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Circadian variation in the head twitch response produced by 5-methoxy-N1,N1-dimethyltryptamine and p-chloroamphetamine in the mouse.

C Singleton, C A Marsden

Psychopharmacology January 1, 1981 DOI: 10.1007/BF00432688 (opens in new tab) via PubMed

Summary

AI-generated from the abstract

In male mice, the head twitch response caused by two different drugs that affect serotonin (5-HT) shows a daily rhythm. Depleting brain serotonin with PCPA increased the response to the direct serotonin receptor agonist 5-MeODMT on days 3 and 5, when serotonin levels were low, but not on day 12 when levels had recovered. PCPA reduced the response to PCA, which releases serotonin from neurons. Under a 12-hour light-dark cycle, the response to the direct agonist peaked near the end of the dark period when serotonin was lowest, while the response to the serotonin-releasing drug peaked in the middle of the light period when serotonin was highest.

Study at a glance

Characteristics Experimental study Peer reviewed
Population Male BK.TO mice
Interventions 5-methoxy-N1 N1-dimethyltryptamine (5-MeODMT) p-chloroamphetamine (PCA) p-chlorophenylalanine (PCPA)
Dose 5 mg/kg IV (5-MeODMT), 400 mg/kg IP twice on consecutive days (PCPA)
Duration Up to 12 days after initial PCPA injection
Citations 28
Key finding Serotonin receptor response shows a circadian rhythm related to both pre-synaptic availability of serotonin and post-synaptic receptor sensitivity.

Abstract

Circadian fluctuations were measured in the head twitch response produced by 5-methoxy-N1,N1-dimethyltryptamine (5-MeODMT) and p-chloroamphetamine (PCA) in male BK. TO mice. The effects of depleting brain 5-hydroxytryptamine (5-HT) with p-chlorophenylalanine (PCPA) on the 5-MeODMT in the mouse were also studied. Changes in brain 5-HT and 5-hydroxyindoleacetic (5-HIAA) were concomitantly determined. PCPA (400 mg/kg IP twice on consecutive days) significantly increased the number of head twitches induced by 5-MeODMT (5 mg/kg IV) on days 3 and 5 after the initial injection of PCPA when 5-HT and 5-HIAA were also significantly reduced. On day 12, there was no significant difference in the number of head twitches between mice administered PCPA and those given saline, and 5-HT and 5-HIAA levels were nearly back to normal. PCPA, using the same dose schedule, significantly reduced the number of head twitches induced by PCA when PCA was administered 24 h after the second injection of PCPA (day 3. Mice maintained on a 12-h light-dark cycle showed a maximum response to the direct 5-HT receptor agonist 5-MeODMT (5 mg/kg IV) towards the end of the dark period, when the 5-HT level was at its lowest. p-Chloroamphetamine, which causes release of 5-HT from pre-synaptic neurones, produced a peak head twitch response in the middle of the light period when 5-HT and 5-HIAA levels were maximal, while the response towards the end of the dark period was significantly less than that at other times tested. It is concluded that 5-HT receptor response shows a circadian rhythm related to both pre-synaptic availability of 5-HT and post-synaptic receptor sensitivity.

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