Article ID Journal Published Year Pages File Type
5501473 Experimental Gerontology 2017 44 Pages PDF
Abstract
Cardiovascular alterations are the most prevalent cause of impaired physiological function in aged individuals with kidney being one the most affected organs. Aging-induced alterations in renal circulation are associated with a decrease in endothelium-derived relaxing factors such as nitric oxide (NO) and with an increase in contracting factors such as endothelin-1(ET-1). As caloric restriction (CR) exerts beneficial effects preventing some of the aging-induced alterations in cardiovascular system, the aim of this study was to analyze the effects of age and caloric restriction in the vascular response of renal arteries to ET-1 in aged rats. Vascular function was studied in renal arteries from 3-month-old Wistar rats fed ad libitum (3 m) and in renal arteries from 8-and 24-month-old Wistar rats fed ad libitum (8 m and 24 m), or subjected to 20% caloric restriction during their three last months of life (8 m-CR and 24 m-CR). The contractile response to ET-1 was increased in renal arteries from 8 m and 24 m compared to 3 m rats. ET-1-induced contraction was mediated by ET-A receptors in all experimental groups and also by ET-B receptors in 24 m rats. Caloric restriction attenuated the increased contraction to ET-1 in renal arteries from 8 m but not from 24 m rats possibly through NO release proceeding from ET-B endothelial receptors. In 24 m rats, CR did not attenuate the aging-increased response of renal arteries to ET-1, but it prevented the aging-induced increase in iNOS mRNA levels and the aging-induced decrease in eNOS mRNA levels in arterial tissue. In conclusion, aging is associated with an increased response to ET-1 in renal arteries that is prevented by CR in 8 m but not in 24 m rats.
Related Topics
Life Sciences Biochemistry, Genetics and Molecular Biology Ageing
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