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Associative processes in addiction and reward. The role of amygdala-ventral striatal subsystems.

Only recently have the functional implications of the organization of the ventral striatum, amygdala, and related limbic-cortical structures, and their neuroanatomical interactions begun to be clarified. Processes of activation and reward have long been associated with the NAcc and its dopamine innervation, but the precise relationships between these constructs have remained elusive. We have sought to enrich our understanding of the special role of the ventral striatum in coordinating the contribution of different functional subsystems to confer flexibility, as well as coherence and vigor, to goal-directed behavior, through different forms of associative learning. Such appetitive behavior comprises many subcomponents, some of which we have isolated in these experiments to reveal that, not surprisingly, the mechanisms by which an animal sequences responding to reach a goal are complex. The data reveal how the different components, pavlovian approach (or sign-tracking), conditioned reinforcement (whereby pavlovian stimuli control goal-directed action), and also more general response-invigorating processes (often called "activation," "stress," or "drive") may be integrated within the ventral striatum through convergent interactions of the amygdala, other limbic cortical structures, and the mesolimbic dopamine system to produce coherent behavior. The position is probably not far different when considering aversively motivated behavior. Although it may be necessary to employ simplified, even abstract, paradigms for isolating these mechanisms, their concerted action can readily be appreciated in an adaptive, functional setting, such as the responding by rats for intravenous cocaine under a second-order schedule of reinforcement. Here, the interactions of primary reinforcement, psychomotor activation, pavlovian conditioning, and the control that drug cues exert over the integrated drug-seeking response can be seen to operate both serially and concurrently. The power of our analytic techniques for understanding complex motivated behavior has been evident for some time. However, the crucial point is that we are now able to map these components with increasing certainty onto discrete amygdaloid, and other limbic cortical-ventral striatal subsystems. The neural dissection of these mechanisms also serves an important theoretical purpose in helping to validate the various hypothetical constructs and further developing theory. Major challenges remain, not the least of which is an understanding of the operation of the ventral striatum together with its dopaminergic innervation and its interactions with the basolateral amygdala, hippocampal formation, and prefrontal cortex at a more mechanistic, neuronal level.

Amygdala↗

Nimodipine prevents hyperglycemia-induced cerebral acidosis in middle cerebral artery occluded rats.

The effects of acute moderate hyperglycemia on local cerebral pH (LCpH) and local cerebral blood flow (LCBF) were studied in rats infused with glucose before middle cerebral artery (MCA) occlusion, and compared with findings in MCA occlusion alone. The effects of nimodipine infusion on LCBF and LCpH in MCA-occluded hyperglycemic rats were also studied. LCpH and LCBF were determined simultaneously by a double-label autoradiographic technique. Hyperglycemia was induced by an intraperitoneal injection of 2 g/kg D-glucose before MCA occlusion. Nimodipine-treated rats received the drug as an intravenous infusion of 0.5 micrograms/kg/min starting 15 min after occlusion, and ending at decapitation 4 h postocclusion. Cortical LCpH of five structures in the MCA territory of hyperglycemic rats varied between 6.64 +/- 0.04 and 6.72 +/- 0.02 (mean +/- SEM). These values were significantly lower than LCpH in the same ischemic structures in the control rats, which varied between 6.76 +/- 0.04 and 6.82 +/- 0.03 (p less than 0.05 for four of five structures). Cortical LCpH of hyperglycemic nimodipine-treated rats ranged between 6.94 +/- 0.02 and 7.05 +/- 0.02, indicating significant elevations in LCpH (p less than 0.001) compared with the untreated ischemic hyperglycemic animals. LCBF in the ischemic structures was not modified by hyperglycemia or nimodipine treatment. This suggests that nimodipine, by mechanisms other than improvement in blood flow, can prevent the enhanced cerebral tissue acidosis produced by hyperglycemia before incomplete focal ischemia.

Acidosis↗

Molecular features of hypothalamic plaques in Alzheimer's disease.

