Regional binding to corticotropin releasing factor receptors in brain of rats exposed to chronic cocaine and cocaine withdrawal

• Published in: Synapse (New York, N.Y.) N.Y.), 1997-03, Vol.25 (3), p.272-276
• Main Authors: Ambrosio, Emilio, Sharpe, Lawrence G., Pilotte, Nancy S.
• Format: Article
• Language: English
• Subjects: 125I-Tyr-oCRF; amygdala; Animals; autoradiography; Brain - metabolism; Cocaine - adverse effects; CRF1 receptors; CRF1 receptors, autoradiography; Drug Administration Schedule; Infusions, Intravenous; Male; Radioligand Assay; Rats; Rats, Inbred Lew; Receptors, Corticotropin-Releasing Hormone - metabolism; Substance Withdrawal Syndrome - metabolism
• ISSN: 0887-4476; 1098-2396
• DOI: 10.1002/(SICI)1098-2396(199703)25:3<272::AID-SYN6>3.0.CO;2-8

Cocaine, as does exposure to other physiological stressors, releases brain corticotropin releasing factor (CRF), and this release habituates during the course of repeated cocaine administration in animals. Due to the many signs of anxiety and responses to stress that are produced by cocaine withdrawal in humans, the present study was designed to assess the effects of chronic cocaine and its withdrawal on regional 125I‐Tyr‐oCRF binding to the CRF1 receptor in brains of male Lewis rats. Cocaine or saline was intravenously infused for 10 days in a regimen that resembled a self‐administration paradigm (1 mg/kg every 12 min for 2 h each day). Tissues were harvested either 15 min after or 10 days after the last cocaine infusion, and the brains were sectioned and prepared for CRF1 receptor autoradiography. Compared with findings in saline controls, there was a 31% lower level of CRF binding sites in the basolateral nucleus of the amygdala immediately after the last cocaine infusion, but not 10 days later. Neuroendocrine and non‐neuroendocrine mechanisms associated with CRF1 receptors do not appear to contribute to long‐term withdrawal effects. Synapse 25:272–276, 1997. © 1997 Wiley‐Liss, Inc.