Prenatal MAM exposure raises kynurenic acid levels in the prefrontal cortex of adult rats.

IF 3.6 3区 医学 Q2 PHARMACOLOGY & PHARMACY
Pharmacological Reports Pub Date : 2024-08-01 Epub Date: 2024-05-24 DOI:10.1007/s43440-024-00604-6
Francesca Frescura, Tibor Stark, Edoardo Tiziani, Serena Di Martino, Jana Ruda-Kucerova, Filippo Drago, Luca Ferraro, Vincenzo Micale, Sarah Beggiato
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引用次数: 0

Abstract

Background: Elevated brain levels of kynurenic acid (KYNA), a metabolite in the kynurenine pathway, are associated with cognitive dysfunctions, which are nowadays often considered as fundamental characteristics of several psychopathologies; however, the role of KYNA in mental illnesses, such as schizophrenia, is not fully elucidated. This study aimed to assess KYNA levels in the prefrontal cortex (PFC) of rats prenatally treated with methylazoxymethanol (MAM) acetate, i.e., a well-validated neurodevelopmental animal model of schizophrenia. The effects of an early pharmacological modulation of the endogenous cannabinoid system were also evaluated.

Methods: Pregnant Sprague-Dawley rats were treated with MAM (22 mg/kg, ip) or its vehicle at gestational day 17. Male offspring were treated with the cannabinoid CB1 receptor antagonist/inverse agonist AM251 (0.5 mg/kg/day, ip) or with the typical antipsychotic haloperidol (0.6 mg/kg/day, ip) from postnatal day (PND) 19 to PND39. The locomotor activity and cognitive performance were assessed in the novel object recognition test and the open field test in adulthood. KYNA levels in the PFC of prenatally MAM-treated rats were also assessed.

Results: A significant cognitive impairment was observed in prenatally MAM-treated rats (p < 0.01), which was associated with enhanced PFC KYNA levels (p < 0.05). The peripubertal AM251, but not haloperidol, treatment ameliorated the cognitive deficit (p < 0.05), by normalizing the PFC KYNA content in MAM rats.

Conclusions: The present findings suggest that the cognitive deficit observed in MAM rats may be related to enhanced PFC KYNA levels which could be, in turn, mediated by the activation of cannabinoid CB1 receptor. These results further support the modulation of brain KYNA levels as a potential therapeutic strategy to ameliorate the cognitive dysfunctions in schizophrenia.

Abstract Image

产前接触 MAM 会提高成年大鼠前额叶皮层中的犬尿氨酸水平。
背景:犬尿氨酸(KYNA)是犬尿氨酸途径中的一种代谢产物,其脑水平的升高与认知功能障碍有关,而认知功能障碍如今通常被认为是几种精神病理学的基本特征;然而,KYNA在精神疾病(如精神分裂症)中的作用尚未完全阐明。本研究旨在评估经醋酸甲唑甲醇(MAM)产前处理的大鼠前额叶皮层(PFC)中的 KYNA 水平,醋酸甲唑甲醇是一种经过验证的精神分裂症神经发育动物模型。此外,还评估了早期药理调节内源性大麻素系统的效果:方法:在妊娠第 17 天对妊娠 Sprague-Dawley 大鼠进行 MAM(22 毫克/千克,ip)或其药物治疗。从出生后第 19 天到出生后第 39 天,雄性后代接受大麻素 CB1 受体拮抗剂/逆激动剂 AM251(0.5 毫克/千克/天,ip)或典型抗精神病药物氟哌啶醇(0.6 毫克/千克/天,ip)治疗。成年后对运动活动和认知能力进行了评估,包括新物体识别测试和开阔地测试。此外,还评估了产前服用MAM的大鼠PFC中的KYNA水平:结果:经产前 MAM 处理的大鼠出现了明显的认知障碍(p 结论:经产前 MAM 处理的大鼠在成年后出现了认知障碍:本研究结果表明,在 MAM 大鼠身上观察到的认知缺陷可能与 PFC KYNA 水平升高有关,而 PFC KYNA 水平升高又可能是通过激活大麻素 CB1 受体介导的。这些结果进一步支持将调节大脑 KYNA 水平作为改善精神分裂症认知功能障碍的一种潜在治疗策略。
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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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