Identifying nicotinic and muscarinic cholinoreceptors at the soma of neuron RPa4 inHelix lucorum

Cholinoreceptors were identified at the somatic membrane of theHelix lucorum RPa4 neuron using intracellular recording techniques. Application of specific agonists of nicotinic (nicotine, cytisine) and muscarinic (muscarine, arecoline) cholinoreceptors to the soma produced neuronal depolarization. The depolarization produced by applying acetylcholine to the cell was of short duration and was often replaced by hyperpolarization. Both selective desensitization of receptors by nicotine and muscarine as well as receptor occupancy by cytisine and arecoline reduced acetylchloline-induced response. The nicotinic cholinoblocker d-tubocurarine substantially inhibited responses to nicotinic cholinomimetics, while atropine, a muscarinic cholinoblocker, depressed response to muscarinic cholinomimetics. Acetylcholine-induced response was inhibited by both cholinoblockers more or less equally. The presence at the RPa4 neuronal somatic membrane is postulated of standard nicotinic and muscarinic cholinoreceptors similar to those found in vertebrates.M. V. Lomonsov State University, Moscow. Translated from Neirofiziologiya, Vol. 20, No. 2, pp. 203–212, March–April, 1988.     

Electrophysiological investigation of the properties of acetylcholine receptors of frog sympathetic ganglionic neurons

Changes in membrane potential and conductance were studied in neurons of isolated sympathetic ganglia ofRana ridibunda during perfusion with cholinomimetics and cholinolytics. Activation of nicotinic (N) acetylcholine receptors by carbachol, suberyldicholine, and tetramethylammonium led to depolarization with an increase in conductance, whereas activation of muscarinic (M) acetylcholine receptors by perfusion with carbachol or 5-methylfurmethide, led to depolarization with a decrease or (less frequently) an increase in conductance. The M-cholinolytic atropine was shown to cause depolarization with an increase in conductance if perfusion with atropine was preceded by perfusion with carbachol.A. A. Bogomolets Institute of Physiology, Academy of Sciences of the Ukrainian SSR, Kiev. Translated from Neirofiziologiya, Vol. 11, No. 5, pp. 475–482, September–October, 1979.     

Protein kinase C is not involved in regulating the short-term cholinoreceptor plasticity of the PPa3 and LPa3 neurons of the edible snail

A voltage clamp technique on identified Helix lucorum's RPa3 and LPa3 neurons has been used to negate the effect of protein kinase C on extinction of response to repeated iontophoretic applications of acetylcholine to soma. Extracellular influence of phorbol ether, protein kinase C activator (12-O-tetradecanoylphorbol-13-acetate, 0.1-10 mumol/l), or polymyxin B, its blocker (100-500 mumol/l), do not affect the extinction of acetylcholine-induced neuronal response. The data show that protein kinase C is not involved into molecular mechanisms responsible for the regulation of short-term plasticity of RPa3 and LPa3 neuronal cholinoreceptors in Helix lucorum.     

Role of calcium ions in processes of serotonin-induced modulation of neuronal response to acetylcholone application in Helix pomatia

The role of calcium ions in modulating serotonin action on acetylcholine (ACh) response in nonidentified and identified (LPa3 and RPa3) neurons ofHelix pomatia was investigated using voltage-clamping at the neuronal membrane. Exposure for 1 min to serotonin prior to ACh application reduced response to ACh in neuron LPa3 and raised it in RPa3. The same two patterns of modulating ACh-induced response were produced by extracellular application of theophylline and dibutyryl c-AMP. Injecting calcium ions into neuron LPa3 led to reinforcement of ACh-induced current in the presence of serotonin, thus changing the pattern of serotonin-induced modulation of ACh response in this unit. In neuron RPa3, the same process enhanced the serotonin-induced modulating effect on ACh response but without changing the pattern of modulation, while injected EDTA produced the reverse effects. Increased intracellular concentration of calcium ions brought about a reduction in the degree of serotonin-induced modulation of ACh response in neuron RPa3. Possible reasons are discussed for changes in serotonin-induced bimodal modulation of ACh response in test neurons produced by altering the extracellular concentration of calcium ions.A. A. Bogomolets Institute of Physiology, Academy of Sciences of the Ukrainian SSR, Kiev. Translated from Neirofiziologiya, Vol. 20, No. 5, pp. 666–671, September–October, 1988.     

