. Direct stimulation of these presynaptic neurones produced not only the classical types of post-synaptic potentials known as e.p.s.p. or i.p.s.p. but also a slow e.p.s.p. and more complex post-synaptic potentials consisting of a rapid depolarizing or hyperpolarizing component (e for excitatory; i for inhibitory). According the p.s.p.s. which have been found were classified as being of eight different types: e.p.s.p., slow e.p.s.p., pseudo-slow e.p.s.p., e.i.p.s.p., i.e.p.s.p., i.i.p.s.p., to which is added the biphasic p.s.p. (b.p.s.p.) of electrical origin. 4. The monosynaptic nature of each of these p.s.p.s. was established by four criteria: (a) ability to follow one to one the presynaptic spike, (b) short and constant latency, (c) change of p.s.p. with the presynaptic spike when the duration is prolonged by iontophoretic injection of TEA, (d) sensitivity of the synaptic efficacy to presynaptic polarization. 5. For all p.s.p.s., the hyperpolarization of the interneurone was followed by a decrease in the corresponding amplitude; on the contrary depolarization produced an increase in p.s.p. amplitude. 6. The physiological role of these p.s.p.s. and their possible mechanism are discussed.

Action Potentials↗
PubMed1975

Heterosynaptic facilitation in the giant cell of Aplysia.

1. Heterosynaptic facilitation, defined as an increase of the efficacy of synaptic transmission between a test interneurone and a post-synaptic neurone, produced by the stimulation of a separate pathway, was studied in the left pleural ganglion. The experimental procedure consisted of detecting the effects of a brief tetanus, applied to tentacular and tegumentary nerves, on the amplitude of monosynaptic and unitary post-synaptic potentials (p.s.p.s) recorded in the left giant cell and generated by stimulating the test interneurone every 10 sec. The membrane potential of the test interneurone was simultaneously recorded. 2. Following heterosynaptic stimulation, the amplitude of the test p.s.p. increased, after a delay of about 30 sec, up to 250% of its original size; this increase subsided after 2-3 min or more. 3. Only the interneurones producing in the giant cell the e.i.p.s.p. (excitatory-inhibitory post-synaptic potential) were affected by hetero-synaptic facilitation. Other interneuronal types showed no changes in their synaptic transmission on the giant cell after heterosynaptic stimulation. 4. Heterosynaptic stimulation did not produce either orthodromic or antidromic spikes in the test interneurones clearly indicating that facilitation of test p.s.p. did not result from increased spike activity in the test interneurone. 5. Often heterosynaptic facilitation of the test p.s.p. was observed due to spontaneous activity in the heterosynaptic pathway, demonstrating the normal occurrence of the phenomenon. 6. Iontophoretic injection of 5-HT at critical, presumably synaptic, sites in the neuropil, evoked a facilitation of the test p.s.p. similar to heterosynaptic facilitation. Only the e.i.p.s.p.s. were so affected by 5-HT. On the contrary, other p.s.p. types were depressed by 5-HT as a result of conductance changes in the left giant cells. 7. Both heterosynaptic facilitation and 5-HT facilitation were suppressed by the presence in the bath of 5-HT (10(-5) M) and of LSD-25 (3 X 10(-4) M). The action of injected 5-HT on the membrane conductance of the left giant cell was also depressed in the pressence of 5-HT in the bath, but was unaffected by LSD-25 (3 X 10(-4) M). 8. From the parallelism of properties of heterosynaptic and 5-HT facilitation, it is suggested that 5-HT is the probable transmitter mediating heterosynaptic facilitation. It seems likely that 5HT is released from the heterosynaptic pathway at the level of the synaptic ending of the test interneurone on to the giant cell and that it increases the efficacy of this synapse, probably acting on the quantity of synaptic transmitter liberated.

Animals↗
PubMed1975

Polyphasic synaptic potentials in the ganglion of the mollusc, Navanax.

1. Included in the ensemble of synaptic input received by identified neurones in the ganglion of the marine mollusc Navanax are biphasic synaptic potentials, consisting of a depolarization followed by a hyperpolarization. 2. Both phases are chemically mediated as judged by their susceptibility to a high magnesium medium and neither exhibits depression with repetition. 3. The hyperpolarizing phase has a reversal potential of about -50mV, which varies only with changes in the external chloride concentration. This phase is unaffected by cholinolytics. 4. The depolarizing phase reverses at a more positive potential, is probably the result of a change in sodium conductance and is blocked by hexamethonium and high concentrations of eserine. 5. The biphasic synaptic potentials are therefore similar in many respects to the biphasic response evoked by iontophoretic application of acetylcholine on to these cells, suggesting that the two types of cholinergic receptors previously characterized on these neurones are both functional.

Animals↗
PubMed1972

Acetylcholine receptors: topographic distribution and pharmacological properties of two receptor types on a single molluscan neurone.

