Evidence map›Paper›PMID 34032876›Full record

ArticlePsychopharmacology2021

Tolerance to neurochemical and behavioral effects of the hallucinogen 25I-NBOMe.

Monika Herian, Mateusz Skawski, Adam Wojtas, Małgorzata K Sobocińska, Karolina Noworyta, Krystyna Gołembiowska

Open access · hybridAbstract read
In one paragraph

Article in Psychopharmacology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 1 pooled it
3.7field-weighted citation impact, top 7% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

12 citing papers in PubMed, 1 synthesis or guideline pooled it, 29 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Molecular and Medical Aspects of Psychedelics.International journal of molecular sciences · 2023
    Review
  8. Article
  9. Review
  10. Article
  11. Article
  12. Effect ofFrontiers in psychiatry · 2022
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 1 institution in 1 country.

Monika HerianDepartment of Pharmacology, Polish Academy of Sciences, Maj Institute of Pharmacology, 12 Smętna, 31-343, Kraków, Poland.
Mateusz SkawskiDepartment of Pharmacology, Polish Academy of Sciences, Maj Institute of Pharmacology, 12 Smętna, 31-343, Kraków, Poland.
Adam WojtasDepartment of Pharmacology, Polish Academy of Sciences, Maj Institute of Pharmacology, 12 Smętna, 31-343, Kraków, Poland.
Małgorzata K SobocińskaDepartment of Pharmacology, Polish Academy of Sciences, Maj Institute of Pharmacology, 12 Smętna, 31-343, Kraków, Poland.
Karolina NoworytaDepartment of Pharmacology, Polish Academy of Sciences, Maj Institute of Pharmacology, 12 Smętna, 31-343, Kraków, Poland.
Krystyna GołembiowskaDepartment of Pharmacology, Polish Academy of Sciences, Maj Institute of Pharmacology, 12 Smętna, 31-343, Kraków, Poland. nfgolemb@cyf-kr.edu.pl.ORCID http://orcid.org/0000-0002-5018-1394
Maj Institute of Pharmacology · PL

Funding

InterDokMed POWR.03.02.00-00-I013/16Maj Institute of Pharmacology Polish Academy of Sciences statutory fundNarodowe Centrum Nauki 2016/21/B/NZ7/01131
6 · The paper itself

Abstract

rationale4-Iodo-2,5-dimethoxy-N-(2-methoxybenzyl)phenethylamine (25I-NBOMe) is a potent serotonin 5-HT

objectivesWe examined the effect of a 7-day treatment with 25I-NBOMe (0.3 mg/kg/day) on neurotransmitters' release and rats' behavior in comparison to acute dose.

methodsChanges in dopamine (DA), serotonin (5-HT), acetylcholine (ACh), and glutamate release were studied using microdialysis in freely moving rats. The hallucinogenic activity was measured in the wet dog shake (WDS) test. The animal locomotion was examined in the open field (OF) test, short-term memory in the novel object recognition (NOR) test. The anxiogenic/anxiolytic properties of the drug were tested using the light/dark box (LDB) test.

resultsRepeated administration of 25I-NBOMe decreased the response to a challenge dose of DA, 5-HT, and glutamatergic neurons in the frontal cortex as well as weakened the hallucinogenic activity in comparison to acute dose. In contrast, striatal and accumbal DA and 5-HT release and accumbal but not striatal glutamate release in response to the challenge dose of 25I-NBOMe was increased in comparison to acute treatment. The ACh release was increased in all brain regions. Behavioral tests showed a motor activity reduction and memory deficiency in comparison to a single dose and induction of anxiety after the drug's chronic and acute administration.

conclusionsOur findings suggest that multiple injections of 25I-NBOMe induce tolerance to hallucinogenic activity and produce alterations in neurotransmission. 25I-NBOMe effect on short-term memory, locomotor function, and anxiety seems to be the result of complex interactions between neurotransmitter pathways.

Indexed as

AnimalsBrain ChemistryDimethoxyphenylethylamineDopamineFrontal LobeGlutamic AcidHallucinogensLocomotionMaleMicrodialysisRatsRats, WistarSerotonin2-(4-iodo-2,5-dimethoxyphenyl)-N-(2-methoxybenzyl)ethanamineDimethoxyphenylethylamineDopamineGlutamic AcidHallucinogensSerotonin25I-NBOMeBehaviorNeurotransmitter releaseTolerance

Identifiers

PMID34032876
PMCPMC8292280
OpenAlexW3164016075

What OpenQuestion holds

Textmetadata
LicenceCC BY
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.