TY - JOUR
T1 - Repeated ketamine exposure induces an enduring resilient phenotype in adolescent and adult rats
AU - Parise, Eric M.
AU - Alcantara, Lyonna F.
AU - Warren, Brandon L.
AU - Wright, Katherine N.
AU - Hadad, Roey
AU - Sial, Omar K.
AU - Kroeck, Kyle G.
AU - Iñiguez, Sergio D.
AU - Bolaños-Guzmán, Carlos A.
N1 - Funding Information:
This work was supported by Grant Nos. R21DA022351 and R01DA026854 from the National Institute on Drug Abuse (NIDA) and the Developing Scholar Award from Florida State University to CABG. BLW was supported by a Neuroscience Fellowship from Florida State University and by Training Grant No. T32MH093311 from the National Institute of Mental Health. SDI was supported by a McKnight Fellowship from the Florida Education Fund, a Neuroscience Fellowship from Florida State University, and National Research Service Award Grant No. F31DA027300 from NIDA. KNW is currently affiliated with the Department of Biomedical Sciences and Program in Neuroscience, Florida State University, Tallahassee, Florida. SDI is currently affiliated with the Department of Psychology, California State University, San Bernardino, California.
PY - 2013/11/15
Y1 - 2013/11/15
N2 - Background Major depressive disorder afflicts up to 10% of adolescents. However, nearly 50% of those afflicted are considered nonresponsive to available treatments. Ketamine, a noncompetitive N-methyl-D-aspartate receptor antagonist has shown potential as a rapid-acting and long-lasting treatment for major depressive disorder in adults. Thus, the effectiveness and functional consequences of ketamine exposure during adolescence were explored. Methods Adolescent male rats (postnatal day [PD] 35) received two ketamine (0, 5, 10, or 20 mg/kg) injections, 4 hours apart, after exposure to day 1 of the forced swim test (FST). The next day, rats were reexposed to the FST to assess ketamine-induced antidepressant-like responses. Separate groups were exposed to chronic unpredictable stress to confirm findings from the FST. After these initial experiments, adolescent naive rats were exposed to either 1 or 15 consecutive days (PD35-49) of ketamine (20 mg/kg) twice daily. Ketamine's influence on behavioral reactivity to rewarding (i.e., sucrose preference) and aversive (i.e., elevated plus-maze, FST) circumstances was then assessed 2 months after treatment. To control for age-dependent effects, adult rats (PD75-89) were exposed to identical experimental conditions. Results Ketamine (20 mg/kg) reversed the chronic unpredictable stress-induced depression-like behaviors in the FST. Repeated ketamine exposure resulted in anxiolytic- and antidepressant-like responses 2 months after drug exposure. None of the ketamine doses used were capable of inducing drug-seeking behaviors as measured by place preference conditioning. Conclusions Repeated ketamine exposure induces enduring resilient-like responses regardless of age of exposure. These findings point to ketamine, and its repeated exposure, as a potentially useful antidepressant during adolescence.
AB - Background Major depressive disorder afflicts up to 10% of adolescents. However, nearly 50% of those afflicted are considered nonresponsive to available treatments. Ketamine, a noncompetitive N-methyl-D-aspartate receptor antagonist has shown potential as a rapid-acting and long-lasting treatment for major depressive disorder in adults. Thus, the effectiveness and functional consequences of ketamine exposure during adolescence were explored. Methods Adolescent male rats (postnatal day [PD] 35) received two ketamine (0, 5, 10, or 20 mg/kg) injections, 4 hours apart, after exposure to day 1 of the forced swim test (FST). The next day, rats were reexposed to the FST to assess ketamine-induced antidepressant-like responses. Separate groups were exposed to chronic unpredictable stress to confirm findings from the FST. After these initial experiments, adolescent naive rats were exposed to either 1 or 15 consecutive days (PD35-49) of ketamine (20 mg/kg) twice daily. Ketamine's influence on behavioral reactivity to rewarding (i.e., sucrose preference) and aversive (i.e., elevated plus-maze, FST) circumstances was then assessed 2 months after treatment. To control for age-dependent effects, adult rats (PD75-89) were exposed to identical experimental conditions. Results Ketamine (20 mg/kg) reversed the chronic unpredictable stress-induced depression-like behaviors in the FST. Repeated ketamine exposure resulted in anxiolytic- and antidepressant-like responses 2 months after drug exposure. None of the ketamine doses used were capable of inducing drug-seeking behaviors as measured by place preference conditioning. Conclusions Repeated ketamine exposure induces enduring resilient-like responses regardless of age of exposure. These findings point to ketamine, and its repeated exposure, as a potentially useful antidepressant during adolescence.
KW - Adolescence
KW - anxiety
KW - depression
KW - ketamine
KW - rats
KW - resilience
KW - stress
UR - http://www.scopus.com/inward/record.url?scp=84886722040&partnerID=8YFLogxK
U2 - 10.1016/j.biopsych.2013.04.027
DO - 10.1016/j.biopsych.2013.04.027
M3 - Article
C2 - 23790225
AN - SCOPUS:84886722040
SN - 0006-3223
VL - 74
SP - 750
EP - 759
JO - Biological Psychiatry
JF - Biological Psychiatry
IS - 10
ER -