Amira Flores

Effects of auditory noise on the psychophysical detection of visual signals: Cross-modal stochastic resonance

Harper [D.W. Harper, Signal detection analysis of effect of white noise intensity on sensitivity to visual flicker, Percept. Mot. Skills 48 (1979) 791-798] demonstrated that the visual flicker sensitivity was an inverted U-like function of the intensity of different levels of auditory noise from 50 to 90dB (SPL), without concomitant changes in the response bias. The aim of the present study was to extend these observations in the context of the stochastic resonance, a counterintuitive phenomenon in which a particular level of noise enhances the response of a nonlinear system to a weak input signal. We show psychophysical evidence in a yes-no paradigm for the existence of a stochastic resonance-like phenomenon in the auditory-visual interactions. We show that the detection of a weak visual signal was an inverted U-like function of the intensity of different levels of auditory noise. Nevertheless, for a strong visual signal the auditory noise acts in detriment of the ability of visual detection. Our results suggest that auditory noise could be employed in vision rehabilitation interventions in order to improve the detection of weak visual signals.

Internal stochastic resonance in the coherence between spinal and cortical neuronal ensembles in the cat.

Internal stochastic resonance is a phenomenon in which the coherence of a non-linear system is enhanced by the presence of a particular, non-zero level of noise generated by internal or external sources without a periodic input signal. The aim of this study was to demonstrate the experimental occurrence of internal stochastic resonance in the coherence between spinal and cortical neuronal ensembles. Simultaneous recordings of spinal and cortical evoked potentials were made in the somatosensory system of the anaesthetized cat. Evoked potentials were produced by input noise introduced in the tactile stimulation of the hindpaw skin. Coherence between the spinal and cortical evoked activity recorded during different levels of input noise was calculated. All animals showed distinct internal stochastic resonance like behavior. We found that the mean coherence was an inverted U-like function of the level of input noise with a mean coherence peak of 0.43. To our knowledge, this is the first documented evidence of such phenomenon in an in vivo preparation of the central nervous system.

Stochastic resonance in human electroencephalographic activity elicited by mechanical tactile stimuli

Stochastic resonance (SR) is a phenomenon in which the response of a non-linear system to a weak input signal is optimized by the presence of noise. The aim of this study was to demonstrate the experimental occurrence of SR in electroencephalographic (EEG) activity elicited by mechanical tactile stimuli. Our experiments show that EEG responses evoked by mechanical tactile stimuli in the region overlying the somatosensory cortical area were optimized by the addition of certain noise amplitudes. All subjects showed distinct SR behavior. The signal-to-noise ratio (SNR) of the response evoked by mechanical indentations of the skin was an inverted U-like function of the input noise. As the noise amplitude increased, SNR values became larger. A maximum value was reached with a particular noise amplitude value. Beyond such peak, with higher noise amplitudes, the curve subsided gradually. To our knowledge, this is the first documented evidence that such remarkable phenomenon embodies electrical processes of the human brain. Such behavior might explain related findings described in psychophysical studies.

Evidence for NMDA receptor in the afferent synaptic transmission of the vestibular system.

This study aimed to define the pharmacology and physiological role of the N-methyl-D-aspartate (NMDA) receptor in the synapse between the hair cells and primary afferent neurons in the vestibular system. The spontaneous and mechanically evoked spike discharges of vestibular nerve fibers were extracellularly recorded in isolated inner ear from the axolotl (Ambystoma tigrinum). Pressure ejection of NMDA (10(-6) to 10(-3) M) elicited a dose-dependent increase of the basal spike discharge from the vestibular nerve fibers. Extracellular magnesium antagonized the NMDA effect in a dose-dependent manner. D(-)-2-amino-5-phosphonovaleric acid (AP5, 10(-5) to 10(-3) M) and 7-chloro-kynurenic acid (7ClKyn, 10(-6) to 10(-3) M) inhibited the basal activity of the vestibular nerve fibers. 7ClKyn also diminished the responses elicited by the mechanical stimulation of the preparation. Glycine (10(-9) to 10(-6) M) applied by bath substitution enhanced the NMDA response, and the glycine agonist D-serine partially reversed the 7ClKyn inhibitory action. These results suggest that NMDA receptors participate in the generation of the basal spike discharge of vestibular system primary afferent neurons, but its activation is not critical for the response to brief mechanical stimuli.

