The effect of phencyclidine-mediated blockade of NMDA receptors in the early postnatal period on glutathione and sulfur amino acid levels in the rat brain as a potential causative factor of schizophrenia-like behavior in adulthood.

IF 3.6 3区 医学 Q2 PHARMACOLOGY & PHARMACY
Pharmacological Reports Pub Date : 2024-08-01 Epub Date: 2024-06-21 DOI:10.1007/s43440-024-00607-3
Elżbieta Lorenc-Koci, Magdalena Górny, Grażyna Chwatko, Kinga Kamińska, Małgorzata Iciek, Zofia Rogóż
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引用次数: 0

Abstract

Background: Phencyclidine, an NMDA receptor antagonist, is frequently used to model behavioral and neurochemical changes correlated with schizophrenia in laboratory animals. The present study aimed to examine the effects of repeated administration of phencyclidine during early postnatal development on the contents of glutathione and sulfur-containing amino acids, as well as the activity of antioxidant enzymes in the brain of 12-day-old rats, and schizophrenia-like symptoms in adulthood.

Methods: Male Sprague-Dawley pups were administered phencyclidine (10 mg/kg) or saline subcutaneously on the postnatal days p2, p6, p9 and p12. In 12-day-old pups, 4 h after the last dose of phencyclidine, the levels of glutathione, cysteine, methionine, and homocysteine, and the enzymatic activity of superoxide dismutase (SOD), glutathione peroxidase (GPx), and glutathione reductase (GR) were measured in the frontal cortex, hippocampus, and striatum. In 70-72-day-old rats, schizophrenia-like symptoms were assessed using behavioral tests.

Results: Biochemical data showed that perinatal phencyclidine treatment significantly reduced glutathione and cysteine levels in all brain structures studied, methionine was diminished in the striatum, and homocysteine in both the frontal cortex and striatum. GR activity was increased in the frontal cortex while SODactivity was decreased in the hippocampus. Behaviorally, perinatal phencyclidine induced long-term deficits in social and cognitive function and a decrease in locomotor activity assessed as the time of walking. Finally, perinatal treatment with phencyclidine resulted in a significant reduction in body weight gain over time.

Conclusion: Our research provides further evidence for the usefulness of the phencyclidine-induced neurodevelopmental model of schizophrenia for studying the pathogenesis of schizophrenia.

Abstract Image

出生后早期苯环利定介导的 NMDA 受体阻断对大鼠脑内谷胱甘肽和硫氨基酸水平的影响是成年期精神分裂症样行为的潜在致病因素。
背景:苯环利定是一种NMDA受体拮抗剂,常用于模拟与精神分裂症相关的实验动物行为和神经化学变化。本研究旨在探讨在出生后早期发育过程中反复给予苯环利定对 12 日龄大鼠脑内谷胱甘肽和含硫氨基酸含量以及抗氧化酶活性的影响,以及对成年后精神分裂症样症状的影响:方法:在出生后第 2、6、9 和 12 天,给雄性 Sprague-Dawley 幼鼠皮下注射苯环利定(10 毫克/千克)或生理盐水。在给 12 天大的幼鼠注射最后一剂苯环利定 4 小时后,测量额叶皮层、海马和纹状体中谷胱甘肽、半胱氨酸、蛋氨酸和同型半胱氨酸的水平,以及超氧化物歧化酶(SOD)、谷胱甘肽过氧化物酶(GPx)和谷胱甘肽还原酶(GR)的酶活性。对 70-72 天大的大鼠进行行为测试,评估其精神分裂症样症状:生化数据显示,围产期苯环利定治疗会显著降低所有研究脑结构中的谷胱甘肽和半胱氨酸水平,减少纹状体中的蛋氨酸,以及额叶皮层和纹状体中的同型半胱氨酸。额叶皮质的 GR 活性增加,而海马的 SOD 活性降低。在行为方面,围产期苯环利定会诱发社交和认知功能的长期缺陷,以及以步行时间评估的运动活动的减少。最后,围产期使用苯环利定治疗会导致体重随时间的推移显著减少:我们的研究进一步证明了苯环利定诱导的精神分裂症神经发育模型在研究精神分裂症发病机制方面的实用性。
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来源期刊
Pharmacological Reports
Pharmacological Reports 医学-药学
CiteScore
8.40
自引率
0.00%
发文量
91
审稿时长
6 months
期刊介绍: Pharmacological Reports publishes articles concerning all aspects of pharmacology, dealing with the action of drugs at a cellular and molecular level, and papers on the relationship between molecular structure and biological activity as well as reports on compounds with well-defined chemical structures. Pharmacological Reports is an open forum to disseminate recent developments in: pharmacology, behavioural brain research, evidence-based complementary biochemical pharmacology, medicinal chemistry and biochemistry, drug discovery, neuro-psychopharmacology and biological psychiatry, neuroscience and neuropharmacology, cellular and molecular neuroscience, molecular biology, cell biology, toxicology. Studies of plant extracts are not suitable for Pharmacological Reports.
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