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Biomedical subjects

J Masur

Publications and source records attributed to J Masur.

At least 19 recordsLinked to original sources

Reversible effects of acute and long-term administration of delta-9-tetrahydrocannabinol (THC) on memory in the rat.

A study was designed to develop a measure of both acute and chronic effects of THC administration on memory in the rat. Errors in an 8-arm radial maze, before and after two delay intervals (5 s and 1 h, introduced between the fourth and the fifth arm choice), constituted the principal dependent measures. The first experiment involved testing the animals shortly after administration of 1.25 mg/kg THC. The drug did not affect performance in the pre-delay tests, although a significant effect was observed after the 5-s delay but not after 1-h delay. In the second experiment, 5 mg/kg THC or saline were administered 6 days/week for 90 days. Testing was conducted 18 h after each drug administration. During chronic administration the pre-delay performance did not differ between groups but the post-delay performance of the THC group deteriorated in a gradual manner, relative to their controls, in both the 5-s and 1-h delay conditions. After discontinuation of drug administration, the differences between groups reversed only after 30 days. The results provided evidence that both acute and chronic administration of THC affected working-memory in the radial arm maze test, although it did not interfere with the general cues of the task (reference memory). Chronic drug effects on memory were reversible after prolonged abstinence. Thus, the 8-arm radial maze task proved to be a useful measure of THC effects on memory and could be further used to investigate more thoroughly the mechanisms involved in such drug effects.(ABSTRACT TRUNCATED AT 250 WORDS)

Animals

Amygdaloid kindling and kindled seizures in rats receiving chronic ethanol administration.

The effects of chronic ethanol administration were studied in rats receiving amygdaloid kindling. Daily ethanol administration 10 min prior to kindling stimulation delayed acquisition of kindling without affecting the electrical afterdischarge. For the lowest tested dose of ethanol (0.5 g/kg), this delay was restricted to kindling stages 1 and 2. For the higher doses of ethanol (1.0 and 1.5 g/kg) this delay became more severe and stages 3 and 4 were blocked. Ethanol produced a clear dose-related anticonvulsant effect upon kindled seizures. After repeated exposure to kindling stimulation and ethanol this anticonvulsant effect vanished. After a 15-day interval without stimulation or ethanol application kindled animals were insensitive to ethanol's anticonvulsant effect. In conclusion, it is suggested that the anticonvulsant effects of low ethanol doses are restricted to kindling stages 1 and 2 and that anticonvulsant effects of high ethanol doses are limited by tolerance and by the level of consolidation of the kindled seizure. Finally, we suggest that the anticonvulsant properties of ethanol are not due to its general depressant effect but to some rather specific action.

Amygdala

The unofficial history of drug use: a study in a Brazilian sample.

Interviews were conducted with 59 former intensive users of illicit drugs with no evidence of current social or behavioural dysfunction. Data were gathered by in-depth standardized interviews through which, past and current psychoactive substance use (including alcohol, tobacco and tranquillizers) were assessed. Special attention was given to the subjects' attributions as to what had caused the change in the drug use pattern. Events attributed for ending or substantially decreasing drug use were categorized as follows: 'physical-mental problems/disliked side effects' (27.1% of respondents), 'developmental/maturational/existential reasons' (27.1%), 'formal or informal drug treatment system' (11.8%), 'interpersonal reasons' (10.2%), 'job or school/performance lowering' (10.2%), 'religious/spiritual involvement' (6.8%), and 'legal/financial problems' (6.8%). The major finding was that only 7 out of the 59 respondents (11.8%) reported having ever been in any formal or informal drug treatment system.

Adult

Ethanol decreases choice accuracy in a radial maze delayed test.

1. The effect of acute ethanol on memory was studied in an eight-arm radial maze by interposing a 15-s or 1-h delay between the rat's fourth and fifth arm choices. 2. Ethanol (1.0 g/kg) was injected intraperitoneally 5 min prior to the first set of 4-arm choices, therefore being present since the acquisition of the trial-unique event. 3. The results showed 1) a decrease in choice accuracy only in the final 4 arm choices after the 1-h delay, and 2) that errors consisted of re-entries into arms chosen before the delay was imposed. The data further support the contention that ethanol impairs retention of working memory.

Animals

Learning impairment in chronic epileptic rats following pilocarpine-induced status epilepticus.

Male Wistar rats were subjected to pilocarpine-induced status epilepticus and allowed to recover. After reaching the chronic state with spontaneous seizures they were tested in an 8-arm radial maze. During learning trials, epileptic rats made significantly more errors than controls. Even in the last trials epileptic rats did not improve their performance, indicating severe learning disability. These results suggest that spontaneous seizures after pilocarpine-induced status epilepticus are a useful model for studying the learning and memory impairment detected in some cases of symptomatic epilepsy.

