Chronic Antipsychotic Treatment Modulates Aromatase (CYP19A1) Expression in the Male Rat Brain

被引:6
作者
Bogus, Katarzyna [1 ]
Palasz, Artur [1 ]
Suszka-Switek, Aleksandra [1 ]
Worthington, John J. [2 ]
Krzystanek, Marek [3 ]
Wiaderkiewicz, Ryszard [1 ]
机构
[1] Med Univ Silesia, Sch Med Katowice, Dept Histol, Ul Medykow St 18, PL-40752 Katowice, Poland
[2] Univ Lancaster, Fac Hlth & Med, Div Biomed & Life Sci, Lancaster LA1 4YQ, England
[3] Med Univ Silesia, Sch Med Katowice, Dept & Clin Psychiat Rehabil, Ul Ziolowa 45-47, PL-40635 Katowice, Poland
关键词
Aromatase; Brain; Olanzapine; Clozapine; Neuroleptics; LONG-TERM TREATMENT; NEUROACTIVE STEROIDS; SYNAPTIC PLASTICITY; PREFRONTAL CORTEX; HALOPERIDOL; INHIBITION; CLOZAPINE; METABOLISM; NEUROSTEROIDS; GLUTAMATE;
D O I
10.1007/s12031-019-01307-x
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Antipsychotic drugs, known as the antagonists of dopaminergic receptors, may also affect a large spectrum of other molecular signaling pathways in the brain. Despite the numerous ongoing studies on neurosteroid action and regulation, there are no reports regarding the influence of extended treatment with typical and atypical neuroleptics on brain aromatase (CYP19A1) expression. In the present study, we assessed for the first time aromatase mRNA and protein levels in the brain of rats chronically (28days) treated with olanzapine, clozapine, and haloperidol using quantitative real-time PCR, end-point RT-PCR, and Western blotting. Both clozapine and haloperidol, but not olanzapine treatment, led to an increase of aromatase mRNA expression in the rat brain. On the other hand, aromatase protein level remained unchanged after drug administration. These results cast a new light on the pharmacology of examined antipsychotics and contribute to a better understanding of the mechanisms responsible for their action. The present report also underlines the complex nature of potential interactions between neuroleptic pharmacological effects and physiology of brain neurosteroid pathways.
引用
收藏
页码:311 / 317
页数:7
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