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C Harnois

Publications and source records attributed to C Harnois.

29 records · Page 2Linked to original sources

Temporal frequency-dependent VEP changes in Parkinson's disease.

We recorded steady-state (4.19 and 8.41 Hz) VEPs in 17 Parkinson's Disease (PD) patients and 18 control observers using on-off temporal modulation of a 2.3 c/deg sinusoidal grating. With 4.19 Hz, 20 out of 33 PD patient eyes had abnormal VEPs. However, only 8 of 33 eyes were abnormal with 8.41 Hz. "Routine" (counterphase) transient VEPs revealed delayed VEPs for only 7 out of 24 eyes of the patients. These findings suggest an "input" temporal frequency-dependent abnormality in the foveal pathway.

Adult↗

Ocular toxicity of Anandron in patients treated for prostatic cancer.

Approximately 65% of patients with prostatic cancer treated by the combination therapy using a gonadorelin (LHRH) agonist or orchidectomy in association with the antiandrogen Anandron complained of a delay in recovering vision after bright illumination (sun, television, bright light). Detailed ophthalmological examination revealed an increase in the photostress recovery time to an average of 9 min, while the upper limit of normal is 1 min 20 s. When treatment was changed from Anandron to the other pure antiandrogen flutamide, the value of the photostress recovery time markedly decreased and the visual symptoms rapidly disappeared. Since uninterrupted administration of the antiandrogen is of the outmost importance for the successful therapy of prostatic cancer, the availability of a compound such as flutamide that has no side effect other than those due to hypoandrogenicity should greatly facilitate compliance by the patients and the success of the treatment.

Aged↗

The hemispheric distribution of the transient rat VEP: a comparison of flash and pattern stimulation.

We investigated the hemispheric distribution of the rat visual evoked potential (VEP) to pattern reversal and flash stimuli, presented monocularly at a rate of 1 Hz. Pattern VEP components could be recorded only over an area bounded by the anatomical coordinates of area 17, while some flash VEP components were recordable outside the primary visual area. Monocular pattern stimulation, as expected, evoked dominant contralateral VEPs. Surprisingly, ipsilateral responses could be also recorded with the reference electrode near the nasal bone. These VEPs showed partial polarity inversion compared to the contralateral EPs. To assess the origin of the ipsilateral EPs, we also recorded EPs following surgical deafferentation of the ipsilateral cortex. Our data reveal that ipsilateral VEPs represent volume conducted potentials.

Animals↗

Electroretinographic signs of experimental chronic ischemia in the rabbit retina.

Chronic retinal ischemia was induced in rabbits by clamping the retrobulbar neurovascular pedicle of one eye. The other eye was used as a control. Electroretinograms (ERGs) were recorded for up to 32 weeks. The amplitude of the b-wave and of the oscillatory potentials showed a biphasic change: first a rapid drop below normal for 4 to 9 weeks, then an increase to above normal. The hyperresponsiveness was maintained up to the 32nd week. The implicit time of response was significantly modified only for the responses evoked by a low to moderate intensity of stimulation.

Animals↗

The effect of contrast and spatial frequency on the visual evoked potential of the hooded rat.

Transient and steady-state visual evoked potentials, obtained with counterphase modulated grating patterns, were recorded through chronically implanted electrodes in lightly anesthetized and unanesthetized hooded rats. As a function of spatial frequency, the latency of the major positive wave (P1) of the transient VEP was minimal with a 0.1 cycles per degree (cpd) grating as stimulus. The amplitude of the P1-N2 component remained constant from 0.04 to 0.20 cpd and then decreased with higher spatial frequencies. The function relating amplitude of steady-state VEP to spatial frequency at high contrast depended on temporal frequency: It had a band-pass form at 5.0 Hz and a low-pass form at 8.4 Hz. As a function of contrast, the latency of the P1 wave linearly decreased and its amplitude increased with increments of contrast up to 55%. The contrast function of the amplitude of the second harmonic of the steady-state VEP (8.4 Hz) showed two linear segments: one for low contrasts with a shallow slope and one for high contrasts with a steep slope, suggesting two distinct contrast mechanisms.

Animals↗

VEPs in humans reveal high and low spatial contrast mechanisms.

The effect of contrast on visual evoked potential (VEP) amplitude was examined in nine observers. A 6.0 cycles/deg (cpd) grating was modulated in an "on-off" mode at 7.5 Hz. The VEP response contains significant first and second harmonic components: their growth with contrast is parallel, each function consisting of two limbs. The data are consistent with the hypothesis that the pattern VEP obtained with "on-off" presentation may reflect the contributions of "low" and "high" contrast neuronal populations demonstrated in physiological studies of the primate.

