Comparison of Antidepressant‐Like and Abuse‐Related Effects of Phencyclidine in Rats. Issue 8 (15th October 2014)
- Record Type:
- Journal Article
- Title:
- Comparison of Antidepressant‐Like and Abuse‐Related Effects of Phencyclidine in Rats. Issue 8 (15th October 2014)
- Main Title:
- Comparison of Antidepressant‐Like and Abuse‐Related Effects of Phencyclidine in Rats
- Authors:
- Hillhouse, Todd M.
Porter, Joseph H.
Negus, S. Stevens - Abstract:
- <abstract abstract-type="main"> <title>Abstract</title> <p> <table-wrap position="anchor" orientation="portrait"> <table border="1"> <colgroup span="1"> <col align="left" span="1" /> </colgroup> <tbody> <tr> <td align="left" rowspan="1" colspan="1">Preclinical Research</td> </tr> </tbody> </table> </table-wrap> </p> <p> <italic>N</italic>‐methyl‐D‐aspartate (NMDA) receptor antagonists, such as ketamine, have emerged as novel candidate treatments for major depressive disorder, but abuse potential of these agents is a concern. The NMDA antagonist phencyclidine has known abuse liability but undefined efficacy as an antidepressant. To further evaluate the relationship between antidepressant‐like and abuse‐related effects of NMDA antagonists, this study evaluated the effects of phencyclidine (1.0–10.0 mg/kg) in male Sprague‐Dawley rats responding under two procedures that have been used to assess antidepressant‐like effects (differential‐reinforcement‐of‐low‐rate [DRL] 72 s schedule of food reinforcement; <italic>n</italic> = 9) and abuse‐related drug effects (intracranial self‐stimulation [ICSS]; <italic>n</italic> = 6). Under the DRL 72 s schedule, phencyclidine (10.0 mg/kg) increased reinforcers and decreased responses without shifting the peak location of the interresponse time (IRT) distribution. Ketamine (10.0 mg/kg) also increased reinforcers and decreased responses, but unlike phencyclidine, it produced a rightward shift in the peak location of the IRT distribution. The<abstract abstract-type="main"> <title>Abstract</title> <p> <table-wrap position="anchor" orientation="portrait"> <table border="1"> <colgroup span="1"> <col align="left" span="1" /> </colgroup> <tbody> <tr> <td align="left" rowspan="1" colspan="1">Preclinical Research</td> </tr> </tbody> </table> </table-wrap> </p> <p> <italic>N</italic>‐methyl‐D‐aspartate (NMDA) receptor antagonists, such as ketamine, have emerged as novel candidate treatments for major depressive disorder, but abuse potential of these agents is a concern. The NMDA antagonist phencyclidine has known abuse liability but undefined efficacy as an antidepressant. To further evaluate the relationship between antidepressant‐like and abuse‐related effects of NMDA antagonists, this study evaluated the effects of phencyclidine (1.0–10.0 mg/kg) in male Sprague‐Dawley rats responding under two procedures that have been used to assess antidepressant‐like effects (differential‐reinforcement‐of‐low‐rate [DRL] 72 s schedule of food reinforcement; <italic>n</italic> = 9) and abuse‐related drug effects (intracranial self‐stimulation [ICSS]; <italic>n</italic> = 6). Under the DRL 72 s schedule, phencyclidine (10.0 mg/kg) increased reinforcers and decreased responses without shifting the peak location of the interresponse time (IRT) distribution. Ketamine (10.0 mg/kg) also increased reinforcers and decreased responses, but unlike phencyclidine, it produced a rightward shift in the peak location of the IRT distribution. The 10.0 mg/kg phencyclidine dose that decreased DRL 72 s responding also decreased rates of ICSS for 50 min after its administration; however, abuse‐related ICSS facilitation was observed at later times (100–300 min) or after a lower phencyclidine dose (3.2 mg/kg). These results suggest that phencyclidine produces weaker antidepressant‐like effects, but stronger abuse‐related effects than ketamine in these procedures.</p> </abstract> … (more)
- Is Part Of:
- Drug development research. Volume 75:Issue 8(2014)
- Journal:
- Drug development research
- Issue:
- Volume 75:Issue 8(2014)
- Issue Display:
- Volume 75, Issue 8 (2014)
- Year:
- 2014
- Volume:
- 75
- Issue:
- 8
- Issue Sort Value:
- 2014-0075-0008-0000
- Page Start:
- 479
- Page End:
- 488
- Publication Date:
- 2014-10-15
- Subjects:
- Drug development -- Periodicals
Drugs -- Research -- Periodicals
615.19 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1098-2299 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/ddr.21228 ↗
- Languages:
- English
- ISSNs:
- 0272-4391
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3629.119000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 4272.xml