Medial septal lesions mimic effects of both selective dorsal and ventral hippocampal lesions

D M Bannerman1, P Matthews, R M J Deacon

  • 1Department of Experimental Psychology, University of Oxford, South Parks Road, Oxford OX1 3UD, United Kingdom. david.bannerman@psy.ox.ac.uk.

Behavioral Neuroscience
|October 28, 2004
PubMed

Insights

Electrolytic medial septal lesions impact spatial memory and anxiety-related behaviors. These findings suggest combined dorsal and ventral hippocampal deafferentation underlies medial septal lesion effects.

Area of Science:

  • Neuroscience
  • Behavioral Neuroscience
  • Neuroanatomy

Background:

  • The medial septal area (MS) plays a crucial role in hippocampal function.
  • Previous studies on MS lesions have yielded varied results, potentially due to different lesioning techniques.
  • Understanding the specific contributions of MS projections to dorsal and ventral hippocampus is essential.

Purpose of the Study:

  • To investigate the behavioral consequences of electrolytic medial septal (MS) lesions.
  • To determine if MS lesions affect dorsal and ventral hippocampus similarly or distinctly.
  • To clarify the role of MS deafferentation in observed behavioral changes.

Main Methods:

  • Electrolytic lesions were made in the medial septal area (MS) of rodents.
  • Acetylcholinesterase staining was used to assess the extent of hippocampal deafferentation.
  • A battery of behavioral tests was employed, including the T-maze, successive alleys, social interaction, and a fear conditioning paradigm (post-shock freezing).

Main Results:

  • MS lesions impaired spatial working memory, similar to dorsal hippocampal lesions.
  • MS lesions reduced anxiety-like behaviors (successive alleys, social interaction, hyponeophagia) and fear responses (post-shock freezing), mirroring ventral hippocampal lesion effects.
  • Histological analysis confirmed depletion of acetylcholinesterase in both dorsal and ventral hippocampus following MS lesions.

Conclusions:

  • Electrolytic MS lesions induce a unique behavioral profile by simultaneously deafferenting dorsal and ventral hippocampal regions.
  • The observed behavioral effects are likely due to the combined impact on both hippocampal subfields.
  • These findings challenge the notion that dorsal hippocampal lesion effects are solely due to demyelination of fibers of passage through the septal pole.