دورية أكاديمية

Effect of Lipopolysaccharide on the Duration of Zolpidem-Induced Loss of Righting Reflex in Mice.

التفاصيل البيبلوغرافية
العنوان: Effect of Lipopolysaccharide on the Duration of Zolpidem-Induced Loss of Righting Reflex in Mice.
المؤلفون: Wada Y; Department of Clinical Pharmacy, Okayama University, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences., Ushio S; Department of Pharmacy, Okayama University Hospital.; Department of Physiology and Pharmacology, Faculty of Pharmaceutical Sciences, Fukuoka University., Kitamura Y; Department of Clinical Pharmacy, Okayama University, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences.; Department of Pharmacy, Okayama University Hospital.; Department of Pharmacotherapy, School of Pharmacy, Shujitsu University., Zamami Y; Department of Clinical Pharmacy, Okayama University, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences.; Department of Pharmacy, Okayama University Hospital., Sendo T; Department of Clinical Pharmacy, Okayama University, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences.; Department of Pharmacy, Okayama University Hospital.
المصدر: Acta medica Okayama [Acta Med Okayama] 2024 Jun; Vol. 78 (3), pp. 227-235.
نوع المنشور: Journal Article
اللغة: English
بيانات الدورية: Publisher: Okayama University Medical School Country of Publication: Japan NLM ID: 0417611 Publication Model: Print Cited Medium: Internet ISSN: 0386-300X (Print) Linking ISSN: 0386300X NLM ISO Abbreviation: Acta Med Okayama Subsets: MEDLINE
أسماء مطبوعة: Original Publication: Okayama : Okayama University Medical School
مواضيع طبية MeSH: Zolpidem*/pharmacology , Lipopolysaccharides* , Pyridines*/pharmacology , Receptors, GABA-A*/metabolism , Receptors, GABA-A*/drug effects , Symporters*/genetics , Symporters*/metabolism , Reflex, Righting*/drug effects, Animals ; Mice ; Male ; Hippocampus/drug effects ; Hippocampus/metabolism ; K Cl- Cotransporters ; Hypnotics and Sedatives/pharmacology ; Inflammation/chemically induced ; Frontal Lobe/drug effects ; Frontal Lobe/metabolism
مستخلص: Zolpidem, a non-benzodiazepine hypnotic, is primarily used to treat insomnia. In a previous study, pior treatment with non-benzodiazepine receptor agonists was associated with inflammation. The present study aimed to clarify the association between the effects of zolpidem and inflammation in mice treated with lipopolysaccharide (LPS), a known model of inflammation. We assessed the zolpidem-induced loss of righting reflex (LORR) duration 24 h after LPS treatment in mice. Additionally, the expressions of γ-aminobutyric acid (GABA)A receptor subunit and K+-Cl- cotransporter isoform 2 (KCC2) mRNA in the hippocampus and frontal cortex were examined in LPS-treated mice. Pretreatment with LPS was associated with significantly prolonged duration of zolpidem-induced LORR compared to control mice. This effect was significantly attenuated by administering bicuculline, a GABAA receptor antagonist, or flumazenil, a benzodiazepine receptor antagonist, in LPS-treated mice. Compared to controls, LPS-treated mice showed no significant change in the expression of GABAA receptor subunits in the hippocampus or frontal cortex. Bumetanide, an Na+-K+-2Cl- cotransporter isoform 1 blocker, attenuated the extended duration of zolpidem-induced LORR observed in LPS-treated mice. LPS significantly decreased Kcc2 mRNA expression in the hippocampus and the frontal cortex. These findings suggest that inflammation increases zolpidem-induced LORR, possibly through a reduction in KCC2 expression.
Competing Interests: No potential conflict of interest relevant to this article was reported.
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فهرسة مساهمة: Keywords: GABAA receptor; K+-Cl− cotransporters; lipopolysaccharide; zolpidem
المشرفين على المادة: 7K383OQI23 (Zolpidem)
0 (Lipopolysaccharides)
0 (Pyridines)
0 (Receptors, GABA-A)
0 (Symporters)
0 (K Cl- Cotransporters)
0 (Hypnotics and Sedatives)
تواريخ الأحداث: Date Created: 20240620 Date Completed: 20240620 Latest Revision: 20240620
رمز التحديث: 20240621
DOI: 10.18926/AMO/67197
PMID: 38902210
قاعدة البيانات: MEDLINE
الوصف
تدمد:0386-300X
DOI:10.18926/AMO/67197