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Biomedical subjects

A Oliverio

Publications and source records attributed to A Oliverio.

At least 55 records · Page 3Linked to original sources

Enhancement of radial maze performances in CD1 mice after prenatal exposure to oxiracetam: possible role of sustained investigative responses developed during ontogeny.

A longitudinal study aimed at analyzing the behavioral effects of prenatal exposure to the nootropic compound oxiracetam was carried out in CD1 mice. Two groups of females were injected either with oxiracetam or saline from the beginning of pregnancy until parturition. Examination of pups from birth until the first month of age revealed no-influence of the treatment on litter size, body weights, sensory motor reflexes and motility. When placed in the open field at one month of age, mice born by mothers exposed to oxiracetam displayed more self grooming and spent less time in freezing than control mice. Prenatally treated mice were then found more interactive with their environment since the introduction of a novel object in the open field was followed by increased ambulation and higher sniffing object and rearing object scores. At three months of age, mice from both groups were tested in a radial six-arm maze task. Choice accuracy was significantly higher in prenatally treated mice which also tended to optimize their exploratory sequences by frequently running the maze in a clock-wise fashion. These results suggest that the better learning performances observed in the experimental group could be viewed as a consequence of an enhanced cognitive development based upon the higher rate of interactions with the environment shown by prenatally treated mice during ontogeny.

Animals↗

New analogs of physostigmine: alternative drugs for Alzheimer's disease?

The synthesis of a series of physostigmine analogs, in which the methylcarbamyl group has been substituted with monoalkylcarbamyl, dimethyl- and diethylcarbamyl groups, is reported. These compounds were prepared with the aim of investigating their possible therapeutic effects in the treatment of Alzheimer's type dementia. The new analogs of physostigmine are inhibitors of acetylcholinesterase from Electroforus electricus, with a value of the reactivation constant, k3 smaller than the one of physostigmine. The percentage of anticholinesterase activity in vitro and in vivo, the acute toxicity and some behavioural effects were also evaluated for selected derivatives. The reactivation constant, in vitro, supports the view that the derivatives described would be more suitable for therapeutic use than physostigmine.

Alzheimer Disease↗

A long-lasting cholinesterase inhibitor affecting neural and behavioral processes.

A series of analogues of physostigmine were prepared with the aim of investigating their inhibitory effects on acetylcholinesterase in the treatment of Alzheimer's disease. One of the isomers prepared was evaluated for its anticholinesterase activity in vivo, acute toxicity, and some behavioral effects. This compound was a competitive inhibitor of the enzyme and was found to antagonize the stimulating effect produced by scopolamine on locomotor activity and to facilitate memory consolidation.

Acetylcholinesterase↗

Strain-dependent effects of shock-induced release of opioids: dissociation between analgesia and behavioral seizures.

Intermittent, but not continuous, footshock resulted in naltrexone-reversible analgesia in two strains of mice: C57BL/6 (C57) and BALB/c (BALB). While no strain differences were evident in relation to analgesia, a clear strain effect appeared when the protective action of intermittent footshock on electroconvulsive shock-induced seizures was considered. In fact naltrexone-reversible protection exerted by intermittent footshock on behavioral seizures was much higher in C57 than in BALB mice. The reason of this dissociation between the effects of endogenous opioids on analgesia and seizures is discussed.

Analgesia↗

Avoidance facilitation in adult mice by prenatal administration of the nootropic drug oxiracetam.

CD-1 mice prenatally exposed to saline solution or to the nootropic drug oxiracetam (50 mg/kg during the whole pregnancy) were tested, when adults, for locomotor activity and for shuttle-box avoidance acquisition. Prenatal drug exposure produced long-lasting effects, evident in mature offspring. At the age of two months, mice prenatally exposed to oxiracetam showed a slight but significant reduction in locomotor activity. At the age of three months, these animals exhibited higher performances than control mice in avoidance acquisition.

Animals↗

Transfer of conditioning in stress-induced analgesia.

Classical conditioning of stress-induced analgesia (SIA) resulted in higher tail flick latencies in BALB/c mice. Transfer of classical conditioning of SIA was evident when the same repetition rate (pulsed light or pulsed tone) characterized stimuli in different sensory modalities. This finding is discussed in terms of opioid production and of generalization of emotional reactions.

Animals↗

Pharmacological evidence for a protective role of the endogenous opioid system on electroshock-induced seizures in the mouse.