Animals

Response variability of ethanol-induced locomotor activation in mice.

Mice from a randomly bred strain were divided into two groups according to their locomotor responses to ethanol (0.8-3.0 g/kg): in two thirds of the tested animals ethanol increased locomotor activity (ethanol activated-EA), whereas in the remaining one third it did not (ethanol non-activated-ENA). Both groups did not differ in their locomotor activity after saline administration. Furthermore, EA and ENA mice presented a similar increase in locomotor activity after challenge with 1.0 and 2.0 mg/kg d-amphetamine. Chronic exposure to ethanol increased the ethanol-induced locomotor activation in both EA and ENA groups. The possibility that the lack of responsiveness of ENA mice to ethanol's acute activating effect could be due to a higher sensitivity to the depressant effect of ethanol is discussed.

Animals

Interference of expectancy and attention demanding tasks on alcohol intoxication.

Seventy-nine undergraduate social drinkers were the subjects in two studies. Both studies had two experimental sessions and followed a blind design. The subjects in experiment I (expectancy manipulation) were informed they would certainly receive an alcoholic beverage in one session, while in the other one they were told the beverage possibly contained alcohol. Thus, the different expectancy on the beverage content was evaluated. The volunteers in experiment II (attention demanding tasks) were submitted to attention tests in one session and in another one they were not. Thus, the assumption that tasks would motivate the subjects to stay more sober and rate themselves as less intoxicated was studied. Each subject received one of three alcohol doses (0.0; 0.4 or 0.6 g/kg): the same dose in both sessions of each experiment. Blood alcohol level (BAL), reaction time, and self-rating intoxication scores were recorded. The variables studied did not alter either BAL or reaction time values. The expectancy manipulation changed the self-rated intoxication with the lower alcohol dose (0.4 g/kg). So when doubt had been raised the subjects rated themselves as less intoxicated. However, this change was only found with a verbal scale. The attention demanding tasks manipulation did not change the self-rating evaluations. It is suggested that the tasks performed were not appropriate to motivate the subjects to stay sober. The differential sensitivity of the self-rating intoxication scales utilized, and the role of alcohol dose in the study of nonpharmacological variables are discussed.

Adolescent

The excitatory effect of ethanol: absence in rats, no tolerance and increased sensitivity in mice.

Three questions related to ethanol's stimulating effect (ESE) were studied. The first referred to the reported absence of tolerance to ESE in mice. It was determined whether tolerance would develop if the period of ethanol treatment were extended significantly beyond those normally found in the literature. No evidence of tolerance to ESE was found over a 5-month period of treatment. The second issue related to the possibility that mice not only do not develop tolerance but actually become more responsive to ESE after chronic exposure. A dose of ethanol that acutely did not produce a significant activating effect did induce a marked excitation after the animals were chronically treated with ethanol. Finally, the issue was addressed of whether the absence of ESE in some strains of rats could in part be due to a masking effect by the depressant component of this drug. To test this possibility rats were treated with ethanol for a 4-month period. Tolerance to the depressant effect was observed but no ESE was detected.

Animals

Hypoglycemia and hypothermia induced by ethanol: antagonism by indomethacin.

The influence of pretreatment with 5.0 or 10.0 mg/kg of indomethacin, a prostaglandin synthetase inhibitor, on the alterations in body temperature produced by 3.0 and 4.0 g/kg of ethanol, was studied in food-deprived and free-feeding rats. A partial antagonism of ethanol's hypothermic effect resulted from indomethacin pretreatments and this effect was found to be ethanol dose-dependent. This result could account for the conflicting reports in the literature on the effectiveness of indomethacin in antagonizing ethanol-induced hypothermia. Indomethacin (5.0 mg/kg) also antagonized ethanol-induced hypoglycemia in 48 hr starved rats. The relationship between two effects of ethanol, hypothermia and hypoglycemia, is discussed.

Animals

Alcohol use among adolescents in São Paulo, Brazil.

Drinking habits was studied in a sample of 3114 students from a low socioeconomic level and aging from 9 to 18 years. Males and females were equally represented in the sample. The survey showed that 27% were non-drinkers, 54% experimental drinkers, 14% moderate regular drinkers and 5% excessive regular drinkers. The excessive regular drinkers reported a higher proportion of heavy alcohol consumption among close relatives, mainly fathers. Sex and age-related differences were found in the drinking pattern. Males as well as oldest students were over represented among the drinkers excepted for excessive regular drinkers where no age difference was detected. This finding (same proportion of excessive regular drinkers in all age groups) was discussed taking into account the possibility that the high drop out rates in Brazilian schools could be introducing a bias in the figures found for the oldest adolescent groups. Beliefs about drinking consequences and location where most drinking occurs were also studied.

