Structure and financing of health care.
Explore the source record for details and available documents.
Health Care Reform↗
Biomedical subjects
R Gillette
Publications and source records attributed to R Gillette.
From Polyplacophora to Cephalopoda: comparative analysis of nitric oxide signalling in mollusca.
The distribution of putative nitric oxide synthase (NOS)-containing cells has been analysed using NADPH-d histochemistry in the CNS and peripheral tissues in more than 2D ecologically and systematically different molluscan genera representing 3 main classes of the phylum MOLLUSCA: Polyplacophora (Lepidopleurus, Lepidozona, Katharina), Gastropoda (Littorina, Lymnaea, Aplexa, Physa, Planorbarius, Planorbis, Helisoma, Biomphalaria, Helix, Limax, Cepaea, Bulla, Aplysia, Phyllaplysia, Philine, Pleurobranchea, Tritonia, Armina, Flabellina, Cadlina) and Cephalopoda (Octopus, Sepia, Rossia, Loligo). Several species were used for more detailed immunohistochemical, biochemical, biophysical and physiological studies to further assay of NOS activity and to analyse functional roles of nitric oxide (NO) in these animals. The main conclusions of our comparative analysis and literature survey can be summarised as following: (i) There is strong evidence for the presence of NO-dependent signalling pathways in different molluscan species. (ii) We hypothesise that a general tendency in the evolution of NADPH-d-reactive cells in Mollusca is a migration of nitrergic function from periphery to the CNS. Also, different isoforms of NOS appear to be present in any one species. (iii) One of the main functional targets of NO signalling is the feeding system. However, there are obvious differences between predators (many labelled central motoneurons) and herbivorous species (many labelled peripheral putative sensory cells) as well as between land/freshwater and marine animals. Nevertheless, in all species tested NO-activated feeding-like motor patterns in the buccal ganglia. Additional functional and cellular targets for NO in molluscs are also considered. We briefly review neuromodulatory mechanisms of NO action and we consider molluscs as useful model systems for investigations of the roles of NO.
Animals↗
Primary care needs.
Explore the source record for details and available documents.
Delivery of Health Care↗
Co-regulation of cAMP-activated Na+ current by Ca2+ in neurones of the mollusc Pleurobranchaea.
1. The cAMP-gated Na+ current (INa, cAMP) was studied in axotomized neurons of the pedal ganglion of the sea slug Pleurobranchaea. INa, cAMP responses were elicited by iontophoretic injection of cAMP and recorded in voltage clamp. 2. The current-voltage relation for INa, cAMP was flat between -90 and -50 mV, but declined steeply with depolarization from -50 to -30 mV. Depolarizing pulses also suppressed the INa, cAMP response, which recovered slowly over tens of seconds. 3. The inactivating effects of depolarization on the current were abolished both by blockade of Ca2+ current and intracellular injection of Ca2+ chelator. Thus, Ca2+ influx through voltage-dependent Ca2+ channels probably mediates inactivation of INa, cAMP within its normal physiological range of action. 4. Increasing intracellular cAMP levels antagonized the effects of Ca2+ influx on INa, cAMP. The mutual antagonism of the ions suggests that cAMP and Ca2+ act competitively in regulation of the INa, cAMP channel. 5. Measures of fractional inactivation of INa, cAMP provided evidence for the existence of an appreciable basal level of current, and hence cAMP, in the unstimulated neuron. Since INa, cAMP is a direct function of cAMP activity, measures of fractional inactivation permit quantification of cAMP levels in the living neuron. 6. Calcium inactivation of INa, cAMP completes a negative feedback loop that can contribute to endogenous burst activity. Over the burst cycle, depolarization and action potential activity driven by INa, cAMP would lead to Ca2+ influx, consequent inactivation of the inward current, and hyperpolarization. This mechanism of endogenous bursting resembles other in which the burst cycle has been found to be regulated by kinetics of Ca2+ influx and removal. However, INa, cAMP may vary in its Ca2+ sensitivity in different neurons and these variations may affect the functional expression of endogenous oscillatory activity.
Animals↗
cAMP-activated Na+ current of molluscan neurons is resistant to kinase inhibitors and is gated by cAMP in the isolated patch.
