•  
  •  
 

Abstract

Regional cerebral blood flow (CBF) decreases with aging. This reduction may be due to a diminished endothelium-dependent vasodilation in large cerebral arteries with aging in the absence of disease. The posterior communicating arteries (PCoA) supply blood flow to the midbrain areas where age-related regional decreases in blood flow have been observed. Furthermore, the PCoA appear to be clinically relevant in age-related cerebrovascular disorders. However, age-related changes in the vasoreactivity of PCoA have not been investigated in the absence of disease. The purpose of this study was to determine the effect of aging on endothelium-dependent vasodilation of PCoA in rats. Posterior communicating arteries (PCoA) were isolated from the brain of 4 month old (n = 4) and 24 month old (n = 4) male Fischer 344 rats. The isolated arteries were cannulated and pressurized to 90 cm H2O via hydrostatic reservoirs. Luminal diameter changes were determined in response to the endothelium-dependent vasodilator, Bradykinin (BK) (10-13 – 10-7 M) and the direct vascular smooth muscle dilator, sodium nitroprusside (SNP, 10-10 – 10-4 M). Responsiveness to the endothelium-dependent vasodilator BK was diminished in PCoA of aged rats compared to young rats, whereas responsiveness to the endothelium-independent vasodilator SNP was not different between PCoA of young and old rats. These data demonstrate that aging is associated with diminished endothelium-dependent vasodilation in PCoA, whereas vascular smooth muscle responsiveness remains intact. Thus, regional age-related reductions in cerebral blood flow may be related to diminished endothelium-dependent vasodilation in PCoA.

Share

COinS
 

To view the content in your browser, please download Adobe Reader or, alternately,
you may Download the file to your hard drive.

NOTE: The latest versions of Adobe Reader do not support viewing PDF files within Firefox on Mac OS and if you are using a modern (Intel) Mac, there is no official plugin for viewing PDF files within the browser window.