-
Something wrong with this record ?
Psilocybin has a narrow therapeutic window as an antidepressant treatment
L. Seillier, B. Čechová, A. Seillier, R. Šlamberová
Language English Country England, Great Britain
Document type Journal Article
- MeSH
- Antidepressive Agents * pharmacology therapeutic use MeSH
- Hallucinogens * pharmacology MeSH
- Hippocampus drug effects metabolism MeSH
- Rats MeSH
- Disease Models, Animal MeSH
- Brain-Derived Neurotrophic Factor metabolism MeSH
- Swimming psychology MeSH
- Motor Activity drug effects MeSH
- Rats, Wistar MeSH
- Prefrontal Cortex drug effects metabolism MeSH
- Psilocybin * pharmacology therapeutic use MeSH
- Body Temperature drug effects MeSH
- Dose-Response Relationship, Drug MeSH
- Animals MeSH
- Check Tag
- Rats MeSH
- Male MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
Psilocybin, a naturally occurring psychedelic compound in magic mushrooms, shows promise as a novel intervention with a single administration inducing rapid and long-lasting antidepressant effects. However, there are limited studies on the optimal dosing required for the beneficial effects of psilocybin given its side effects. To address this gap, we investigated in Wistar rats whether a single psilocybin administration (0.1, 0.32, 1.0, and 3.2 mg/kg) had antidepressant-like effects in the forced swim test (FST), a pro-social effect in the social interaction test (SIT), and the ability to alter pleasure using the sucrose preference test (SPT). We also examined the dose-response relationships of psilocybin on the head-twitch response (HTR), locomotor activity, body temperature, and weight gain. Furthermore, we explored whether the brain-derived neurotrophic factor (BDNF) levels in the hippocampus and prefrontal cortex (PFC) paralleled the behavioral changes observed after psilocybin. In the FST, psilocybin induced dose-dependent inverted-U-shaped responses with only the intermediate dose of 0.32 mg/kg producing short and long-term antidepressant-like effects. A similar pattern was observed for the SIT, the SPT, and the HTR. In contrast, the high doses of psilocybin (1.0 and 3.2 mg/kg), while deprived of anti-depressant-like activity, significantly reduced body temperature, locomotor activity, and body weight gain. BDNF levels in the hippocampus and PFC increased dose-dependently after psilocybin, but linearly suggesting a dissociation between high BDNF levels and the observed antidepressant-like behaviors. Our results indicated that there is a narrow window for the therapeutic potential of psilocybin, with 0.32 mg/kg effectively producing antidepressant-like effects without the accompanying adverse effects observed only at higher doses.
References provided by Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc25016181
- 003
- CZ-PrNML
- 005
- 20250731091556.0
- 007
- ta
- 008
- 250708e20250415enk f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.1016/j.pnpbp.2025.111368 $2 doi
- 035 __
- $a (PubMed)40246053
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a enk
- 100 1_
- $a Seillier, Lenka $u Department of Physiology, Third Faculty of Medicine, Charles University, Ke Karlovu 4, 120 00 Prague 2, Czech Republic. Electronic address: lenka.seillier@lf3.cuni.cz
- 245 10
- $a Psilocybin has a narrow therapeutic window as an antidepressant treatment / $c L. Seillier, B. Čechová, A. Seillier, R. Šlamberová
- 520 9_
- $a Psilocybin, a naturally occurring psychedelic compound in magic mushrooms, shows promise as a novel intervention with a single administration inducing rapid and long-lasting antidepressant effects. However, there are limited studies on the optimal dosing required for the beneficial effects of psilocybin given its side effects. To address this gap, we investigated in Wistar rats whether a single psilocybin administration (0.1, 0.32, 1.0, and 3.2 mg/kg) had antidepressant-like effects in the forced swim test (FST), a pro-social effect in the social interaction test (SIT), and the ability to alter pleasure using the sucrose preference test (SPT). We also examined the dose-response relationships of psilocybin on the head-twitch response (HTR), locomotor activity, body temperature, and weight gain. Furthermore, we explored whether the brain-derived neurotrophic factor (BDNF) levels in the hippocampus and prefrontal cortex (PFC) paralleled the behavioral changes observed after psilocybin. In the FST, psilocybin induced dose-dependent inverted-U-shaped responses with only the intermediate dose of 0.32 mg/kg producing short and long-term antidepressant-like effects. A similar pattern was observed for the SIT, the SPT, and the HTR. In contrast, the high doses of psilocybin (1.0 and 3.2 mg/kg), while deprived of anti-depressant-like activity, significantly reduced body temperature, locomotor activity, and body weight gain. BDNF levels in the hippocampus and PFC increased dose-dependently after psilocybin, but linearly suggesting a dissociation between high BDNF levels and the observed antidepressant-like behaviors. Our results indicated that there is a narrow window for the therapeutic potential of psilocybin, with 0.32 mg/kg effectively producing antidepressant-like effects without the accompanying adverse effects observed only at higher doses.
- 650 _2
- $a zvířata $7 D000818
- 650 12
- $a psilocybin $x farmakologie $x terapeutické užití $7 D011562
- 650 12
- $a antidepresiva $x farmakologie $x terapeutické užití $7 D000928
- 650 _2
- $a mužské pohlaví $7 D008297
- 650 _2
- $a potkani Wistar $7 D017208
- 650 _2
- $a vztah mezi dávkou a účinkem léčiva $7 D004305
- 650 _2
- $a mozkový neurotrofický faktor $x metabolismus $7 D019208
- 650 _2
- $a krysa rodu Rattus $7 D051381
- 650 _2
- $a prefrontální mozková kůra $x účinky léků $x metabolismus $7 D017397
- 650 _2
- $a hipokampus $x účinky léků $x metabolismus $7 D006624
- 650 _2
- $a pohybová aktivita $x účinky léků $7 D009043
- 650 _2
- $a modely nemocí na zvířatech $7 D004195
- 650 _2
- $a tělesná teplota $x účinky léků $7 D001831
- 650 12
- $a halucinogeny $x farmakologie $7 D006213
- 650 _2
- $a plavání $x psychologie $7 D013550
- 655 _2
- $a časopisecké články $7 D016428
- 700 1_
- $a Čechová, Barbora $u Department of Physiology, Third Faculty of Medicine, Charles University, Ke Karlovu 4, 120 00 Prague 2, Czech Republic
- 700 1_
- $a Seillier, Alexandre $u Schizophrenia Models for Advancing Research and Treatment, Preclinical Research Program, National Institute of Mental Health, Topolova 748, 250 67 Klecany, Czech Republic
- 700 1_
- $a Šlamberová, Romana $u Department of Physiology, Third Faculty of Medicine, Charles University, Ke Karlovu 4, 120 00 Prague 2, Czech Republic
- 773 0_
- $w MED00003930 $t Progress in neuro-psychopharmacology & biological psychiatry $x 1878-4216 $g Roč. 138 (20250415), s. 111368
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/40246053 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y - $z 0
- 990 __
- $a 20250708 $b ABA008
- 991 __
- $a 20250731091550 $b ABA008
- 999 __
- $a ok $b bmc $g 2366781 $s 1253306
- BAS __
- $a 3
- BAS __
- $a PreBMC-MEDLINE
- BMC __
- $a 2025 $b 138 $c - $d 111368 $e 20250415 $i 1878-4216 $m Progress in neuro-psychopharmacology & biological psychiatry $n Prog Neuropsychopharmacol Biol Psychiatry $x MED00003930
- LZP __
- $a Pubmed-20250708