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Biomedical subjects

E Hård

Publications and source records attributed to E Hård.

At least 37 records · Page 2Linked to original sources
PubMed1977

Influence of maternal stress on offspring sexual behaviour.

During the last trimester of gestation, pregnant rats were exposed to crowded living conditions, or to immobilization combined with intense illumination. In adulthood, male offspring of mothers exposed to either condition of stress showed increased readiness to display feminine sexual behaviour (lordosis) while no deficits were observed in their masculine sexual behaviour. It was concluded that prenatal stress adversely affects sexual differentiation by causing a feminization but not a demasculinization of male offspring.

Animals↗
PubMed1977

Open field behavior and gross motor development in offspring of nursing rat mothers given penfluridol.

Nursing rat mothers were injected with penfluridol, a dopamine receptor blocking agent, at Day 1, 3, 5 and 7 after delivery, and their offspring were investigated at 6-18 days of age for various aspects of motor behavior development, and at 4, 8 and 12 weeks of age for open field behavior. No deficits were found in the development of locomotion, air righting, startle response and eye opening. Open field ambulation decreased from an abnormally high level at 4 weeks of age to an abnormally low level at 8 and 12 weeks of age. The ability to habituate to an open field decreased from a normal level at 4 weeks of age to an abnormally low level after 8 weeks of age. The behavior deficits were related to a decreased functional activity of the mesolimbic dopamine neuron system, and the possible relation to a clinical dysfunction among children - minimal brain dysfunction - was discussed.

Age Factors↗
PubMed1975

Development of air righting in rats.

Rats aged between 13 and 18 days were dropped from different heights in order to establish the height at which 50% of the animals were able to perform complete air righting. The proportion of animals showing complete air righting abruptly increased at 16 days of age indicating maturation of the response at this age. No necessary relationship was observed between eye opening and air righting. At 15 days of age, when normally only a minority of the rats are able to display complete air righting, a marked effect of training was observed.

Age Factors↗
PubMedDate not supplied

Effects of the 5-HT receptor agonist, 8-OH-DPAT, on ethanol preference in the rat.

Clinical and animal studies have suggested that consumption of ethanol is influenced by the central serotonergic (5-HT) transmission system. In the present study this hypothesis was tested by observing the effects of a selective 5-HT receptor agonist, 8-OH-DPAT, on ethanol preference in the rat. The rats had access to a 6% (v/v) ethanol solution and water during baseline and treatment periods. Based on the baseline recordings, 2 groups of rats were formed: A high preference group (ethanol intake greater than 50% of total fluid intake) and a low preference group (ethanol intake less than 30%). Both groups were treated SC with 0.125 mg/kg 8-OH-DPAT twice daily for 3 days. The treatment caused a significant reduction of ethanol consumption in the high preference group, but no change in the low preference group. The findings support the hypothesis that activation of the 5-HT system reduces ethanol intake. This effect was restricted to the high preferring rats, suggesting that 8-OH-DPAT interferes only with the positive reinforcing effect of ethanol.

8-Hydroxy-2-(di-n-propylamino)tetralin↗
PubMedDate not supplied

Audiogenic immobility reaction and open-field behavior in AA and ANA rat lines.

Individual predispositions in emotional reactivity have been suggested as factors involved in the development of alcoholism. To approach this problem, we assessed emotional reactivity in alcohol-naive animals from the alcohol-preferring (AA) and alcohol-avoiding (ANA) rat lines of Alko Ltd. AA rats are known to have higher brain levels of 5-hydroxytryptamine (5-HT) than ANA rats. Emotional reactivity was therefore assessed by an audiogenic immobility reaction (freezing), which is specifically sensitive to and shortened by depletion of 5-HT. The results showed that AA rats of both sexes displayed increased immobility reactions compared to the corresponding sex of the ANA rats. During the period of adaptation to the test cage ANA rats of both sexes showed increased locomotor activity compared to the corresponding sex of the AA rats. Levels of plasma corticosterone did not differ between the rat lines, either during resting or stressful conditions. The present results suggest that a passive, inhibited style of defensive behavior is associated with a high alcohol consumption.

Acoustic Stimulation↗
PubMedDate not supplied

Involvement of the serotonergic system in ethanol intake in the rat.

A two-bottle, free-choice paradigm was used to investigate the influence of the serotonergic (5-HT) system on ethanol intake in genetically heterogeneous Wistar rats. Systemic administration of the 5-HT1A agonist ipsapirone (1.25-5.0 mg/kg) caused a dose-dependent decrease in ethanol preference and intake, while the 5-HT2 antagonist ritanserin (1.25-5.0 mg/kg) and the 5-HT3 antagonists ondansetron (0.01-1.0 mg/kg) and granisetron (0.5-1.0 mg/kg) failed to alter ethanol consumption. The effect of ipsapirone treatment on ethanol intake was more pronounced in high-preferring animals than in low-preferring. A closer look at the microstructure of the rat's drinking behaviour by means of a microcomputer-controlled data acquisition system showed that ipsapirone treatment caused a significant decrease in the number of licks recorded at the ethanol-containing bottle and a decrease in the time spent at this bottle. Furthermore, ipsapirone treatment caused a significant increase in the number of breaks in licking behaviour recorded at this bottle. The drinking behaviour at the water-containing bottle was not affected by the ipsapirone treatment. Neither was the rat's eating behaviour altered by this treatment. These findings support the hypothesis that the 5-HT system is involved in the regulation of ethanol intake, with special emphasis on the involvement of the 5-HT1A receptor subtype, and may indicate that central reward-mediating mechanisms are influenced.

Alcohol Drinking↗
PubMedDate not supplied

Involvement of corticosterone in the modulation of ethanol consumption in the rat.

Several studies report that rats exposed to stressful conditions may increase their ethanol consumption. Stress is accompanied by a rise in the secretion of adrenocortical hormones, and the possibility that these hormones exert an influence on ethanol consumption should be considered. The present investigation addressed this issue by studying the effect of adrenalectomy (ADX) and subsequent corticosterone (CORT) or aldosterone (ALDO) treatment on ethanol intake. The results showed that ADX rats decreased their ethanol intake compared to the sham-operated controls and that treatment with CORT restored the intake of ethanol to the preoperative level. In contrast, treatment with ALDO (0.25 or 0.75 mg/kg) had no effect on ethanol intake. Biochemical analyses showed increases in monoamine turnover in the brain stem and limbic forebrain after ADX. The reduction of ethanol consumption caused by ADX may thus be specifically attributed to the loss of one of the adrenal hormones, CORT. The results indicate that CORT may be a factor of importance in the modulation of alcohol consumption.

Adrenalectomy↗
PubMedDate not supplied

Taste reactivity to ethanol in rats: influence of adrenalectomy or ipsapirone.

The affective mimetic responses of male Wistar rats with prior access to 6% ethanol in their home cages were observed during intraoral infusions of an equivalent alcohol solution. Ethanol preference in the home cage appeared unrelated to measures of aversion and ingestion in the taste reactivity tests in normal rats. Adrenalectomy, which significantly reduced home cage ethanol preference, failed to influence the taste reactions elicited by ethanol or water. On the other hand, treatment of intact rats with the 5-HT1A receptor agonist ipsapirone (2.5 mg/kg), a drug that also decreases ethanol drinking in two-bottle intake tests, did increase the duration of aversive groomings, whereas measures of ingestion remained unaffected. These results suggest that ipsapirone, but not adrenalectomy, may alter the palatability of ethanol; this perceptual change may partly underlie the ability of ipsapirone to reduce home cage alcohol drinking in the rat.

Adrenalectomy↗