Ionic mechanisms of the transmembrane current evoked by injection of cyclic amp into identified Helix pomatia neurons

Ionic mechanisms of the transmembrane current evoked by injection of cyclic AMP into identified neurons ofHelix pomatia were investigated by the voltage clamp method. Injection of cyclic AMP into neurons RPa3, LPa2, LPa3, and LPl1 was shown to cause the development of a two-component transmembrane (cyclic AMP) current. The current-voltage characteristic curve of the early component is linear in the region from –40 to –90 mV; the reversal potential of the early component, determined by extrapolation, lies between –5 and +20 mV; the current-voltage characteristic curve of the late component also is linear and has a reversal potential between –55 and –60 mV. A decrease in the sodium concentration in the external medium from 100 to 25 mM led to a decrease in amplitude of the cyclic AMP current and to a shift of the reversal potential for the early component by 30–32 mV toward hyperpolarization. It is suggested that the early component of the cyclic AMP current in neurons RPa3, LPa2, LPa3, and LPl1 is associated with an increase in permeability of the neuron membrane chiefly for sodium ions, whereas the late component is correspondingly connected with permeability for potassium ions. Injection of cyclic AMP also caused the appearance of a transmembrane inward current in neuron LPa8, but it was independent of the holding potential and was unaccompanied by any change in membrane permeability. It is suggested that this current may be due to a change in the activity of the electrogenic ion pump.A. A. Bogomolets Institute of Physiology, Academy of Sciences of the Ukrainian SSR, Kiev. Translated from Neirofiziologiya, Vol. 12, No. 5, pp. 526–532, September–October, 1980.     

The role of cyclic 3',5'-adenosine monophosphate in the extinction of the reaction of identified neurons in the edible snail to acetylcholine

The recording of transmembrane currents and intracellular potentials has been used to show on Helix lucorum identified neurons RPa4, RPa3 and LPa3, that pharmacologic effects on adenylate cyclase system do not influence the extinction of neuronal response to repeated local iontophoretic applications of acetylcholine to the soma. Neither cAMP-raising adenylate cyclase activator forskolin (2-6 x 10(-5) mol/l), nor cAMP-lowering phosphodiesterase activator imidazole (5 x 10(-3) mol/l) alter the dynamics of extinction of response to acetylcholine. A conclusion has been made that shortterm plasticity of cholinoreceptors in the investigated neurons is independent of intracellular cAMP level.     

Dose-response dependence of the excitatory effect of acetylcholine on Helix lucorum neurons after orthodromic tetanization

Hill numbers before and after tetanic stimulation were calculated from dose-response dependence between the amplitude of the acetylcholine-induced inward current and the amplitude of the iontophoretic current through a micropipette filled with acetylcholine. Semi-intact Helix lucorum preparation was used. Acetylcholine-induced inward currents were recorded using two-electrode voltage clamp technique. Tetanic stimulation evoked changes in dose-response dependence but did not modify the slopes of dose-response plots (Hill numbers were 1.42 + 0.15 before and 1.41 + 0.15 after tetanization). It was concluded that increase in cholinosensitivity in LPa3 and RPa3 neurons after the orthodromic tetanic stimulation of nervus intestinalis is not accompanied by changes in the number of ligand-binding sites per acetylcholine receptor molecule or proportion of nicotinic and muscarinic cholinoreceptors.     

Action of local iontophoretic application of acetylcholine and serotonin to neurons of the rabbit superior cervical ganglion

The action of ionotophoretic application of acetylcholine and serotonin (5-hydroxytryptamine) on neurons of the isolated rabbit superior cervical ganglion was investigated by intracellular recording. The soma of neurons in the ganglion was shown to have no muscarinic receptors and to have only nicotinic receptors scattered irregularly over the whole surface of the neuron soma membrane. Acetylcholine has an excitatory action on presynaptic endings. In about half of the neurons of the ganglion the soma was shown to possess serotonin receptors.A. A. Bogomolets Institute of Physiology, Academy of Sciences of the Ukrainian SSR, Kiev. Translated from Neirofiziologiya, Vol. 10, No. 5, pp. 519–524, September–October, 1978.     

