Effects of isolation rearing and early antipsychotic intervention on oxidative stress-induced apoptosis and brain-derived neurotrophic factor in hippocampus in a rat model of schizophrenia
Autor: | Chuen-Lin Huang, Szu-Nian Yang, Yia-Ping Liu, Fang-Jung Wan, Yu-Yin Yang |
---|---|
Jazyk: | angličtina |
Rok vydání: | 2017 |
Předmět: |
0301 basic medicine
Olanzapine medicine.medical_specialty medicine.medical_treatment lcsh:Medicine medicine.disease_cause Brain-derived neurotrophic factor 03 medical and health sciences 0302 clinical medicine Neurotrophic factors Internal medicine early antipsychotic intervention medicine Hippocampus (mythology) oxidative stress isolation rearing Antipsychotic Psychiatry Risperidone business.industry lcsh:R lcsh:Medical emergencies. Critical care. Intensive care. First aid General Medicine lcsh:RC86-88.9 medicine.disease schizophrenia 030104 developmental biology Endocrinology Schizophrenia business 030217 neurology & neurosurgery Oxidative stress medicine.drug |
Zdroj: | Journal of Medical Sciences, Vol 37, Iss 4, Pp 155-162 (2017) |
ISSN: | 1011-4564 |
Popis: | Background: Oxidative stress-induced neuronal dysfunction has been considered an essential factor for the development of schizophrenia. However, a longitudinal and causal relation between the impacts of developmental stress and oxidative stress remains unsolved. The present study aimed to examine whether the oxidative stress-relevant dysfunctions of the apoptotic index can be induced in rats of isolation rearing (IR, a rodent model of schizophrenia) and to see if the intervention of antipsychotics can reverse these dysfunctions. Materials and Methods: Pharmacological manipulation (risperidone [RIS] [1 mg/kg/day], olanzapine [OLA] [2.5 mg/kg/day], or saline [SAL] vehicle) was introduced 4 weeks (adolescence) or 8 weeks (young adulthood) after IR (i.e., rats were 7- or 11-week-old). The regime of RIS, OLA, or SAL was continued for 9 weeks. Locomotor activity was employed to validate the IR effect. Rats' hippocampus immediately after sacrifice was removed to measure messenger RNA expression of Bax, Bcl-2, brain-derived neurotrophic factor (BDNF) and the plasma level of nitric oxide (NO). Results: The results showed: (i) IR rats were more hyperactive. (ii) RIS may exert anti-apoptotic effects on IR rats, particularly at their adolescent age (as indexed by increased Bcl-2 and decreased Bax/Bcl-2 ratio). (iii) The therapeutic potential of RIS can be also observed in the change of BDNF in an age-independent manner, in which RIS effectively increased the BDNF level in IR but not social (SOC) rats. (iv) Plasma NO was not altered. Conclusion: The study results support the utility of the IR paradigm in exploring mental disorders with neurodevelopmental origin in which early pharmacological intervention may provide a therapeutic benefit in the overloaded oxidative stress and the dysfunction of BDNF. |
Databáze: | OpenAIRE |
Externí odkaz: |