Chronic deafferentation in monkeys differentially affects nociceptive and nonnociceptive pathways distinguished by specific calcium-binding proteins and down-regulates gamma-aminobutyric acid type A receptors at thalamic levels.

Chronic deafferentation of skin and peripheral tissues is associated with plasticity of representational maps in cerebral cortex and with perturbations of sensory experience that include severe "central" pain. This study shows that in normal monkeys the nonnociceptive, lemniscal component of the somatosensory pathways at spinal, brainstem, and thalamic levels is distinguished by cells and fibers immunoreactive for the calcium-binding protein parvalbumin, whereas cells of the nociceptive component at these levels are distinguished by immunoreactivity for 28-kDa calbindin. Long-term dorsal rhizotomies in monkeys lead to transneuronal degeneration of parvalbumin cells at brainstem and thalamic sites accompanied in the thalamus by a down-regulation of gamma-aminobutyric acid type A receptors and an apparent increase in activity of calbindin cells preferentially innervated by central pain pathways. Release from inhibition and imbalance in patterns of somatosensory inputs from thalamus to cerebral cortex may constitute subcortical mechanisms for inducing changes in representational maps and perturbations of sensory perception, including central pain.     

Thalamic Reorganization in Chronic Patients With Intracerebral Hemorrhage: A Retrospective Cross-Sectional Study

The aim of this study was to investigate changes of synaptic area of the spinothalamic tract and its thalamocortical pathway (STT) in the thalamus in chronic patients with putaminal hemorrhage.Twenty four patients with a lesion in the ventral posterior lateral nucleus (VPL) of the thalamus following putaminal hemorrhage were recruited for this study. The subscale for tactile sensation of the Nottingham Sensory Assessment (NSA) was used for the determination of somatosensory function. Diffusion tensor tractography of the STT was reconstructed using the Functional Magnetic Resonance Imaging of the Brain Software Library. We classified patients according to 2 groups: the VPL group, patients whose STTs were synapsed in the VPL; and the non-VPL group, patients whose STTs were synapsed in other thalamic areas, except for the VPL.Thirteen patients belonged to the VPL group, and 8 patients belonged to the non-VPL group. Three patients were excluded from grouping due to interrupted integrity of the STTs. The tactile sensation score of the NSA in the non-VPL group (10.50 ± 0.93) was significantly decreased compared with that of the VPL group (19.45 ± 1.33) (P < 0.05).We found that 2 types of patient had recovered via the VPL area or other areas of the STT. It appears that patients who showed shifting of the thalamic synaptic area of the STT might have recovered by the process of thalamic reorganization following thalamic injury. In addition, thalamic reorganization appears to be related to poorer somatosensory outcome.     

Immediate thalamic sensory plasticity depends on corticothalamic feedback

Multiple neuron ensemble recordings were obtained simultaneously from both the primary somatosensory (SI) cortex and the ventroposterior medial thalamus (VPM) before and during the combined administration of reversible inactivation of the SI cortex and a reversible subcutaneous block of peripheral trigeminal nerve fibers. This procedure was performed to quantify the contribution of descending corticofugal projections on (i) the normal organization of thalamic somatosensory receptive fields and (ii) the thalamic somatosensory plastic reorganization that immediately follows a peripheral deafferentation. Reversible inactivation of SI cortex resulted in immediate changes in receptive field properties throughout the VPM. Cortical inactivation also significantly reduced but did not completely eliminate the occurrence of VPM receptive field reorganization resulting from the reversible peripheral deafferentation. This result suggests that the thalamic plasticity that is seen immediately after a peripheral deafferentation is dependent upon both descending corticofugal projections and ascending trigeminothalamic projections.     

Maintenance of a somatotopic cortical map in the face of diminishing thalamocortical inputs

This study addresses the extent of divergence in the ascending somatosensory pathways of primates. Divergence of inputs from a particular body part at each successive synaptic step in these pathways results in a potential magnification of the representation of that body part in the somatosensory cortex, so that the representation can be expanded when peripheral input from other parts is lost, as in nerve lesions or amputations. Lesions of increasing size were placed in the representation of a finger in the ventral posterior thalamic nucleus (VPL) of macaque monkeys. After a survival period of 1–5 weeks, area 3b of the somatosensory cortex ipsilateral to the lesion was mapped physiologically, and the extent of the representation of the affected and adjacent fingers was determined. Lesions affecting less than 30% of the thalamic VPL nucleus were without effect upon the cortical representation of the finger whose thalamic representation was at the center of the lesion. Lesions affecting about 35% of the VPL nucleus resulted in a shrinkage of the cortical representation of the finger whose thalamic representation was lesioned, with concomitant expansion of the representations of adjacent fingers. Beyond 35–40%, the whole cortical representation of the hand became silent. These results suggest that divergence of brainstem and thalamocortical projections, although normally not expressed, are sufficiently great to maintain a representation after a major loss of inputs from the periphery. This is likely to be one mechanism of representational plasticity in the cerebral cortex.     

