دورية أكاديمية

Oleoylethanolamide decreases frustration stress-induced binge-like eating in female rats: a novel potential treatment for binge eating disorder

التفاصيل البيبلوغرافية
العنوان: Oleoylethanolamide decreases frustration stress-induced binge-like eating in female rats: a novel potential treatment for binge eating disorder
المؤلفون: Romano, Adele, Micioni Di Bonaventura, Maria Vittoria, Gallelli, Cristina Anna, Koczwara, Justyna Barbara, Smeets, Dorien, Giusepponi, Maria Elena, De Ceglia, Marialuisa, Friuli, Marzia, Micioni Di Bonaventura, Emanuela, Scuderi, Caterina, Vitalone, Annabella, Tramutola, Antonella, Altieri, Fabio, Lutz, Thomas A, Giudetti, Anna Maria, Cassano, Tommaso, Cifani, Carlo, Gaetani, Silvana
المصدر: Romano, Adele; Micioni Di Bonaventura, Maria Vittoria; Gallelli, Cristina Anna; Koczwara, Justyna Barbara; Smeets, Dorien; Giusepponi, Maria Elena; De Ceglia, Marialuisa; Friuli, Marzia; Micioni Di Bonaventura, Emanuela; Scuderi, Caterina; Vitalone, Annabella; Tramutola, Antonella; Altieri, Fabio; Lutz, Thomas A; Giudetti, Anna Maria; Cassano, Tommaso; Cifani, Carlo; Gaetani, Silvana (2020). Oleoylethanolamide decreases frustration stress-induced binge-like eating in female rats: a novel potential treatment for binge eating disorder. Neuropsychopharmacology, 45(11):1931-1941.
بيانات النشر: Nature Publishing Group
سنة النشر: 2020
المجموعة: University of Zurich (UZH): ZORA (Zurich Open Repository and Archive
مصطلحات موضوعية: Institute of Veterinary Physiology, 570 Life sciences, biology, Pharmacology, Psychiatry and Mental health
الوصف: Binge eating disorder (BED) is the most frequent eating disorder, for which current pharmacotherapies show poor response rates and safety concerns, thus highlighting the need for novel treatment options. The lipid-derived messenger oleoylethanolamide (OEA) acts as a satiety signal inhibiting food intake through the involvement of central noradrenergic and oxytocinergic neurons. We investigated the anti-binge effects of OEA in a rat model of binge-like eating, in which, after cycles of intermittent food restrictions/refeeding and palatable food consumptions, female rats show a binge-like intake of palatable food, following a 15-min exposure to their sight and smell (“frustration stress”). Systemically administered OEA dose-dependently (2.5, 5, and 10 mg kg−1) prevented binge-like eating. This behavioral effect was associated with a decreased activation (measured by mapping the expression of c-fos, an early gene widely used as a marker of cellular activation) of brain areas responding to stress (such as the nucleus accumbens and amygdala) and to a stimulation of areas involved in the control of food intake, such as the VTA and the PVN. These effects were paralleled, also, to the modulation of monoamine transmission in key brain areas involved in both homeostatic and hedonic control of eating. In particular, a decreased dopaminergic response to stress was observed by measuring dopamine extracellular concentrations in microdialysates from the nucleus accumbens shell, whereas an increased serotonergic and noradrenergic tone was detected in tissue homogenates of selected brain areas. Finally, a decrease in corticotropin-releasing factor (CRF) mRNA levels was induced by OEA in the central amygdala, while an increase in oxytocin mRNA levels was induced in the PVN. The restoration of a normal oxytocin receptor density in the striatum paralleled the oxytocinergic stimulation produced by OEA. In conclusion, we provide evidence suggesting that OEA might represent a novel potential pharmacological target for the treatment of ...
نوع الوثيقة: article in journal/newspaper
وصف الملف: application/pdf
اللغة: English
تدمد: 0893-133X
العلاقة: https://www.zora.uzh.ch/id/eprint/188160/1/s41386-020-0686-z.pdfTest; info:pmid/32353860; urn:issn:0893-133X
DOI: 10.5167/uzh-188160
DOI: 10.1038/s41386-020-0686-z
الإتاحة: https://doi.org/10.5167/uzh-18816010.1038/s41386-020-0686-zTest
https://www.zora.uzh.ch/id/eprint/188160Test/
https://www.zora.uzh.ch/id/eprint/188160/1/s41386-020-0686-z.pdfTest
حقوق: info:eu-repo/semantics/openAccess ; Creative Commons: Attribution 4.0 International (CC BY 4.0) ; http://creativecommons.org/licenses/by/4.0Test/
رقم الانضمام: edsbas.58851A8B
قاعدة البيانات: BASE
الوصف
تدمد:0893133X
DOI:10.5167/uzh-188160