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Repeated lysergic acid diethylamide in an animal model of depression: Normalisation of learning behaviour and hippocampal serotonin 5-HT2 signalling

Tobias Buchborn, H. Schröder, V. Höllt, G. Grecksch

Journal of Psychopharmacology April 30, 2014 DOI: 10.1177/0269881114531666 (opens in new tab)

Study at a glance

AI-extracted from the abstract
Characteristics Animal model study Peer reviewed
Population Male rats (olfactory bulbectomised and sham-operated)
Intervention LSD
Dose 0.13 mg/kg/d for 11 days
Duration 11 days
Measures active avoidance learning, [(35)S]-GTP-gamma-S binding
Topics Depression LSD Serotonin
Citations 71
Key points Repeated LSD treatment reverses behavioral deficits and normalizes hippocampal 5-HT2 signaling in bulbectomised rats, suggesting antidepressant-like effects.

Abstract

A re-balance of postsynaptic serotonin (5-HT) receptor signalling, with an increase in 5-HT1A and a decrease in 5-HT2A signalling, is a final common pathway multiple antidepressants share. Given that the 5-HT1A/2A agonist lysergic acid diethylamide (LSD), when repeatedly applied, selectively downregulates 5-HT2A, but not 5-HT1A receptors, one might expect LSD to similarly re-balance the postsynaptic 5-HT signalling. Challenging this idea, we use an animal model of depression specifically responding to repeated antidepressant treatment (olfactory bulbectomy), and test the antidepressant-like properties of repeated LSD treatment (0.13 mg/kg/d, 11 d). In line with former findings, we observe that bulbectomised rats show marked deficits in active avoidance learning. These deficits, similarly as we earlier noted with imipramine, are largely reversed by repeated LSD administration. Additionally, bulbectomised rats exhibit distinct anomalies of monoamine receptor signalling in hippocampus and/or frontal cortex; from these, only the hippocampal decrease in 5-HT2 related [(35)S]-GTP-gamma-S binding is normalised by LSD. Importantly, the sham-operated rats do not profit from LSD, and exhibit reduced hippocampal 5-HT2 signalling. As behavioural deficits after bulbectomy respond to agents classified as antidepressants only, we conclude that the effect of LSD in this model can be considered antidepressant-like, and discuss it in terms of a re-balance of hippocampal 5-HT2/5-HT1A signalling.

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  • Repeated LSD treatment reversed behavioral deficits and normalized hippocampal 5-HT2 signaling in bulbectomised rats, suggesting antidepressant-like effects.

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Comparable studies

Other preclinical and animal studies on LSD for depression, most cited first.

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