Selective interhemispheric circuits account for a cardinal bias in spontaneous activity within early visual areas.

Ongoing brain activity exhibits patterns resembling neural ensembles co-activated by stimulation or task performance. Such patterns have been attributed to the brain's functional architecture, e.g. selective long-range connections. Here, we directly investigate the contribution of selective connections between hemispheres to spontaneous and evoked maps in cat area 18 close to the 17/18 border. We recorded voltage-sensitive dye imaging maps and spiking activity while manipulating interhemispheric input by reversibly deactivating corresponding contralateral areas. During deactivation, spontaneous maps continued to be generated with similar frequency and quality as in the intact network but a baseline cardinal bias disappeared. Consistently, neurons preferring either horizontal (HN) or vertical (VN), as opposed to oblique contours, decreased their resting state activity. HN decreased their rates also when stimulated visually. We conclude that structured spontaneous maps are primarily generated by thalamo- and/or intracortical connectivity. However, selective long-range connections through the corpus callosum - in perpetuation of the long-range intracortical network - contribute to a cardinal bias, possibly, because they are stronger or more frequent between neurons preferring horizontal and/or cardinal contours. As those contours are easier perceived and appear more frequently in natural environment, long-range connections might provide visual cortex with a grid for probabilistic grouping operations in a larger visual scene.

High-order motor cortex in rats receives somatosensory inputs from the primary motor cortex via cortico-cortical pathways.

The motor cortex of rats contains two forelimb motor areas; the caudal forelimb area (CFA) and the rostral forelimb area (RFA). Although the RFA is thought to correspond to the premotor and/or supplementary motor cortices of primates, which are higher-order motor areas that receive somatosensory inputs, it is unknown whether the RFA of rats receives somatosensory inputs in the same manner. To investigate this issue, voltage-sensitive dye (VSD) imaging was used to assess the motor cortex in rats following a brief electrical stimulation of the forelimb. This procedure was followed by intracortical microstimulation (ICMS) mapping to identify the motor representations in the imaged cortex. The combined use of VSD imaging and ICMS revealed that both the CFA and RFA received excitatory synaptic inputs after forelimb stimulation. Further evaluation of the sensory input pathway to the RFA revealed that the forelimb-evoked RFA response was abolished either by the pharmacological inactivation of the CFA or a cortical transection between the CFA and RFA. These results suggest that forelimb-related sensory inputs would be transmitted to the RFA from the CFA via the cortico-cortical pathway. Thus, the present findings imply that sensory information processed in the RFA may be used for the generation of coordinated forelimb movements, which would be similar to the function of the higher-order motor cortex in primates.

Neural correlates of perceptual similarity masking in primate V1.

Visual detection is a fundamental natural task. Detection becomes more challenging as the similarity between the target and the background in which it is embedded increases, a phenomenon termed 'similarity masking'. To test the hypothesis that V1 contributes to similarity masking, we used voltage sensitive dye imaging (VSDI) to measure V1 population responses while macaque monkeys performed a detection task under varying levels of target-background similarity. Paradoxically, we find that during an initial transient phase, V1 responses to the target are enhanced, rather than suppressed, by target-background similarity. This effect reverses in the second phase of the response, so that in this phase V1 signals are positively correlated with the behavioral effect of similarity. Finally, we show that a simple model with delayed divisive normalization can qualitatively account for our findings. Overall, our results support the hypothesis that a nonlinear gain control mechanism in V1 contributes to perceptual similarity masking.

Optogenetic Manipulation of Postsynaptic cAMP Using a Novel Transgenic Mouse Line Enables Synaptic Plasticity and Enhances Depolarization Following Tetanic Stimulation in the Hippocampal Dentate Gyrus.

cAMP is a positive regulator tightly involved in certain types of synaptic plasticity and related memory functions. However, its spatiotemporal roles at the synaptic and neural circuit levels remain elusive. Using a combination of a cAMP optogenetics approach and voltage-sensitive dye (VSD) imaging with electrophysiological recording, we define a novel capacity of postsynaptic cAMP in enabling dentate gyrus long-term potentiation (LTP) and depolarization in acutely prepared murine hippocampal slices. To manipulate cAMP levels at medial perforant path to granule neuron (MPP-DG) synapses by light, we generated transgenic (Tg) mice expressing photoactivatable adenylyl cyclase (PAC) in DG granule neurons. Using these Tg(CMV-Camk2a-RFP/bPAC)3Koka mice, we recorded field excitatory postsynaptic potentials (fEPSPs) from MPP-DG synapses and found that photoactivation of PAC during tetanic stimulation enabled synaptic potentiation that persisted for at least 30 min. This form of LTP was induced without the need for GABA receptor blockade that is typically required for inducing DG plasticity. The paired-pulse ratio (PPR) remained unchanged, indicating the cAMP-dependent LTP was likely postsynaptic. By employing fast fluorescent voltage-sensitive dye (VSD: di-4-ANEPPS) and fluorescence imaging, we found that photoactivation of the PAC actuator enhanced the intensity and extent of dentate gyrus depolarization triggered following tetanic stimulation. These results demonstrate that the elevation of cAMP in granule neurons is capable of rapidly enhancing synaptic strength and neuronal depolarization. The powerful actions of cAMP are consistent with this second messenger having a critical role in the regulation of synaptic function.

Evaluation of acute anodal direct current stimulation-induced effects on somatosensory-evoked responses in the rat.

Transcranial direct current stimulation (tDCS) is a non-invasive tool used to treat brain disorders. The DC electric field is thought to modulate neuronal excitability and it has been reported to exert effects within the localized treatment area under the electrode, as well as in diffuse brain regions extending beyond the electrode. However, the manner in which tDCS influences neural transmission in the cortex and modulates neural activity in distant interconnected cortical regions remains unclear. Thus, the present study investigated the effects of anodal DCS (aDCS) on the forelimb-evoked sensory response that initially appears in the primary sensorimotor cortex (S1-M1) and then propagates to the secondary motor cortex (M2). When aDCS application was confined to the S1-M1 region, local field potential (LFP) recordings and voltage-sensitive dye (VSD) imaging revealed that the forelimb-evoked response in the S1-M1 was clearly enhanced. In contrast, the neural response in the M2 remained almost unchanged. On the other hand, aDCS application confined to the M2 increased the forelimb-evoked response in the M2 but not the S1-M1. Taken together, these results suggest that, when applied to the cortex, the aDCS may have intrinsic local effects, influencing afferent neural activity immediately underneath the stimulation site. Thus, the present results indicate that aDCS has less influence on neural activity in distant cortical areas interconnected to the stimulation site than at the stimulation site itself. Therefore, the findings do not support the idea of DCS remote activation via cortico-cortical connections, at least between the S1-M1 and M2 regions in rats.