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Endozepines in recurrent stupor

Authors :
Pasquale Montagna
M.L. Zeneroli
Pietro Cortelli
Rossella Avallone
Elio Lugaresi
Mario Baraldi
Roberto Riva
Jessica Mandrioli
Agostino Baruzzi
Lorenzo Corsi
Paolo Tinuper
Cortelli P.
Avallone R.
Baraldi M.
Zeneroli M.L.
Mandrioli J.
Corsi L.
Riva R.
Tinuper P.
Lugaresi E.
Baruzzi A.
Montagna P.
Publication Year :
2005

Abstract

Summary Stupor is a condition from which the subject can be aroused only by vigorous stimuli. Most patients with stupor have a diffuse organic cerebral dysfunction. Rarely stupor is recurrent and no specific causes can be found. Patients with idiopathic recurrent stupor were awakened by i.v. administration of an antagonist (flumazenil) of the benzodiazepine recognition site located in the GABA A receptor. Since no exogenous benzodiazepines were detected in plasma and cerebrospinal fluid by high performance liquid chromatography, an excess of endogenous benzodiazepine-like compounds (endozepines) was proposed as the cause of stupor. The existence of endozepines, their widespread distribution in the CNS and their involvement in hepatic encephalopathy are established. However, the origin of these compounds, how biosynthesis occurs and the mechanisms and causes through which they alter brain functions are poorly understood. The fact that a number of synthetic benzodiazepines are difficult to detect using conventional techniques and the discovery that some cases of recurrent stupor were caused by fraudulent administration of lorazepam question whether the concept of endozepine recurrent stupor can be sustained. This review summarizes the state of endozepine physiology and pharmacology and the clinical syndromes attributed to their involvement. A diagnostic work-up to define endozepine-induced recurrent stupor is suggested.

Details

Language :
English
Database :
OpenAIRE
Accession number :
edsair.doi.dedup.....5ba224a20541b6cfbd5a6b6b87ce73b4