Functional Hippocampal Assessment with Depth Electrodes

  • David W. Loring
  • Kimford J. Meador
  • Gregory P. Lee
Part of the Critical Issues in Neuropsychology book series (CINP)

Abstract

Mesial temporal lobe (MTL) structures, from which seizures commonly originate, are crucial for acquisition of new material into memory. The reason for this relationship is unknown but may be related to the tissue excitability necessary for memory encoding. For information to be encoded into memory and the recent memory systems (i.e., episodic memory) to be constantly updated, a system with sufficient sensitivity and constant, active processing of the environment is necessary to allow continual information updating. However, a balance between the sensitivity and stability of functionally connected cell assemblies is also required (Freeman, 1975). As neurons become excited by background input, the neural gain increases, driving the neurons to an operating point closer to their firing threshold; subsequent input is more likely to trigger a response. However, as sensitivity increases, there is a concomitant increase in instability. Thus, the requirement for a memory system to possess the ability to rapidly lay down memory traces makes it less stable and perhaps predisposed to develop seizures.

Keywords

Verbal Memory Seizure Onset Temporal Lobectomy Recent Memory Depth Electrode 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

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References

  1. Brazier, M. A. B. (1966). Stimulation of the hippocampus in man using implanted electrodes. In M. A. B. Brazier (Ed.), RNA and brain function, memory and learning. Berkeley: University of California Press.Google Scholar
  2. Chapman, L. G., Walter, R. D., Markham, C. H., Rand, R. W., & Crandall, R H. (1967). Memory changes induced by stimulation of the hippocampus or amygdala in epilepsy patients with implanted electrodes. Transactions of the American Neurological Association, 92, 50–56.PubMedGoogle Scholar
  3. Davis, A., & Wada, J. (1977). Hemispheric asymmetries in human infants: Spectral analysis of flash and click evoked potentials. Brain and Language, 4, 23–31.PubMedCrossRefGoogle Scholar
  4. Engel, J., Jr., Rausch, R., Lieb, J. R, Kuhl, D. E., & Crandall, R H. (1981). Correlation of criteria used for localizing epileptic foci in patients considered for surgical therapy of epilepsy. Archives of Neurology, 9, 215–224.Google Scholar
  5. Flanigin, H. E, & Smith, J. R. (1987). Depth electrode implantation at the Medical College of Georgia. In J. Engel (Ed.), Surgical treatment of the epilepsies (pp. 609–612). New York: Raven Press.Google Scholar
  6. Flanigin, H. E, King, D. W, & Gallagher, B. B. (1984). Surgical treatment of epilepsy. In T. Pedley & B. Meldrum (Eds.), Recent advances in epilepsy, Vol. 2 (pp. 297–339). New York: Churchill-Livingstone.Google Scholar
  7. Freeman, W. Y. (1975). Mass action in the nervous system. New York: Academic Press.Google Scholar
  8. Halgren, E., & Wilson, C. L. (1985). Recall deficits produced by afterdischarges in the human hippocampal formation and amygdala. Electroencephalography and Clinical Neurophysiology, 61, 375–380.PubMedCrossRefGoogle Scholar
  9. Halgren, E., Walter, R. D, Cherlow, D. G., & Crandall, R H. (1978). Mental phenomena evoked by electrical stimulation of the human hippocampal formation and amygdala. Brain, 101, 83–117.PubMedCrossRefGoogle Scholar
  10. Halgren, E., Squires, N. K., Wilson, C. L., Rorbaugh, I. W, Babb, T. L., & Crandall, P. H. (1981). Endogenous potentials generated in the human hippocampal formation by infrequent events. Science, 210, 803–805.CrossRefGoogle Scholar
  11. Halgren, E., Squires, N. K., Wilson, C. L., & Crandall, R H. (1982). Brain generators of evoked potentials: The late (endogenous) components. Bulletin of Los Angeles Neurological Society, 47, 108–123.Google Scholar
