PMID- 23873577 OWN - NLM STAT- MEDLINE DCOM- 20141105 LR - 20211021 IS - 1476-3524 (Electronic) IS - 1029-8428 (Linking) VI - 25 IP - 3 DP - 2014 Apr TI - Foraging activity is reduced in a mouse model of depression. PG - 235-47 LID - 10.1007/s12640-013-9411-6 [doi] AB - Depression interferes with the human ability to make decisions. Multiple criteria have been adopted for the diagnosis of depression in humans, but no clear indicators are available in animal models to reflect the depressive mood, involving higher cognitive functions. The act of foraging is a species-specific behaviour which is believed to involve the decision-making and higher cognitive functions. We previously established a method to detect the foraging behaviour of rodents, in which our results demonstrated that NMDA and dopamine receptors were involved. Conversely, increased NMDA receptors and reduced dopamine have been reported in depression model rodents. However, we hypothesise that foraging activities may also be impaired in depression. To test the theory, we successfully established a mouse model of depression using the chronic unpredictable mild stress (CUMS) paradigm. Most interestingly, the food foraging activity of mice after CUMS was significantly reduced. In addition, the treatment of anti-depressant fluoxetine reversed most depressive symptoms and reduced glial fibrillary associated protein (GFAP) expression in the hippocampus, but was less effective in the reduction of foraging activities. However, clozapine reversed all symptoms of CUMS-exposed mice including reduction of GFAP expression in the hippocampus and impaired foraging activity. Our findings of GFAP expression as a marker to validate the CUMS protocol provide further validation of our hypothesis, that the reduced food foraging is probably a new behavioural finding of depression in which the serotoninergic system could not be singly involved. Our study suggests that NMDA receptors, serotoninergic and dopaminergic systems are differentially involved in these food foraging behaviours. Our data suggest that the foraging test in rodents can be a useful tool to assess the ability of decision-making in depression. FAU - Yang, C R AU - Yang CR AD - Yunnan Key Laboratory of Regenerative Medicine and Stem Cells, Institute of Molecular and Clinical Medicine, Kunming Medical University, Kunming, Yunnan, People's Republic of China. FAU - Zhang, Z G AU - Zhang ZG FAU - Bai, Y Y AU - Bai YY FAU - Zhou, H Fiona AU - Zhou HF FAU - Zhou, L AU - Zhou L FAU - Ruan, C S AU - Ruan CS FAU - Li, F AU - Li F FAU - Li, C Q AU - Li CQ FAU - Zheng, H Y AU - Zheng HY FAU - Shen, L J AU - Shen LJ FAU - Zhou, X F AU - Zhou XF LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't DEP - 20130720 PL - United States TA - Neurotox Res JT - Neurotoxicity research JID - 100929017 RN - 0 (Antidepressive Agents) RN - 0 (Glial Fibrillary Acidic Protein) RN - 0 (RNA, Messenger) RN - 01K63SUP8D (Fluoxetine) RN - J60AR2IKIC (Clozapine) SB - IM MH - Animals MH - Antidepressive Agents/*pharmacology MH - *Appetitive Behavior/drug effects MH - Body Weight MH - Cerebral Cortex/drug effects/metabolism MH - Chronic Disease MH - Clozapine/*pharmacology MH - Depressive Disorder/drug therapy/*metabolism MH - Disease Models, Animal MH - Exploratory Behavior/drug effects/physiology MH - Feeding Behavior/drug effects/physiology MH - Fluoxetine/*pharmacology MH - Freezing Reaction, Cataleptic/drug effects/physiology MH - Glial Fibrillary Acidic Protein/metabolism MH - Hippocampus/drug effects/metabolism MH - Male MH - Mice MH - Mice, Inbred C57BL MH - RNA, Messenger/genetics/metabolism MH - Stress, Psychological EDAT- 2013/07/23 06:00 MHDA- 2014/11/06 06:00 CRDT- 2013/07/23 06:00 PHST- 2013/04/22 00:00 [received] PHST- 2013/06/28 00:00 [accepted] PHST- 2013/06/26 00:00 [revised] PHST- 2013/07/23 06:00 [entrez] PHST- 2013/07/23 06:00 [pubmed] PHST- 2014/11/06 06:00 [medline] AID - 10.1007/s12640-013-9411-6 [doi] PST - ppublish SO - Neurotox Res. 2014 Apr;25(3):235-47. doi: 10.1007/s12640-013-9411-6. Epub 2013 Jul 20.