Evoked Potentials, Visual↗

Pattern electroretinograms and visual-evoked potentials in glaucoma and multiple sclerosis.

Steady-state visual-evoked potentials and electroretinograms were simultaneously recorded in four patients with glaucoma and in five patients with multiple sclerosis. The stimuli included a homogenous field and a 2.3 cycles per degree sinusoidal grating that were counter-phase modulated at the rate of 7.5 Hz. We used narrow bandwidth spectral analysis to measure the response amplitudes and signal-to-noise ratios. Transient pattern visual-evoked potentials (1 Hz) were also measured for latency in each eye. We found abnormal pattern electroretinograms, based on the absence of a significant second harmonic component, in three of the four glaucomatous eyes although the homogenous field electroretinograms were normal. In the patients with multiple sclerosis, the pattern electroretinograms were abnormal in two eyes, but the transient visual-evoked potential latency had the highest diagnostic yield (seven of ten eyes).

Adult↗

On the possible role of temporal delays of afferent processing in Parkinson's disease.

Visual evoked potential (VEP) latency is one measure of afferent delays in Parkinson's disease. New aspects of temporal processing were studied in the VEP of 7 patients and 10 normals. For this analysis the patterned stimulus was simultaneously modulated at two temporal frequencies. Phase shifts of non-linear VEP components in patients, compared to normals, revealed that an abnormality of temporal processing in this disease must be caused by altered neuronal interactions, not only by simple conduction defects.

Adult↗

Pallidofugal projections to thalamus and midbrain: a quantitative antidromic activation study in monkeys and cats.

The projections of monkey medial globus pallidus (and of cat entopeduncular nucleus) to thalamus and midbrain were studied with antidromic activation in order to determine the number of pallidal neurons sending axonal branches to the two sites. The animals were anesthetized with pentobarbital and several movable electrodes were used to stimulate the thalamic nuclear complex ventralis anterior - ventralis lateralis (VA-VL), the nucleus "centre médian" (CM), and the midbrain nucleus tegmenti pedunculopontinus (TPP). The responses of pallidal neurons were recorded with extracellular microelectrodes. In 3 monkeys 99% and 87% of 145 medial pallidal neurons responded antidromically to stimulation of VA-VL and TPP respectively. Reciprocal collision tests demonstrated that 86% of the 145 neurons sent axonal branches to the two sites. By comparison in 2 cats the tests demonstrated that 72% of 46 entopeduncular neurons branched to VA-VL and TPP. In 2 monkeys 68% of 53 medial pallidal neurons were shown to branch to VA-VL and CM thalamic nuclei. In the monkeys, the latencies of responses indicate that all pallidofugal fibers have the same mean conduction rate: 6 m/s. The fibers appear to branch profusely in VA-VL where less current was required to activate neurons antidromically than in TPP. The location of neurons in the medial pallidum is weakly correlated with the location of stimulation points in VA-VL activating the neurons antidromically at low threshold, suggesting some topography in the pallidothalamic projection. However there is no particular localization of medial pallidal neurons with and without branching projections. Apart from one exception, the 162 neurons recorded in the lateral pallidum failed to respond antidromically to the stimulation sites. We conclude that the great majority of medial pallidal neurons can send signals to both the thalamus and the midbrain in the cat and in the monkey.

Animals↗

A comparison of projections of entopeduncular neurons to the thalamus, the midbrain and the habenula in the cat.

Anatomical studies have demonstrated that the output of the striopallidal system is distributed to two areas of the thalamus: the ventrolateral-ventroanterior and the centromedian nuclei. The two areas are involved in different ways in the control of somatic motor activity. Pallidal efferents are also distributed to a still obscure tegmental area in the midbrain, the pedunculopontine nucleus, and to the lateral habenular nucleus, a structure of the limbic system. The present study compares the projections of entopeduncular neurons to the four sites in cats. The comparison is based on an estimation of the number of entopeduncular neurons sending fibers to each site and branching to more than one site. The four projection sites were stimulated electrically in anesthetized cats and the number of entopeduncular neurons excited antidromically were counted. At least 68% of entopeduncular neurons were excited antidromically by stimulation of the ventrolateral nucleus, an equal number were excited antidromically by stimulation of the nucleus centromedian and slightly fewer but still more than 50% by stimulation of the pedunculopontine nucleus. The three sites gave rise to antidromic responses of the same entopeduncular neuron in at least 33% of the cases. Only 25% of entopeduncular neurons responded antidromically to stimulation of the lateral habenular nucleus exclusively (one-third) or not (two-thirds). Some neurons recorded incidentally in the globus pallidus responded antidromically to the stimulation sites. Neurons were also recorded in the preoptico-hypothalamic area and 67% responded antidromically exclusively to the stimulation of the lateral habenular nucleus.

Action Potentials↗