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24 - Future research: an experimental perspective

from Part V - Conclusions and future perspectives

Published online by Cambridge University Press:  07 September 2009

Rob A. Voskuyl
Affiliation:
LACDR, Division of Pharmacology, Gorlaeus Laboratories, Leiden, The Netherlands; Epilepsy Institute of the Netherlands (SEIN), Achterweg, Heemstede, The Netherlands
Daniel M. Jonker
Affiliation:
LACDR, Division of Pharmacology, Gorlaeus Laboratories, Leiden, The Netherlands; Epilepsy Institute of the Netherlands (SEIN), Achterweg, Heemstede, The Netherlands
Fernando H. Lopes da Silva
Affiliation:
Epilepsy Institute of the Netherlands (SEIN), Achterweg, Heemstede, The Netherlands; Swammerdom Institute of Life Sciences (SILS), University of Amsterdam, The Netherlands
Jerzy Majkowski
Affiliation:
Foundation of Epileptology, Warsaw
Blaise F. D. Bourgeois
Affiliation:
Harvard University, Massachusetts
Philip N. Patsalos
Affiliation:
Institute of Neurology, London
Richard H. Mattson
Affiliation:
Yale University, Connecticut
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Summary

Introduction

The previous chapters have amply demonstrated both the need for effective combinations of antiepileptic drugs (AEDs) and the problems associated with the use of such combinations. The first problem is to choose which drugs should be combined and in which dose ratio. To be superior to monotherapy, the drug combination should either act synergistically with respect to the antiepileptic effect or antagonistically with respect to adverse effects, or both. The second major task is assessment of the efficacy of a combination and the experimental demonstration that the efficacy is significantly better than monotherapy.

It is the challenge for basic research:

  1. To provide the theoretical basis to design effective combinations for specific epilepsies.

  2. To provide new tools to assess whether the effect of a combination is synergistic, additive or antagonistic.

In this chapter, we will focus only on achieving maximal synergy for the antiepileptic effect. Alternatively, aiming at achieving maximal antagonism could be applied to minimize adverse effects.

Ultimately, the advantage of a combination of drugs over a single drug can be demonstrated only in in vivo experiments. In vitro experiments are highly useful for the analysis of interactions at specific targets, but can never take into account all aspects that contribute to the final efficacy in the intact organism. Therefore, studies on combination therapy should include both approaches. When designing in vivo experiments and choosing an experimental animal model to demonstrate synergy (or antagonism) of drug combinations, a number of points should be taken into consideration.

Type
Chapter
Information
Antiepileptic Drugs
Combination Therapy and Interactions
, pp. 441 - 457
Publisher: Cambridge University Press
Print publication year: 2005

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  • Future research: an experimental perspective
    • By Rob A. Voskuyl, LACDR, Division of Pharmacology, Gorlaeus Laboratories, Leiden, The Netherlands; Epilepsy Institute of the Netherlands (SEIN), Achterweg, Heemstede, The Netherlands, Daniel M. Jonker, LACDR, Division of Pharmacology, Gorlaeus Laboratories, Leiden, The Netherlands; Epilepsy Institute of the Netherlands (SEIN), Achterweg, Heemstede, The Netherlands, Fernando H. Lopes da Silva, Epilepsy Institute of the Netherlands (SEIN), Achterweg, Heemstede, The Netherlands; Swammerdom Institute of Life Sciences (SILS), University of Amsterdam, The Netherlands
  • Edited by Jerzy Majkowski, Blaise F. D. Bourgeois, Harvard University, Massachusetts, Philip N. Patsalos, Institute of Neurology, London, Richard H. Mattson, Yale University, Connecticut
  • Book: Antiepileptic Drugs
  • Online publication: 07 September 2009
  • Chapter DOI: https://doi.org/10.1017/CBO9780511545023.026
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  • Future research: an experimental perspective
    • By Rob A. Voskuyl, LACDR, Division of Pharmacology, Gorlaeus Laboratories, Leiden, The Netherlands; Epilepsy Institute of the Netherlands (SEIN), Achterweg, Heemstede, The Netherlands, Daniel M. Jonker, LACDR, Division of Pharmacology, Gorlaeus Laboratories, Leiden, The Netherlands; Epilepsy Institute of the Netherlands (SEIN), Achterweg, Heemstede, The Netherlands, Fernando H. Lopes da Silva, Epilepsy Institute of the Netherlands (SEIN), Achterweg, Heemstede, The Netherlands; Swammerdom Institute of Life Sciences (SILS), University of Amsterdam, The Netherlands
  • Edited by Jerzy Majkowski, Blaise F. D. Bourgeois, Harvard University, Massachusetts, Philip N. Patsalos, Institute of Neurology, London, Richard H. Mattson, Yale University, Connecticut
  • Book: Antiepileptic Drugs
  • Online publication: 07 September 2009
  • Chapter DOI: https://doi.org/10.1017/CBO9780511545023.026
Available formats
×

Save book to Google Drive

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Google Drive.

  • Future research: an experimental perspective
    • By Rob A. Voskuyl, LACDR, Division of Pharmacology, Gorlaeus Laboratories, Leiden, The Netherlands; Epilepsy Institute of the Netherlands (SEIN), Achterweg, Heemstede, The Netherlands, Daniel M. Jonker, LACDR, Division of Pharmacology, Gorlaeus Laboratories, Leiden, The Netherlands; Epilepsy Institute of the Netherlands (SEIN), Achterweg, Heemstede, The Netherlands, Fernando H. Lopes da Silva, Epilepsy Institute of the Netherlands (SEIN), Achterweg, Heemstede, The Netherlands; Swammerdom Institute of Life Sciences (SILS), University of Amsterdam, The Netherlands
  • Edited by Jerzy Majkowski, Blaise F. D. Bourgeois, Harvard University, Massachusetts, Philip N. Patsalos, Institute of Neurology, London, Richard H. Mattson, Yale University, Connecticut
  • Book: Antiepileptic Drugs
  • Online publication: 07 September 2009
  • Chapter DOI: https://doi.org/10.1017/CBO9780511545023.026
Available formats
×