Effects of neuropeptide Y and corticotropin-releasing factor on ethanol intake in Wistar rats: interaction with chronic ethanol exposure

• Published in: Behavioural brain research Vol. 161; no. 1; pp. 133 - 140
• Main Authors: Thorsell, Annika, Slawecki, Craig J., Ehlers, Cindy L.
• Format: Journal Article
• Language: English
• Published: Shannon Elsevier B.V 03.06.2005; Elsevier Science
• Subjects: Alcohol Drinking; Animals; Behavior, Animal - drug effects; Behavioral psychophysiology; Biological and medical sciences; Body Weight - drug effects; Central Nervous System Depressants - administration & dosage; Corticotropin-Releasing Hormone - pharmacology; CRF; Dependence; Drinking Behavior - drug effects; Drug Administration Schedule; Drug Interactions; Ethanol; Ethanol - administration & dosage; Ethanol - blood; Fundamental and applied biological sciences. Psychology; Male; Motor Activity - drug effects; Neuropeptide Y - pharmacology; Neurotransmission and behavior; NPY; Psychology. Psychoanalysis. Psychiatry; Psychology. Psychophysiology; Rat; Rats; Rats, Wistar; Self Administration - methods; Self-administration; Stereotyped Behavior - drug effects; Time Factors; Self-administration; Ethanol; Rat; NPY; CRF; Dependence; Neuropeptide Y; Interaction; Rodentia; Corticotropin releasing factor; Exposure; Self administration; Hypothalamic hormone; Vertebrata; Chronic; Mammalia; Animal; Hormone releasing factor
• ISSN: 0166-4328; 1872-7549; 1872-7549
• DOI: 10.1016/j.bbr.2005.01.016

Neuropeptide Y (NPY) and corticotropin-releasing factor (CRF) have opposing effects on stress-associated and consummatory behaviors in rodents. Recent studies also suggest that both peptides influence ethanol intake. In the present study, the effects of administration of CRF and NPY into the lateral ventricle on ethanol intake in naive and ethanol-vapor-exposed Wistar rats were examined. A limited access paradigm was used to measure intake of a 10% (v/v) ethanol solution in Wistar rats trained to drink using a sucrose fading procedure. Ethanol vapor exposure for 8 weeks significantly elevated ethanol intake in this limited access paradigm relative to pre-exposure levels. The effects of icv administration of CRF (1 μg), NPY (10 μg) or NPY/CRF combined (10 and 1 μg, respectively) on ethanol intake were then assessed. In non-vapor-exposed subjects, icv infusion of NPY had no effect on ethanol intake, while a significant suppression of drinking was seen following icv administration of CRF. Administration of NPY in combination with CRF had no effect on ethanol intake in non-ethanol-vapor-exposed rats. In vapor-exposed subjects, both NPY and CRF reduced ethanol intake, but when given in combination, no difference from vehicle was detected. Locomotor activity was measured during drinking sessions and was unaffected by peptide administration. These studies underscore the importance of a history of exposure to chronic ethanol vapor in the regulation of ethanol intake by NPY. Furthermore, the results presented here suggest that a balance between the stress-related peptides NPY and CRF may be involved in the regulation of ethanol intake.