Finger kinaesthesia: cognitive electrogeneses to attended joint input.

Study of brain mechanisms subserving perception of passive finger movements revealed an unexpected contrast between cutaneous and deep inputs from fingers. Selective attention to tactile inputs from finger tips did not change the first response of primary area 3b, but elicited a cognitive P40 in second order postcentral cortex. For finger joint inputs, attention enhanced the very first cortical response elicited by thalamo-cortical input in postcentral area 2 whereby finger kinaesthesia information was integrated with the cutaneous features information received from primary somatic areas via corticocortical connections.

The challenge of non-invasive cognitive physiology of the human brain: how to negotiate the irrelevant background noise without spoiling the recorded data through electronic averaging.

Brain mechanisms involved in selective attention in humans can be studied by measures of regional blood flow and metabolism (by positron emission tomography) which help identify the various locations with enhanced activities over a period of time of seconds. The physiological measures provided by scalp-recorded brain electrical potentials have a better resolution (milliseconds) and can reveal the actual sequences of distinct neural events and their precise timing. We studied selective attention to sensory inputs from fingers because the brain somatic representations are deployed over the brain convexity under the scalp thereby making it possible to assess distinct stages of cortical processing and representation through their characteristic scalp topographies.

Non-averaged human brain potentials in somatic attention: the short-latency cognition-related P40 component.

1. Non-averaged scalp-recorded brain potentials were studied in humans during selective attention to randomly intermixed series of stimuli to fingers. Physiological tests were use for validating the presence or absence of the short-latency cognition-related P40 electrogeneses in parietal cortex in the response to a single-target stimulus (P40 signifies a positive polarity of about 40 ms peak latency).

Transient phase-locking of 40 Hz electrical oscillations in prefrontal and parietal human cortex reflects the process of conscious somatic perception.

Electrical potential oscillations in the range of 35-45 Hz (gamma waves) have recently been shown to occur rather ubiquitously in the brain of awake humans. During selective somatic attention, we demonstrate a transient phase-locking of the gamma waves generated in the contralateral prefrontal and parietal cortical areas that we had previously shown to be involved in such selective attention tasks. In line with other microphysiological evidence obtained on mammalian visual cortex, this selective functional synchronization between critical human brain areas (as far as about 9 cm apart) is proposed to reflect the transient 'binding' of discrete cognitive features that are processed in distributed neuronal assemblies of the brain whereby the conscious perception of an object or event can be achieved.

A method for identifying short-latency human cognitive potentials in single trials by scalp mapping.

Studies of scalp-recorded brain event-related potentials in humans currently depend on the electronic averaging of many responses to the stimulus. In non-averaged single responses, it is sometimes possible to see late components such as the so-called P300, but not the shorter latency components that are much smaller and masked in background noise. We tried to identify short-latency cognitive potentials evoked by finger stimulation by comparing single trial responses that are concomitantly recorded at the contralateral and ipsilateral parietal scalp respectively.

Right or left ear reference changes the voltage of frontal and parietal somatosensory evoked potentials.

Short-latency cortical somatosensory evoked potentials (SEPs) to left median nerve stimulation were recorded with either the left or right earlobe as reference. With a right earlobe reference the voltage of the parietal N20 and P27 was reduced while the voltage of the frontal P20 and N30 was enhanced. The effects were consistent, but their size varied with the SEP component considered and also among the subjects.

Mapping early somatosensory evoked potentials in selective attention: critical evaluation of control conditions used for titrating by difference the cognitive P30, P40, P100 and N140.

Detailed procedures are described for the study of somatosensory event-related potentials (ERPs) to electric stimulation of fingers. Control responses to homogeneous (100%) series of identical stimuli (thus eliminating input mismatch) while the subject reads a novel (thus providing a distinct attention-capturing activity and maintaining vigilance level) are validated as reflecting the exogenous obligatory profiles required for assessing cognitive component in ERPs to target relevant stimuli. With these 'neutral' conditions, the control responses have a similar profile even at larger ISIs such as those separating the infrequent targets in Attention runs.

Automated measurement of kidney lysosomes by light microscopy. Influence of cyclosporine treatment.

After staining for acid phosphatase, video images were acquired from 1-micron sections of the kidneys of rats treated with cyclosporine. Automated segmentation of the lysosomes was followed by measurements of their area, number and optical density; tubular area was delineated manually. In addition to small lysosomes, representing more than 80% of the total number, all kidneys contained a second population of larger organelles.