Boguszewska-Czubara Anna, Kurzepa Jacek, Biała Grażyna, Kaszubska Katarzyna, Grot Karolina, Tarkowski Piotr, Kowalczyk Joanna, Silvestro Serena, Faggio Caterina, Budzyńska Barbara
Department of Medicinal Chemistry, 4a Chodzki Str., Medical University of Lublin, Lublin, Poland.
Department of Pharmacology and Pharmacodynamics, 4a Chodzki Str., Medical University of Lublin, Lublin, Poland.
Curr Mol Pharmacol. 2019;12(2):115-121. doi: 10.2174/1874467212666190114154307.
The use of drugs of addiction, as mephedrone, is associated with functional neuronal disorders due to remodeling of the nervous tissue. Key enzymes in remodeling are extracellular matrix (ECM) proteases like matrix metalloproteases (MMPs). Recently, MMPs have been of great interest as some studies point to a fact that the alterations in structural remodeling of synaptic connections modify learning-dependent changes, which remain active even after a prolonged period of abstinence. This entails a continuous development of dependence.
The aim of the study was to determine the influence of subchronic exposure to three different doses of mephedrone on the activity of MMP-2 and 9 in hippocampus and prefrontal cortex and how this was correlated with memory processes in mice.
The homogenates of hippocampus and cortex were assayed for MMP-2 and MMP-9 activity by gelatin zymography. Memory consolidation processes were evaluated in the passive avoidance (PA) test.
The study confirmed the dose-dependent increase in activity of MMP-2 and -9 exerted by subchronic administration of mephedrone. Moreover, the highest dose of mephedrone attenuated consolidation of memory and learning processes.
We could hypothesize that inhibition of MMPs can be considered as a therapeutic option for the treatment of addictive behaviors associated with cognitive processes. Moreover, further studies are required to find out if elevated activities of MMPs contribute to brain damage or recovery from brain damage caused directly by mephedrone.
使用成瘾性药物,如甲麻黄碱,会因神经组织重塑而导致功能性神经元紊乱。重塑过程中的关键酶是细胞外基质(ECM)蛋白酶,如基质金属蛋白酶(MMPs)。最近,MMPs引起了极大关注,因为一些研究指出,突触连接结构重塑的改变会改变依赖学习的变化,即使在长时间戒断后这些变化仍然存在。这导致了依赖性的持续发展。
本研究的目的是确定亚慢性暴露于三种不同剂量的甲麻黄碱对小鼠海马体和前额叶皮质中MMP-2和MMP-9活性的影响,以及这与记忆过程的相关性。
通过明胶酶谱法检测海马体和皮质匀浆中MMP-2和MMP-9的活性。在被动回避(PA)试验中评估记忆巩固过程。
该研究证实了亚慢性给予甲麻黄碱会导致MMP-2和MMP-9活性呈剂量依赖性增加。此外,最高剂量的甲麻黄碱减弱了记忆巩固和学习过程。
我们可以推测,抑制MMPs可被视为治疗与认知过程相关的成瘾行为的一种治疗选择。此外,还需要进一步研究以确定MMPs活性升高是否会导致脑损伤或由甲麻黄碱直接引起的脑损伤的恢复。