  12. Halgren, E., Wilson, C. L., & Stapleton, J. M. (1985). Human medial temporal-lobe stimulation disrupts both formation and retrieval of recent memories. Brain and Cognition, 4, 287–295.PubMedCrossRefGoogle Scholar
  13. Jones-Gotman, M. (1987). Commentary: Psychological evaluation—testing hippocampal function. In J. Engel (Ed.), Surgical treatment of the epilepsies (pp. 203–211). New York: Raven Press.Google Scholar
  14. Lee, G. P., Loring, D. W, Meador, K. J., Flanigan, H. F., & Brooks, B. S. (1988). Severe behavioral complications following intracarotid sodium amobarbital injection: Implications for hemispheric asymmetry of emotion. Neurology, 38, 1233–1236.PubMedCrossRefGoogle Scholar
  15. Loring, D. W, Meador, K. J., Sherman, C. J., King, D.W., & Gallagher, B. B. (1987). Abulia and impaired responsiveness during the intracarotid sodium Amytal procedure. Journal of Clinical and Experimental Psychology, 9, 31.Google Scholar
  16. Loring, D. W, Lee, G. R, Flanigin, H. E, Meador, K. J., Smith, J. R., Gallagher, B. B., & King, D. W. (1988a). Verbal memory deficits following unilateral electrical stimulation of the human hippocampus. Journal of Epilepsy, 1, 79–85.CrossRefGoogle Scholar
  17. Loring, D. W, Meador, K. J., King, D. W, Gallagher, B. B., Smith, J. R., and Flanigin, H. E (1988b). Relationship of limbic evoked potentials to recent memory performance. Neurology, 38, 45–48.PubMedCrossRefGoogle Scholar
  18. Meador, K. J., Loring, D. W., King, D. W, Gallagher, B. B., Gould, J., & Flanigin, H. E (1987a). Limbic evoked potentials predict site of epileptic focus. Neurology, 37, 494–497.PubMedCrossRefGoogle Scholar
  19. Meador, K. J., Loring, D. W, King, D. W., Gallagher, B. B., Smith, J. R., & Flanigin, H. E (1987b). Spectral power of human limbic evoked responses: Relationship to seizure onset. Annals of Neurology, 22, 131–132.Google Scholar
  20. Milner, B. (1972). Disorders of learning and memory after temporal lobe lesions in man. Clinical Neurosurgery, 19, 421–946.PubMedGoogle Scholar
  21. Papanicolaou, A. C, Loring, D. W., Raz, N., & Eisenberg, H. M. (1985). Relationship between stimulus intensity and the P300. Psychophysiology, 22, 326–329.PubMedCrossRefGoogle Scholar
  22. Penfield, W., & Mathieson, G. (1974). Memory: Autopsy findings and comment on the role of hippocampus in experiential recall. Archives of Neurology, 31, 145–154.PubMedCrossRefGoogle Scholar
  23. Pritchard, W. S. (1981). Psychophysiology of P300. Psychological Bulletin, 89, 506–540.PubMedCrossRefGoogle Scholar
  24. Sem-Jacobsen, C. W. (1968). Depth electrode stimulation of the human brain and behavior. Springfield, Ill: Charles C. Thomas.Google Scholar
  25. Squires, N. K., Halgren, E., Wilson, C, & Crandall, R (1983). Human-endogenous limbic potentials: Cross-modality and depth/surface comparisons in epileptic subjects. In A. Gaillard & W. Ritter (Eds.), Tutorials in event related potential research: Endogenous components (pp. 217–232). New York: North-Holland.CrossRefGoogle Scholar
  26. Wood, C., McCarthy, G., Squires, N., Vaughn, H., Woods, D., & McCallum, W (1984). Anatomical and physiological substrates of event-related potentials. Annals of the New York Academy of Sciences, 425, 681–721.PubMedCrossRefGoogle Scholar

Copyright information

© Springer Science+Business Media New York 1992

Authors and Affiliations

  • David W. Loring
    • 1
  • Kimford J. Meador
    • 2
  • Gregory P. Lee
    • 3
  1. 1.Section of Behavioral Neurology, Department of NeurologyMedical College of GeorgiaAugustaUSA
  2. 2.Section of Behavioral Neurology, Department of NeurologyMedical College of GeorgiaAugustaUSA
  3. 3.Department of Psychiatry, and Section of Neurosurgery, Department of SurgeryMedical College of GeorgiaAugustaUSA

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