The pathology of Alzheimer's disease (AD) involves subcortical as well as cortical structures. The authors have used immunohistochemical methods to study the molecular composition of AD plaques in the hypothalamus. In contrast to previous studies using histochemical methods, the authors observed large numbers of diffuse plaques in the AD hypothalamus labeled with an antiserum to the beta-amyloid, or A4 peptide, of the beta-amyloid precursor proteins (beta APPs), whereas A4-immunoreactive plaques were uncommon in the hypothalamus of patients without AD. Unlike plaques in the cortex and hippocampus of AD patients, hypothalamic plaques did not contain epitopes corresponding to other regions of the beta APPs, nor did they contain tau-, neurofilament-, or microtubule-associated protein-reactive epitopes, and did not disrupt the neuropil or produce astrogliosis. These findings demonstrate that there are substantial molecular and cellular differences in the pathologic features of AD in the hypothalamus compared with those observed in hippocampal and cortical structures, which may provide insight into the pathogenetic mechanisms of AD.

Aged↗

Contrast and stereoscopic visual stimuli yield lateralized scalp potential fields associated with different neural generators.

The use of dynamic random-dot stereograms (RDS) allows to investigate evoked potential components generated exclusively by cortical structures. We analyzed the scalp distribution of stereoscopically evoked or contrast evoked potential field by recording electrical brain activity in 20 channels simultaneously from an electrode array covering the occipital scalp areas. Evoked brain activity was obtained from 13 healthy adults with dynamic RDS stimuli presented as a stereoscopic checkerboard pattern in the center, or in the right or left visual half-field. Such stereoscopically evoked scalp potential distributions were compared to those elicited by a conventional 2-dimensional checkerboard reversal stimulus of the same mean luminance and retinal extent. We found that the latencies of the major evoked components were similar for contrast and stereoscopic stimuli, while significant differences were observed when we compared the strength of the evoked potential fields or the topographical pattern elicited by lateralized stereoscopic and contrast stimuli. The functional relation of evoked electrical brain activity to the retinal stimulus location was significantly different for stereoscopic and contrast stimuli. We present evidence that stereoscopic perception relies on the activation of cortical structures in the human visual system that are different from those activated by comparable contrast stimuli, supporting the conclusions derived from our earlier electrophysiological experiments on stereoscopic vision. These data on the physiological correlates of processing of stereoscopic information in humans are in line with the results obtained with single neuron recordings from the cat and monkey visual cortex.

Adolescent↗

Expression of a monoclonal antibody (3G5) defined ganglioside antigen in the renal cortex.

The monoclonal antibody (mAb) 3G5 was found, by indirect immunofluorescence, to bind to renal cortical structures in frozen sections of human, rat and calf kidneys. Double indirect immunofluorescence studies on frozen sections of rat kidneys showed that 3G5 stained only the glomerulus and the distribution of the 3G5 antigen on the glomerulus was more extensive than the staining observed with antibodies to Factor VIII antigen. 3G5 stained the proximal convoluted tubules and collecting tubules in bovine renal sections but glomeruli did not stain with 3G5. The 3G5 mAb did not stain tissue cultured bovine glomerular endothelial cells or mesangial cells, but did stain bovine glomerular epithelial cell cultures. 3G5 did not stain MDCK cell cultures. The binding of mAb 3G5 to glomeruli was investigated by immunoelectron microscopy of rat renal tissue. In contrast to the podocyte specificity on bovine glomerular cells in vitro, it was found that the specificity of 3G5 expression on rat glomerular cells in vivo was broader. No binding of mAb 3G5 was found outside the glomerulus in the rat renal cortex. Podocytes, endothelial cells and capsular epithelial cells expressed the 3G5 antigen most strongly. A lesser amount of binding was found in the glomerular basement membrane. The mesangium showed a little binding of mAb 3G5 and no binding at all was found to other cortical structures. The 3G5 antigen in rat renal tissue was found to be a glycolipid that migrated between the ganglioside markers GM2 and GM1 by immunostaining of thin layer chromatograms.(ABSTRACT TRUNCATED AT 250 WORDS)

Animals↗

An investigation of collateral projections of the dorsal lateral geniculate nucleus and other subcortical structures to cortical areas V1 and V4 in the macaque monkey: a double label retrograde tracer study.

