Catherine F. Moore , Cecilia L. Bergeria , Cristina Sempio , Jost Klawitter , Uwe Christians , Elise M. Weerts
{"title":"High doses of orally administered cannabigerol produce deficits in sustained attention in female rats","authors":"Catherine F. Moore , Cecilia L. Bergeria , Cristina Sempio , Jost Klawitter , Uwe Christians , Elise M. Weerts","doi":"10.1016/j.pbb.2026.174154","DOIUrl":null,"url":null,"abstract":"<div><div>Cannabigerol (CBG) is a phytocannabinoid found in cannabis that is increasingly being sold and used as an isolate product or as the dominant cannabinoid in cannabis products for purported cognitive enhancement (attention, focus, and memory). The purpose of this study was to evaluate the effects of orally administered CBG on sustained attention, motivation, and memory. In a series of experiments, separate groups of male and female adult Sprague Dawley rats received oral CBG (30–600 mg/kg, per os [p.o.]) or sesame oil vehicle prior to testing in 1) the rodent psychomotor vigilance test; 2) progressive ratio responding for food; 3) spontaneous alternation test of working memory (selected doses: 300–600 mg/kg, p.o.). Blood plasma was collected 60 min following oral administration for assessments of circulating CBG levels. CBG produced deficits in sustained attention at the highest doses (300–600 mg/kg) in female, but not male, rats. CBG did not affect motivation to respond for a food reward nor working memory, indicating an effect specific to attention in females. Finally, females showed significantly higher circulating CBG in plasma compared with males following oral CBG. In sum, these data suggest a sex-specific effect of CBG on sustained attention in females.</div></div>","PeriodicalId":19893,"journal":{"name":"Pharmacology Biochemistry and Behavior","volume":"260 ","pages":"Article 174154"},"PeriodicalIF":2.5000,"publicationDate":"2026-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Pharmacology Biochemistry and Behavior","FirstCategoryId":"102","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0091305726000092","RegionNum":3,"RegionCategory":"心理学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/1/12 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"BEHAVIORAL SCIENCES","Score":null,"Total":0}
引用次数: 0
Abstract
Cannabigerol (CBG) is a phytocannabinoid found in cannabis that is increasingly being sold and used as an isolate product or as the dominant cannabinoid in cannabis products for purported cognitive enhancement (attention, focus, and memory). The purpose of this study was to evaluate the effects of orally administered CBG on sustained attention, motivation, and memory. In a series of experiments, separate groups of male and female adult Sprague Dawley rats received oral CBG (30–600 mg/kg, per os [p.o.]) or sesame oil vehicle prior to testing in 1) the rodent psychomotor vigilance test; 2) progressive ratio responding for food; 3) spontaneous alternation test of working memory (selected doses: 300–600 mg/kg, p.o.). Blood plasma was collected 60 min following oral administration for assessments of circulating CBG levels. CBG produced deficits in sustained attention at the highest doses (300–600 mg/kg) in female, but not male, rats. CBG did not affect motivation to respond for a food reward nor working memory, indicating an effect specific to attention in females. Finally, females showed significantly higher circulating CBG in plasma compared with males following oral CBG. In sum, these data suggest a sex-specific effect of CBG on sustained attention in females.
期刊介绍:
Pharmacology Biochemistry & Behavior publishes original reports in the areas of pharmacology and biochemistry in which the primary emphasis and theoretical context are behavioral. Contributions may involve clinical, preclinical, or basic research. Purely biochemical or toxicology studies will not be published. Papers describing the behavioral effects of novel drugs in models of psychiatric, neurological and cognitive disorders, and central pain must include a positive control unless the paper is on a disease where such a drug is not available yet. Papers focusing on physiological processes (e.g., peripheral pain mechanisms, body temperature regulation, seizure activity) are not accepted as we would like to retain the focus of Pharmacology Biochemistry & Behavior on behavior and its interaction with the biochemistry and neurochemistry of the central nervous system. Papers describing the effects of plant materials are generally not considered, unless the active ingredients are studied, the extraction method is well described, the doses tested are known, and clear and definite experimental evidence on the mechanism of action of the active ingredients is provided.