The cAMP-dependent Na+ current (INa,cAMP) modulates excitability in many molluscan neurons. Rapid activation of INa,cAMP by cyclic nucleotide, its ion dependence, and its blockade by divalent cations resemble cyclic nucleotide-activated cation currents in vertebrate photoreceptors and olfactory receptors, where activation has been found to be independent of kinase activity. We tested the phosphorylation dependence of INa,cAMP in neurons of the feeding and locomotory networks of the predatory marine snail Pleurobranchaea. Identified neurons of pedal and buccal ganglia were axotomized for recording the INa,cAMP response to iontophoretic injection of cAMP under two-electrode voltage clamp. Intracellular injections of specific peptide inhibitor of protein kinase A had no blocking effects on activation of INa,cAMP by iontophoretic injection of cAMP. Inward single-channel currents were activated in excised inside-out patches during exposure to cAMP in salines without added ATP. Sodium was the major current carrying ion. Two distinct types of INa,cAMP channel activity were observed, where opening probability and open times differed, but conductance was similar, 36.7 pS. These observations suggest that INa,cAMP activation occurs by direct binding of cAMP to a regulatory site at the channel, rather than by phosphorylation.
Animals↗
Kinetic analysis of cAMP-activated Na+ current in the molluscan neuron. A diffusion-reaction model.
cAMP-activated Na+ current (INa,cAMP) was studied in voltage-clamped neurons of the seaslug Pleurobranchaea californica. The current response to injected cAMP varied in both time course and amplitude as the tip of an intracellular injection electrode was moved from the periphery to the center of the neuron soma. The latency from injection to peak response was dependent on the amount of cAMP injected unless the electrode was centered within the cell. Decay of the INa,cAMP response was slowed by phosphodiesterase inhibition. These observations suggest that the kinetics of the INa,cAMP response are governed by cAMP diffusion and degradation. Phosphodiesterase inhibition induced a persistent inward current. At lower concentrations of inhibitor, INa,cAMP response amplitude increased as expected for decreased hydrolysis rate of injected cAMP. Higher inhibitor concentrations decreased INa,cAMP response amplitude, suggesting that inhibitor-induced increase in native cAMP increased basal INa,cAMP and thus caused partial saturation of the current. The Hill coefficient estimated from the plot of injected cAMP to INa,cAMP response amplitude was close to 1.0. An equation modeling INa,cAMP incorporated terms for diffusion and degradation. In it, the first-order rate constant of phosphodiesterase activity was taken as the rate constant of the exponential decay of the INa,cAMP response. The stoichiometry of INa,cAMP activation was inferred from the Hill coefficient as 1 cAMP/channel. The equation closely fitted the INa,cAMP response and simulated changes in the waveform of the response induced by phosphodiesterase inhibition. With modifications to accommodate asymmetric INa,cAMP activation, the equation also simulated effects of eccentric electrode position. The simple reaction-diffusion model of the kinetics of INa,cAMP may provide a useful conceptual framework within which to investigate the modulation of INa,cAMP by neuromodulators, intracellular regulatory factors, and pharmacological agents.
1-Methyl-3-isobutylxanthine↗
pH-sensitive, Ca2+/calmodulin-dependent phosphorylation of unique protein in molluscan nervous system.
Intracellular pH and Ca2+ are prominent co-regulators of neuron excitability that act on ion channels. In looking for a possible mechanism of their action, we tested their combinatorial effect on the phosphorylation state of nervous system proteins. 32PO4 labelling in endogenous phosphorylation reactions of homogenates of nervous tissue of the sea-slug Pleurobranchaea showed steep pH sensitivity in protein migrating at a molecular mass of 108 kDa with pI 6.9-7.0 (pp108). Phosphorylation of pp108 was highest below reaction pH 7.0 and declined steeply as pH rose to 7.4 pp108 phosphorylation was Ca2+/calmodulin-dependent. pp108 constituted a significant part of the total protein (0.15%) and phosphoprotein (8.9%) of the nervous system. The specifically and uniquely combinatorial pH and Ca2+ sensitivity of the phosphorylation of pp108, and its relative abundance, suggest that it could mediate integrated actions of H+ and Ca2+ in the molluscan neuron.
Animals↗
Enhancement of cyclic AMP-dependent sodium current by the convulsant drug pentylenetetrazol.
The convulsant drug pentylenetetrazol (PTZ) causes paroxysmal depolarizing shifts (PDS) and bursting in molluscan neurons. PDS has been found to be accompanied by increased levels of cyclic AMP (cAMP) and supported by persistent Na+ current. In neurons of the snail Lymnaea stagnalis the blocker of cAMP degradation isobutylmethylxanthine (IBMX) mimicks PTZ action. Na+ dependence of PTZ-induced inward shift in holding current in voltage-clamped cells supports the potential Na+ current origin of PDS. Intracellular cAMP injection elicits a transient Na+ current whose amplitude and duration are enhanced by both PTZ and IBMX. PTZ may cause PDS partly through slowing cAMP degradation, thus enhancing the cAMP-dependent Na+ current. PDS-generated bursts cause partial inactivation of the Na+ current, which may contribute towards burst termination.