Changes in corticothalamic modulation of receptive fields during peripheral injury-induced reorganization

The influence of corticothalamic projections on the thalamus during different stages of reorganization was determined in anesthetized raccoons that had undergone previous removal of a single forepaw digit. Single-unit recordings were made from 522 sites in the somatosensory nucleus of the thalamus (ventroposterior lateral nucleus) before and after lesioning parts of primary somatosensory cortex. In those parts of ventroposterior lateral nucleus that had intact input from the periphery, the cortical lesion resulted in an immediate 85% increase in receptive field (RF) size. In animals studied 2-6 weeks after digit amputation, peripherally denervated thalamic neurons had unique RFs that were larger than normal, and these were not further enlarged by cortical lesion. However, at longer periods of reorganization (>4 mo), when the new RFs of denervated neurons had decreased in size, cortical lesion again produced expansion of RF size. These data demonstrate that corticothalamic fibers modulate the spatial extent of thalamic RFs in intact animals, probably by controlling intrathalamic inhibition. This corticothalamic modulation is ineffective during the early stages of injury-induced reorganization when new RFs are being formed, but is reinstated after the new RFs have become stabilized. The fact that neurons in the denervated thalamic region retained their unique RFs after cortical lesion indicates that their new inputs are not being relayed from a reorganized cortex and support the view that some plasticity occurs in or below the thalamus.     

The effect of thiamine deficiency on the structure and physiology of the rat forebrain

Dietary thiamine deficiency, enhanced by pyrithiamine administration in adult rats, produces overt lesions in the brain that are especially prominent in the thalamus. The present study was undertaken to determine whether the thalamic lesions could be correlated with alterations in the physiological properties of neurons in the thalamus and somatosensory cortex. The regimen for experimentally inducing thiamine deficiency produced large lesions in the thalamus of every case; the lesions included most, if not all, of the neurons in the intralaminar thalamic nuclei. The extent of the lesion in the intralaminar thalamus was highly correlated with the loss of bilaterally synchronous spontaneous activity in the cerebral cortex. This correlation was seen in animals analyzed as early as 1–18 hr after the appearance of opisthotonus, the crisis state of thiamine deficiency, and as late as 2–9 weeks of recovery following thiamine replacement therapy. The loss of bilateral synchronous bursting neuronal activity following intralaminar thalamic lesions is consistent with the proposed role of the intralaminar thalamus as a pacemaker for rhythmic cortical activity (Armstrong-Jameset al.,Exp. Brain Res., 1985; Fox and Armstrong-James,Exp. Brain Res. 63: 505–518, 1986). The location and size of the central lesions within the thalamus suggest that the observed neuronal loss could result from a nonhemorrhagic infarction in the ventromedial branches of the superior cerebellar arteries. Experimental thiamine deficiency also produced alterations in the receptive field properties of the somatosensory cortex neurons in all animals examined. Changes in cortical receptive field properties were correlated with the destruction of sensory relay neurons in the thalamic ventrobasal complex. The loss of the central lateral thalamic input to the cortex and the loss of somatosensory relay neurons in the ventrobasal thalamus in experimental thiamine deficiency produce alterations in cortical function which may contribute to deficits in memory and cognition analogous to those which characterize Korsakoff's psychosis in humans.     

Peripheral nerve damage facilitates functional innervation of brain grafts in adult sensory cortex.

The neural pathways that relay information from cutaneous receptors to the cortex provide the somatic sensory information needed for cortical function. The last sensory relay neurons in this pathway have cell bodies in the thalamus and axons that synapse on neurons in the somatosensory cortex. After cortical lesions that damage mature thalamocortical fibers in the somatosensory cortex, we have attempted to reestablish somatosensory cortical function by grafting embryonic neocortical cells into the lesioned area. Such grafts survive in adult host animals but are not innervated by thalamic neurons, and consequently the grafted neurons show little if any spontaneous activity and no responses to cutaneous stimuli. We have reported that transection of peripheral sensory nerves prior to grafting "conditions" or "primes" the thalamic neurons in the ventrobasal complex so that they extend axons into grafts subsequently placed in the cortical domain of the cut nerve. In this report we present evidence that the ingrowth of ventrobasal fibers leads to graft neurons that become functionally integrated into the sensory circuitry of the host brain. Specifically, the conditioning lesions made prior to grafting produce graft neurons that are spontaneously active and can be driven by natural activation of cutaneous receptors or electrical stimulation of the transected nerve after it regenerates. Furthermore, oxidative metabolism in these grafts reaches levels that are comparable to normal cortex, whereas without prior nerve cut, oxidative metabolism is abnormally low in neocortical grafts. We conclude that damage to the sensory periphery transsynaptically stimulates reorganization of sensory pathways through mechanisms that include axonal elongation and functional synaptogenesis.     

