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[Value of the Remedi chromatography automate for the analytic diagnosis of drug poisoning].

The aim of this study was to evaluate the liquid chromatographic system Remedi (Biorad) in comparison with traditional immunological and colorimetric methods, for the diagnosis of acute drug overdose. 469 blood samples and 95 stomach cleaning liquid samples have been analysed during 1995. The usual toxicologic analysis was composed of the benzodiazepines, tricyclic antidepressants and barbiturates research. Ethanol, meprobamate and acetaminophen assays were performed only on physician's request. Only three pharmacological classes can be analysed both with immunological methods and Remedi: benzodiazepines, tricyclic antidepressants and barbiturates. Remedi has been found to be less sensitive than immunological method for benzodiazepines, it sometimes gave false negative results for barbiturates, but it was very efficient for antidepressants. Remedi often identified drugs other than the 3 previous classes: sedatives, antipsychotic, beta-blockers, antiarythmics. Furthermore these drugs are of clinical importance due to the fact that they are able to modify the symptomatology. In every case Remedi was able to give an estimation of the blood concentration of the toxic molecule matched. Remedi can not replace traditional methods but is a good complementary tool, available in emergency. This is particularly useful when clinical signs do not correspond to the toxics suspected by questioning the patient or relatives.

Antidepressive Agents, Tricyclic↗

Synthesis of some indane derivatives of central muscle relaxant and anticonvulsant profiles.

A series of 2,2-bis(hydroxymethyl)indane derivatives 1a-f, 2a-e and 3a-f were synthesized to investigate their central muscle relaxant and anticonvulsant activities. The synthesized compounds 1a-f, 2a-e and 3a-f were found to be devoid of central muscle relaxant activity using meprobamate (100 mg/kg) as a reference standard. However, they showed remarkable anticonvulsant properties in a dose of 80 mg/kg (s.c.) compared with diphenylhydantoin sodium (80 mg/kg) as a reference standard.

Animals↗

Effect of leaf extract from Clerodendron colebrookianum on CNS function in mice.

Effect of acute multiple (20, 40 and 80 mg/kg body wt, i.p.) doses of C. colebrookianum leaf extract on behaviour, convulsion, analgesia and sedative-hypnosis was studied in mice. A marginal reduction of awareness and motor activity was observed in low (20 mg) and moderate (40 mg) dose level of extract. However, 80 mg dose caused marked inhibition of awareness and motor activity. Grip strength and stereotypy was observed in all the dose levels. The extract alone did not show loss of righting reflex but it prolonged the effect of meprobamate, diazepam, chlorpromazine and pentobarbitone significantly in a dose dependent manner. The extract neither produced analgesia alone nor it altered analgesic effect of morphine and pethidine. Pretreatment of the extract caused significant protection of strychnine and leptazol induced convulsion and mortality. The results suggest a mild (or dose dependent) CNS depressant action of leaf extract of C. colebrookianum in mice.

Animals↗

[Effect of psychopharmaceutic agents on cortical potentials and long-lasting post-tetanic changes in excitability released through stimulation of the dental pulp].

Short-time tetanic stimulation of the tooth pulp with square pulses affords, depending on the stimulation parameters selected, a long-lasting facilitation in the response of subsequently applied test stimuli in the sensomotor cortex of rabbits. The benzodiazepin derivatives, chlorodiazepoxide, nitrazepam (10 mg/kg i.p.) and clonazepam (1 mg/kg i.p.) caused suppression of posttetanic facilitation with partly different influences on cortical potentials following individual stimulation. Meprobamate (200 mg/kg i.p.) had no effect on the processes of posttetanic facilitation, while the amplitudes of sensomotor potentials showed a long-lasting reduction on single stimulation. Chloropromazine (2 mg/kg i.p.) showed a rapid and transient inhibition of posttetanic facilitation and reduced the amplitudes of evoked potentials following single stimulation.

Animals↗