Acute administration of morphine produced a protective effect on electroshock (ECS)-induced seizures in mice, while naloxone and naltrexone decreased ECS seizure threshold. Chronic morphine administration in mice resulted in a decrease of ECS-induced seizure threshold evident within 24 h following the end of drug treatment. This effect disappeared 5 days after the end of chronic morphine treatment. Moreover, tolerance to the anticonvulsant effect of morphine was evident in mice chronically treated with morphine and subjected to ECS 30 min after the last injection of the drug, as well as in mice subjected to ECS 24 h after the end of chronic treatment.

Animals↗

D-Amino acids influence ultrasonic calling in mice pups: effects of D-phenylalanine and D-leucine.

6-day-old mice pups were injected with D-amino acids (D-phenyl-alanine + D-leucine), and their ultrasonic distress vocalizations were measured. D-Amino acids, which exert opioid-like effects, reduce the number of ultrasonic calls without affecting the activity of the pups. This effect is reversed by naloxone, an opioid antagonist. The role of endogenous opioids in modulating early attachment is discussed.

Animals↗

Diurnal variations in electroconvulsive shock-induced seizures: involvement of endogenous opioids.

Electroconvulsive shock (ECS)-induced seizures present a clear cut diurnal rhythmicity when BALB/c mice are subjected to a light-dark (L/D) schedule. On the contrary, in the absence of external synchronizers no evident fluctuations in epileptic behaviour were evident. Naloxone decreased the threshold of ECS-induced convulsions, thus confirming an involvement of opioids in this type of behaviour. These findings indicate that opioids present a diurnal (L/D) but not circadian (L/L) rhythmicity in BALB/c mice.

Adaptation, Physiological↗

Genetic differences in daily rhythms of pain sensitivity in mice.

A dark phase increase in pain sensitivity was evident in C57BL/6 inbred mice. On the contrary Swiss mice are characterized by decreased nocturnal pain sensitivity. The latter finding is in agreement with a number of previous studies based on albino mice. However, our findings indicate that (1) nocturnal decreased pain sensitivity is not the rule in the mouse and (2) large differences are evident when the onset in peak nocturnal analgesia is considered.

Animals↗

Effects of sauvagine on behavioural arousal of mice.

The effects of natural and synthetic sauvagine on locomotor activity and ECS-induced seizures were studied in DBA/2 mice. A dose-dependent activity depression was evident following the administration of both compounds. Moreover they exerted a protective effect against ECS-induced seizures. This effect was naloxone-reversible, suggesting the involvement of endogenous opioids. In both series of experiments natural sauvagine was more effective than the synthetic compound.

Amphibian Proteins↗

A genetic analysis of stereotypy in the mouse: dopaminergic plasticity following chronic stress.

After repeated stressful experiences, DBA/2 (DBA) mice showed an increase in apomorphine-induced climbing while C57BL/6 (C57) mice showed a clear-cut decrease of this behavior. Genetic analysis involving F1 and F2 hybrids and the backcross populations (F1 X C57; F1 X DBA) indicated complete dominance of the C57 genotype and a significant genotype X environment interaction. These findings are discussed in terms of dopaminergic plasticity and of the heuristic value of this animal model in relation to disturbed behaviors triggered by stressful experiences.

Animals↗

Interaction between nootropic drugs and methamphetamine on avoidance acquisition but not on locomotor activity in mice.

Two nootropic drugs, oxiracetam and piracetam, were tested, alone or in combination with methamphetamine, on locomotor activity and shuttle-box avoidance acquisition in mice of the C57BL/6 strain. Oxiracetam (50 mg/kg/day) and piracetam (100 mg/kg/day) had no effect when given alone, but significantly increased avoidance responses when combined with methamphetamine (0.5, 1 and 2 mg/kg). On the contrary, the two nootropic agents did not affect locomotor stimulation induced by methamphetamine. The results suggest that nootropic drugs may interact with methamphetamine in behavioural tests in which learning and memory processes are involved.

Animals↗

Opioid antagonism of electroshock-induced seizures.

Morphine, beta-endorphin and [D-Ala2, D-Leu5] enkephalin administered intracerebroventricularly exerted a protective effect on electroconvulsive shock (ECS)-induced seizures in mice. This effect was reversed by intraperitoneal injections of naltrexone. The role of mu and delta receptors in ECS-induced convulsions is discussed.

Animals↗

Anticonvulsant effects of stress: role of endogenous opioids.

Mice subjected to immobilization stress were protected against electrconvulsive shock-induced seizures in comparison to non-stressed mice. Pretreatment with naltrexone antagonized the effects of stress indicating that the protective effects of stress on seizures involved a release of endogenous opioids.

Animals↗