Department of Neurobiology, Maj Institute of Pharmacology, Polish Academy of Sciences, 12 Smętna Street, 31-343 Kraków, Poland.
Department of Medical Laboratory Diagnostics-Fahrenheit Biobank BBMRI.pl, Medical University of Gdańsk, 7 Dębinki Street, 80-211 Gdańsk, Poland.
Int J Mol Sci. 2021 Nov 13;22(22):12282. doi: 10.3390/ijms222212282.
MK-801, an NMDA receptor antagonist, and scopolamine, a cholinergic receptor blocker, are widely used as tool compounds to induce learning and memory deficits in animal models to study schizophrenia or Alzheimer-type dementia (AD), respectively. Memory impairments are observed after either acute or chronic administration of either compound. The present experiments were performed to study the nitric oxide (NO)-related mechanisms underlying memory dysfunction induced by acute or chronic (14 days) administration of MK-801 (0.3 mg/kg, i.p.) or scopolamine (1 mg/kg, i.p.). The levels of L-arginine and its derivatives, L-citrulline, L-glutamate, L-glutamine and L-ornithine, were measured. The expression of constitutive nitric oxide synthases (cNOS), dimethylaminohydrolase (DDAH1) and protein arginine N-methyltransferases (PMRTs) 1 and 5 was evaluated, and the impact of the studied tool compounds on cGMP production and NMDA receptors was measured. The studies were performed in both the cortex and hippocampus of mice. S-nitrosylation of selected proteins, such as GLT-1, APP and tau, was also investigated. Our results indicate that the availability of L-arginine decreased after chronic administration of MK-801 or scopolamine, as both the amino acid itself as well as its level in proportion to its derivatives (SDMA and NMMA) were decreased. Additionally, among all three methylamines, SDMA was the most abundant in the brain (~70%). Administration of either compound impaired eNOS-derived NO production, increasing the monomer levels, and had no significant impact on nNOS. Both compounds elevated DDAH1 expression, and slight decreases in PMRT1 and PMRT5 in the cortex after scopolamine (acute) and MK-801 (chronic) administration were observed in the PFC, respectively. Administration of MK-801 induced a decrease in the cGMP level in the hippocampus, accompanied by decreased NMDA expression, while increased cGMP production and decreased NMDA receptor expression were observed after scopolamine administration. Chronic MK-801 and scopolamine administration affected S-nitrosylation of GLT-1 transport protein. Our results indicate that the analyzed tool compounds used in pharmacological models of schizophrenia or AD induce changes in NO-related pathways in the brain structures involved in cognition. To some extent, the changes resemble those observed in human samples.
MK-801 是一种 NMDA 受体拮抗剂,东莨菪碱是一种胆碱能受体阻滞剂,它们被广泛用作工具化合物,以诱导动物模型中的学习和记忆缺陷,分别用于研究精神分裂症或阿尔茨海默病(AD)。无论是急性还是慢性给药,这两种化合物都会导致记忆损伤。本实验旨在研究急性或慢性(14 天)给予 MK-801(0.3mg/kg,ip)或东莨菪碱(1mg/kg,ip)引起的记忆功能障碍与一氧化氮(NO)相关的机制。测量了 L-精氨酸及其衍生物 L-瓜氨酸、L-谷氨酸、L-谷氨酰胺和 L-鸟氨酸的水平。评估了组成型一氧化氮合酶(cNOS)、二甲基氨基水解酶(DDAH1)和蛋白精氨酸 N-甲基转移酶(PMRTs)1 和 5 的表达,并测量了研究工具化合物对 cGMP 产生和 NMDA 受体的影响。研究在小鼠的皮质和海马中进行。还研究了选定蛋白质(如 GLT-1、APP 和 tau)的 S-亚硝基化。我们的结果表明,慢性给予 MK-801 或东莨菪碱后,L-精氨酸的可用性降低,因为氨基酸本身及其与衍生物(SDMA 和 NMMA)的比例均降低。此外,在所有三种甲基胺中,SDMA 在大脑中含量最丰富(约 70%)。两种化合物均损害 eNOS 衍生的 NO 产生,增加单体水平,对 nNOS 无显著影响。两种化合物均增加 DDAH1 的表达,在 PFC 中,急性给予东莨菪碱后观察到皮质中 PMRT1 和 PMRT5 的表达略有下降,慢性给予 MK-801 后则观察到 PMRT5 的表达略有下降。MK-801 给药导致海马中环磷酸鸟苷水平降低,同时 NMDA 表达减少,而东莨菪碱给药后则导致环磷酸鸟苷生成增加和 NMDA 受体表达减少。慢性 MK-801 和东莨菪碱给药影响 GLT-1 转运蛋白的 S-亚硝基化。我们的结果表明,用于精神分裂症或 AD 药理学模型的分析工具化合物在参与认知的脑结构中引起与 NO 相关的途径变化。在某种程度上,这些变化类似于在人类样本中观察到的变化。