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1.
Eur J Pharmacol ; 842: 231-238, 2019 Jan 05.
Article in English | MEDLINE | ID: mdl-30391741

ABSTRACT

Benzodiazepine receptor agonists are widely prescribed therapeutic agents, alter gamma-aminobutyric acid (GABA)A receptor function, and have hypnotic, anxiolytic, anticonvulsant, and antispastic effects. GABAA receptor activity increases under systemic inflammatory conditions. We investigated the effect of benzodiazepine receptor agonists on pentobarbital-induced loss of righting reflex (LORR) duration using a mouse model of lipopolysaccharide (LPS)-induced inflammation. We assessed pentobarbital-induced LORR duration 24 h after LPS treatment in mice. Additionally, we examined the microglial response by immunohistochemistry and serum IL-6 and TNF-α concentrations in mice. LPS treatment significantly increased the duration of pentobarbital-induced LORR in mice treated with benzodiazepine receptor agonists (diazepam and brotizolam) and a GABAA receptor agonist (muscimol) compared to that of mice treated with vehicle. These effects were blocked by bicuculline, a GABAA receptor antagonist. LPS significantly increased the number of ionized calcium binding adapter molecule-1-positive hippocampal cells 2 and 24 h after treatment. The enhancing effect of diazepam in LPS-treated mice was significantly reduced by minocycline. These findings suggest that LPS enhances pentobarbital-induced LORR duration in mice treated with benzodiazepine via GABAA receptor activity.


Subject(s)
Diazepam/pharmacology , Lipopolysaccharides/pharmacology , Pentobarbital/pharmacology , Reflex, Righting/drug effects , Animals , Dentate Gyrus/drug effects , Dentate Gyrus/metabolism , Frontal Lobe/drug effects , Frontal Lobe/metabolism , Gene Expression Regulation/drug effects , Hippocampus/drug effects , Hippocampus/metabolism , Interleukin-6/blood , Interleukin-6/genetics , Mice , RNA, Messenger/genetics , RNA, Messenger/metabolism , Time Factors , Tumor Necrosis Factor-alpha/blood , Tumor Necrosis Factor-alpha/genetics
2.
Article in English | MEDLINE | ID: mdl-26819715

ABSTRACT

BACKGROUND: Delirium is an acute change in cognition and concentration that complicates the postoperative course. Patients who suffer delirium after surgery have an increased risk of persistent cognitive impairment, functional decline, and death. Postoperative delirium is also associated with an increased length of hospital stay and higher costs. With the goal of preventing delirium in postoperative patients, we organized a medical team from the Delirium Management and Assessment Center (D-mac) at Okayama University Hospital in January 2012. The team members consisted of physicians, pharmacists, nurses, and clinical psychologists. METHODS: We retrospectively reviewed the medical records of patients with delirium to examine risk factors related to the patients' background. RESULTS: Fifty-nine postoperative patients with lung or esophageal cancer were investigated; 25% exhibited delirium during hospitalization. Multiple logistic regression analysis showed significant associations between the presence of delirium and a past history of delirium (odds ratio, 4.22; 95% CI, 1.10-16.2; p = 0.09) and use of benzodiazepine receptor agonists (odds ratio, 3.97; 95% CI, 1.09-14.5; p = 0.03). Intervention by the D-mac significantly reduced the rate of delirium episodes in lung cancer patients (p =0.01). Notably, prior to intervention, the incidence of delirium was 100% when three high-risk factors for delirium were present. In contrast, the incidence of delirium in patients with three high-risk factors decreased following implementation of the D-mac intervention. CONCLUSIONS: These findings suggest that active participation by various staff in the medical team managing delirium had a marked therapeutic impact.

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