Effect of intracellular injection of cyclic amp on electrical characteristics of identified neurons in Helix pomatia

The effect of intracellular iontophoretic injection of cyclic AMP on electrical activity of neurons RPa1, RPa3, LPa2, LPa3, and LPl1 in the corresponding ganglia ofHelix pomatia was investigated. Injection of cyclic AMP into neuron LPl1 was found to cause the appearance of rhythmic activity (if the neuron was originally "silent"), an increase in the frequency of spike generation (if the neuron had rhythmic activity), and a decrease in amplitude of waves of membrane potential, in the duration of the interval between bursts, and in the number of action potentials in the burst (if the neuron demonstrated bursting activity). In the remaining "silent" neurons injection of cyclic AMP led to membrane depolarization. Injection of cyclic AMP into neurons whose membrane potential was clamped at the resting potential level evoked the development of an inward transmembrane current (cyclic AMP current), the rate of rise and duration of which increased proportionally to the size and duration of the injection. Theophylline in a concentration of 1 mM led to an increase in the amplitude and duration of the cyclic AMP current by about 50%. It is concluded that a change in the cyclic AMP concentration within the nerve cell may modify the ionic permeability of its membrane and, correspondingly, its electrical activity.A. A. Bogomolets Institute of Physiology, Academy of Sciences of the Ukrainian SSR, Kiev. Translated from Neirofiziologiya, Vol. 12, No. 5, pp. 517–525, September–October, 1980.     

Distribution of the LPa3 and PPa3 neuronal processes in the pedal ganglia of the edible snail

By means of intracellular injection of the dye Lucifer yellow processes were revealed of the snail command neurones of escape behaviour LPa3 and RPa3 in pedal nerves ipsilateral to these neurones. A process of the neurone LPa3 was also found in the contralateral Nervus cutaneus pedalis secundus. Blockade of central chemical synapses by cadmium chloride did not lead to disappearance of motor reactions evoked by electrical stimulation of LPa3 and RPa3 neurones both on ipsi- and contralateral sides of the animal foot; this allowed to suggest a presence in the contralateral muscular pedal nerves of these neurones processes unrevealed by the used dyeing method.     

The role of cGMP in extinguishing the reactions of identified neurons in the edible snail to acetylcholine

Possible role of cGMP is studied in control of extinction of snail neurones RPa4, RPa3 and LPa3 reactions to acetylcholine (ACh), applied rhythmically to neurone soma by means of microiontophoresis. It is shown that guanylate cyclase activators which raise the cGMP level in the cell--Na nitroprusside and Na azide (5,10(-4)-10(-3) mol/l)--intensify at extracellular application the extinction of inward transmembrane current and membrane depolarization in response to ACh. Suggestion is made about participation of cGMP-dependent phosphorylation of membrane proteins in control of the development rate, depth and duration of neurone cholinoreceptors short-term plasticity.     

Ca-dependent regulation by Na, K-pump of post-tetanic sensitization of extrasynaptic choline receptors in Helix lucorum neurons

Posttetanic potentiation (by orthodromic stimulation) of cholinosensitivity in LPa3 and RPa3 Helix lucorum neurons that are command in respect to withdrawal behavior was shown earlier (Pivovarov et al., 1999). Now we studied the regulatory role of the Na,K-pump and intracellular free Ga2+ in the posttetanic potentiation (PTP) of cholinosensitivity in command neurons. Semiintact Helix preparation "CNS-visceral bag" was used in experiments. Acetylcholine-induced inward currents were recorded using two-electrode voltage clamp technique. Acetylcholine was applied to somata of the identified LPa3 and RPa3 neurons with a 10-min interval before and after electrical tetanic stimulation of the n. intestinalis (10.5 mA; 0.1 s; 2/s; 2 min). Ouabain (extracellular application, 70 mcM) blocked the PTP. Intracellular injection of BAPTA (1 mM), chelator of Ca2+ ions, prevented the PTP. The PTP was absent after the ouabain application against the background of preliminary intracellular injection of BAPTA. A conclusion war drawn about Ca-dependent participation of Na,K-pump in posttetanic potentiation of cholinosensitivity in command Helix lucorum neurons of withdrawal behavior.     

Ionic mechanisms underlying acetylcholine-, nicotine-, and muscarine-induced depolarization of Helix lucorum neuron RPa4

Research was carried out into the ionic aspects of depolarization potentials produced inHelix lucorum neuron RPa4 by injecting three cholinomimetics into the soma: acetylcholine, nicotine, and muscarine. Substances were used suppressing Na⁺, K⁺, Ca²⁺, and Cl^– conductance at the membrane. Acetylcholine brought about increased Na⁺, Ca²⁺; and Cl^– conductance. As the choline component was only slight, due to the similarity of membrane and resting potential for chloride, it might be deduced that the prevailing response to acetylcholine is associated with chemically controlled input of Na⁺ and Ca²⁺ into the cell. Nicotine and muscarine induced mainly sodium and calcium conductance respectively.M. V. Lomonosov State University, Moscow. Translated from Neirofiziologiya, Vol. 21, No. 3, pp. 305–314, May–June, 1989.     

