Mechanism Underlying the Therapeutic Effects of Electroconvulsive Therapy (ECT) on Depression

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Author(s)

Abstract

Electroconvulsive therapy (ECT) is used to treat drug-resistant depressive disorders. The results of studies on the mechanism underlying the effectiveness of ECT on depression are still controversial. ECT stimulus is usually larger than the threshold of induction of seizures and activation of whole-brain is believed to be necessary to produce therapeutic effects. A single ECT session induces alterations of the electroencephalogram (EEG) including initial epileptic discharges, then slow waves, and finally flattened EEG. Repeated ECT results in an increasing number of slower waves in the EEG for as long as a month. ECT-induced changes in various neurotransmitter systems have also been reported. Serotonin (5-hydroxytryptamine, 5-HT) is one of the most important neurotransmitters involved in depressive illness, and ECT alters several 5-HT-receptor subtypes in the central nervous system. 5-HT<SUB>1A</SUB> receptors in post-synaptic neurons are sensitized by repeated ECT, but those in pre-synaptic neurons (auto-receptors) are not changed. In addition, our electrophysiological studies have shown that ECT increases sensitivity to 5-HT of 5-HT<SUB>3</SUB> receptors in the hippocampus, resulting in an increase in release of neurotransmitters such as glutamate and γ-aminobutyric acid. In contrast, ECT decreases the auto-receptor functions in noradrenergic and dopaminergic neurons in the locus coeruleus and substantia nigra, respectively, resulting in an increase in release of noradrenaline and dopamine. In conclusion, 5-HT<SUB>1A</SUB>-receptor sensitization may be important for explaining the effectiveness of ECT, as this change induces a decrease in the number of 5-HT<SUB>2A</SUB> receptors that are elevated in depressive patients. Facilitation of neurotransmitter releases due to 5-HT<SUB>3</SUB>-receptor sensitization by ECT may also play an important role in effective treatment of depressive patients refractory to therapeutic drugs.

Journal

  • The Japanese Journal of Pharmacology

    The Japanese Journal of Pharmacology 80(3), 185-189, 1999-07

    The Japanese Pharmacological Society

References:  40

Cited by:  2

Codes

  • NII Article ID (NAID)
    10008195077
  • NII NACSIS-CAT ID (NCID)
    AA00691188
  • Text Lang
    ENG
  • Article Type
    Journal Article
  • ISSN
    00215198
  • NDL Article ID
    4806211
  • NDL Source Classification
    ZS51(科学技術--薬学)
  • NDL Call No.
    Z53-D199
  • Data Source
    CJP  CJPref  NDL  J-STAGE 
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