Leptin increases L-type Ca2+ channel expression and GnRH-stimulated LH release in LβT2 gonadotropes

Leptin, a mediator of long-term regulation of energy balance, has been implicated in the release of adenohypophyseal gonadotropins by regulating gonadotropin-releasing hormone (GnRH) secretion from the hypothalamus. However, a direct effect of leptin on hormone release from gonadotropes remains virtually unexplored. In the current report, we assessed the long-term (48 h) actions of leptin on voltage-gated channel activity and luteinizing hormone (LH) production in mouse pituitary gonadotrope LbetaT2 cells. Electrophysiological recordings showed that leptin treatment significantly increased whole-cell patch-clamp Ba(2+) current through L-type Ca(2+) channels. Quantitative RT-PCR analysis revealed increased levels of L-type (alpha(1D)) Ca(2+) channel mRNA. Likewise, radioimmunoassays using specific antibodies provided evidence that leptin alone had no effect on LH release but did enhance GnRH-induced secretion of the hormone. Leptin had no apparent effects on LH gene transcription in absence of GnRH, as measured by transient transfection assays using a LH promoter-reporter gene and real-time RT-PCR. These observations suggest that leptin might affect LH release by acting directly on the gonadotropes, favoring hormone production by enhancing responsiveness to GnRH as a result of increased Ca(2+) channel expression.

Computing the center of mass for traveling alpha waves in the human brain.

The phenomenon of traveling waves of the brain is an intriguing area of research, and its mechanisms and neurobiological bases have been unknown since the 1950s. The present study offers a new method to compute traveling alpha waves using the center of mass algorithm. Electroencephalographic alpha waves are oscillations with a characteristic frequency range and reactivity to closed eyes. Several lines of evidence derived from qualitative observations suggest that the alpha waves represent a spreading wave process with specific trajectories in the human brain. We found that during a certain alpha wave peak recorded with 30 electrodes the trajectory starts and ends in distinct regions of the brain, mostly frontal-occipital, frontal-frontal, or occipital-frontal, but the position of the trajectory at the time in which the maximal positivity of the alpha wave occurs has a definite position near the central regions. Thus we observed that the trajectory always crossed around the central zones, traveling from one region to another region of the brain. A similar trajectory pattern was observed for different alpha wave peaks in one alpha burst, and in different subjects, with a mean velocity of 2.1+/-0.29 m/s. We found that all our results were clear and reproducible in all of the subjects. To our knowledge, the present method documents the first explicit description of a spreading wave process with a singular pattern in the human brain in terms of the center of mass algorithm.

Cortical neuronal ensembles driven by dorsal horn spinal neurones with spontaneous activity in the cat

Simultaneous recordings of cortical activity, recorded as the cortical local field potential (CLFP) in the contralateral posterior sigmoid gyrus, and the spinal activity, recorded as the cord dorsum potential (CDP) of the L6 lumbar segment, were made in the anaesthetized cat. The electrodes were positioned in somatosensory regions where the largest spontaneous negative CLFPs and CDPs were recorded. We found that spontaneous negative CLFPs were preceded by spontaneous negative CDPs with a mean latency of 14.4+/-3.5 ms. Amplitude of these spontaneous negative CLFPs was abolished after section of the dorsal columns and ipsilateral dorsolateral funiculus. It is concluded that the neurones of the primary somatosensory cortex can be driven by dorsal horn spinal neurones producing the spontaneous negative CDPs. This suggests very strongly that spontaneous neuronal activity in somatosensory regions of the brain is generated not only by ongoing activity of neurones located at supraspinal sites, but also by ongoing activity of spinal neurones.

Absence of effects of contralateral group I muscle afferents on presynaptic inhibition of Ia terminals in humans and cats.

