The ventral hippocampus, but not the dorsal hippocampus is critical for learned approach-avoidance decision making

Hippocampus. 2016 Apr;26(4):530-42. doi: 10.1002/hipo.22542. Epub 2015 Oct 23.

Abstract

The resolution of an approach-avoidance conflict induced by ambivalent information involves the appraisal of the incentive value of the outcomes and associated stimuli to orchestrate an appropriate behavioral response. Much research has been directed at delineating the neural circuitry underlying approach motivation and avoidance motivation separately. Very little research, however, has examined the neural substrates engaged at the point of decision making when opposing incentive motivations are experienced simultaneously. We hereby examine the role of the dorsal and ventral hippocampus (HPC) in a novel approach-avoidance decision making paradigm, revisiting a once popular theory of HPC function, which posited the HPC to be the driving force of a behavioral inhibition system that is activated in situations of imminent threat. Rats received pre-training excitotoxic lesions of the dorsal or ventral HPC, and were trained to associate different non-spatial cues with appetitive, aversive and neutral outcomes in three separate arms of the radial maze. On the final day of testing, a state of approach-avoidance conflict was induced by simultaneously presenting two cues of opposite valences, and comparing the time the rats spent interacting with the superimposed 'conflict' cue, and the neutral cue. The ventral HPC-lesioned group showed significant preference for the conflict cue over the neutral cue, compared to the dorsal HPC-lesioned, and control groups. Thus, we provide evidence that the ventral, but not dorsal HPC, is a crucial component of the neural circuitry concerned with exerting inhibitory control over approach tendencies under circumstances in which motivational conflict is experienced.

Keywords: conditioned cue avoidance; conditioned cue preference; decision making; hippocampus; incentive motivation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Appetitive Behavior / physiology
  • Association Learning / physiology
  • Avoidance Learning / physiology*
  • Conditioning, Psychological / physiology
  • Conflict, Psychological
  • Cues
  • Decision Making / physiology*
  • Hippocampus / physiology*
  • Hippocampus / physiopathology
  • Inhibition, Psychological*
  • Male
  • Maze Learning / physiology
  • N-Methylaspartate
  • Neural Pathways / physiology
  • Neural Pathways / physiopathology
  • Neuropsychological Tests
  • Rats, Long-Evans
  • Reward

Substances

  • N-Methylaspartate