Modulatory effect of olanzapine on SMIM20/phoenixin, NPQ/spexin and NUCB2/nesfatin-1 gene expressions in the rat brainstem.

Pharmacological reports : PR Pub Date : 2021-08-01 Epub Date: 2021-04-29 DOI:10.1007/s43440-021-00267-7
Artur Pałasz, Piotr Żarczyński, Katarzyna Bogus, Kinga Mordecka-Chamera, Alessandra Della Vecchia, Jakub Skałbania, John J Worthington, Marek Krzystanek, Małgorzata Żarczyńska
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引用次数: 5

Abstract

Background: Phoenixin, spexin and nesfatin-1 belong to a family of newly discovered multifunctional neuropeptides that play regulatory roles in several brain structures and modulate the activity of important neural networks. However, little is known about their expression and action at the level of brainstem. The present work was, therefore, focused on gene expression of the aforementioned peptides in the brainstem of rats chronically treated with olanzapine, a second generation antipsychotic drug.

Methods: Studies were carried out on adult, male Sprague-Dawley rats that were divided into 2 groups: control and experimental animals treated with olanzapine (28-day-long intraperitoneal injection, at dose 5 mg/kg daily). All individuals were killed under anesthesia and the brainstem excised. Total mRNA was isolated from homogenized samples of both structures and the RT-PCR method was used for estimation of related SMIM20/phoenixin, NPQ/spexin and NUCB2/nesfatin-1 gene expression.

Results: Long-term treatment with olanzapine is reflected in qualitatively different changes in expression of examined neuropeptides mRNA in the rat brainstem. Olanzapine significantly decreased NPQ/spexin mRNA expression, but increased SMIM20/phoenixin mRNA level in the rat brainstem; while NUCB2/nesfatin-1 mRNA expression remained unchanged.

Conclusions: Olanzapine can affect novel peptidergic signaling in the rat brainstem. This may cautiously suggest the presence of an alternative mode of its action.

Abstract Image

Abstract Image

奥氮平对大鼠脑干SMIM20/phoenixin、NPQ/spexin、NUCB2/nesfatin-1基因表达的调节作用
背景:Phoenixin, spexin和nesfatin-1属于新发现的多功能神经肽家族,在多种脑结构中发挥调节作用,并调节重要神经网络的活性。然而,对它们在脑干水平上的表达和作用知之甚少。因此,目前的工作集中在长期服用第二代抗精神病药物奥氮平的大鼠脑干中上述肽的基因表达。方法:以成年雄性Sprague-Dawley大鼠为研究对象,将其分为对照组和实验动物2组,分别给予奥氮平(5 mg/kg / d)腹腔注射,持续28 d。所有人都在麻醉下死亡,脑干被切除。从两种结构的均质样品中分离总mRNA,采用RT-PCR方法估计相关SMIM20/phoenixin、NPQ/spexin和NUCB2/nesfatin-1基因的表达。结果:奥氮平长期给药后,大鼠脑干内所测神经肽mRNA表达发生了质的不同变化。奥氮平显著降低大鼠脑干NPQ/spexin mRNA表达,升高SMIM20/phoenixin mRNA表达;而NUCB2/nesfatin-1 mRNA表达不变。结论:奥氮平可影响大鼠脑干的新型肽能信号传导。这可能谨慎地暗示其作用的另一种模式的存在。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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