Coding perceptual discrimination in the somatosensory thalamus

The sensory thalamus is classically viewed as a relay station of sensory information to cortex, but recent studies suggest that it is sensitive to cognitive demands. There are, however, few experiments designed to test whether this is so. We addressed this problem by analyzing the responses of single neurons recorded in the somatosensory thalamus while trained monkeys reported a decision based on the comparison of two mechanical vibration frequencies applied sequentially to one fingertip. In this task, monkeys must hold the first stimulus frequency (f1) in working memory and compare it to the current sensory stimulus (f2) and must postpone the decision report until a cue triggers the decision motor report, i.e., whether f2 > f1 or f2 < f1. We found that thalamic somatosensory neurons encoded the stimulus frequency either in their periodicity and firing-rate responses, but only during the stimulus periods and not during the working memory and decision components of this task. Furthermore, correlation analysis between behavior and stimulus coding showed that only the firing rate modulations accounted for the overall psychophysical performance. However, these responses did not predict the animal’s decision reports on individual trials. Moreover, the sensitivity to changes in stimulus frequency was similar when the monkeys performed the vibrotactile discrimination task and when they were not required to report discrimination. These results suggest that the somatosensory thalamus behaves as a relay station of sensory information to the cortex and that it is insensitive to the cognitive demands of the task used here.     

Integration of signals from different cortical areas in higher order thalamic neurons

Higher order thalamic neurons receive driving inputs from cortical layer 5 and project back to the cortex, reflecting a transthalamic route for corticocortical communication. To determine whether or not individual neurons integrate signals from different cortical populations, we combined electron microscopy “connectomics” in mice with genetic labeling to disambiguate layer 5 synapses from somatosensory and motor cortices to the higher order thalamic posterior medial nucleus. A significant convergence of these inputs was found on 19 of 33 reconstructed thalamic cells, and as a population, the layer 5 synapses were larger and located more proximally on dendrites than were unlabeled synapses. Thus, many or most of these thalamic neurons do not simply relay afferent information but instead integrate signals as disparate in this case as those emanating from sensory and motor cortices. These findings add further depth and complexity to the role of the higher order thalamus in overall cortical functioning.

Until relatively recently, the view of thalamic neurons is that they simply relay information to the cortex with little or no integrative processing. This view drew heavily on lessons learned from the dominant model of the thalamus: the lateral geniculate nucleus (LGN), where receptive fields of geniculate relay cells closely match those of their retinal inputs. However, recent evidence has dramatically changed this view. There are three main reasons for this.First, there is considerable evidence that modulatory input to the thalamus can strongly affect the response properties of thalamic relay cells (reviewed in ref. 1). Examples include the different tonic and burst firing modes, gain of response to driving inputs, etc.Second, new evidence demonstrates that driver inputs that convey different types of peripheral sensory information converge onto single thalamic relay cells, therefore suggesting the possibility of significant integration of information prior to relaying to the cortex. These studies include evidence of retinal inputs with very different receptive fields converging onto single geniculate relay cells (2, 3), of driving inputs from retina and superior colliculus converging onto single geniculate relay cells (4), and of cortical layer 5 and brainstem driver inputs converging onto single cells of the posterior medial nucleus [POm (5)]. However, these examples are few, and each is limited in scale. There is also recent evidence that some thalamic relays may function without traditional driver input (6).Third, the recent division of thalamic nuclei into two functional types, first order and higher order (reviewed in ref. 1), offers potentially new views on the extent to which thalamic neurons transform received information prior to transmission. Unlike first order thalamic relays, which receive driving input from a subcortical source (e.g., the retina for the LGN) and transmit that to the cortex, higher order relays receive inputs primarily from layer 5 of the cortex and thus serve as a transthalamic route for corticocortical communication. Therefore, the distinct functional organization of higher order thalamic relays offers an interesting substrate for thalamic integration of disparate information (7–9). Specifically, since higher order thalamic nuclei commonly receive overlapping projections from layer 5 neurons of multiple, distinct cortical areas (10), we can ask whether these multiple driving inputs containing different types of information converge to synapse onto single relay cells. Because most of thalamus by volume seems to be higher order (1) and because most or all cortical areas send layer 5 projections to the thalamus as the afferent limb in transthalamic pathways (10), such convergence would have major significance for thalamocortical functioning.To provide morphological evidence for such convergence, we employed modern viral tracing techniques to disambiguate multiple long-distance pathways in large volume serial electron microscope (EM) reconstructions (i.e., “connectomics”) in the mouse; by this approach, we could identify possible convergence of layer 5 inputs from somatosensory and motor cortices onto single relay cells of the POm, which is a higher order somatosensory thalamic nucleus. The viral tracing makes use of orthograde labeling of long pathways with an ascorbate peroxidase (APX) from the pea plant (11) that has allowed us to identify separately synaptic terminals from sensory and motor cortices onto neurons of the POm. Our results indicate significant convergence of presumptive driver inputs onto single thalamic neurons from layer 5 cells of disparate sensory and motor cortices.     