Disulfide bonds in acetylcholine receptors of frog sympathetic ganglion neurons

Changes in responses of frog sympathetic ganglion neurons to perfusion with cholinomimetics were studied during modification of acetylcholine receptors by dithiothreitol and ferricyanide. Perfusion with dithiothreitol suppressed responses to carbachol, suberyldicholine, and 5-methylfurmethide, whereas subsequent perfusion with ferricyanide partly restored responses to suberyldicholine but suppressed responses to 5-methylfurmethide. Acetylcholine and tetramethylammonium, used as protectors, protected nicotinic and muscarinic receptors against the action of dithiothreitol, but acetylcholine was more effective than tetramethylammonium for nicotinic acetylcholine receptors. It is suggested that disulfide bonds, some of them located in the anionic centers of the receptors, are present in the recognition sites of acetylcholine receptors of the frog sympathetic ganglion.A. A. Bogomolets Institute of Physiology, Academy of Sciences of the Ukrainian SSR, Kiev. Translated from Neirofiziologiya, Vol. 11, No. 6, pp. 593–600, November–December, 1979.     

Interactions of endogenous lectin from theHelix pomatia reproductive system (HPA) with the surface of CNS neurons of the snail

The surface of unidentified cultured neurons and electrophysiologically identified units RPa1, RPa2, and LPa3 of the snailHelix pomatia was studied using a colloidal gold-labelled endogenous gonad lectin of this molluse (Helix pomatia agglutinin -HPA), which is specific to -anomer N-acetyl-D-galactosamine, and some other lectins. It was found that only two populations of cultured neurons with a specific ultrastructure typical of peptidergic cells and differing from the ultrastructure of other peptidergic and non-peptidergic neurons possessHPA receptors. These neurons average about 1% of cultured nerve cells. Using a variety of plant lectins withHPA-like specificity (LBA, VVA, SBA) showed that the surface of many peptidergic neurons contains -anomer-like structures, yet it does not bindHPA. These data were supported in the experiments on identified snall neurons with the use ofSBA. The results suggest a putative role of endogenous lectins in regulation of activity of neurons participating in processes of secretion in the gonads.Neirofiziologiya/Neurophysiology, Vol. 28, No. 1, pp. 17–29, January–February, 1996.     

The negative shift in the reversal potential of the acetylcholine-induced incoming current in the RPa3 and LPa3 neurons of the edible snail during its extinction

A negative shift of reversal potential at its extinction has been found with the current-voltage relation of acetylcholine-induced inward current in Helix lucorum's RPa3 and LPa3 neurons. An assumption has been made on a nonuniform extinction of acetylcholine-induced currents which is due to the motion of different ions. Ion flow with a more positive equilibrium potential decreases to a greater degree than reversal potential. It can be a current of Ca2+ and/or Na+ ions.     

The duration of the storage of the electrical characteristics of command neurons in the acquisition of long-term sensitization in the snail

The retention of the long-term sensitization (LTS) of defensive reflex and dynamics of change in electric characteristics (membrane potential (Vm) and action potential generation threshold (Vt)) of command neurons of defensive reflex was studied in a snail during behavioral tests. The membrane mechanisms were analyzed by measuring electrical characteristics of the LPa3, RPa3, LPa2, and RPa2 command neurons on the 1st, 4th, 7th, 10th, and 14th days after the LTS formation and 1 month later. The membrane potential and threshold potential in sensitized snails (-54.1 +/- 2.0 and 24.5 +/- 1.4 microV, respectively) were significantly (p < 0.001) decreased in comparison with the control animals (-60.9 +/- 0.8 and 19.9 +/- 0.6 microV respectively). These changes retained within 14 days after the LTS formation. The results suggest the long-term retention of the increased excitability of command neurons. A month after the LTS formation, the duration of the defensive reflex returned to the initial level and the electric characteristics of command neurons did not significantly differ from the control (-61.1 +/- 2.0 and 19.3 +/- 1.4 microV, respectively).     

