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Exploring the role of zolpidem in alleviating cognitive and motor impairments in chronic cerebral hypoperfusion: a rat model study with in vivo and in silico insights

Choo, Sherilyn M.T. and Mohamad, Fatin H. and Sayed Mohamad, Syarifah Maisarah and Abd Halim, Khairul Bariyyah and Abdul Hamid, Azzmer Azzar and Abdullah, Jafri Malin and Che Has, Ahmad Tarmizi (2025) Exploring the role of zolpidem in alleviating cognitive and motor impairments in chronic cerebral hypoperfusion: a rat model study with in vivo and in silico insights. Experimental Animals, 75 (1). pp. 23-39. ISSN 1881-7122

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Abstract

The ε-containing GABA(A) receptors (GABAARs), a lesser-studied subtype within the GABAAR family, have garnered attention due to their distinct pharmacological properties and potential involvement in brain injury. Zolpidem (ZPM), a widely used Z-drug, is known to induce paradoxical effects in patients with brain injury, although the underlying molecular mechanisms remain unclear. In this study, a chronic cerebral hypoperfusion (CCH) rat model was established using Permanent Bilateral Occlusion of the Common Carotid Arteries (PBOCCA), followed by administration of ZPM at doses of 1.0, 2.0, and 4.0 mg/kg. Behavioral assessments demonstrated that the 1.0 mg/kg dose of ZPM significantly improved spatial learning and memory acquisition (P<0.01) and enhanced memory retention (P<0.001), whereas higher doses resulted in sedation and cognitive impairment. Immunohistochemical analysis revealed an upregulation of the ε subunit expression in the hippocampal CA1 and CA3 regions of CCH rats (P<0.05), suggesting alterations in receptor composition in response to cerebral hypoperfusion. Further investigation of ZPM’s interaction with ε-containing GABAARs (specifically the α1β2ε subtype) was conducted using in silico techniques. Molecular docking identified the α1+/ε- binding interface as a favorable ZPM binding site, with key residues being either conserved or suitably replaced. Molecular dynamics simulations demonstrated that ZPM stabilizes the receptor while permitting conformational flexibility, consistent with its role as a positive allosteric modulator. These findings provide evidence that ZPM interacts with ε-containing GABAARs, potentially explaining its paradoxical effects observed in brain injury models

Item Type: Article (Journal)
Uncontrolled Keywords: chronic cerebral hypoperfusion (CCH), GABA(A) receptors (GABAARs), in silico, in vivo, zolpidem
Subjects: Q Science > QP Physiology
Kulliyyahs/Centres/Divisions/Institutes (Can select more than one option. Press CONTROL button): Kulliyyah of Science
Kulliyyah of Science > Department of Biotechnology
Depositing User: AP. Dr. Azzmer Azzar Abdul Hamid
Date Deposited: 08 Jan 2026 12:24
Last Modified: 08 Jan 2026 12:24
Queue Number: 2026-01-Q1565
URI: http://irep.iium.edu.my/id/eprint/126749

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