Insights into the suanzaoren mechanism—From constructing the 3D structure of GABA-A receptor to its binding interaction analysis

Abstract

Gamma aminobutyric acid type A (GABA-A) receptors are an important therapeutic target in insomnia treatment. The GABA-A protein structure is still not available. In this study, a reliable structure of GABA-A receptor was built and validated by several criteria. Zolpidem was predicted to gain the highest binding affinity at the BZ-binding site and be surrounded by α 1-His129, α 1-Tyr187, α 1-Gly228, α 1-Thr234, α 1-Tyr237, γ 2-Met96, γ 2-Phe116, and γ 2-Met169. In addition, GABA formed five hydrogen bonds with α 1-Arg159, β 2-Glu179, and β 2-Tyr181 and was surrounded by the residues α 1-Phe92, α 1-Arg147, β 2-Tyr181, β 2-Thr184, β 2-Thr226, and β 2-Tyr229 at the GABA-binding site. The two simulation results were consistent with the experimental assay, which suggested that the simulated GABA-A receptor was reliable. Jujuboside A, which was considered the effective suanzaoren constituent, had difficulty penetrating the blood–brain barrier. Besides, jujuboside A was unable to bind at both binding sites due to its large structural volume. However, jujubogenin that was hydrolyzed from jujuboside A showed the most compatible binding pose and formed five hydrogen bonds with the key residues, β 2-Thr226 and β 2-Tyr229, at the GABA-binding site. In addition, according to a docking study, jujubogenin gained higher scoring values, which indicated a higher binding affinity. Moreover, the adsorption, distribution, metabolism, excretion, and toxicity (ADMET) descriptors predicted that jujubogenin had high blood–brain barrier penetration. Conclusively, jujubogenin was suggested to be the effective suanzaoren constituent for exerting the sedative function via GABA-A receptor.