Synaptic effects of nicotinic and muscarinic agonists in sympathetic ganglia of the frog

Superfusion of the isolated sympathetic ganglia of the frog with nicotinic agonists (suberyldicholine, tetramethylamonium, and dimethylphenylpiperazinium), as well as acetylcholine in the presence of atropine led to a brief depolarization of the neurons and blockade of synaptic transmission. The muscarinic agonists methylfurmethide (MFM) and methyldilvasen, cis^–, L(+), as well as acetylcholine elicited a stable depolarization which is not accompanied by disturbance in transmission. Oxotremorine at a concentration of 1·10^–5 M did not lead to the depolarization of the post-synaptic membrane, but at a concentration of 1·10^–6 M decreased the quantal EPSP content twofold, which indicates that the presynaptic receptors belong to the M₂ subtype. Inhibition of acetylcholinesterase significantly intensified the postsynaptic effect of MFM: a shift of the concentration-effect curve took place toward the side of lower MFM concentrations. It was shown that the post-synaptic muscarinic receptors of the ganglionic neurons possess varied sensitivity to the enantiomers of methyldilvasen and, consequently, are stereospecific. The identified functional properties of the cholinoreceptors of the ganglionic neurons explain the set of changes in synaptic transmission under conditions of the prolonged presence of a mediator in the synaptic cleft.I. M. Sechenov Institute of Evolutionary Physiology and Biochemistry, Academy of Sciences of the USSR, Leningrad. Translated from Neirofiziologiya, Vol. 20, No. 2, pp. 227–234, March–April, 1988.     

Protein Kinase C Is Involved in M1-Muscarinic Receptor-Mediated Facilitation of L-Type Ca2+ Channels in Neurons of the Major Pelvic Ganglion of the Adult Male Rat

We used patch clamp recording techniques to determine if muscarinic signaling mechanisms are present in dissociated autonomic neurons obtained from the major pelvic ganglion, which provides the cholinergic innervation of the urinary bladder and other pelvic organs. The M₁ specific agonist, McN-A-343 (2–30 M) enhanced Ca²⁺ currents in approximately 37% of neurons (by 50–80%). This enhancement was reduced by atropine (5–10 M) or a PKC inhibitor (bisindolylmaleimide, 50–200 nM). In responsive neurons Ca²⁺ currents were also enhanced by the phorbol ester, phorbol-12, 13-dibutyrate (50–300 nM) and the dihydropyridine agonist Bay K 8644 (5 M) and had kinetics of activation and inactivation as expected for L-type Ca²⁺ channels. We conclude that in a subpopulation of MPG neurons, M₁-mediated activation of PKC phosphorylates and enhances L-type Ca²⁺ channel activities. This muscarinic facilitatory mechanism in MPG neurons may be the same as the M₁-mediated facilitation of transmitter release reported previously at the nerve terminals in the urinary bladder.     

EPYLRFamide-mediated reduction of acetylcholine-induced inward currents in Helix lucorum-identified neurones: role of NAADP-dependent and IP3-dependent Ca2+ release from internal stores,calmodulin and Ca2+/calmodulin-dependent protein kinase II

The effect of seven compounds intracellularly applied by spontaneous diffusion were investigated on the EPYLRFamide-induced reduction of acetylcholine-induced inward current (ACh-current) recorded from identified neurones from Helix lucorum. Inward currents were recorded from neurones LPa2, LPa3, RPa3 and RPa2 in isolated ganglia preparations using two-electrode voltage clamp technique. ACh was applied ionophoretically. Heparin, an antagonist of IP(3) receptors (IP(3)Rs), and IP(3), the agonist of IP(3)Rs, decreased the effect of EPYLRFamide. Thio-NADP, a blocker of NAADP-induced Ca(2+) release, beta-NAADP, Ca(2+) releaser, R24571, W-7 (both calmodulin antagonists), and KN-62, a selective inhibitor of Ca(2+)/calmodulin-dependent protein kinase II, did not change the modulatory effect of EPYLRFamide. These data suggest that EPYLRFamide decreases ACh-current through elevation of the basal intracellular level of the putative endogenous agonist of IP(3)Rs which activates release of Ca(2+) from intracellular stores. It is concluded that intracellular free Ca(2+) acts on ACh receptor/ionic channel without activation of calmodulin and Ca(2+)/calmodulin-dependent protein kinase II.