1-Methyl-3-isobutylxanthine↗
Cyclic AMP-stimulated sodium current in identified feeding neurons of Lymnaea stagnalis.
Iontophoretic injection of cAMP elicits a slow, transient inward current in identified buccal feeding motoneurons and in the giant cerebral interneuron of the snail, Lymnaea stagnalis. The current is voltage independent, and is abolished in the absence of extracellular Na+. Application of the phosphodiesterase inhibitor isobutylmethylxanthine (IBMX) causes a marked increase in both amplitude and duration of cAMP-stimulated inward current. The amplitude of the current is reduced following prolonged application of depolarizing pulses to the cell. However, generation of high-frequency bursts of action potentials lasting up to 20 s has no significant effect on the amplitude of the cAMP-induced current measured subsequently. Bath application of the cAMP analogue 8-chlorophenylthio-cAMP or of IBMX leads to enhanced bursting activity in buccal motoneurons. It is suggested that cAMP sensitivity in feeding motoneurons provides a mechanism for adjusting the cells' responsiveness to rhythmic synaptic inputs during the generation of feeding motor output.
1-Methyl-3-isobutylxanthine↗
Regulation of cAMP-stimulated ion current by intracellular pH, Ca2+, and calmodulin blockers.
1. Iontophoretic injection of adenosine 3',5'-cyclic monophosphate (cAMP) into identified neurons elicited a slow transient Na+ current whose amplitude and duration were sensitive to altered intracellular pH (pHi), calmodulin blocking drugs, depolarization, and manipulations of internal and external Ca2+. 2. Intracellular acidification between resting pHi to several tenths of a pH unit increased the amplitude of the cAMP-stimulated current and prolonged its duration. 3. Intracellular alkalinization of similar magnitude also increased the amplitude and duration of the current response. The effects of alkalinization were somewhat labile. In cells alkalinized by NH4+-containing salines, washout of NH4+ with normal saline caused acidification and further enhanced the cAMP current response. The immediacy of the increase and the dual acid/basic sensitivity of the response suggest an accommodative process whereby the responsiveness of the cell to cAMP adapts to a maintained pHi. 4. The calmodulin blockers trifluoperazine and N-(6-aminohexyl)-5-chloro-1-naphthalenesulfonamide increased the amplitude and duration of the current response. Phorbol ester activators of Ca2+/phospholipid-dependent kinase had no effect on the current. 5. Periods of depolarization preceding tests significantly reduced current response amplitude. This effect was dependent on saline Ca2+ and was blocked by Co2+. 6. Intracellular injection of the Ca2+ chelator ethylene glycol-bis(beta-aminoethyl ether)N,N,N',N',-tetraacetic acid also augmented the amplitude and duration of the current response. 7. The above effects are consistent with a possible common site of action on cAMP degradation. This interpretation is consistent with previous evidence for pH-sensitive and Ca2+/calmodulin-dependent cAMP phosphodiesterase activity in Pleurobranchaea nervous tissue.
Animals↗
Calcium dependence of voltage sensitivity in adenosine 3',5'-cyclic phosphate-stimulated sodium current in Pleurobranchaea.
1. Ionophoretic injection of cyclic AMP into a voltage-clamped molluscan neurone caused a transient slow inward current (Isi) whose amplitude was enhanced by depolarization. Na+-replaced salines abolished the current, placing it with cyclic AMP-stimulated Na+ currents of other gastropod species. 2. Isi amplitude was suppressed by extracellular Ca2+. The amplitude increased up to 4-fold at holding potentials of -50 mV in nominally Ca2+-free saline. Ion substitutions showed that Ca2+ suppressed Isi more effectively than Mg2+, Co2+, Cd2+, Mn2+, Ba2+ or Sr2+. 3. Voltage sensitivity of Isi was abolished by low-Ca2+ salines, by the Ca2+ current blocker Co2+ and by substitution of Ba2+ or Sr2+ as Ca2+ channel current carriers. In such salines Isi showed no appreciable change in amplitude at holding potentials between -70 and -25 mV. 4. Intracellular injection of the Ca2+ chelator EGTA both augmented the amplitude of the current and its duration. EGTA injection failed to suppress the Ca2+-dependent voltage sensitivity of Isi. Intracellular injection of concentrated 3-N-(morpholino) propanesulphonic acid (MOPS) pH buffer to inhibit secondary, Ca2+-dependent intracellular acidification also failed to suppress the voltage sensitivity, as did injections of a mixed EGTA and MOPS solution. 5. While the data indicate a requirement for extracellular Ca2+ in conferring voltage sensitivity, they do not support a role for an intracellular action. An extracellular binding site for Ca2+ could mediate the voltage sensitivity, either by local depolarization-dependent changes in extracellular Ca2+ concentration or through direct voltage-sensitive block of the Isi channel.
