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Vol. 286, Issue 3, 1397-1403, September 1998
Departments of
Pharmacology, Universidad Complutense, Madrid 28040 Spain (J.C.L.);
Pharmacology (E.S., G.S., M.W.R.) and
Surgery (J.C.R.),
University of Alberta, Edmonton, AB, Canada, T6G 2H7
We have investigated the effects of early phases of chronic stress on
generation and actions of nitric oxide (NO) in JCR:LA-cp rats both lean
(+/+) and obese (cp/cp). Restraint stress was carried out
for a 15-min single exposure or for 1 hr every day during 4, 9 or 14 days. The stress reaction was evidenced by significant increase in
plasma cortisol. The exposure to stress for 14 days led to a neuronal
damage in lean rats as evidenced by a decrease in glutamate uptake and
an increase in the release of lactate in synaptosomes. This effect was
not observed in obese rats. Concomitantly, the levels of glutamate
increased in the hippocampus at 14 days in lean, but not obese rats,
that showed higher basal levels of glutamate than lean rats. The
activity of NO synthase (NOS) and guanosine cyclic monophosphate levels
increased in the hippocampus preceding the neuronal damage. The
neuronal lesions were prevented by inhibition of NOS without affecting
cortisol levels. In the cardiovascular system, chronic stress exerted
no significant effect on blood pressure, aortic contractility or
platelet aggregation. However, there were significant changes in plasma
nitrite/nitrate that reached maximum at 4 to 9 days. It is concluded
that the generation of NO contributes to the systemic response to the
organism to stress. In the brain, NO appears to be detrimental as this molecule mediates glutamate-dependent hippocampal damage, this effect
being cortisol-independent. In contrast, in the vascular system,
increased generation of NO may attenuate the vasoconstrictor and
platelet aggregatory effects of catecholamines and other mediators of
stress.
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