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At least 271 records · Page 15Linked to original sources

Functions of the frontal cortex of the rat: a comparative review.

This review summarizes the anatomical and functional organization of the frontal cortex of the rat in comparison to primates. Lesions of the primary motor or of the prefrontal cortex of both primates and rodents produce a consistent constellation of symptoms that are strikingly similar across species as diverse as rats and humans. Thus, in spite of the tremendous difference in the relative volume of the frontal cortex of mammals, as well as the obvious diversity of behavioral repertoires across mammalian phylogeny, there appears to be a remarkable unity in frontal cortex function across the class mammalia. Hence, motor and prefrontal lesions produce analogous alterations in motor control in rodents and primates even though humans walk upright and have fine control of digit movement and rats walk on all fours and have less dextrous control of distal movements. Similarly, there are analogous changes in behaviors that can be labeled response inhibition, temporal ordering, spatial orientation, social or affective behavior, behavioral spontaneity, olfaction and habituation following prefrontal cortex lesions in both primates and rodents. Finally, it is proposed that the principal function of the prefrontal cortex of mammals is the temporal organization of behavior.

Animals↗

Field trials of flocoumafen against warfarin-resistant infestations of the Norway rat (Rattus norvegicus Berk.).

The anticoagulant rodenticide flocoumafen was tested against warfarin-resistant Norway rats (Rattus norvegicus Berk.) infesting farm buildings. Complete control was obtained in 10-21 days (mean 14.2 days) in six treatments in which baits poisoned with 0.005% flocoumafen were maintained, in surplus, until rats ceased to feed from them. A further six treatments, in which the application of poisoned bait was restricted to periodic placements of 50 g, were also completely successful in 15-30 days (mean 21.0 days). Less poisoned bait was used in the restricted flocoumafen treatments than in the unrestricted treatments but the time taken to control the rat infestations was significantly longer.

4-Hydroxycoumarins↗

Field trials of bromadiolone against infestations of warfarin-resistant Rattus norvegicus.

Baiting with 0.005% bromadiolone in medium oatmeal or soaked wheat completely controlled infestations of warfarin-resistant rats on farms when surplus amounts of the poisoned baits were maintained until rats ceased to feed on them. The speed with which control was achieved was the same as with other anticoagulants that have been tested in this way.Poison baiting with 0.005% bromadiolone for only 1, 4 or 7 days achieved respectively about 49, 77 and 81% control of similar farm rat infestations.

4-Hydroxycoumarins↗

Pen and field trials of flupropadine against the house mouse (Mus musculus L.).

Laboratory and field trials were conducted to determine the efficacy of the candidate rodenticide flupropadine against the house mouse (Mus musculus L.). In laboratory feeding tests, family groups of wild mice maintained in pens and conditioned to feeding on plain foods were offered flupropadine at either 0.10%, 0.15%, 0.18% or 0.20% in pinhead oatmeal bait. Overall mortalities in replicated 21-day treatments were 66/71 (93.0%), 71/79 (89.9%), 72/76 (94.7%) and 69/75 (92.0%) respectively. In 17 field trials carried out against mice infesting farm buildings, flupropadine was used at 0.10%, 0.15% and 0.18% in oatmeal bait. Mean treatment success, estimated from live-capture and mortality data, was 88.6%, 96.2% and 96.6% respectively. Flupropadine was found to be as near effective against mice as calciferol/warfarin and the second-generation anticoagulant rodenticides difenacoum, bromadiolone and brodifacoum. In further comparison with the anticoagulants, treatment with flupropadine bait achieved markedly quicker control.

Animals↗

Cadmium treatment and lead-induced suppression of splenic erythropoiesis.

Young adult female mice were injected with lead acetate (d 0). Following injection, determinations were made of the percentages of radioactive iron (59Fe) uptake into the hemoglobin of erythrocytes produced by spleen. Control 59Fe uptake percentage vacillated between 4.2 and 5.5 within the 7-d period of observation. On d 4 following lead treatment, splenic percentages were dramatically reduced below those of the saline-injected controls; by d 6 the splenic 59Fe uptake of lead-treated mice was comparable to that of controls. For rodents injected with cadmium chloride on 0, the 59Fe uptake values showed a statistically significant elevation by d 2, which was extended beyond that of the controls' d 4 value. For those animals receiving both lead and cadmium (d 0), the uptake percentages paralleled those of the controls throughout the 7-d period of observation. These data suggest that the inhibitory effect of lead on erythropoiesis of the spleen is blocked by a concurrent cadmium treatment. Results are interpreted in regard to a possible vulnerable target and competition for the target by lead and cadmium.

Animals↗

Laboratory test of seven rodenticides for the control of Mastomys natalensis.

Laboratory feeding tests were carried out to assess the efficacy of seven rodenticides against Mastomys natalensis. The poisons (warfarin, coumatetralyl, difenacoum, brodifacoum, bromadiolone, calciferol and zinc phosphide) were all toxic at the concentrations normally used against Rattus norvegicus (Berk.), although several were unpalatable. Trials are now needed to demonstrate the relative efficacy of these poisons in the field, but it is likely that, given suitable bait formulations, they would all be useful as practical control agents.

4-Hydroxycoumarins↗

Field trials of a new sub-acute rodenticide flupropadine, against wild Norway rats (Rattus norvegicus).

Fifteen experimental treatments with rodenticidal baits containing 0.1, 0.15 or 0.2% flupropadine were conducted on farmsteads against Rattus norvegicus infestations. Eight treatments were completely successful and the others gave kills ranging from 36 to 72% in 28 days. Treatments with 0.1 and 0.15% flupropadine were less successful against large infestations than against small ones. Flupropadine was most successful at 0.2% but still gave incomplete kills on farms where abundant alternative food was available. The compound was more effective than acute poisons in achieving complete control of Norway rat infestations, but was less reliable in doing so than anticoagulants. On the other hand, many flupropadine treatments gave quicker control and used smaller quantities of bait than anticoagulant treatments.

Animals↗