T he petroleum ether (60-80°C) ex tract of OcilllulIl sanCIUln root was tested fo r pentobarbitone induced hypnosis in mice. The root extract or vehicle was admi nistered (i.p. ) and after 30 minutes pentobarbito ne sodium (35 mg/kg) was admini stered. The explo ratory behavi our like Water Maze Test was studi ed by imparting training to mice ill a rec tangular tank ha ving holes to escape, fil...

The oxygen uptake of bovine endometrium was less when perfused with seminal plasma than when perfused with Krebs-Ringer phosphate buffer solution. Dialysing the seminal plasma against Krebs\x=req-\ Ringer phosphate buffer solution did not alter the depressant action of the seminal plasma. The depressant substance was shown to be partially heat labile. Variable mineral concentrations were not re...

The group of drugs known as Benzodiazepines (BDZs) are among the most widely prescribed CNS-depressant drugs. Alprazolam (Alp) is a member BDZs family, commonly an antipsychotic and anxiolytic agent. Induction oxidative stress, impairment cognitive functions psychomotor skills, conformational alterations in hemoglobin structure elevation liver enzymes side effects reported on use alprazolam. Se...

The depressant action of antidromic volleys of impulses on gustatory nerve signals from the tongues of bullfrogs was studied. Electrical stimulation of the glossopharyngeal nerve at a rate of 100 Hz for 10 s and at supramaximal intensity slightly depressed the integrated glossopharyngeal nerve responses to quinine and to mechanical taps to the tongue . The same antidromic stimuli resulted in a ...

Bilastine is a new H1 antagonist with no sedative side effects, no cardiotoxic effects, and no hepatic metabolism. In addition, bilastine has proved to be effective for the symptomatic treatment of allergic rhinoconjunctivitis and urticaria. Pharmacological studies have shown that bilastine is highly selective for the H1 receptor in both in vivo and in vitro studies, and with no apparent affin...

We attempted to identify the antinociceptive and anti-inflammatory actions of the monoterpene p-cymene. Firstly, behavioural screening was carried out to verify the influence of p-cymene [25, 50, and 100 mg/kg intraperitoneal (i.p.)] on the central nervous system (CNS) activity. The antinociceptive activity of p-cymene was evaluated by the acetic acid-induced writhing response, formalin, and ho...

BACKGROUND Grewia carpinifolia is a plant commonly used in the tropics to manage various central nervous system (CNS) disorders. However, despite its widespread use no scientific work has been reported to validate these claims. OBJECTIVES To evaluate the activity of G. carpinifolia as it affects behaviour using animal model. METHODS Twenty five adult Wistar rats were randomly divided into f...

Carvacrol (CARV) is a phenolic monoterpene present in the essential oil of several aromatic spices. The purpose of the present study was to evaluate the antinociceptive effect of CARV on formalin-, capsaicin-, and glutamate-induced orofacial nociception in mice. Male mice were pretreated with CARV [25, 50, and 100 mg/kg body weight (BW), intraperitoneal (i.p.)], morphine (5 mg/kg BW, i.p.), or ...

Since the pioneering discovery of the rapid CNS depressant actions of steroids by the "father of stress," Hans Seyle 70 years ago, brain-derived "neurosteroids" have emerged as powerful endogenous modulators of neuronal excitability. The majority of the intervening research has focused on a class of naturally occurring steroids that are metabolites of progesterone and deoxycorticosterone, which...

tumors of the central nervous system (cns), occur relatively frequently during the early years of life. they are the most common solid tumors of childhood and are second only to leukemia in overall cancer incidence and account for a high proportion of deaths. in different studied performed in several countries, astrocytomas and other gilomas (combined) account for half of the cns malignancies, ...