Biomedical subjects

M A Chaput

Publications and source records attributed to M A Chaput.

15 recordsLinked to original sources

PubMed2004

Taurine action on mitral cell activity in the frog olfactory bulb in vivo.

Taurine (TAU) is a free amino acid that is particularly abundant in the olfactory bulb. In the frog, TAU is located in the terminations of the primary olfactory axons and in the granular cell layer. TAU action seems to be associated with gamma amino butyric acid (GABA), the main inhibitory neurotransmitter involved in the processing of the sensory signal. The present study was designed to assess the action of TAU in vivo during the olfactory network's stimulation by odors. It was performed by recording the single-unit activity of mitral cells, the main bulbar output neurons. TAU effects were tested on both their spontaneous and odor-induced firing activity. Interactions between TAU and GABA were examined by analyzing TAU effects under the selective blocking action of GABAA or GABAB antagonists. TAU was found to suppress the spontaneous firing of mitral cells, mainly without altering their odor response properties. By testing GABA antagonists, we further show that TAU action is associated with GABAergic inhibitory mechanisms mainly via GABAB receptors. Thus, TAU action clearly reduces background activity in favor of the emergence of the odor-induced activity in the same manner as GABA action does via GABAB receptors. As a conclusion, we propose that, in the frog olfactory bulb, the joint actions of TAU and GABA may favor the processing of the primary sensory information by increasing the signal to noise ratio.

Action Potentials↗

PubMed2003

Rats habituated to chronic feeding restriction show a smaller increase in olfactory bulb reactivity compared to newly fasted rats.

During the 1970s, the multiunit reactivity of the olfactory bulb to food odor was extensively shown to increase before their usual meal in rats habituated to having a single 2 h daily meal compared to the same rats recorded after their usual meal. More recently, we reported dramatic modifications of mitral cell single-unit reactivity in adult rats following a simple a manipulation of the olfactory environment--exposure to an odor. The present study aimed at testing the hypothesis that a simple behavioral change such as habituation to chronic food restriction may induce profound changes in olfactory bulb responsiveness compared to occasional fasting. We compared mitral cell reactivity in non-fasted rats, in rats fasted during 22 h for the very first time, and in rats habituated during 15 days to a chronic 22 h food restriction. Mitral cell single-unit reactivity was found to increase less in rats habituated to fasting than in newly fasted rats. Indeed, the proportion of mitral cell responses to food and non-food odors was significantly higher in rats habituated to fasting than in non-fasted rats, but lower than in newly fasted rats. The proportion of simple unsynchronized and synchronized responses of 1b and 2b types was also lower in habituated rats whereas the proportion of complex synchronized responses of 4b type increased. This decreased responsiveness in habituated rats, similar to that observed in rats repeatedly exposed for 20 min per day to an odor during six consecutive days in our previous studies, is discussed with respect to olfactory bulb plasticity.

Animals↗

PubMed2000

Peripheral odor coding in the rat and frog: quality and intensity specification.

In mammals, two recent studies have shown recently that one odor molecule can be recognized by several molecular olfactory receptors (ORs), and a single OR can recognize multiple odor molecules. In addition, one olfactory receptor neuron (ORN) may respond to different stimuli chosen as representative of distinct odor qualities. The aim of the present study was to analyze quality and intensity coding abilities of rat single ORNs, comparing them with previous extensive data gathered in the frog to get insight into the generality of olfactory coding mechanisms over vertebrates. Response properties of 90 rat ORNs to different odors or to one odor at different concentrations were analyzed. In the rat and the frog, odor quality appears to be specified through the identity of activated ORNs. However, rat ORNs have higher response thresholds. This lower sensitivity may be interpreted as an increase in selectivity of rat ORNs for low or medium odor intensities. In these conditions, the lower proportion of activated ORNs could be counterbalanced by their number, as well as by their higher glomerular convergence ratio in the olfactory bulb. From amphibians to mammals, the olfactory system appears to use universal mechanisms based on a combinatorial-coding mode that may allow quasi-infinite possibilities of adaptation to various olfactory environments.

Action Potentials↗

PubMed2000

EOG responses in anesthetized freely breathing rats.

In mammals, access of odor molecules to the olfactory receptor neurons is controlled by respiratory activity. Thus, anesthetized, freely breathing rats were used to record from the olfactory mucosa in the intact nasal cavity (electroolfactogram or EOG) so as to study global response characteristics to odor stimuli. During alternation of the inspiratory phases of odor sampling and expiratory phases, the response was a succession of individual EOG events synchronized with respiration. These were characterized by a steep decrease that started approximately 100-150 ms after the beginning of inhalation, reached its maximum at the transition between inspiration and expiration and was followed by a slower rise until the next inhalation. They were greater during the first respiratory cycles following odor stimulation onset. Thereafter their amplitudes decreased throughout odor delivery, but a significant EOG signal was still present at the end of short (10 s) and long (60 s) odor presentations. Amplitude increased with odor concentration, but much less than expected from concentration changes. Lastly, for some odors EOG responses persisted well beyond the end of stimulation. These results are in agreement with the respiratory synchronization of mitral cell activities observed during short odor presentations and long duration odor exposures. They underline again the importance of taking into account the respiratory activity in studies on the functioning of the olfactory system.