Cortical control of adaptation and sensory relay mode in the thalamus

A major synaptic input to the thalamus originates from neurons in cortical layer 6 (L6); however, the function of this cortico–thalamic pathway during sensory processing is not well understood. In the mouse whisker system, we found that optogenetic stimulation of L6 in vivo results in a mixture of hyperpolarization and depolarization in the thalamic target neurons. The hyperpolarization was transient, and for longer L6 activation (>200 ms), thalamic neurons reached a depolarized resting membrane potential which affected key features of thalamic sensory processing. Most importantly, L6 stimulation reduced the adaptation of thalamic responses to repetitive whisker stimulation, thereby allowing thalamic neurons to relay higher frequencies of sensory input. Furthermore, L6 controlled the thalamic response mode by shifting thalamo–cortical transmission from bursting to single spiking. Analysis of intracellular sensory responses suggests that L6 impacts these thalamic properties by controlling the resting membrane potential and the availability of the transient calcium current I_T, a hallmark of thalamic excitability. In summary, L6 input to the thalamus can shape both the overall gain and the temporal dynamics of sensory responses that reach the cortex.Sensory signals en route to the cortex undergo profound signal transformations in the thalamus. One important thalamic transformation is sensory adaptation. Adaptation is a common characteristic of sensory systems in which neural output adjusts to the statistics and dynamics of past stimuli, thereby better encoding small stimulus changes across a wide range of scales despite the limited range of possible neural outputs (1–3). Thalamic sensory adaptation is characterized by a steep decrease in action potential (AP) activity during sustained sensory stimulation (4–7), decreasing the efficacy at which subsequent sensory stimuli are transmitted to the cortex.The widely reported duality of thalamic response mode is another key property of thalamic information processing which further affects how sensory input reaches the cortex. In burst mode, sensory inputs are relayed as short, rapid clusters of APs; in contrast, in tonic mode the same inputs are translated into single APs. Both tonic and burst modes have been described during anesthesia/sleep and wakefulness/behavior, with a pronounced shift toward the tonic mode during alertness (8–12).Although the exact information content of thalamic bursts is not yet clear, it has been suggested that bursting may signal novel stimuli to the cortex, whereas the tonic mode enables linear encoding of fine stimulus details, e.g., when an object is examined (13, 14). One issue hampering the interpretation of burst/tonic responses is that currently it is unknown if the cortex itself is involved in the rapid changes in firing modes seen in the awake and anesthetized animal (15, 16) and which mechanisms initiate these shifts in vivo.On the biophysical level, the response mode depends on the resting membrane potential (RMP), which controls the availability of the transient low-threshold calcium current (I_T) (17). Depolarization decreases the size of the I_T-mediated low-threshold calcium spike (LTS), and fewer burst spikes are fired (18). Similarly, RMP influences adaptation in that depolarization reduces the voltage distance to the AP threshold, thereby increasing the probability that smaller, depressed inputs will trigger APs (6). Thus, the dynamics of the RMP may govern several key properties of signal transformation in the thalamus, thereby providing a common mechanism for controlling thalamic adaptation and response mode.Although subcortical inputs have been shown to influence thalamic firing modes (7, 9), we investigated the impact of cortical activity on thalamic sensory processing. Cortico–thalamic projections from cortical layer 6 (L6) are a likely candidate for regulating thalamic sensory processing with high spatial and temporal precision, because these projections provide a major input to the thalamus and, as shown by McCormick et al. (19), depolarize and modulate firing of thalamic cells in vitro.However, because of the inability to study sensory signals in brain slices, the role of L6 on thalamic input/output properties during sensory processing is not clear. Here, in the ventro posteromedial nucleus (VPM) of the mouse whisker thalamus, we investigate how L6 impacts the transmission of whisker inputs to the cortex. Recent advances in cell-type–specific approaches to dissect specific circuits in vivo (20–22) allowed us to activate the L6–thalamic pathway specifically and determine its impact on thalamic sensory processing.We found that cortical L6 can change key properties of thalamic sensory processing by controlling the interaction of intrinsic membrane properties and sensory inputs. This mechanism enables the cortex to control the frequency-dependent adaptation and the gain of its own input.     

