Your browser doesn't support javascript.
loading
KU32 prevents 5-fluorouracil induced cognitive impairment.
Sofis, Michael J; Jarmolowicz, David P; Kaplan, Sam V; Gehringer, Rachel C; Lemley, Shea M; Garg, Gaurav; Blagg, Brian S; Johnson, Michael A.
Affiliation
  • Sofis MJ; Department of Applied Behavioral Science, University of Kansas, 4041 Dole Developmental Center, 1000 Sunnyside Ave., Lawrence, KS 66045, USA. Electronic address: sofis@ku.edu.
  • Jarmolowicz DP; Department of Applied Behavioral Science, University of Kansas, 4041 Dole Developmental Center, 1000 Sunnyside Ave., Lawrence, KS 66045, USA. Electronic address: dpj@ku.edu.
  • Kaplan SV; Department of Chemistry, University of Kansas, 2919 Malott Hall, 1251 Wescoe Hall Dr., Lawrence, KS 66045, USA.
  • Gehringer RC; Department of Chemistry, University of Kansas, 2919 Malott Hall, 1251 Wescoe Hall Dr., Lawrence, KS 66045, USA.
  • Lemley SM; Department of Applied Behavioral Science, University of Kansas, 4041 Dole Developmental Center, 1000 Sunnyside Ave., Lawrence, KS 66045, USA.
  • Garg G; Department of Medicinal Chemistry, University of Kansas, 4070 Malott Hall, 1251 Wescoe Hall Dr., Lawrence, KS 66045, USA.
  • Blagg BS; Department of Medicinal Chemistry, University of Kansas, 4070 Malott Hall, 1251 Wescoe Hall Dr., Lawrence, KS 66045, USA.
  • Johnson MA; Department of Chemistry, University of Kansas, 2919 Malott Hall, 1251 Wescoe Hall Dr., Lawrence, KS 66045, USA.
Behav Brain Res ; 329: 186-190, 2017 06 30.
Article in En | MEDLINE | ID: mdl-28359881
ABSTRACT
Chemotherapy induced cognitive impairment (i.e. chemobrain) involves acute and long-term deficits in memory, executive function, and processing speed. Animal studies investigating these cognitive deficits have had mixed results, potentially due to variability in the complexity of behavioral tasks across experiments. Further, common chemotherapy treatments such as 5-fluorouracil (5-FU) break down myelin integrity corresponding to hippocampal neurodegenerative deficits and mitochondrial dysfunction. There is little evidence, however, of pharmacological treatments that may target mitochondrial dysfunction. Using a differential reinforcement of low rates (DRL) task combining spatial and temporal components, the current study evaluated the preventative effects of the pharmacological agent KU32 on the behavior of rats treated with 5-FU (5-FU+Saline vs. 5FU+KU32). DRL performance was analyzed the day after the first set of injections (D1), the day after the second set of injections (D7) and the last day of the experiment (D14). The 5FU+KU32 group earned significantly more reinforcers on the DRL task at D7 and D14 than the 5FU+Saline group. Further, the 5FU+KU32 group showed significantly better temporal discrimination. The 5FU+KU32 showed within-group improvement in temporal discrimination from D7 to D14. No significant differences were observed in spatial discrimination, however, those in the 5FU+Saline group responded more frequently on T3 compared to the 5FU+KU32 group, highlighting temporal discrimination differences between groups. The current data suggest that KU32 shows promise in the prevention of chemotherapy induced impairments in temporal discrimination.
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Novobiocin / Cognition Disorders / Neuroprotective Agents / Fluorouracil / Immunosuppressive Agents Type of study: Prognostic_studies Limits: Animals Language: En Journal: Behav Brain Res Year: 2017 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Novobiocin / Cognition Disorders / Neuroprotective Agents / Fluorouracil / Immunosuppressive Agents Type of study: Prognostic_studies Limits: Animals Language: En Journal: Behav Brain Res Year: 2017 Document type: Article
...