Evidence map›Paper›PMID 41559847›Full record

ArticleJournal of cannabis research2026

Melatonin mitigates hormonal toxicity in cannabis-treated female Wistar rats: involvement of cannabinoid receptor.

A Oluwasola

Abstract read
In one paragraph

Article in Journal of cannabis research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

The trial behind it

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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

1 author.

A OluwasolaDepartment of Physiology, Faculty of Basic Medical Sciences, University of Ilesa, Ilesa, Osun State, Nigeria. dr.amuda19@gmail.com.ORCID http://orcid.org/0000-0002-5950-0179

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundConsumption of Cannabis sativa (CS), a well known psychoactive substance may impose threat on the hormonal activities of the body, hence, a protective measure is needed to prevent this threat. This study investigates the effects of melatonin and CS together with its receptors (cannabinoid receptors 1 and 2) on hormonal toxicity in female rats.

methodsFifty female rats were assigned into ten groups of five animals each, such that the rats in groups 1,2,3,4, 5, 6, 7, 8, 9, and 10 received orally 1mL distilled water, 2 mg/kg of ethanolic extract of Cannabis sativa (EECS), 2 mg/kg of cannabinoid one receptor (CB1R) blocker (rimonabant hydrochloride), 2 mg/kg of cannabinoid two receptor (CB2R) blocker (am630), 2 mg/kg of CB1R blocker + 2 mg/kg of EECS, 2 mg/kg of CB2R blocker + 2 mg/kg of EECS,2 mg/kg of CB1R blocker + 2 mg/kg of CB2R blocker + 2 mg/kg of EECS,4 mg/kg of melatonin,2 mg/kg of CB1R blocker + 2 mg/kg of EECS + 4 mg/kg of melatoninand2mg/kg of CB2R blocker + 2 mg/kg of EECS + 4 mg/kg of melatonin, respectively for 14 days. Gonadotropin-releasing hormone (GnRH), follicle-stimulating hormone (FSH), luteinizing hormone (LH), estradiol (E), progesterone, and prolactin were quantified according to the instruction provided by assay kit manufacturers, using microplateimmunoenzymometric (EMA/ELISA) assays.

resultsCS significantly (p < 0.05) decrease GnRH, FSH, LH, E, progesterone, and prolactin levels respectively when compared with the control. However, blockage of either cannabinoid receptors 1 or 2 significantly (p < 0.05) increase the levels of all these reproductive hormones when compared to the CS-treated group. Although, that of the former was more than the latter. All these effects were ameliorated by melatonin when the cannabinoid receptors (1 and 2) were stimulated and blocked.

conclusionThis study concluded that the gonadotoxic effects of CS could be mediated by endocrine disruption caused by cannabinoid receptors 1 and 2. In addition, CB1 primarily disrupts hypothalamic-pituitary-gonadal axis. Thereby causing more hormonal toxicity than CB2 which mainly influence hormonal imbalance indirectly through immune modulation. However, these effects could be ameliorated by melatonin. The study suggests that melatonin could be used as a supplement to prevent the gonadotoxic effects of CS.

Indexed as

Cannabinoid receptorsCannabis-sativaMelatoninReproductive hormones

Identifiers

PMID41559847
PMCPMC12903301

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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.