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Showing papers by "Angela Clow published in 1999"


Journal ArticleDOI
TL;DR: The present findings do not support a predominantly gluconeogenic role for morning cortisol activation and challenge the view that an oxidisable substrate for energy metabolism is permissive for cortisol responses.

65 citations


Journal ArticleDOI
TL;DR: It is concluded that generation of MAO-AI, which is associated with HPA activation induced by psychological stress, is not a component of the pathways involved in immunological stimulation of the HPA axis.

11 citations


Journal Article
TL;DR: There was a dissociation between effects on locomotor activity and antioxidant enzyme induction and the only potentially neuroprotective effect caused by these drugs was an induction of catalase.
Abstract: The putative neuroprotective drugs (-)-deprenyl and pergolide were administered to rats from 3 to 19 months of age and effects on activity in the Hole Board apparatus monitored. The antioxidant enzymes catalase, glutathione peroxidase (GPx) and CuZn superoxide dismutase (SOD) in the striatum were measured at 6 and 12 months. There was a pronounced age related decrease in line crossing, head dipping and rearing in the control animals. At 6 months the pergolide treated group were more active in line crossing than their controls, and the (-)-deprenyl treated group were less active. However by 19 months there was no difference between either drug treated group and its controls in any activity. In control animals here was a significant decrease in both catalase and CuZnSOD between 6 and 12 months, but not in GPx. Both drugs caused a significant increase in catalase, after both 6 and 12 months, but had no effect on CuZn SOD and GPx activity. Thus there was a dissociation between effects on locomotor activity and antioxidant enzyme induction. The only potentially neuroprotective effect caused by these drugs was an induction of catalase.

5 citations


Journal ArticleDOI
TL;DR: There was a marked decrease in 3H-mazindol binding in the injected controls compared with the untreated controls at both 12 and 20 months, raising the possibility that mild chronic stress may accelerate the aging of the dopamine system.

4 citations