1. The iontophoretic application of acetylcholine (ACh) on to identified neurones in the buccal ganglion of the mollusc Navanax produced a biphasic or monophasic membrane potential change which was a function of the current intensity and site of ACh application.2. Low iontophoretic currents, 200 msec in duration, applied to the somatic surface facing the neuropile, caused a monophasic potential change of 6-10 sec duration, which had a reversal potential of about - 50 mV, varied with changes in the [Cl](o) of the bathing medium, and was not blocked by the cholinolytics tested.3. ACh applied more distal to the soma, in the neuropile, produced a 1-3 sec monophasic response whose reversal potential was more positive than - 30 mV, varied in amplitude with changes in the [Na](o) of the medium, and was blocked by cholinolytics such as tubocurarine, hexamethonium and atropine.4. With larger iontophoretic currents a biphasic response could be obtained, depolarization followed by hyperpolarization, which represented a superposition of the above monophasic potentials.5. The cholinomimetics propionylcholine and butyrylcholine caused a biphasic response like that to ACh. Carbamylcholine and tetramethylammonium also produced a biphasic response but with a more prominent Cl component than that to ACh. Acetyl-beta-methylcholine, oxytremorine and pilocarpine only produced a response comparable to the chloride phase of the ACh response.6. Anticholinesterases prolonged both phases of the ACh response.7. It was concluded that each of the identified neurones possess two types of cholinoceptive sites, which are pharmacologically distinct, produced different changes in membrane permeability and are distributed differently over the axo-somatic membrane complex.

Acetylcholine↗
PubMed1970

Electrical transmission among neurons in the buccal ganglion of a mollusc, Navanax inermis.

The opisthobranch mollusc, Navanax, is carnivorous and cannibalistic. Prey are swallowed whole by way of a sudden expansion of the pharynx. The buccal ganglion which controls this sucking action was isolated and bathed in seawater. Attention was focused upon 10 identifiable cells visible on the ganglion's rostral side. Two cells were observed simultaneously, and each was penetrated with two glass microelectrodes, one for polarizing the membrane and the other for recording membrane potential variations. The coupling coefficients for direct current flow and action potentials of several identified cells were tabulated. Attenuation was essentially independent of the direction of current flow, but depended upon the relative size of the directly and indirectly polarized cells. The attenuation of subthreshold sinusoidally varying voltages increased with frequency above about 1 Hz. The coupling coefficient for spikes was lower than for DC due to greater high frequency attenuation. There is considerable similarity in the spontaneous PSP's of all cells, which is not due to the electrical coupling but to input from a common source. The 10 cells were not chemically interconnected but some were electrically connected to interneurons which fed back chemically mediated PSP's. The feedback can be negative or positive depending upon the membrane potential of the postsynaptic cell. We conclude that electrical coupling among the 10 cells plays a minor role in sudden pharyngeal contractions but that the dual electrical-chemical coupling with interneurons may be important in this respect.

Action Potentials↗
PubMed1970

Heterosynaptic facilitation and post-tetanic potentiation in Aplysia nervous system.

1. Heterosynaptic facilitation was defined as an increase of amplitude of a test excitatory post-synaptic potential (EPSP) after the activation of a pathway (heterosynaptic pathway) different from that which produced the test EPSP. This phenomenon has been studied in Aplysia central nervous system under conditions which excluded the participation of post-tetanic potentiation.2. A unitary test was produced in the left and right giant cells, by indirect stimulation of an interneurone located in the peri-oesophageal ring.3. During heterosynaptic stimulation, orthodromic and antidromic activation of the test interneurone was prevented by (1) isolating the synaptic afferent region of the test interneurone from the tested synapse on the right giant cell by a sucrose block applied on the left pleurovisceral connective, and (2) using physiological stimulation of a piece of skin as a heterosynaptic stimulus. Under these conditions which prevented any firing in the test interneurone, heterosynaptic facilitation is observed as a 200% increase of amplitude of the test EPSP in the right cell which lasted more than 15 min. When instead of the physiological stimulus a supramaximal electrical stimulation of the nerves afferent to the abdominal ganglion was used, the increase of amplitude of the test EPSP could reach as much as 500% of its original amplitude. The effectiveness of such heterosynaptic stimulus was smaller when it was applied in the absence of a block of the left pleuro-visceral connective.4. It was possible to produce heterosynaptic facilitation when the preparation was cooled to 7-9 degrees C or if Li(+) replaced Na(+) in the medium. Both of these changes suppressed post-tetanic potentiation.5. It was concluded that heterosynaptic facilitation is a phenomenon different from post-tetanic potentiation. Heterosynaptic facilitation is similar to heterosynaptic inhibition seen in other cells in the same preparation, except for the polarity of action. Both phenomena seem to result from comparable mechanisms, probably acting on the quantity of transmitter released.

Action Potentials↗