Area-specific regulation of γ-aminobutyric acid type A receptor subtypes by thalamic afferents in developing rat neocortex

Targeting and innervation of the cerebral cortex by thalamic afferents is a key event in the specification of cortical areas. The molecular targets of thalamic regulation, however, have remained elusive. We now demonstrate that thalamic afferents regulate the expression of γ-aminobutyric acid type A (GABA_A) receptors in developing rat neocortex, leading to the area-specific expression of receptor subtypes in the primary visual (V1) and somatosensory (S1) areas. Most strikingly, the α1- and α5-GABA_A receptors exhibited a reciprocal expression pattern, which precisely reflected the distribution of thalamocortical afferents at postnatal day 7. Following unilateral lesions at the birth of the thalamic nuclei innervating V1 and S1 (lateral geniculate nucleus and ventrobasal complex, respectively), profound changes in subunit expression were detected 1 week later in the deprived cortical territories (layers III–IV of V1 and S1). The expression of the α1 subunit was strongly down-regulated in these layers to a level comparable to that in neighboring areas. Conversely, the α5 subunit was up-regulated and areal boundaries were no longer discernible in the lesioned hemisphere. Changes similar to the α5 subunit were also seen for the α2 and α3 subunits. These results indicate that the differential expression of GABA_A receptor subtypes in developing neocortex is dependent on thalamic innervation, contributing to the emergence of functionally distinct areas.     

Oxidation of ethanol in the rat brain and effects associated with chronic ethanol exposure

It has been reported that chronic and acute alcohol exposure decreases cerebral glucose metabolism and increases acetate oxidation. However, it remains unknown how much ethanol the living brain can oxidize directly and whether such a process would be affected by alcohol exposure. The questions have implications for reward, oxidative damage, and long-term adaptation to drinking. One group of adult male Sprague–Dawley rats was treated with ethanol vapor and the other given room air. After 3 wk the rats received i.v. [2-¹³C]ethanol and [1, 2-¹³C₂]acetate for 2 h, and then the brain was fixed, removed, and divided into neocortex and subcortical tissues for measurement of ¹³C isotopic labeling of glutamate and glutamine by magnetic resonance spectroscopy. Ethanol oxidation was seen to occur both in the cortex and the subcortex. In ethanol-naïve rats, cortical oxidation of ethanol occurred at rates of 0.017 ± 0.002 µmol/min/g in astroglia and 0.014 ± 0.003 µmol/min/g in neurons, and chronic alcohol exposure increased the astroglial ethanol oxidation to 0.028 ± 0.002 µmol/min/g (P = 0.001) with an insignificant effect on neuronal ethanol oxidation. Compared with published rates of overall oxidative metabolism in astroglia and neurons, ethanol provided 12.3 ± 1.4% of cortical astroglial oxidation in ethanol-naïve rats and 20.2 ± 1.5% in ethanol-treated rats. For cortical astroglia and neurons combined, the ethanol oxidation for naïve and treated rats was 3.2 ± 0.3% and 3.8 ± 0.2% of total oxidation, respectively. ¹³C labeling from subcortical oxidation of ethanol was similar to that seen in cortex but was not affected by chronic ethanol exposure.     

