Differential effects of anterior and posterior insular cortex lesions on the acquisition of conditioned taste aversion and spatial learning

Neurobiology of Learning and Memory

Volumn 66, Issue 1, 1996, Pages 44-50

  Nerad, Ludìk ^b   Ramírez Amaya, Victor ^a   Ormsby, Christopher E ^a   Bermúdez Rattoni, Federico ^a  

^a UNIVERSIDAD NACIONAL AUTÓNOMA DE MÉXICO   (Mexico)

^b INSTITUTE OF PHYSIOLOGY   (Czech Republic)

Author keywords

[No Author keywords available]

Indexed keywords

N METHYL DEXTRO ASPARTIC ACID;

ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; BRAIN INJURY; CONDITIONING; CONTROLLED STUDY; INSULA; LEARNING; MALE; MAZE TEST; NONHUMAN; RAT; SPATIAL DISCRIMINATION; TASTE AVERSION; TOPOGRAPHY;

EID: 0343026323     PISSN: 10747427     EISSN: None     Source Type: Journal    
DOI: 10.1006/nlme.1996.0042     Document Type: Article

References (27)

1. Aggleton, J. P., Petrides, M., & Iversen, S. D. (1981). Differential effects of amygdaloid lesion on conditioned taste aversion learning by rats. Physiology and Behavior, 27, 397-403.
2. Benjamin, R. M., & Akert, K. (1959). Cortical and thalamic areas involved in taste discrimination in the albino rat. Journal of Comparative Neurology, 111, 231-260.
3. Bermudez-Rattoni, F., Introini-Collison, I. B., & McGaugh, J. L. (1991). Reversible inactivation of the insular cortex by tetrodotoxin produces retrograde and anterograde amnesia for inhibitory avoidance and spatial learning. Proceedings of the National Academy of Sciences USA, 88, 5379-5382.
4. Bermúdez-Rattoni, F., & McGaugh, J. L. (1991). Insular cortex and amygdala lesions differentially affect acquisition on inhibitory avoidance and conditioned taste aversion. Brain Research, 549, 165-170.
5. Bermúdez-Rattoni, F., Sánchez, M. A., & Prado-Alcalá, R. A. (1989). Learning of external and visceral cue consequences may be subserved by different neuroanatomical substrates. In T. Archer & N. Lars-Goran (Eds.), Aversion avoidance and anxiety (pp. 121-138). Hillside, NJ: Erlbaum.
6. Braun, J. J., Kiefer, S. W., & Ouellet, J. V. (1981). Psychic ageusia in rats lacking gustatory neocortex. Experimental Neurology, 72, 711-716.
7. Braun, J. J., Lasiter, P. S., & Kiefer, S. W. (1982). The gustatory neocortex of the rat. Physiological Psychology, 10, 13-45.
8. Braun, J. J., Slick, T. B., & Lorden, J. F. (1972). Involvement of gustatory neocortex in the learning of taste aversions. Physiology and Behavior, 9, 637-641.
9. Garcia, J., Lasiter, P. S., Bermúdez-Rattoni, F., & Deems, D. (1985). A general theory of aversion learning. In N. S. Braveman & P. Bronstein (Eds.) Experimental assessments and clinical applications of conditioned food aversions. Annals of the N.Y. Academy of Science, 443, 8-20.
10. Hankins, W. G., García, J., & Rusiniak, K. W. (1974). Cortical lesions: Flavor-illness and noise-shock conditioning. Behavioral Biology, 10, 173-181.
11. Ito, S. (1992). Multiple projection of vagal non-myelinated afferents to the anterior insular cortex in rats. Neuroscience Letters, 148, 151-154.
12. Kiefer, S. W. (1985). Neural mediation of conditioned food aversions. In N. S. Braveman & P. Bronstein (Eds.), Experimental Assessments and Clinical Applications of Conditioned Food Aversions. Annals of the N.Y. Academy of Science, 443, 100-109.
13. Kosar, E., Grill, H. J., & Norgren, R. (1986). Gustatory cortex in the rat. I. Physiological properties and cytoarchitecture. Brain Research, 379, 329-341.
14. Krusher, L. A., & van der Kooy, D. (1988). Visceral cortex: Integration of the mucosal with limbic information in the rat agranular insular cortex. Journal of Comparative Neurology, 270, 34-541.
15. Lasiter, P. S. (1982). Cortical substrates of taste aversion learning: direct amygdalocortical projections to the gustatory neocortex do not mediate conditioned taste aversion learning. Physiological Psychology, 10, 377-383.
16. Lasiter, P. S., & Glanzman, D. L. (1985). Cortical substrates of taste aversion learning: involvement of the dorsolateral amygdaloid nuclei and temporal neocortex in taste aversion learning, Behavioral Neuroscience, 99, 257-276.
17. Nachman, M., & Ashe, J. H. (1974). Effects of basolateral amygdala lesions on neophobia, learned taste aversions and sodium appetite in rats. Journal of Comparative and Physiological Psychology, 87, 622-643.
18. Paxinos, G., & Watson, C. (1986). The rat brain in stereotaxic coordinates. Orlando, FL: Academic Press.
19. Rosen, J. B., Hitchcock, J. M., Miserendino, M. J., Falls, W. A., Campeau, S., & Davis, M. (1992). Lesions of the perirhinal cortex but not of the frontal, medial prefrontal, visual, or insular cortex block fear-potentiated startle using a visual conditioned stimulus. Journal of Neuroscience, 12, 4624-4633.
20. Saper, C. B. (1982). Convergence of autonomic and limbic connections in the insular cortex of the rat. Journal of Comparative Neurology, 210, 163-173.
21. Takagishi, M., & Chiba, T. (1991). Efferent projections of the infralimbic (area 25) region of the medial prefrontal cortex in the rat: An anterograde tracer PHA-L study. Brain Research. 566, 26-39.
22. van der Kooy, D. L., Koda, L. Y., McGintly, J. F., Gerfen, C. R., & Bloom, F. E., (1984). The organization of projections from the cortex to amygdala, and hypothalamus to the nucleus of the solitary tract in the rat. Journal of Comparative Neurology, 224, 1-24.
23. Wiig, K. A., & Bilkey, D. K. (1994). The effects of perirhinal cortical lesions on spatial reference memory in the rat. Behavioral Brain Research, 63, 101-109.
24. Yamamoto, T., Matsuo, R., & Kawamura, Y. (1980). Localization of cortical gustatory area in rats and its role in taste discrimination. Journal of Neurophysiology, 44, 440-455.
25. Yasui, Y., Breder, C. D., Saper, C. B., & Cechetto, D. F. (1991). Autonomic responses and efferent pathways from the insular cortex in the rat. Journal of Comparative Neurology, 303, 355-374.
26. Zilles, K. (1985). The cortex of the rat: A stereotaxic atlas. Berlin: Springer-Verlag.
27. Zola-Morgan, S., Squire, L. R., Clower, R. P., & Rempel, N. L. (1993). Damage to the perirhinal cortex exacerbates memory impairment following lesions to the hippocampal formation. Journal of Neuroscience, 13, 251-265.