Animals↗

PubMed1999

Odor response properties of rat olfactory receptor neurons.

Molecular biology studies of olfaction have identified a multigene family of molecular receptors that are likely to be involved in odor transduction mechanisms. However, because previous functional data on peripheral coding were mainly collected from inferior vertebrates, it has been difficult to document the degree of specificity of odor interaction mechanisms. As a matter of fact, studies of the functional expression of olfactory receptors have not demonstrated the low or high specificity of olfactory receptors. In this study, the selectivity of olfactory receptor neurons was investigated in the rat at the cellular level under physiological conditions by unitary extracellular recordings. Individual olfactory receptor neurons were broadly responsive to qualitatively distinct odor compounds. We conclude that peripheral coding is based on activated arrays of olfactory receptor cells with overlapping tuning profiles.

Acetophenones↗

PubMed1998

Olfactory bulb output cell temporal response patterns to increasing odor concentrations in freely breathing rats.

This study compares the single-unit responses of 74 mitral/tufted cells recorded in freely breathing rats to step increases of the intensity of five odorants from 2 x 10(-4) to 10(-1) of saturated vapor pressure. It reveals a stability of the responses of these olfactory bulb output cells. Olfactory stimulation has frequently been shown to produce a strong patterning of mitral/tufted cell discharges highly correlated with respiration. In this study, cells were generally found to show the same response type to two consecutive concentrations, and only a few cells switched their response from excitation to suppression or vice versa. Their firing peak and/or trough occupied the same position in a high proportion of respiratory cycles recorded during a stimulation, and they remained significantly time-locked to the same respiratory epoch for the next higher concentration. Increasing odor concentration did not cause the mean firing frequency of individual cells during a peak to change appreciably between successive or extreme concentrations. By contrast, it tended to shift their maximum frequency during this peak towards an earlier respiratory cycle after stimulation onset. These results are compared with data reported in other electrophysiological studies and with results given by olfactory bulb models before being discussed for their implications in odor coding.

Animals↗

PubMed1997

Recording the slow potentials evoked by odors in the olfactory mucosa of awake animals.

The aim of this report is to expose several improvements which are essential for obtaining good recordings from the basal side of the olfactory mucosa of awake rats with Ag-AgCl electrodes implanted through holes drilled in the roof of the nasal bone. In a first step, we present how this minimally invasive method was developed and validated in anesthetized rats. We insist particularly on several important points such as the size and form of the electrode tip, the careful deposit of silver chloride on this tip or the location of the implanting site. Then we demonstrate that the recorded signals have the characteristics of an electro-olfactogram (EOG), i.e that they have a local origin, that they change with odors and concentrations, and that they do not appear during pure air delivery, nor after ipsilateral nostril closure. Lastly we show that this method was successfully utilized in awake rats. In provided data demonstrating the rhythmicity of EOGs in freely-breathing animals and allowed us to study their relationships with respiration.

Anesthesia, General↗

PubMed1996

Similarity of granular-induced inhibitory periods in pairs of neighboring mitral/tufted cells.

1. Neighboring mitral/tufted cells have been previously shown to present temporal correlations of their firings related to the respiratory rhythm, particularly under odor stimulation. This occurs despite the existence of a powerful inhibitory control exerted by granule cells onto mitral/tufted cells. In the present study, we hypothesized that neighboring mitral cells can present granular induced inhibitory periods with similar latencies and durations and that such a similarity would preserve them from a possible suppression of their temporal correlations. 2. To test this hypothesis, we analyzed the latencies and durations of the inhibitory periods induced by granular activation in pairs of simultaneously recorded neighboring mitral cells. The activation of granule cells was achieved by electrical stimulation of the different pathways known to directly activate granule cells [lateral olfactory tract (LOT), anterior limb of the anterior commissure (AC), and piriform cortex (PC)]. Data from this group were compared with those of a control group composed of distant cells also recorded simultaneously. 3. Results first show that the latencies to onset of inhibition or to recovery were more frequently similar in neighboring cells than in control cells and that this similarity was enhanced by odor stimulation. Second, the probability that two cells exhibit similar inhibitory periods (i.e., similar latencies to both onset and to recovery) in response to electrical stimulation of LOT, AC, or PC was significantly higher in neighboring than in control cells. Third, only neighboring cells were found to present similar inhibitory periods in response to the stimulation of all of the three structures. 4. Granular activation was also found to modify the temporal patterns of individual mitral cells. However, although these patterns were not systematically modified similarly in neighboring mitral cells, they remained perfectly synchronized with zero delay if they were already synchronous without electrical stimulation. On the contrary, if patterns were spontaneously uncorrelated, electrical stimulation never produced a synchronization of their firings, even if their temporal relationships could be profoundly modified. 5. These results show that neighboring mitral cells can receive granular-induced inhibition with similar latencies and durations with a probability much higher than control cells. Such similarities allow neighboring mitral cells to preserve their temporal correlation despite the powerful inhibitory input from granule cells. Functional hypotheses about the role of the cortical feedback projections onto the bulb are discussed.

