PubMed Health⌕ Search

PubMed · 12744980

Neural population codes.

Abstract

In many regions of the brain, information is represented by patterns of activity occurring over populations of neurons. Understanding the encoding of information in neural population activity is important both for grasping the fundamental computations underlying brain function, and for interpreting signals that may be useful for the control of prosthetic devices. We concentrate on the representation of information in neurons with Poisson spike statistics, in which information is contained in the average spike firing rate. We analyze the properties of population codes in terms of the tuning functions that describe individual neuron behavior. The discussion centers on three computational questions: first, what information is encoded in a population; second, how does the brain compute using populations; and third, when is a population optimal? To answer these questions, we discuss several methods for decoding population activity in an experimental setting. We also discuss how computation can be performed within the brain in networks of interconnected populations. Finally, we examine questions of optimal design of population codes that may help to explain their particular form and the set of variables that are best represented. We show that for population codes based on neurons that have a Poisson distribution of spike probabilities, the behavior and computational properties of the code can be understood in terms of the tuning properties of individual cells.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Terence D Sanger. 2003. Neural population codes.. https://doi.org/10.1016/s0959-4388(03)00034-5

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related citations

Serial hearing organs in the atympanate grasshopper Bullacris membracioides (Orthoptera, Pneumoridae).

In different insect taxa, ears can be found on virtually any part of the body. Comparative anatomy and similarities in the embryological development of ears in divergent taxa suggest that they have evolved multiple times from ubiquitous stretch or vibration receptors, but the homology of these structures has not yet been rigorously tested. Here we provide detailed analysis of a novel set of hearing organs in a relatively "primitive" atympanate bladder grasshopper (Bullacris membracioides) that is capable of signaling acoustically over 2 km. We use morphological, physiological, and behavioral experiments to demonstrate that this species has six pairs of serially repeated abdominal ears derived from proprioceptive pleural chordotonal organs (plCOs). We demonstrate continuity in auditory function from the five posterior pairs, which are simple forms comprising 11 sensilla and resembling plCOs in other grasshoppers, to the more complex anterior pair, which contains 2000 sensilla and is homologous to the single pair of tympanate ears found in "modern" grasshoppers. All 12 ears are morphologically differentiated, responsive to airborne sound at frequencies and intensities that are biologically significant (tuned to 1.5 and 4 kHz; 60-98 dB SPL), and capable of mediating behavioral responses of prospective mates. These data provide evidence for the transition in function and selective advantage that must occur during evolutionary development of relatively complex organs from simpler precursors. Our results suggest that ancestral insects with simple atympanate pleural receptors may have had hearing ranges that equal or exceed those of contemporary insects with complex tympanal ears. Moreover, auditory capability may be more prevalent among modern insect taxa than the presence of overt tympana indicates.

Action Potentials↗

Thermal properties of acid-induced depolarization in cultured rat small primary afferent neurons.

Tissue ischemia and inflammation result in localized acidosis, and acidic pH can trigger a sensation of pain. Pain is known to be often modified by the tissue temperature. The purpose of this study is to clarify the thermal behavior of nociceptors in response to acidification using intracellular recordings from cultured rat primary afferent neurons. Extracellular acidification induced depolarization of two types, transient and sustained responses. The former (to pH 6.3 and 5.2) was augmented at lower temperature (26, 16 degrees C) and amiloride blocked the response to pH 6.3 at 26 degrees C. On the other hand, the sustained depolarization, which often followed the transient one, in response to pH 6.3 was greater at 36 degrees C and significantly blocked by capsazepine at 36 degrees C, but not at 26 degrees C. The sustained response to pH 5.2 was blocked even at 26 degrees C. These results suggest that the low pH evoked depolarization is temperature-dependent, and the contribution of transient receptor potential V1 (vanilloid receptor 1) to proton-induced response is greater in the physiological body temperature range, while that of the acid-sensing-ion-channel family is greater at room temperature or lower.

Action Potentials↗

Comparison of reorganization of the somatosensory system in rats that sustained forelimb removal as neonates and as adults.

Studies of sensory pathways in several species indicate that the extent and form of reorganization resulting from deafferentation early in life vs. adulthood are not the same. The reasons for such differences are not well understood. To gain further insight into age-dependent mechanisms of reorganization, this study compared the consequences of neonatal vs. adult forelimb amputation in rats at multiple levels of the sensory pathway, including primary somatosensory cortex, brainstem, and dorsal root ganglia. At the cortical level, the average area of the functional forelimb-stump representation from rats amputated as adults was significantly smaller (P < 0.05) than that of neonatally amputated rats (4.3 +/- 1.3 mm(2) vs. 6.6 +/- 1.5 mm(2), respectively). At the brainstem level, neonatally amputated rat cuneate neurons possessed the following responsivities: 20% stump responsive, 40% responsive to both stump and hindlimb, 30% responsive to another body region, and 10% unresponsive. In contrast, cuneate neurons of adult amputated rats were 70% stump responsive, 2% responsive to both stump and hindlimb, and 30% unresponsive. A significantly (P < 0.001) greater percentage of the C(6)-C(8) dorsal root ganglia neurons of adult amputated rats were unresponsive to peripheral stimulation vs. neurons from neonatally amputated rats (48% vs. 16%, respectively). These results indicate that the reorganization that occurs in response to forelimb amputation at birth vs. adulthood is distinctly different at each of these levels of the dorsal column-medial lemniscal pathway. Possible mechanisms to account for these differences are considered.

Action Potentials↗