Unconditioned stimulus pathways to the amygdala: effects of posterior thalamic and cortical lesions on fear conditioning

• Published in: Neuroscience 2004, Vol.125 (2), p.305-315
• Main Authors: Lanuza, E, Nader, K, Ledoux, J.E
• Format: Article
• Language: English
• Subjects: Amygdala - physiology; Analysis of Variance; Animals; Behavior, Animal; Biological and medical sciences; Brain Diseases - physiopathology; Conditioning, Classical - drug effects; Conditioning, Classical - physiology; Electrolysis - methods; Electroshock - adverse effects; emotional learning; Fear - physiology; footshock pathways; Fundamental and applied biological sciences. Psychology; Immobilization; Intralaminar Thalamic Nuclei - injuries; Intralaminar Thalamic Nuclei - physiology; Male; Neural Networks (Computer); neurotoxic lesions; Neurotoxins - toxicity; pain; Parietal Lobe - injuries; Parietal Lobe - physiology; posterior intralaminar thalamic complex; Rats; Rats, Sprague-Dawley; Time Factors; Vertebrates: nervous system and sense organs
• ISSN: 0306-4522; 1873-7544
• DOI: 10.1016/j.neuroscience.2003.12.034

Plasticity in the lateral nucleus of the amygdala is thought to be critical for the acquisition of Pavlovian fear conditioning. The pathways that transmit auditory conditioned stimulus information originate in auditory processing regions of the thalamus and cortex, but the pathways mediating transmission of unconditioned stimuli to the amygdala are poorly understood. Recent studies suggest that somatosensory (footshock) unconditioned stimulus information is also relayed in parallel to the lateral nucleus of the amygdala from the thalamus (the posterior intralaminar thalamic complex, PIT) and the cortex (parietal insular cortex). In the present study we reexamined this issue. Our results showed that bilateral electrolytic lesions of the PIT alone blocked fear conditioning, whereas bilateral excitotoxic PIT lesions had no effect. These electrolytic PIT lesions did not affect fear conditioning using a loud noise as unconditioned stimulus, defining the effects of PIT lesions as a disruption of somatosensory as opposed to auditory processing. Finally, we performed combined bilateral excitotoxic lesions of the PIT nuclei and electrolytic lesions of the parietal insular cortex. These, like excitotoxic lesions of PIT alone, had no effect on the acquisition of fear conditioning. Thus, somatosensory regions of the thalamus and cortex may well be important routes of unconditioned stimulus transmission to the amygdala in fear conditioning, but information about the unconditioned somatosensory stimulus is also transmitted from other sources that send fibers through, but do not form essential synapses in, the thalamus en route to the amygdala.