Previous anterograde studies in the macaque monkey have shown that, in addition to the projection to striate cortex (V1), the dorsal lateral geniculate nucleus (DLG) has a sparse, horizontally segregated projection to layers IV and V of prestriate cortex (V4). However, the distribution and degree of axon collateralization of DLG cells which give rise to these projections are unknown. This study was designed to answer these questions. The DLG (along with the pulvinar and other subcortical regions) was examined for the presence of single- or double-labeled cells after injections of two different (fluorescent or HRP) retrograde tracers into corresponding retinotopic points in visual cortical areas V1 and V4. In the DLG, it was found that cells projecting to V4, which reside in or near the tectorecipient interlaminar zones of the DLG, do not project to V1 and thus represent a separate population of cells. The organization of the macaque geniculo-prestriate projection thus seems quite different from that of carnivores. Both single- and double-labeled cells were found in other subcortical areas, e.g., single-labeled cells were found in the claustrum, hypothalamus and lateral pulvinar, and a double-labeled cell population was found in the inferior pulvinar.

Animals↗

Continuum limit of discrete neuronal structures: is cortical tissue an "excitable" medium?

As a simple model of cortical tissue, we study a locally connected network of spiking neurons in the continuum limit of space and time. This is to be contrasted with the usual numerical simulations that discretize both of them. Refractoriness, noise, axonal delays, and the time course of excitatory and inhibitory postsynaptic potentials have been taken into account explicitly. We pose, and answer, the question of whether the continuum limit presents a full description of scenarios found numerically (the answer is no, not quite). In other words, can the numerics be reduced to a continuum description of a well-known type? As a corollary, we derive some classical results such as those of Wilson and Cowan (1973), thus indicating under what conditions they are valid. Furthermore, we show that spatially discrete objects may be fragile due to noise arising from the stochasticity of the individual neurons, whereas they are not once the continuum limit has been taken. This, then, resolves the above question. Finally, we indicate how one can directly incorporate orientation preference of the neurons.

Action Potentials↗

Divergent anatomical pattern of D1 and D3 binding and dopamine- and cyclic AMP-regulated phosphoprotein of 32 kDa mRNA expression in the Roman rat strains: Implications for drug addiction.

Autoradiography analysis of D1, D2 and D3 dopamine receptors and in situ hybridization analysis of mRNA for dopamine and cAMP regulated phosphoprotein of 32 kDa (DARPP-32) were performed in brains of naïve Roman high avoidance (RHA) and Roman low avoidance (RLA) inbred rats. These strains, genetically selected for high (RHA) or extremely low (RLA) active avoidance acquisition in the two-way shuttle box, differ in indices of dopaminergic activity along with sensation/novelty and substance-seeking behavioral profiles. The present study shows no differences in D2 receptor binding between the two strains. In contrast, the D1 and D3 receptor binding in the nucleus accumbens was higher in RHA-I rats, whereas RLA-I rats show higher D3 binding in the Calleja islands. Together with previous evidence showing behavioral and presynaptic differences related to the dopamine system, the present results suggest a higher dopaminergic tone at the nucleus accumbens shell in RHA-I rats. Besides, the comparison of the expression pattern of DARPP-32 mRNA with that of dopamine receptor binding revealed a mismatch in some amygdala nuclei. In some cortical structures (prelimbic and cingulate cortices, the dentate gyrus) as well as in the central amygdala, RHA-I rats showed higher DARPP-32 mRNA expression than RLA-I rats. Hence, RHA-I and RLA-I rats may be a useful tool to identify dopamine-related mechanisms that predispose to drug and alcohol dependence.

Animals↗

Spatial pooling in the second-order spatial structure of cortical complex cells.

We investigate what computational mechanisms give rise to the nonlinearity of complex cell responses in the primary visual cortex. Complex cells are characterized by their nonlinear spatial properties such as spatial phase invariance and nonlinear spatial additivity. We carried out network simulations to estimate the second-order Wiener-like kernels for several different models. Models with nonlinear spatial pooling of simple-cell-like linear subunits reproduce the second-order kernels in good agreement with physiologically estimated kernels, while models without the pooling mechanism fail to reproduce the kernel. The results support the cascade mechanism consisting of simple cells' local feature extraction followed by spatial pooling.

Humans↗

Modelling studies on the computational function of fast temporal structure in cortical circuit activity.

