Skip to main content
Log in

The effect of repeated electroconvulsive shock on corticosterone responses to centrally acting pharmacological stimuli in the male rat

  • Original Investigations
  • Published:
Psychopharmacology Aims and scope Submit manuscript

Abstract

The effect of repeated and single electroconvulsive shocks (ECS) on the corticosterone response to pharmacological stimuli has been studied in male rats. Plasma corticosterone concentrations are elevated by oxotremorine, a muscarinic agonist, and by 5-hydroxy-l-tryptophan, a precursor of serotonin. Both these agonists probably stimulate corticotrophinreleasing-factor release from the hypothalamus. The log dose-response curves of the corticosterone response to oxotremorine and to 5-hydroxy-l-tryptophan are shifted to the left after a single ECS given daily for 10 days compared with sham-shocked controls. Plasma corticosterone concentrations are elevated by treatment with α-methyl-p-tyrosine methyl ester (400 mg/kg IP). This rise is suppressed by clonidine. The log dose-response curve for the corticosterone response to clonidine after α-methyl-p-tyrosine methyl ester is also shifted to the left by repeated ECS, compared with controls. There is no difference in the corticosterone response of ECS and sham-treated groups given vasopressin, which is thought to act directly on the pituitary to release ACTH.

A single ECS produces a slight enhancement of the response to 5-hydroxy-l-tryptophan, a slight decrease in the response to oxotremorine and no change in the response to clonidine after α-methyl-p-tyrosine.

The disappearance of the difference in response between ECS and sham-treated animals was also studied 1,3, and 6 days after a series of ten ECS or sham procedures. Significant differences in the corticosterone responses to oxotremorine, 5-hydroxy-l-tryptophan and clonidine after α-methyl-p-tyrosine between ECS and sham-treated animas were found 24 h after the last ECS or sham shock. These differences were in decline 3 days after the last procedure and had completely disappeared by day 6. The decline was largely due to an increase in plasma corticosterone responsiveness to pharmacological stimuli of the shamshocked controls. Responses in the ECS-treated groups remained constant.

It is apparent that the anaesthetic procedure suppresses the effect of oxotremorine, 5-hydroxy-l-tryptophan and clonidine after α-methyl-p-tyrosine on corticosterone concentrations in plasma. This effect is spontaneously reversible. Repeated ECS reverses the effect of the anaesthetic procedure but produces no reversible enhancement of its own.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  • Bergstrom DA, Kellar KF (1979) Effect of electroconvulsive shock on monoaminergic binding sites in rat brain. Nature 278:464–466

    Google Scholar 

  • Carroll BJ (1972) Control of plasma cortisol levels in depression: studies with the dexamethasone suppression test. In: Carroll BJ, (ed) Depressive illness: some research studies. Thomas, Springfield III, p 87

    Google Scholar 

  • Chang CC (1964) A sensitive method for spectrophotoflurometric assay of catecholamines. Int J Neuropharmacol 3:643–649

    Google Scholar 

  • Edén S, Modigh K (1977) Effects of apomorphine and clonidine on rat plasma growth hormone after pretreatment with reserpine and electroconvulsive shock. Brain Res 129:379–384

    Google Scholar 

  • Evans JPM, Grahame-Smith DG, Green A, Tordoff AFC (1976) Electroconvulsive shock increases the behavioural responses of rats to brain 5-hydroxytryptamine accumulation and central nervous system stimulant drugs. Br. J Pharmacol 56:193–199

    Google Scholar 

  • Freeman CPL, Barson JV, Crighton A (1978) Double-blind controlled trial of electroconvulsive therapy (E.C.T.) and simulated E.C.T. in depressive illness. Lancet I:738–740

    Google Scholar 

  • Green AR, Heal DJ, Grahame-Smith DG (1977) Further observations on the effect of repeated electroconvulsive shock on the behavioural responses of rats producd by increases in the functional action of brain 5-hydroxy-tryptamine and dopamine. Psychopharmacology 52:195–200