Animals↗

PubMed1992

Temporal pattern analyses in pairs of neighboring mitral cells.

1. Neighboring mitral cells in the rat olfactory bulb have been previously shown to give similar response profiles to a series of odorants. We now analyze their temporal patterns of activity before and during stimulation to evaluate to what extent soma proximity may act on their temporal correlation and to what extent olfactory stimulation may force two close cells to fire with similar patterns. 2. In anesthetized adult rats, we recorded simultaneously the extracellular single-unit activities of two mitral cells with the use of twin micropipettes with tips separated by less than 40 microns. These activities were recorded before and during stimulation by a series of five odorants. 3. Activities were classified into nine types according to their temporal pattern along the respiratory cycle. These types comprised nonrhythmic patterns and rhythmic ones, the latter being simple or complex. A phase parameter was also calculated to compare the positions of maximal activity within respiratory cycles of pairs of cells that had rhythmic activities. 4. All analyses were made by comparing data from pairs of close cells with data from pairs of control cells obtained by pairing each first cell of all recorded pairs with the second units of all other pairs. Results reveal a probability of similar activity types significantly higher in pairs of close cells than in control ones before stimulation. Odorant stimulation enhances this difference by reducing the probability of similar associations in control pairs. Close cells present similar patterns as frequently before, as during, stimulation; however, the probability of double nonrhythmic firings decreases whereas the probability of double rhythmic ones increases.(ABSTRACT TRUNCATED AT 250 WORDS)

Animals↗

PubMed1991

Mitral cell-to-glomerulus connectivity: an HRP study of the orientation of mitral cell apical dendrites.

It has been suggested that the principal output cells of the main olfactory bulb, the mitral cells, along with the glomerulus they enter, form an anatomical and functional column. To test the extent to which mitral cell somata lying close together in the mitral cell layer are connected to the same glomerulus, we reconstructed 267 mitral cells labeled by extracellular injections of horseradish peroxidase (HRP) in the external plexiform layer. Results show that apical dendrites tilt rostrally from the somata to the glomeruli and this tilt is gradually greater as the somata are located more and more rostrally in the olfactory bulb. The apical dendrites of most mitral cells in the same region of the bulb are parallel. We analyzed the degree to which dendrites were parallel by measuring the difference in angle of all pairs of apical dendrites in each section, with the restriction that no cells were separated by more than 500 microns. About half of these pairs of dendrites differed in angle by 20 degrees or less and were therefore said to be parallel. The degree of parallelism did not vary with the cell pair location or with intercell distance. Study of glomerular connections of pairs of mitral cells as a function of intercell distance revealed that 96% of mitral cells connected to the same glomerulus were separated by less than 120 microns, while 72% of cells connected to adjacent glomeruli and only 29% of cells connected to distant, i.e., nonadjacent, glomeruli were separated by less than 120 microns.(ABSTRACT TRUNCATED AT 250 WORDS)

Animals↗

PubMed1990

Response similarity to odors in olfactory bulb output cells presumed to be connected to the same glomerulus: electrophysiological study using simultaneous single-unit recordings.

1. The glomeruli of the olfactory bulb are discrete anatomic structures in which the terminals of receptor cell axons make extensive contacts with the primary dendrites of the mitral and tufted output cells. In mammals, each mitral and deep tufted (M/T) cell possesses a single primary dendrite and sends it toward the glomerulus situated just in front of its somata. 2. We tested the hypothesis that the glomeruli, which appear to form anatomic units, could act to some extent as functional units. A unitary functioning implies that the M/T cells connected to the same glomerulus will more often display similar responses to odorants than cells having no common glomerular relationships, including cells related to adjacent glomeruli. 3. In anesthetized adult rats, we recorded the extracellular single-unit responses of pairs of M/T cells to a series of five odorants. Recordings were performed with the use of twin microelectrodes whose tips were separated either by less than 40 or by 150-200 microns. Because of the olfactory bulb organization, we assumed that the close cells, recorded at a distance less than 40 microns, were more often connected to the same glomerulus, whereas the distant cells, recorded at a distance of 150-200 microns, were more often connected to adjacent glomeruli. 4. Stimulus-evoked changes in firing rate were classified as either excitatory (+), suppressive (-), or null (0) responses. The collection of response types of a given cell to the 5 odorants composed its response profile. Response profiles were used to compare the responsiveness within close and within distant cell pairs with that observed within control pairs of cells.(ABSTRACT TRUNCATED AT 250 WORDS)

Action Potentials↗

PubMed1987

Influence of stimulus intensity on the categories of single-unit responses recorded from olfactory bulb neurons in awake freely-breathing rabbits.

