Evidence mapPaperPMID 40852923Full record

ArticleCNS neuroscience & therapeutics2025

Cannabinoid Receptors CB1 and CB2 Activation Restores Hippocampal Lipid Profiles and Alleviates Autism-Like Behaviors in Valproic Acid-Induced ASD Rats.

Haoran Wang, Mengyuan Zhang, Sen Yang, Yi Jiang, Lijie Wu, Caihong Sun

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Article in CNS neuroscience & therapeutics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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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

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Haoran WangDepartment of Children's and Adolescent Health, Public Health College, Harbin Medical University, Harbin, China.
Mengyuan ZhangDepartment of Children's and Adolescent Health, Public Health College, Harbin Medical University, Harbin, China.
Sen YangDepartment of Children's and Adolescent Health, Public Health College, Harbin Medical University, Harbin, China.
Yi JiangDepartment of Children's and Adolescent Health, Public Health College, Harbin Medical University, Harbin, China.
Lijie WuDepartment of Children's and Adolescent Health, Public Health College, Harbin Medical University, Harbin, China.ORCID 0000-0002-0631-5076
Caihong SunDepartment of Children's and Adolescent Health, Public Health College, Harbin Medical University, Harbin, China.ORCID 0000-0002-1798-0768

Funding

National Natural Science Foundation of China 82173535Natural Science Foundation of Heilongjiang Province No.LH2023H017
6 · The paper itself

Abstract

objectiveEmerging evidence suggests lipid metabolism dysregulation contributes to autism spectrum disorders (ASD), with the endocannabinoid system (cannabinoid receptors CB1R/CB2R) implicated in lipid homeostasis. This study investigated whether CB1R/CB2R activation improves hippocampal lipid metabolism and ASD-like behaviors in a valproic acid (VPA)-induced ASD rat model.

methodsMale offspring from dams exposed to VPA (600 mg/kg, i.p.) received the CB1R agonist ACPA (0.1 mg/kg) or the CB2R agonist AM1241 (3 mg/kg) from postnatal days 21-27. ASD-like behaviors (marble burying, self-grooming, social interaction, open-field tests) and hippocampal lipid profiles (UPLC-MS/MS) were analyzed.

resultsVPA-exposed rats displayed heightened repetitive behaviors, social deficits, and hyperactivity, all significantly alleviated by ACPA and AM1241. Lipidomics revealed marked reductions in hippocampal phosphatidylcholines, lysophosphatidylcholines, fatty acids, sphingomyelins, ceramides, and phosphatidylethanolamines in VPA rats. Both agonists restored lipid levels to near normal, comparable to controls.

conclusionsCB1R/CB2R activation ameliorates behavioral abnormalities and rectifies hippocampal lipid dysregulation in VPA-induced ASD models, highlighting cannabinoid receptors as potential therapeutic targets for ASD-associated metabolic disturbances.

Indexed as

Autism Spectrum DisorderHippocampusLipid MetabolismReceptor, Cannabinoid, CB1Receptor, Cannabinoid, CB2Valproic AcidAnimalsBehavior, AnimalCannabinoid Receptor AgonistsFemaleMalePregnancyRatsRats, Sprague-DawleyCannabinoid Receptor AgonistsCnr2 protein, ratReceptor, Cannabinoid, CB1Receptor, Cannabinoid, CB2Valproic Acidautism spectrum disorderscannabinoid receptor 1cannabinoid receptor 2lipidomics

Identifiers

PMID40852923
PMCPMC12376063

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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 Socratic graph.