Adolescent

Lack of agreement between two questionnaires that evaluate the severity of the alcohol dependence syndrome.

The Short-Alcohol Dependence Data (SADD) and the Alcohol Dependence Scale (ADS) questionnaires, both designed to evaluate the degree of severity of alcohol dependence, were compared in a sample of 201 known alcoholics. Although a significant correlation was found between the scores obtained on the two scales (r = 0.61; P less than 0.01), respondents were classified differently by the two questionnaires (Kappa = 0.20). Subjects were generally considered less dependent by the ADS than by the SADD. Different possibilities that could explain the differential classification are discussed.

Adult

Reversal of abnormal dexamethasone suppression test in alcoholics abstinent for four weeks.

Fourteen of 64 alcoholic inpatients (22%) showed a nonsuppression postdexamethasone response when tested between the second and fifth days of admission. No association with alterations of hepatic enzymes (GGT, SGOT, SGPT) was observed. At retest (in the fourth week of abstinence), no abnormal response to the Dexamethasone Suppression Test (DST) was detected. The nonsuppressor alcoholics did not meet the criteria for major depression according to the Research Diagnostic Criteria (RDC). The data indicate a lack of specificity of the DST for the diagnosis of depression in alcoholics during the first days of withdrawal.

Adult

Diagnostic of alcoholism: how useful is the combination of gamma glutamyl transferase with different biochemical markers?

The present paper analyses the alterations in sensitivity, specificity and in the positive predictive value (PPV) of GGT as a state marker of alcohol abuse when used either alone or in combination with glutamate pyruvate transaminases (SGPT), glutamate oxalacetate (SGOT) and mean corpuscular volume (MCV). The results obtained with an alcoholic (n = 70) and non-alcoholic sample (n = 63) showed that the best combination considering sensitivity was obtained when GGT was combined with MCV (80%). However, this combination produced the largest decrease in PPV. The relevance of taking into account not only sensitivity but also PPV when the markers are to be used as screening tests in unselected populations is discussed.

Adult

An attempt to improve the identification of alcohol-dependent patients in a teaching general hospital.

The information on drinking habits contained in medical records with that obtained through the CAGE alcoholism screening test was compared for 124 inpatients of a teaching general hospital. This survey was followed by testing the possibility of introducing the CAGE test into the routine clinical interview. A second analysis of 110 medical records performed 2 months later indicated the failure of this attempt, as the general pattern of information on drinking habits remained unaltered and characterized by either no information at all or information that was too ambiguous to be of clinical value. Among the different hypotheses that could account for the negative results is the possibility that physicians are not sufficiently informed on the wide spectrum of clinical disorders associated to alcohol abuse. Another important factor is the lack of motivation shown by attending physicians to detect less obvious cases of alcohol dependence as they feel pessimistic about dealing with this condition.

Alcoholism

Ethanol induces hyper and hypoglycemia in both fasted and nonfasted rats dependent on the ambient temperature.

An experiment was undertaken to characterize the influence of ambient temperature on ethanol-induced glycemic alterations in rats. Animals under two different feeding conditions (nonfasted or 48-hr fasted) were IP injected with 4.0 g/kg of ethanol. Blood glucose and body temperature were measured before, 90 and 180 min after drug administration. The rats were tested under ambient temperatures of 16, 21 and 32 degrees C. Fed animals with a mean pre-drug glycemia of near 105 mg/100 ml presented a variation of blood glucose ranging from 50 mg/100 ml at 16 degrees C to 140 mg/100 ml at 32 degrees C. The glycemia from fasted rats, with a starting value of 70 mg/100 ml ranged from 20 to 115 mg/100 ml at 16 and 32 degrees C, respectively. It was concluded that the administration of ethanol can render nonfasted as well as fasted rats hypo or hyperglycemic, depending upon the environmental temperature.

Animals

Nephrectomy enhances alcohol-induced hypoglycemia in fasted rats.

Male Wistar rats (N = 84) weighing 230-270 g were fasted 48 hr. Equal groups were controls, nephrectomized bilaterally and sham-operated. Equal subgroups were then given 4.0, 6.0 or 7.5 g of alcohol per kg of body weight or water by orogastric intubation. Blood glucose levels did not decrease significantly after nephrectomy alone or after the 4.0 g/kg dose. Blood glucose declined significantly more in the nephrectomized than in the sham-operated rats at 90 and 180 min after the 6.0 g/kg dose. Blood glucose decreased significantly in both the nephrectomized and sham-operated rats after the 7.5 g/kg dose.

Alcohol Drinking