HUN-REN-SZTE Neuroscience Research Group, Hungarian Research Network, University of Szeged, Danube Neuroscience Research Laboratory, Tisza Lajos krt. 113, H-6725 Szeged, Hungary.
Institute of Pharmaceutical Chemistry and HUN-REN-SZTE Stereochemistry Research Group, University of Szeged, Eötvös u. 6, H-6720 Szeged, Hungary.
Int J Mol Sci. 2024 Mar 16;25(6):3394. doi: 10.3390/ijms25063394.
The central nervous system (CNS) is the final frontier in drug delivery because of the blood-brain barrier (BBB), which poses significant barriers to the access of most drugs to their targets. Kynurenic acid (KYNA), a tryptophan (Trp) metabolite, plays an important role in behavioral functions, and abnormal KYNA levels have been observed in neuropsychiatric conditions. The current challenge lies in delivering KYNA to the CNS owing to its polar side chain. Recently, C-3 side chain-modified KYNA analogs have been shown to cross the BBB; however, it is unclear whether they retain the biological functions of the parent molecule. This study examined the impact of KYNA analogs, specifically, SZR-72, SZR-104, and the newly developed SZRG-21, on behavior. The analogs were administered intracerebroventricularly (i.c.v.), and their effects on the motor domain were compared with those of KYNA. Specifically, open-field (OF) and rotarod (RR) tests were employed to assess motor activity and skills. SZR-104 increased horizontal exploratory activity in the OF test at a dose of 0.04 μmol/4 μL, while SZR-72 decreased vertical activity at doses of 0.04 and 0.1 μmol/4 μL. In the RR test, however, neither KYNA nor its analogs showed any significant differences in motor skills at either dose. Side chain modification affects affective motor performance and exploratory behavior, as the results show for the first time. In this study, we showed that KYNA analogs alter emotional components such as motor-associated curiosity and emotions. Consequently, drug design necessitates the development of precise strategies to traverse the BBB while paying close attention to modifications in their effects on behavior.
中枢神经系统(CNS)是药物输送的最后一个前沿领域,因为血脑屏障(BBB)对大多数药物到达其靶点构成了重大障碍。犬尿酸(KYNA)是色氨酸(Trp)的代谢产物,在行为功能中发挥着重要作用,并且在神经精神疾病中观察到异常的 KYNA 水平。当前的挑战在于由于其极性侧链,将 KYNA 递送到 CNS。最近,已经表明 C-3 侧链修饰的 KYNA 类似物可以穿过 BBB;然而,尚不清楚它们是否保留了母体分子的生物学功能。本研究检查了 KYNA 类似物,特别是 SZR-72、SZR-104 和新开发的 SZRG-21,对行为的影响。类似物通过脑室内(i.c.v.)给药,并将其对运动域的影响与 KYNA 进行了比较。具体来说,使用开放式场(OF)和旋转轮(RR)测试来评估运动活动和技能。SZR-104 在 0.04 μmol/4 μL 剂量下增加了 OF 测试中的水平探索性活动,而 SZR-72 在 0.04 和 0.1 μmol/4 μL 剂量下降低了垂直活动。然而,在 RR 测试中,KYNA 及其类似物在任何剂量下均未显示出运动技能的任何显着差异。侧链修饰会影响情感运动表现和探索行为,这是首次表明。在这项研究中,我们表明 KYNA 类似物改变了与运动相关的好奇心和情绪等情感成分。因此,药物设计需要制定精确的策略来穿越 BBB,同时密切注意其对行为的影响的修饰。