对具有显著情绪调节活性的 1,3-二甲基嘌呤-2,6-二酮衍生物(GR-14)进行大鼠高级药理学和药代动力学评估。

IF 3.6 3区 医学 Q2 PHARMACOLOGY & PHARMACY Pharmacological Reports Pub Date : 2025-02-01 Epub Date: 2024-12-16 DOI:10.1007/s43440-024-00686-2
Agnieszka Cios, Grażyna Chłoń-Rzepa, Magdalena Jastrzębska-Więsek, Krzysztof Pociecha, Katarzyna Wójcik-Pszczoła, Elżbieta Pękala, Anna Wesołowska
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引用次数: 0

摘要

背景:从以1,3-二甲基嘌呤-2,6-二酮为末端酰胺片段的长链芳基哌嗪(LCAPs)基团中寻找抗抑郁/抗焦虑药物的新候选物符合现代探索的趋势。本研究首次在雄性Wistar大鼠中研究了7-(5-(4-(3-氯苯基)哌嗪-1-基)戊基)-1,3-二甲基-3,7-二氢-1 h -嘌呤-2,6-二酮盐酸(GR-14)的药效学(抗抑郁和抗焦虑样)和药代动力学特性。方法:分别用强迫游泳试验(FST)和Vogel冲突饮酒试验评估抗抑郁药和焦虑样活动。确定了GR-14的药代动力学特征、在大鼠组织中的分布以及ADME-Tox的几个体外参数(肝细胞毒性、神经细胞毒性、代谢稳定性)。结果:GR-14在使用的两种测试中产生强烈的剂量依赖性抗抑郁药和抗焦虑药样作用。药代动力学结果表明,GR-14在静脉注射(iv)后呈线性药代动力学,口服(po)后迅速吸收。它迅速穿过血脑屏障(BBB),这对精神疾病、抑郁症和焦虑症的体内治疗效果至关重要。此外,它会慢慢地从大脑中消失,维持比上次测量时血浆中的浓度更高的浓度。进一步的研究也表明,GR-14在大鼠肝微粒体中是一种平均高清除率的药物,在体外不产生肝细胞毒性和神经细胞毒性作用。结论:所测衍生物GR-14在大鼠体内具有明显的情绪调节活性,具有良好的药动学参数和安全性。GR-14在体内的有益药理学和药代动力学与其在体外的情况高度一致,因此强调了非常有希望支持早期发育过程的特性。
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Advanced pharmacological and pharmacokinetic evaluation of 1,3 dimethylpurine-2,6-dione derivative (GR-14) with prominent mood-modulating activity in rats.

Background: Research on new candidates for antidepressant/anxiolytic drugs from the long-chain arylpiperazines (LCAPs) group containing a 1,3-dimethylpurine-2,6-dione as a terminal amide fragment fits into the modern exploration trend. This study aimed to examine, for the first time in male Wistar rats, pharmacodynamic (antidepressant- and anxiolytic-like) and pharmacokinetic properties of 7-(5-(4-(3-chlorophenyl)piperazin-1-yl)pentyl)-1,3-dimethyl-3,7-dihydro-1 H-purine-2,6-dione hydrochloride (GR-14).

Methods: Antidepressant- and anxiolytic-like activities have been assessed in the forced swim test (FST) and Vogel conflict drinking test, respectively. The pharmacokinetic characteristics of GR-14, its distribution into rat tissues, and several in vitro ADME-Tox parameters (hepatocytotoxic, neurocytotoxic, metabolic stability) have been defined.

Results: GR-14 produces strong and dose-dependent antidepressant- and anxiolytic-like effects in both tests used. Pharmacokinetic findings demonstrate that GR-14 reveals linear pharmacokinetics tested after intravenous (iv) and was rapidly absorbed after oral (po) administration. It rapidly crosses the blood-brain barrier (BBB) which is vital for therapeutic effects in vivo in psychiatric diseases, depression, and anxiety. Moreover, it is slowly eliminated from the brain, maintaining concentrations higher than those in plasma at the last time point measured. Further studies have also shown that GR-14 is an average high-clearance drug in rat liver microsomes and exerts neither hepatocytotoxic nor neurocytotoxic effects in vitro.

Conclusion: The tested derivative GR-14 presents prominent mood-modulating activity in rats and has promising pharmacokinetic parameters and a good safety profile. The beneficial pharmacology and pharmacokinetics of GR-14 in vivo are in high concordance with its profile in vitro, thus underlining very hopeful properties to support the early development process.

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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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