Cellular organization of cortical barrel columns is whisker-specific

The cellular organization of the cortex is of fundamental importance for elucidating the structural principles that underlie its functions. It has been suggested that reconstructing the structure and synaptic wiring of the elementary functional building block of mammalian cortices, the cortical column, might suffice to reverse engineer and simulate the functions of entire cortices. In the vibrissal area of rodent somatosensory cortex, whisker-related “barrel” columns have been referred to as potential cytoarchitectonic equivalents of functional cortical columns. Here, we investigated the structural stereotypy of cortical barrel columns by measuring the 3D neuronal composition of the entire vibrissal area in rat somatosensory cortex and thalamus. We found that the number of neurons per cortical barrel column and thalamic “barreloid” varied substantially within individual animals, increasing by ∼2.5-fold from dorsal to ventral whiskers. As a result, the ratio between whisker-specific thalamic and cortical neurons was remarkably constant. Thus, we hypothesize that the cellular architecture of sensory cortices reflects the degree of similarity in sensory input and not columnar and/or cortical uniformity principles.Two major concepts of cortical neuronal organization have been proposed. Structurally, correlations between stereology-based measurements (1) of neuron density and cortical thickness resulted in the hypothesis of structural uniformity, arguing that the number of neurons beneath a square millimeter of cortical surface is constant and independent of cortical area and species (2, 3). Functionally, cortex is organized in a columnar fashion, reflecting similar neuronal activity along the vertical cortex axis in response to peripheral stimuli (4–8). Similar spatial extents of functional cortical columns in the horizontal plane, combined with the idea of cortical uniformity, resulted in the notion that a stereotypic columnar network may also represent the elementary structural building block of sensory cortices (9). In combination, the two concepts thus suggested a common organization of all sensory cortices, which led to reverse engineering and simulation efforts that build up large-scale network models of repeatedly occurring identical cortical circuits (10, 11).The ideal model system for investigating columnar structure and function is the vibrissal area of rodent somatosensory cortex. There, “barrels” of neurons in layer 4 (L4) have been identified as somatotopically organized structural correlates of peripheral receptor organs (i.e., facial whiskers). Whisker/barrel columns have thus been regarded as both structural and functional elementary cortical units (12–14). To investigate the structural stereotypy of cortical barrel columns, independent of the drawbacks associated with stereology (i.e., extrapolations from small sampling regions), we decided to locate each excitatory and inhibitory neuron soma within the entire volume of interest. Using high-resolution, large-scale confocal microscopy (15) and automated image-processing routines (16), we found that the number of neurons per barrel column increased by ∼2.5-fold from columns that correspond to the dorsal facial whiskers (A-row) to columns corresponding to the ventral whiskers (E-row). Moreover, cortical thickness increased by ∼500 μm from A- to E-rows, resulting in whisker-specific laminar neuron profiles, layer locations, and thicknesses. Further, the distributions of excitatory and inhibitory neurons outside the L4 barrels were indistinguishable between barrel columns, the septa (the cortex separating the barrel columns) (14) and the dysgranular zones (DZ) surrounding the vibrissal cortex (17).We performed the same analyses for the ventral posterior medial division (VPM) of rat thalamus, which provides whisker-specific input to the vibrissal cortex (18–20). Again, we found that the number of neurons per whisker (i.e., within so-called “barreloids”) (21) was constant within a whisker row, but increased by ∼2.5-fold from the A- to the E-row. Consequently, the ratio between neurons per barrel (column) and respective barreloid was remarkably constant. This whisker-specific cellular organization is in contrast to the ideas of columnar and cortical uniformity, questioning the stereology-based concept that mammalian cortices are composed of stereotypical elementary building blocks.     

A Simple and Efficient Method for Preparing High-Purity α-CaSO4·0.5H2O Whiskers with Phosphogypsum

A simple and efficient approach for the high-purity CaSO₄·2H₂O (DH) whiskers and α-CaSO₄·0.5H₂O (α-HH) whiskers derived from such phosphogypsum (PG) was proposed. The impact of different experimental parameters on supersaturated dissolution–recrystallization and preparation processes of α-CaSO₄·0.5H₂O was elaborated. At 3.5 mol/L HCl concentration, the dissolution temperature and time were 90 °C and 20 min, respectively. After eight cycles and 5–8 times cycles, total crystallization amount of CaSO₄·2H₂O was 21.75 and 9.97 g/100 mL, respectively, from supersaturated HCl solution. The number of cycles affected the shape and amount of the crystal. Higher HCl concentration facilitated CaSO₄·2H₂O dissolution and created a much higher supersaturation, which acted as a larger driving force for phase transformation of CaSO₄·2H₂O to α-CaSO₄·0.5H₂O. The HCl solution system’s optimum experimental conditions for HH whiskers preparation involved acid leaching of CaSO₄·2H₂O sample, with HCl concentration 6.0 mol/L, reaction temperature 80 °C, and reaction time 30 min–60 min. Under the third cycle conditions, α-CaSO₄·0.5H₂O whiskers were uniform in size, clear, and distinct in edges and angles. The length range of α-CaSO₄·0.5H₂O whiskers was from 106 μm to 231 μm and diameter range from 0.43 μm to 1.35 μm, while the longest diameter ratio was 231. Purity of α-CaSO₄·0.5H₂O whiskers was approximately 100%, where whiteness reached 98.6%. The reuse of the solution enables the process to discharge no waste liquid. It provides a new reference direction for green production technology of phosphogypsum.     

