Bio-behavioural changes in treatment-resistant socially isolated FSL rats show variable or improved response to combined fluoxetine-olanzapine versus olanzapine treatment.

Journal: IBRO neuroscience reports

Volume: 13

Issue: 

Year of Publication: 

Affiliated Institutions:  Centre of Excellence for Pharmaceutical Sciences (PharmaCen), Division of Pharmacology, School of Pharmacy, North-West University (Potchefstroom Campus), South Africa.

Abstract summary 

Exposure of Flinders Sensitive Line (FSL) rats to post-weaning social isolation rearing (SIR) causes depressive- and social anxiety-like symptoms resistant to, or worsened by, fluoxetine. SIR typically presents with psychotic-like symptoms, while the paradoxical response to fluoxetine suggests unaddressed psychotic-like manifestations. Psychotic depression (MDpsy) is invariably treatment resistant. To further explore the mood-psychosis continuum in fluoxetine resistant FSL-SIR rats (Mncube et al., 2021), mood-, psychotic-, anxiety-, and social-related behaviour and biomarker response to antidepressant/antipsychotic treatment was studied in FSL-SIR rats. Methods: Sprague Dawley (SD) and FSL pups were subjected to social rearing or SIR from postnatal day (PND) 21. Thereafter FSL-SIR rats received olanzapine (5 mg/kg x 14 days) or olanzapine+fluoxetine (OLZ+FLX; 5 mg/kg + 10 mg/kg for 14 days) from PND 63. Psychotic-like, depressive, anxiety, and social behaviour were assessed from PND 72, versus saline-treated FSL-SIR rats, using the prepulse inhibition (PPI), forced swim, open field and social interaction tests. Post-mortem cortico-hippocampal norepinephrine (NE), serotonin (5-HT), and dopamine (DA), as well as plasma corticosterone and dopamine-beta-hydroxylase levels were evaluated. Results: SD-SIR and FSL-SIR rats present with significant depressive-like behaviour ( < 0.01) as well as significantly reduced sensorimotor gating ( < 0.01), although exacerbation versus SIR alone was not observed. Anxiety was significant in FSL-SIR ( < 0.01) but not SD-SIR rats. No deficit in social behaviour was evident. Cortico-hippocampal monoamines (NE, 5-HT, DA;  < .05) and dopamine beta hydroxylase ( = 1.13) were reduced in FSL-SIR rats, less so in SD-SIR rats. Except for dopamine-beta-hydroxylase, these deficits were reversed by both olanzapine and OLZ+FLX ( < 0.01). OLZ+FLX was superior to reverse hipocampal NE and DA changes ( < 0.01). However, OLZ (p < .05) and OLZ+FLX (p < .01) worsened depressive-like behaviour and failed to reverse PPI deficits in FSL-SIR rats.SIR-exposed FSL rats display worsened anxiety, as well as depressive and psychotic-like symptoms, variably responsive to olanzapine or OLZ+FLX. Depleted monoamines are reversed by OLZ+FLX, less so by olanzapine. FSL-SIR rats show promising face and construct but limited predictive validity for MDpsy, perhaps more relevant for bipolar disorder.

Authors & Co-authors:  Mncube K K Harvey B H BH

Study Outcome 

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Citations :  Rush A.J., Fava M., Wisniewski S.R., Lavori P.W., Trivedi M.H., Sackeim H.A., et al. Sequenced treatment alternatives to relieve depression (STAR*D): rationale and design. Control. Clin. Trials. 2004;25(1):119–142. doi: 10.1016/s0197-2456(03)00112-0.
Authors :  2
Identifiers
Doi : 10.1016/j.ibneur.2022.08.009
SSN : 2667-2421
Study Population
Male,Female
Mesh Terms
Other Terms
5-HT, serotonin;Animal model;Bipolar disorder, dual hit;DA, dopamine;FSL, Flinders Sensitive Line;Fluoxetine plus olanzapine;Inflammation;NE, norepinephrine;OLZ+FLX, olanzapine plus fluoxetine co-therapy;PPI, prepulse inhibition;Psychotic depression;SAL, saline;SD, Sprague-Dawley;SIR, social isolation rearing;SOC, socially-reared;Social anxiety
Study Design
Cross Sectional Study
Study Approach
Country of Study
Publication Country
Netherlands