ABSTRACT
Experimental drugs and/or plant extracts are often dissolved in solvents, including propylene glycol. Nevertheless, there is evidence for psychoactive properties of this alcohol. In this study we found that in the hole-board test 10 percent propylene glycol did not modify the head-dipping behavior. However, 30 percent propylene glycol induced an increase in the number of head-dips (46.92 + or - 2.37 compared to 33.83 + or - 4.39, P<0.05, ANOVA/Student-Newman-Keuls), an effect comparable to that obtained with 0.5 mg/kg diazepam (from 33.83 + or - 4.39 to 54 + or - 3.8, P<0.01, ANOVA/Student-Newman-Keuls). These results demonstrate that 30 percent propylene glycol has significant anxiolytic effects in this model and therefore cannot be used as an innocuous solvent
Subject(s)
Animals , Male , Mice , Anti-Anxiety Agents/pharmacology , Behavior, Animal/drug effects , Propylene Glycol/pharmacology , Solvents/pharmacology , Anti-Anxiety Agents/pharmacology , Diazepam/pharmacology , Exploratory Behavior/drug effects , Head Movements/drug effects , Locomotion/drug effectsABSTRACT
Although recently developed drugs have brought significant improvement, the treatment of psychotic disorders still presents serious drawbacks. Since inherent complexity and lack of satisfactory understanding of the underlying pathophysiology impose limits for rational drug design, resourceful approaches in the search for antipsychotics are pertinent. This paper reports pharmacological properties of alstonine, a heteroyohimbine type alkaloid, Which exbitited an antipsychotic-like profile, inhibiting amphetamine-induced lethaly, apomorphine-induced steotypy and potentiating barbiturate-induced slleping time. Atypical features of alstonine were the prevention of haloperidol-induced catalepsy and lack of direct interaction with D1, D2 and 5-HT2A receptors, classically linked to antipsychotic mechanism of action.