The interplay between modelling and experimental studies can support the exploration of the function of neuronal circuits in the cortex. We exemplify such an approach with a study on the role of spike timing and gamma-oscillations in associative memory in strongly connected circuits of cortical neurones. It is demonstrated how associative memory studies on different levels of abstraction can specify the functionality to be expected in real cortical neuronal circuits. In our model overlapping random configurations of sparse cell populations correspond to memory items that are stored by simple Hebbian coincidence learning. This associative memory task will be implemented with biophysically well tested compartmental neurones developed by Pinsky and Rinzel . We ran simulation experiments to study memory recall in two network architectures: one interconnected pool of cells, and two reciprocally connected pools. When recalling a memory by stimulating a spatially overlapping set of cells, the completed pattern is coded by an event of synchronized single spikes occurring after 25-60 ms. These fast associations are performed even at a memory load corresponding to the memory capacity of optimally tuned formal associative networks (>0.1 bit/synapse). With tonic stimulation or feedback loops in the network the neurones fire periodically in the gamma-frequency range (20-80 Hz). With fast changing inputs memory recall can be switched between items within a single gamma cycle. Thus, oscillation is not a primary coding feature necessary for associative memory. However, it accompanies reverberatory feedback providing an improved iterative memory recall completed after a few gamma cycles (60-260 ms). In the bidirectional architecture reverberations do not express in a rigid phase locking between the pools. For small stimulation sets bursting occurred in these cells acting as a supportive mechanism for associative memory.

Animals↗

Calcium-binding proteins immunoreactivity in the human subcortical and cortical visual structures.

The distribution of neurons and fibers immunoreactive (ir) to the three calcium-binding proteins parvalbumin (PV), calbindin D-28k (CB), and calretinin (CR) was studied in the human lateral geniculate nucleus (LGN), lateral inferior pulvinar, and optic radiation, and related to that in the visual cortex. In the LGN, PV, CR, and CB immunoreactivity was present in all laminae, slightly stronger in the magnocellular than in the parvocellular laminae for CB and CR. PV-ir puncta, representing transversally cut axons, and CR-ir fibers were revealed within the laminae and interlaminar zones, and just beyond the outer border of lamina 6 in the geniculate capsule. In the optic radiation both PV- and CR-immunoreactive neurons, puncta, and fibers were present. CB immunoreactivity was revealed in neurons of all laminae of the lateral geniculate nucleus, including S lamina and interlaminar zones. There were hardly any CB-ir puncta or fibers in the laminae, interlaminar zones, geniculate capsule, or optic radiation. In the lateral inferior pulvinar, immunoreactive neurons for the three calcium-binding proteins were present in smaller number than in the LGN, as well as PV-ir puncta and CR-ir fibers within the nucleus and in the pulvinar capsule. In the white matter underlying area 17, fibers intermingled with a few scattered neurons were stained for both PV and CR, but very rarely for CB. These fibers stopped at the limit between areas 17 and 18. Area 17 showed a dense plexus of PV-ir puncta and neurons in the thalamo-receptive layer IV and CR-ir puncta and neurons both in the superficial layers I-II, IIIC, and in layer VA. Cajal-Retzius CR-ir neurons were present in layer I. CB-ir puncta were almost confined to layer I-III and CB-ir neurons to layer II. Finally the superior colliculus exhibited mostly populations of PV and CR pyramidal-like immunoreactive neurons, mainly in the intermediate tier. These data suggest that in the visual thalamus most calcium-binding protein immunoreactive neurons project to the visual cortex, while in the superior colliculus a smaller immunoreactive population represent projection neurons.

Adult↗

Physical limits to spatial resolution of optical recording: clarifying the spatial structure of cortical hypercolumns.

Neurons in macaque primary visual cortex are spatially arranged by their global topographic position and in at least three overlapping local modular systems: ocular dominance columns, orientation pinwheels, and cytochrome oxidase (CO) blobs. Individual neurons in the blobs are not tuned to orientation, and populations of neurons in the pinwheel center regions show weak orientation tuning, suggesting a close relation between pinwheel centers and CO blobs. However, this hypothesis has been challenged by a series of optical recording experiments. In this report, we show that the statistical error associated with photon scatter and absorption in brain tissue combined with the blurring introduced by the optics of the imaging system has typically been in the range of 250 microm. These physical limitations cause a systematic error in the location of pinwheel centers because of the vectorial nature of these patterns, such that the apparent location of a pinwheel center measured by optical recording is never (on average) in the correct in vivo location. The systematic positional offset is approximately 116 microm, which is large enough to account for the claimed misalignment of CO blobs and pinwheel centers. Thus, optical recording, as it has been used to date, has insufficient spatial resolution to accurately locate pinwheel centers. The earlier hypothesis that CO blobs and pinwheel centers are coterminous remains the only hypothesis currently supported by reliable observation.

Animals↗