Discontinuity of cortical gradients reflects sensory impairment

Topographic maps and their continuity constitute a fundamental principle of brain organization. In the somatosensory system, whole-body sensory impairment may be reflected either in cortical signal reduction or disorganization of the somatotopic map, such as disturbed continuity. Here we investigated the role of continuity in pathological states. We studied whole-body cortical representations in response to continuous sensory stimulation under functional MRI (fMRI) in two unique patient populations—patients with cervical sensory Brown-Séquard syndrome (injury to one side of the spinal cord) and patients before and after surgical repair of cervical disk protrusion—enabling us to compare whole-body representations in the same study subjects. We quantified the spatial gradient of cortical activation and evaluated the divergence from a continuous pattern. Gradient continuity was found to be disturbed at the primary somatosensory cortex (S1) and the supplementary motor area (SMA), in both patient populations: contralateral to the disturbed body side in the Brown-Séquard group and before repair in the surgical group, which was further improved after intervention. Results corresponding to the nondisturbed body side and after surgical repair were comparable with control subjects. No difference was found in the fMRI signal power between the different conditions in the two groups, as well as with respect to control subjects. These results suggest that decreased sensation in our patients is related to gradient discontinuity rather than signal reduction. Gradient continuity may be crucial for somatotopic and other topographical organization, and its disruption may characterize pathological processing.The somatotopic “homunculus” representation in the human cortex is one of the most important discoveries of modern neuroscience (1, 2). The early electrophysiological findings of Penfield and coworkers (1, 2) have been confirmed and extended in several neuroimaging studies in healthy individuals (3–7) and have been further explored in patients and nonhuman primates with different pathologies using both electrophysiology and neuroimaging (8–14). The latter elicited changes in the cortical pattern of activity after a damage to the somatosensory system, manifested as functional cortical reorganization. Kaas, Merzenich, and Killackey suggested that there may be “several types of cortical reorganization, including (i) the somatotopic expansion of previously existing representations of body parts, (ii) the development of ‘new’ representations, (iii) the activation of large regions of the cortex from a very limited region of a receptive field surface, and (iv) a ‘nonsomatotopic’ activation of the cortex from scattered receptive fields” (9). The first three reorganization options were established whereas non-somatotopic representation remains understudied and unclear. A potential explanation is that most previous studies focused on the reorganization of single organ representation or changes in limited cortical area without exploring large scale topographical changes. We hypothesized that large scale nonsomatotopic reorganization may be associated to the relationship between the representation of the disturbed body part and the whole-body representation. In fact, the whole-body representation may have particular importance because continuous somatotopic organization reflects not only adjacency of different body parts, but also the general principle that neural populations that are involved in similar computational tasks are located in close spatial proximity (15, 16). Nonsomatotopic discontinuous whole-body representation may thus reflect a general pathological principle.To examine the role of continuity and discontinuity in somatosensory processing, we searched for a model that would enable us to compare processing of physiological and pathological whole-body continuous signals in the same study subject. One such model is the cervical partial (sensory) Brown-Séquard syndrome. This syndrome is characterized by injury to one half of the spinal cord, which disturbs sensory signal conduction from half of the body below the lesion to the contralateral hemisphere (17, 18). Patients with Brown-Séquard syndrome experience a reduction in sensation of one side of their body (hemihypoesthesia). Cervical Brown-Séquard syndrome is unique, involving a unilateral representation of the body, but in patients without brain pathology, thus serving as an ideal model to compare physiological and pathological cortical patterns from the disturbed and nondisturbed body sides in each individual patient. Another model that may causally demonstrate the role of continuity and discontinuity in somatosensory processing is one involving patients before and after surgical repair of cervical disk protrusion. This model enables examination of continuity in the same study subjects before and after intervention. Notably, whereas studies in nonhuman primates compare response to lesion before and after induction, no such study, to our knowledge, has examined response to surgical repair. We therefore used functional MRI (fMRI) in these two patient populations to compare responses in the most prominent somatosensory homunculi—the primary somatosensory cortex (S1) and supplementary motor area (SMA) (1, 19)—with continuous sensory stimulation of the whole body.To describe a sequential change in cortical activation coinciding with continuous sensory stimulation, we use the term “gradient” (20, 21). We quantified the continuity of gradients by analyzing a one-dimensional series of functional cluster geometric centroids that represent responses to sensory input from different body parts. Signal power was measured as well because somatosensory deficit that results in hypoesthesia may be reflected in signal reduction. We hypothesize that somatotopic representation in the hemisphere contralateral to the sensory deficit exhibits functional reorganization manifested as gradient discontinuity.     

Growth of new brainstem connections in adult monkeys with massive sensory loss

Somatotopic maps in the cortex and the thalamus of adult monkeys and humans reorganize in response to altered inputs. After loss of the sensory afferents from the forelimb in monkeys because of transection of the dorsal columns of the spinal cord, therapeutic amputation of an arm or transection of the dorsal roots of the peripheral nerves, the deprived portions of the hand and arm representations in primary somatosensory cortex (area 3b), become responsive to inputs from the face and any remaining afferents from the arm. Cortical and subcortical mechanisms that underlie this reorganization are uncertain and appear to be manifold. Here we show that the face afferents from the trigeminal nucleus of the brainstem sprout and grow into the cuneate nucleus in adult monkeys after lesions of the dorsal columns of the spinal cord or therapeutic amputation of an arm. This growth may underlie the large-scale expansion of the face representation into the hand region of somatosensory cortex that follows such deafferentations.     