Crossed effects from group I afferents on reflex excitability and their mechanisms of action are not yet well understood. The current view is that the influence is weak and takes place indirectly via oligosynaptic pathways. We examined possible contralateral effects from group I afferents on presynaptic inhibition of Ia terminals in humans and cats. In resting and seated human subjects the soleus (SO) H-reflex was conditioned by an electrical stimulus to the ipsilateral common peroneal nerve (CPN) to assess the level of presynaptic inhibition (PSI_control). A brief conditioning vibratory stimulus was applied to the triceps surae tendon at the contralateral side (to activate preferentially Ia muscle afferents). The amplitude of the resulting H-reflex response (PSI_conditioned) was compared to the H-reflex under PSI_control, i.e., without the vibration. The interstimulus interval between the brief vibratory stimulus and the electrical shock to the CPN was -60 to 60 ms. The H-reflex conditioned by both stimuli did not differ from that conditioned exclusively by the ipsilateral CPN stimulation. In anesthetized cats, bilateral monosynaptic reflexes (MSRs) in the left and right L(7) ventral roots were recorded simultaneously. Conditioning stimulation applied to the contralateral group I posterior biceps and semitendinosus (PBSt) afferents at different time intervals (0-120 ms) did not have an effect on the ipsilateral gastrocnemius/soleus (GS) MSR. An additional experimental paradigm in the cat using contralateral tendon vibration, similar to that conducted in humans, was also performed. No significant differences between GS-MSRs conditioned by ipsilateral PBSt stimulus alone and those conditioned by both ipsilateral PBSt stimulus and contralateral tendon vibration were detected. The present results strongly suggest an absence of effects from contralateral group I fibers on the presynaptic mechanism of MSR modulation in relaxed humans and anesthetized cats.

NITRIC OXIDE IN THE AFFERENT SYNAPTIC TRANSMISSION OF THE AXOLOTL VESTIBULAR SYSTEM

This study was performed using intracellular and multiunit extracellular recording techniques in order to characterize the role of nitric oxide in the afferent synaptic transmission of the vestibular system of the axolotl (Ambystoma tigrinum). Bath application of nitric oxide synthase inhibitors N(G)-nitro-L-arginine (0.01microM to 10microM) and N-nitro-L-arginine methyl ester hydrochloride (0.1microM to 1000microM) elicited a dose-dependent decrease in the basal discharge of the semicircular canal afferent fibers. N(G)-Nitro-L-arginine also diminished the response to mechanical stimuli. Moreover, N(G)-nitro-L-arginine (1microM) produced a hyperpolarization associated with a decrease in the spike discharge and diminished the frequency of the excitatory postsynaptic potentials on afferent fibers recorded intracellularly. Nitric oxide donors were also tested: (i) S-nitroso-N-acetyl-DL-penicillamine (0.1microM to 100microM) increased the basal discharge and the response to mechanical stimuli. At the maximum effective concentration (100microM) this drug affected neither the amplitude nor the frequency of the excitatory postsynaptic potentials. However, it slightly depolarized the afferent neurons and decreased their input resistance. (ii) 3-Morpholino-sydnonimine hydrochloride did not significantly affect the basal discharge or the mechanically evoked peak response of afferent neurons at any of the concentrations used (1microM to 1000microM). However, after 10min of perfusion in the bath, 1microM and 10microM 3-morpholino-sydnonimine hydrochloride significantly modified the baseline of the mechanically evoked response, producing an increase in the mean spike discharge of the afferent fibers. These results indicate that nitric oxide may have a facilitatory role on the basal discharge and on the response to mechanical stimuli of the vestibular afferent fibers. Thus, nitric oxide probably participates in the sensory coding and adaptative changes of vestibular input in normal and pathological conditions.

Histochemistry and role of nitric oxide synthase in the amphibian (Ambystoma tigrinum) inner ear

Nicotinamide adenine dinucleotide phosphate reduced-diaphorase (NADPH-d) histochemistry was investigated in the axolotl (Ambystoma tigrinum) inner ear. Hair cells showed an intense NADPH-d reaction; afferent neurones also stained but less intensely than hair cells. Effects of NG-nitro-L-arginine (L-NOARG) on the basal discharge and mechanical responses of semicircular canal afferent neurones recorded extracellularly were also studied. L-NOARG (1 mu M) diminished the basal discharge and the response of afferent neurones to sinusoidal mechanical stimuli to 45 +/- 6.4% and 65 +/- 5.3% (mean +/- SEM) of control value, respectively. These findings suggest that production of nitric oxide (NO) by hair cells and probably also by afferent neurones contributes to the basal discharge and the response of afferent neurones to mechanical stimuli.