Influences of vestibular and visual motion information on the spatial firing patterns of hippocampal place cells.

نویسندگان

  • P E Sharp
  • H T Blair
  • D Etkin
  • D B Tzanetos
چکیده

Hippocampal place cells show location-specific firing as animals locomote in an environment. A possible explanation for these place fields is that each cell is simply driven by environmental sensory inputs available in its field. This cannot provide the full explanation, however, since cells can maintain stable place fields even in the absence of reliable environmental orienting cues. This suggests the cells are also influenced by movement-related information, since this is the only available, ongoing indicator of current location when external orienting cues are not present. Two candidates for the movement-related information are vestibular activation, and visual motion. To test for these influences, place cells were recorded as animals locomoted in a cylindrical apparatus that was made so that its wall (painted with vertical black and white stripes) and floor could be independently rotated, to provide visual motion and vestibular inputs, respectively. The results showed that both these inputs could influence place fields. Sometimes they caused a predictable locational shift, so that the field rotated its location on the apparatus floor in a way that was compatible with the movement indicated by the vestibular and/or visual motion input. This updating was most reliably obtained when the two inputs were presented in combination. In other cases, the apparatus rotations caused unpredictable changes in firing characteristics, so that cells either stopped firing, or developed place fields that were altered in overall size, shape, and eccentricity. Interestingly, the probability of these changes increased with experience with the rotational manipulations, suggesting a learned component.

برای دانلود رایگان متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Hippocampal spatial representations require vestibular input.

The hippocampal formation is essential for forming declarative representations of the relationships among multiple stimuli. The rodent hippocampal formation, including the entorhinal cortex and subicular complex, is critical for spatial memory. Two classes of hippocampal neurons fire in relation to spatial features. Place cells collectively map spatial locations, with each cell firing only when...

متن کامل

Modelling Path Integrator Recalibration Using Hippocampal Place Cells

The firing activities of place cells in the rat hippocampus exhibit strong correlations to the animal’s location. External (e.g. visual) as well as internal (proprioceptive and vestibular) sensory information take part in controlling hippocampal place fields. Previously it has been observed that when rats shuttle between a movable origin and a fixed target the hippocampus encodes position in tw...

متن کامل

Spatial information outflow from the hippocampal circuit: distributed spatial coding and phase precession in the subiculum.

Hippocampal place cells convey spatial information through a combination of spatially selective firing and theta phase precession. The way in which this information influences regions like the subiculum that receive input from the hippocampus remains unclear. The subiculum receives direct inputs from area CA1 of the hippocampus and sends divergent output projections to many other parts of the b...

متن کامل

مدل شبکه ی عصبی از نگاشت سلول‌های شبکه به سلول‌های مکانی

Abstract: Medial entorhinal cortex is known to be the hub of a brain system for navigation and spatial representation. These cells increase firing frequency at multiple regions in the environment, arranged in regular triangular grids. Each cell has some properties including spacing, orientation, and phase shift of the nodes of its grid. Entorhinal cortex is commonly perceived to be the major in...

متن کامل

How vision and movement combine in the hippocampal place code.

How do external environmental and internal movement-related information combine to tell us where we are? We examined the neural representation of environmental location provided by hippocampal place cells while mice navigated a virtual reality environment in which both types of information could be manipulated. Extracellular recordings were made from region CA1 of head-fixed mice navigating a v...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

عنوان ژورنال:
  • The Journal of neuroscience : the official journal of the Society for Neuroscience

دوره 15 1 Pt 1  شماره 

صفحات  -

تاریخ انتشار 1995