Action Potentials↗
pH sensitivity of calmodulin distribution in nervous tissue fractions.
Alkalinization of nervous system extracts of the mollusk, Pleurobranchaea, from pH 7.0 to 8.0 markedly increases the ratio of soluble to total calmodulin. This effect is independent of pH effects on free Ca2+ concentration and is pronounced at micromolar (near intracellular) levels of Ca2+. These data may relate to recent evidence that Ca2+/calmodulin-activated cyclic nucleotide phosphodiesterase mediates the effects of small changes in intracellular pH (0.1-0.2 units) on the electrical activity of neurons. Calmodulin redistribution could reflect altered availability to stimulate phosphodiesterase activity and supports a role for calmodulin in mediating effects of intracellular pH fluxes on cellular activity.
Animals↗
Functional roles and circuitry in an inhibitory pathway to feeding command neurones in Pleurobranchaea.
The paracerebral neurones (PCNs) of the brain of Pleurobranchaea californica serve a command role in the initiation of feeding behaviour (Gillette, Kovac & Davis, 1978). The PCNs are synaptically excited by food stimuli applied to the oral veil of hungry, naive animals. In food avoidance-conditioned animals, the PCNs are inhibited by a barrage of inhibitory postsynaptic potentials concomitant with the suppression of feeding (Davis & Gillette, 1978). In this paper, an interneuronal pathway is described which causes inhibition of the PCNs and potentially mediates the effects of learning. The inhibitory pathway consists of three serially connected interneurones. One population, designated the Interneurone 1s (Int-1s), monosynaptically inhibits the PCNs. A second population, the Interneurone 2s (Int-2s), excites the Int-1 population. They also excite other neurones of the brain including the metacerebral giant neurones. A third population, the Interneurone 3s (Int-3s), monosynaptically excites the Interneurone 2 population. Dual intracellular recordings and current injection show that ipsilateral members of the Int-2 population are electrically coupled via a nonrectifying connection. Contralateral members of the Int-2 population are excitatorily coupled via a polysynaptic pathway. The Int-1 population is phasically active during the rhythmic motor activity that underlies feeding. In the isolated nervous system Int-1 activity is phase-locked with rhythmic PCN activity; Int-1 activity occurs maximally at the end of a PCN burst, during the retraction phase of the cycle. Int-2 activity also occurs during the retraction phase. During actual feeding in the whole animal preparation, the Int-2s are also phasically active; maximal excitation occurs during buccal mass retraction and maximal inhibition during protraction and the bite. Stimulated activity in a single Int-2 can entirely suppress the rhythmic motor activity of the feeding network evoked by electrical stimulation of the stomatogastric nerve. The suppressant effects of Int-2 activity must be mediated widely within the feeding network because the rhythmic motor output so driven is not dependent on PCN spiking. Application of an appetitive chemosensory stimulus to whole and semi-intact animal preparations initiated feeding and elicited excitation of the Int-1 and Int-2 populations. Noxious chemosensory stimuli, such as a dilute soap solution or ethanol, elicited oral veil withdrawal and inhibition of the Int-2s by multiple inhibitory postsynaptic potentials.(ABSTRACT TRUNCATED AT 400 WORDS)
Action Potentials↗
Phenothiazines mimic the action of cAMP in potentiating slow inward current in a bursting molluscan neuron.
Trifluoperazine and chlorpromazine, blockers of calmodulin action, potentiate slow inward current in molluscan neurons identically to the action of cAMP. The sulfoxide derivative of chloropromazine does not appreciably bind to calmodulin and also fails to enhance the inward current. The likelihood that these effects are mediated by cAMP via inhibition of a Ca2+-calmodulin-activated phosphodiesterase is discussed and related to other data.
Animals↗
Ca2+ activated and pH sensitive cyclic AMP phosphodiesterase in the nervous system of the mollusc Pleurobranchaea.
