Abstract:
The putative endogenous tripeptide ligand of the translocator protein (TSPO) l-phenylalanyl-l-tryptophanyl-l-leucine amide was obtained using the drug-based peptide design strategy and molecular modeling. This tripeptide demonstrated anxiolytic activity in the elevated plus-maze test and antidepressant-like activity in the forced swimming test in BALB/c mice at the doses of 10 mg kg−1 (i.p.) and also showed neuroprotective activity in the concentration range of 10−5–10−7 m in vitro under conditions of oxidative stress using HT-22 neuronal cell line.
Citation:
O. A. Deeva, A. S. Pantileev, O. Yu. Kravtsova, S. V. Nikolaev, N. A. Zefirov, P. Yu. Povarnina, T. A. Antipova, T. A. Gudasheva, V. L. Dorofeev, “Tripeptide Phe-Trp-Leu-NH2 as a putative endogenous ligand of TSPO: molecular modeling, synthesis and pharmacological activity”, Mendeleev Commun., 34:5 (2024), 682–684