This study analyzes the influence of increasing odor intensity on the single-unit activity of olfactory bulb neurons recorded in awake freely-breathing rabbits. Five odorants were delivered at four concentrations over a range of 2 log units. Inspiration-and expiration-related firing activities were analyzed separately to categorize the odor-evoked responses into excitation, suppression and no response. Increasing the odor concentration caused more neurons to show excitatory responses during the inspiratory phase of the respiratory cycle and/or suppressive responses during the expiratory phase. The highest concentration of each odor also caused several units to give suppressive responses during inspiratory phases or excitatory responses during expiratory phases. However, increasing odor concentration caused few responses (less than 2%) to change from excitation to suppression or vice versa. How these results relate to those from studies performed in anaesthetized animals and the implications of the results for olfactory coding will be discussed.

Animals↗

PubMed1986

Respiratory-phase-related coding of olfactory information in the olfactory bulb of awake freely-breathing rabbits.

The "across-neuron pattern" theory of olfactory information coding states that odorants are represented by spatial patterns of activity produced across-neurons in the olfactory bulbs. The present study analyzes the different response patterns encoding olfactory information in both the inspiratory and expiratory phases of the respiratory cycles of awake freely-breathing rabbits. We recorded the single-unit responses of 31 neurons to 5 different odorants, 3 of which were repeatedly delivered 5 times each. These responses were characterized by the change in their mean firing activity during the inspiratory and expiratory phases of the respiratory cycles respectively. Their processing using principal component analyses revealed that both the inspiration- and the expiration-related across-neuron profiles of responses contained information appropriate to the specification of each odorant. It was therefore concluded that there was a dynamic representation of odorants in the olfactory bulb of awake freely-breathing animals. This alternate representation of odorants by two profiles and its physiological significance are discussed.

Acetophenones↗

PubMed1985

Responses of olfactory bulb neurons to repeated odor stimulations in awake freely-breathing rabbits.

Thirty-one olfactory bulb neurons were recorded in the olfactory bulbs of unanaesthetized rabbits during repeated stimulations. Their single-unit activity associated with the inspiratory phases of the respiratory cycles and that associated with the expiratory phases were processed separately. When responses were classified into 3 types, i.e., excitation, inhibition and null, it was found that a large number of neurons presented variable responses to repeated stimulations with the same stimulus. However, the passage from one type to another was found to be limited: responses by excitation or inhibition to the first stimulation turned into null responses only; null responses turned into either excitation or inhibition. Inspiration- and expiration-related responses were also subjected to a principal component analysis in order to determine whether changes in responses were compatible with a reliable coding of the qualitative properties of a stimulus. The results indicated that the repeated presentations of an odorant induced fairly similar profiles of activity across the set of neurons while different odorants induced clearly discriminable profiles. It is concluded that repeated stimulations do not blur the characteristic features of the across-neuron profile of response of an odorant in the olfactory bulb despite the variability of the responses of the neurons which compose the profile.

Animals↗

PubMed1982

Effects of long duration odor exposure on the unit activity of olfactory bulb cells in awake rabbits.

Recordings of single unit activity before, during and after a 1-h continuous exposure were made from the mitral cell layer of the olfactory bulbs of awake rabbits. Thirteen complete 1-h exposures were performed using 8 neurons, while a further 6 neurons were lost before the end of the exposure. During the first few minutes of exposure, a respiration-related synchronization of firing activity occurred which was similar to that of the pre-exposure 5-s stimulations with the same odor. This discharge patterning continued for the full duration of some exposures but disappeared within a few minutes for others. In all cases, a response to the exposure odor, although reduced in amplitude, was evident 6 min after the exposure had been terminated. This reduction was also observed for stimulations with other odors that had induced a response prior to exposure, and was always followed by a gradual recovery in the amplitude of the response. The relation between the changes in the firing activity of mitral cells during and after 1-h exposures, and adaptation phenomena observed using psychophysical methods are discussed. The absence of gross changes in firing activity are discussed with reference to 'mitral cell selective degeneration' and autoradiographic 2-deoxyglucose experiments.

Animals↗