Regulation of cyclic AMP through its synthesis is known to be important in modulating the activity of molluscan neurons; however, no data exists regarding the regulation of cyclic AMP degradation. We find that cyclic AMP phosphodiesterase (PDE) activity in homogenates of the nervous system of the mollusc Pleurobranchaea is significantly stimulated by calcium ion. Ca2+ stimulation is suppressed by the calmodulin antagonist trifluoperazine (TFP), indicating resemblance to the Ca2+-calmodulin PDEs of mammalian neurons. Ca2+ also accentuates the pH sensitivity of PDE. The qualities of Ca2+ and pH sensitivity of PDE are fitted into a model for cAMP regulation of neuronal activity in an identified feeding command neuron; the postulated role of PDE is consistent with effects of cAMP, TFP, and pH on the neuron's activity.
3',5'-Cyclic-AMP Phosphodiesterases↗
Intracellular alkalinization potentiates slow inward current and prolonged bursting in a molluscan neuron.
1. The bilaterally paired ventral white cells (VWCs) of the buccal ganglion of Pleurobranchaea drive the cyclic motor output of ingestive feeding behavior during prolonged and endogenously sustained burst episodes (7). The capacity to support burst episodes is specifically induced by appetitive (food) stimulation of chemosensory pathways (5). Cyclic 3',5'-adenosine monophosphate (cAMP) and its agonists also induce prolonged burst episodes (8) through potentiation of a slow inward current (6). 2. Intracellular alkalinization of the VWC by externally applied ammonium ion and methylamine (5-20 mM) induces bursting and enhances slow inward current measured under voltage-clamp conditions. The enhancement of slow inward current is seen in the induction or augmentation of a negative slope resistance region in the current-voltage relation and in the enhancement of slowly decaying inward current tails recorded near the K+ equilibrium potential following depolarizing voltage commands. 3. Intracellular injection of alkalinizing agents, bicarbonate ion and a strong buffer solution at pH 8.1, also enhance the inward current. In ammonium saline, enhancement of inward current is dependent on NH3 content, not NH4+; NH3 is the intracellular alkalinizing agent of ammonium saline. Therefore, the change in slow inward current is an effect specific to intracellular pH. 4. The time courses of inward current enhancement and intracellular pH change in NH4+ saline are similar. The results of this study suggest that normal fluctuations in intracellular pH may be significant determinants of the excitability and consequent activity of these and perhaps other neurons. The potential interaction of intracellular pH and cyclic AMP metabolism is discussed.
Acid-Base Equilibrium↗
Organization of synaptic inputs to paracerebral feeding command interneurons of Pleurobranchaea californica. III. Modifications induced by experience.
Phasic paracerebral feeding command interneurons (PCP's) were studied in whole-animal preparations of Pleurobranchaea drawn from four populations with different behavioral histories: food avoidance conditioned, yoked controls, food satiated, and naive. PCP responses to chemosensory food stimuli (liquefied squid) and mechanosensory touch stimuli (tactile stimulation of anterior and posterior structures) were recorded intracellularly, scored blind, and compared quantitatively across the four populations. PCP's from avoidance-conditioned specimens (10, 18, 19) showed decreased excitatory and increased inhibitory responses to food and touch in comparison with naive (untrained) specimens. Control animals did not show these effects. PCP's from satiated specimens showed decreased excitatory and increased inhibitory responses to food and touch in comparison with PCP's from control, naive, and conditioned specimens. Inhibitory postsynaptic potentials (IPSPs) induced in PCP's of conditioned and satiated specimens by food and touch are indistinguishable in amplitude and waveform from IPSPs produced in the same PCP's by the previously described cyclic inhibitory network (CIN; Ref. 13). In addition, tonic paracerebral neurons (PCT's) that lack input from the CIN, are not inhibited but rather are excited in trained and satiated animals. Therefore the inhibitory responses to food and touch by PCP's of conditioned and satiated specimens appear to be mediated by the CIN. This study demonstrates that associative and nonassociative processes (learning and food satiation, respectively) manifest similarly at the level of command interneurons. The findings furnish a neurophysiological explanation for behavioral motivation in Pleurobranchaea, namely, modulation of the balance of excitation/inhibition in command neurons controlling the corresponding behavior. A cellular model of food avoidance learning and food satiation is formulated to account for these data, based on the identified neural circuitry of the paracerebral command system (15, 17).
Animals↗
Bursting neurons command consummatory feeding behavior and coordinated visceral receptivity in the predatory mollusk Pleurobranchaea.
Explore the source record for details and available documents.
Action Potentials↗