Abstract 2487: Ischemia/Reperfusion Injury Impairs Myogenic Tone of Cerebral Vessels in both Ischemic and Nonischemic Hemispheres: Differential Role of Oxidative Stress.
Cerebrovascular autoregulation and reactivity are critical to maintain constant perfusion during ischemic brain injury. It is known that ischemia/ reperfusion (I/R) injury and resulting oxidative stress impair vessel reactivity in ischemic hemisphere. Yet the behavior of vessels in nonischemic hemisphere is still unexplored. Hypothesis: I/R injury impairs myogenic tone of vessels in both ischemic and nonischemic hemispheres via increased peroxynitrite (ONOO - ) generation. Methods: Middle cerebral arteries (MCA) isolated from age matched male Wistar rats (n=6) subjected to 30 min MCA occlusion (MCAO)/45 min reperfusion, or MCAO followed by treatment with ONOO - scavenger FeTPPs (20mg/kg) at reperfusion were pressurized in arteriograph chamber. In another set of animals, MCA isolated from control Wistar rats were exposed to ex vivo oxygen-glucose deprivation (OGD) then their myogenic tones across the pressure range were determined. Results: I/R injury impaired myogenic tone of vessels in both ischemic and nonischemic sides albeit to a different degree. Interestingly FeTPPs restored myogenic tone of vessels from ischemic side only ( Table ). Vessels exposed to ex vivo and in vivo hypoxia experienced loss of myogenic tone. The reduction of myogenic tone % by OGD is similar to I/R injury. Conclusion: Our ex vivo model of hypoxia is a valuable method to assess the ischemic insult on vessel reactivity. Increased ONOO - production is one of the underlying mechanisms of loss of tone under I/R injury in ischemic hemisphere, but the impairment of myogenic tone in nonischemic hemisphere involves other mechanisms. Understanding how I/R alters myogenic tone and ultimately cerebral perfusion in both ischemic and nonischemic hemispheres is vital in improving current preventive and therapeutic strategies for acute stroke. + p<0.001, * p< 0.05 vs Sham, # p<0.001 vs ischemic MCA , ** p<0.01 vs nonischemic MCA