Benefit of a low-fat over high-fat diet on vascular health during alternate day fasting

Background:

Alternate day fasting (ADF) with a low-fat (LF) diet improves brachial artery flow-mediated dilation (FMD). Whether these beneficial effects can be reproduced with a high-fat (HF) diet remains unclear.

Objective:

This study compared the effects of ADF-HF to ADF-LF regimens on FMD. The role that adipokines have in mediating this effect was also investigated.

Methods:

Thirty-two obese subjects were randomized to an ADF-HF (45% fat) or ADF-LF diet (25% fat), consisting of two phases: (1) a 2-week baseline weight maintenance period and (2) an 8-week ADF weight loss period. Food was provided throughout the study.

Results:

Body weight was reduced (P<0.0001) in the ADF-HF (4.4±1.0 kg) and ADF-LF group (3.7±0.7 kg). FMD decreased (P<0.05) by ADF-HF relative to baseline (7±1 to 5±2%) and increased (P<0.05) by ADF-LF (5±1 to 7±2%). Blood pressure remained unchanged in both groups. Adiponectin increased (P<0.05) in the ADF-HF (43±7%) and ADF-LF group (51±7%). Leptin and resistin decreased (P<0.05) in the ADF-HF (32±5% 23±5%) and ADF-LF group (30±3% 27±4%). Increases in adiponectin were associated with augmented FMD in the ADF-LF group only (r=0.34, P=0.03).

Conclusion:

Thus, improvements in FMD with ADF may only occur with LF diets and not with HF diets, and adipokines may not have a significant role in mediating this effect.     

Somatosensory cortical plasticity in adult humans revealed by magnetoencephalography.

Microelectrode recordings in adult mammals have clearly demonstrated that somatosensory cortical maps reorganize following peripheral nerve injuries and functional modifications; however, such reorganization has never been directly demonstrated in humans. Using magnetoencephalography, we have been able to demonstrate the somatotopic organization of the hand area in normal humans with high spatial precision. Somatosensory cortical plasticity was detected in two adults who were studied before and after surgical separation of webbed fingers (syndactyly). The presurgical maps displayed shrunken and nonsomatotopic hand representations. Within weeks following surgery, cortical reorganization occurring over distances of 3-9 mm was evident, correlating with the new functional status of their separated digits. In contrast, no modification of the somatosensory map was observed months following transfer of a neurovascular skin island flap for sensory reconstruction of the thumb in two subjects in whom sensory transfer failed to occur.     

Basal ganglia and cerebellum receive different somatosensory information in rats.

There are two great subcortical circuits that relay sensory information to motor structures in the mammalian brain. One pathway relays via the pontine nuclei and cerebellum, and the other relays by way of the basal ganglia. We studied the cells of origin of these two major pathways from the posteromedial barrel subfield of rats, a distinct region of the somatosensory cortex that contains the sensory representation of the large whiskers. We injected tracer substances into the caudate putamen or the pontine nuclei and charted the location of retrogradely filled cortical cells. In preliminary studies, we used double-labeling techniques to determine whether the cells of origin of these two pathways send axon collaterals to other subcortical targets. Lamina V of the rat posteromedial barrel subfield contains two distinct populations of subcortically projecting neurons, which are organized into distinct sublamina. . Corticopontine cells are located exclusively in sublamina Vb, the deeper of two sublamina revealed by cytochrome oxidase staining. Corticostriate cells are located almost exclusively in the more superficial sublamina Va. Experiments using double-labeling fluorescent tracers demonstrate that about one-quarter of the corticopontine cells send a collateral branch to the superior colliculus. Other studies have shown that cells in Vb are activated at very short latency after vibrissal stimulation; hence, they would seem to be an appropriate relay for the rapid transmission of sensory information to the cerebellum for use in sensory guidance of movement.     

An anatomical substrate for experience-dependent plasticity of the rat barrel field cortex.

The objective of this study was to examine the influence of sensory experience on the synaptic circuitry of the cortex. For this purpose, the quantitative distribution of the overall and of the gamma-aminobutyric acid (GABA) population of synaptic contacts was investigated in each layer of the somatosensory barrel field cortex of rats which were sensory deprived from birth by continuously removing rows of whiskers. Whereas there were no statistically significant changes in the quantitative distribution of the overall synaptic population, the number and proportion of GABA-immunopositive synaptic contacts were profoundly altered in layer IV of the somatosensory cortex of sensory-deprived animals. These changes were attributable to a specific loss of as many as two-thirds of the GABA contacts targeting dendritic spines. Thus, synaptic contacts made by GABA terminals in cortical layer IV and, in particular, those targeting dendritic spines represent a structural substrate of experience-dependent plasticity. Furthermore, since in this model of cortical plasticity the neuronal receptive-field properties are known to be affected, we propose that the inhibitory control of dendritic spines is essential for the elaboration of these functional properties.