    Google Scholar 

  • Heal DJ, Green AR (1978) Repeated electroconvulsive shock increases the behavioural responses of rats to injection of both dopamine and dibutyryl cyclic AMP into the nucleus accumbens. Neuropharmacology 17:1085–1087

    Google Scholar 

  • Jones MT, Hillhouse EW, Burden J (1976) Effect of various putative neurotransmitters on the secretion of corticotrophin-releasing hormone from the rat hypothalamus in vitro—a model of the neurotransmitters involved. J Endocrinol 69:1–10

    Google Scholar 

  • Kirkegaard C, Smith E (1978) Continuation therapy in endogenous depression controlled by changes in the TRH stimulation test. Psychol Med 8:501–503

    Google Scholar 

  • Langer G (1976) Reduced growth hormone responses to amphetamine in ‘endogenous’ depressive patients: studies in normal, ‘reactive’, and ‘endogenous’ depressive schizophrenic and chronic alcoholic subjects. Arch Gen Psychiat 33:1471–1475

    Google Scholar 

  • Longoni R, Mulas A, Oderfeld Novak B, Marconcini Pepeu I, Pepeu G (1976) Effect of single and repeated electroshock applications on brain acetyl choline levels and choline acetyl transferase activity in the rat. Neuropharmacology 15:283–286

    Google Scholar 

  • Lutz-Bucher B, Koch B, Mialhe C (1977) Comparative in vitro studies on corticotropin releasing activity of vasopressin and hypothalamic median eminence extract. Neuroendocrinology 23:181–192

    Google Scholar 

  • Modigh K (1975) Electroconvulsive shock and postsynaptic catecholamine effects: increased psychomotor stimulant action of apomorphine and clonidine in reserpine pretreated mice by repeated ECS. J Neural Trans 36:19–32

    Google Scholar 

  • Modigh K (1976) Long-term effects of electroconvulsive shock therapy on synthesis turnover and uptake of brain monoamines. Psychopharmacology 49:179–185

    Google Scholar 

  • Paul SM, Skolnick P (1978) Rapid changes in brain benzodiazepine receptors after experimental seizures. Science 202:892–894

    Google Scholar 

  • Roizen MF, Kopin IJ, Palkovits M, Brownstein M, Kizer JS, Jacobowitz DM (1975) The effect of two diverse inhalational anaesthetic agents on serotonin in discrete regions of the rat brain. Exp Brain Res 24:203–207

    Google Scholar 

  • Roizen MF, Kopin IJ, Thoa NB, Zivin J, Muth EA, Jacobowitz DM (1976) The effect of two anesthetic agents on norepinephrine and dopamine in discrete brain nuclei, fiber tracts and terminal regions of the rat. Brain Res 110:515–522

    Google Scholar 

  • Royal College of Psychiatrists' Memorandum on the Use of Electroconvulsive Therapy (1977). Br. J. Psychiat. 131:261–272

    Google Scholar 

  • Sachar EJ (1975) Twenty-four-hour cortisol secretory patterns in depressed and manic patients. Prog Brain Res 42:81–91

    Google Scholar 

  • Steiner JA, Grahame-Smith DG (1980) Central pharmacological control of corticosterone secretion in the intact rat. Demonstration of cholinergic and serotoninergic facilitatory and α-adrenergic inhibitory mechanisms. Psychopharmacology 71: 213–217

    Google Scholar 

  • Takahashi S, Kondo H, Yoshimura M, Ochi Y (1974) Growth hormone responses to administration of l-5-hydroxytryptophan (l-5-HTP) in manic depressive psychoses. In: Hatotani N (ed) Psychoneuroendocrinology. Karger, Basel, p 33

    Google Scholar 

  • Zenker N, Bernstein DS (1958) The estimation of small amounts of corticosterone in rat plasma. J Biol Chem 231:695–701

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Steiner, J.A., Grahame-Smith, D.G. The effect of repeated electroconvulsive shock on corticosterone responses to centrally acting pharmacological stimuli in the male rat. Psychopharmacology 71, 205–212 (1980). https://doi.org/10.1007/BF00433053

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00433053

Key words

Navigation