Department of Synthesis and Chemical Technology of Pharmaceutical Substances with Computer Modeling Laboratory, Faculty of Pharmacy, Medical University of Lublin, 4A Chodzki St., 20-093 Lublin, Poland.
Department of Biotechnology, Institute of Biology and Biotechnology, University of Rzeszow, 1 Pigonia St., 35-310 Rzeszow, Poland.
Int J Mol Sci. 2020 Nov 23;21(22):8849. doi: 10.3390/ijms21228849.
The treatment of memory impairments associated with the central nervous system diseases remains an unmet medical need with social and economic implications. Here we show, that a multi-target ligand of aminergic G protein-coupled receptors with antipsychotic activity in vivo (D2AAK1) stimulates neuron growth and survival and promotes neuron integrity. We focused on the multilevel evaluation of the D2AAK1-related effects on neurons in terms of behavioral, cellular, molecular, and biochemical features in vivo and in vitro, such as memory-related responses, locomotor activity, tissue sections analysis, metabolic activity, proliferation level, neurons morphology, and proteins level involved in intracellular signaling pathways. studies indicate that activation of calcium/calmodulin-dependent protein kinase I (CaMKI) may underline some of the observed activities of the compound. Furthermore, the compound increases hippocampal neuron proliferation via the activation of neurotrophic factors and cooperating signals responsible for cell growth and proliferation. D2AAK1 improves memory and learning processes in mice after both acute and chronic administration. D2AAK1 also causes an increase in the number of hippocampal pyramidal neurons after chronic administration. Because of its neuroprotective properties and pro-cognitive activity in behavioral studies D2AAK1 has the potential for the treatment of memory disturbances in neurodegenerative and mental diseases.
治疗与中枢神经系统疾病相关的记忆损伤仍然是一种未满足的医学需求,具有社会和经济意义。在这里,我们展示了一种具有体内抗精神病活性的多靶标胺能 G 蛋白偶联受体配体(D2AAK1),它能刺激神经元生长和存活,并促进神经元完整性。我们专注于从行为、细胞、分子和生物化学特征等多个层面评估 D2AAK1 对体内和体外神经元的影响,如与记忆相关的反应、运动活性、组织切片分析、代谢活性、增殖水平、神经元形态以及参与细胞内信号通路的蛋白质水平。研究表明,钙/钙调蛋白依赖性蛋白激酶 I(CaMKI)的激活可能是该化合物观察到的一些活性的基础。此外,该化合物通过激活神经营养因子和负责细胞生长和增殖的协同信号,增加海马神经元的增殖。D2AAK1 在急性和慢性给药后均可改善小鼠的记忆和学习过程。D2AAK1 还可导致慢性给药后海马锥体神经元数量增加。由于其神经保护特性和行为研究中的认知促进活性,D2AAK1 有可能治疗神经退行性和精神疾病中的记忆障碍。