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A Rex

Publications and source records attributed to A Rex.

23 records · Page 2Linked to original sources

Effects of BOC-CCK-4 and L 365.260 on cortical 5-HT release in guinea-pigs on exposure to the elevated plus maze.

The elevated plus maze is a well-established model of anxiety, with previous results showing that guinea-pigs handled daily from birth exhibit behaviour in this test similar to rats. In the present microdialysis study exposure of the guinea-pig to the elevated plus maze increased extracellular 5-HT in the lateral prefrontal cortex. The CCK-B receptor agonist BOC-CCK-4 (10 micrograms/kg) produced 'anxious' behaviour and potentiated the rise in 5-HT observed on exposure to the X-maze. The basal release of cortical extracellular 5-HT was not affected by BOC-CCK-4. Pretreatment with the selective CCK-B antagonist L 365.260 (100 micrograms/kg) antagonized both the 'anxious' behaviour and the neurochemical changes induced by BOC-CCK-4 while L 365.260 alone produced 'anxiolytic' behaviour, decreased basal extracellular 5-HT and prevented the increase in extracellular 5-HT seen when the guinea-pigs were exposed to the X-maze. Our results show that CCK-B receptor stimulation and blockade induce changes in central extracellular 5-HT levels associated with 'anxious' and 'anxiolytic' behaviour, respectively.

Animals↗

Different effects of diazepam in Fischer rats and two stocks of Wistar rats in tests of anxiety.

The behaviour of animals in tests of anxiety varies between strains, even in identical tests and surroundings. To evaluate the results obtained, a more detailed knowledge of the behaviour of different rat strains is indispensable. Identically raised Fischer 344 rats and two stocks of Wistar rats were examined in two animal tests of anxiety: the X-maze and a modified open-field test following diazepam treatment (0.5-4.0 mg/kg). Harlan-Wistar rats were the least 'anxious' when the behaviour of vehicle treated controls was compared. The largest effect of the anxiolytic diazepam, however, was observed in Harlan-Fischer rats. To determine possible reasons for strain and stock differences, plasma concentrations of diazepam and metabolites and concentrations of serotonin (5-HT) in the CNS were measured. Plasma concentrations of diazepam and metabolites differed between the strains with the Harlan-Fischer rats showing higher diazepam concentrations. 5-HT levels in discrete brain regions varied with Harlan-Fischer rats having higher 5-HT concentrations. Strain differences influence the anxiety-associated behaviour of untreated animals and the effect of anxiolytics.

Animals↗