Key result
Stroke-prone hypertensive rats demonstrate faster cerebral spin-probe decay, reflecting increased brain oxidative stress.
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A number of researchers have reported that free radicals generated in the brain are involved in various brain dysfunctions, including ischemia-reperfusion injury, brain tumors, and neurodegenerative diseases. It has been reported that the spin probe MC-PROXYL can penetrate the blood-brain barrier and can be useful for evaluating oxidative stress in the brain. Preliminary comparisons were made by ESR imaging of the heads of live mice and isolated rat brains using the spin probe MC-PROXYL and the blood-brain-barrier impermeable probe carbamoyl-PROXYL. The results showed that MC-PROXYL, but not carbamoyl-PROXYL, was widely distributed in the brain. These methods were also applied for the imaging of brains from stroke-prone spontaneously hypertensive rats (SHRSPs). The rapid decay of 2D ESR images of MC-PROXYL in isolated SHRSP-brain was observed, compared to Wistar-Kyoto rats (WKYs), using the ESR imaging system. Furthermore, we provide evidence, by using L-band ESR non-invasively, that the decay rate of MC-PROXYL in the head region is faster in live SHRSPs than in live WKYs. Taken together, the high oxidative stress sustained by oxygen radical generation in SHRSPs may cause the alteration of MC-PROXYL metabolism in the brain. Our results suggest that in vivo ESR could be applied to the assessment of antioxidant effects on oxidative stress in the brain in animal disease models, such as the SHRSP.
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Miyazaki et al. (2002) studied Hypertension / cerebral oxidative stress (animal model). In vivo L-band electron spin resonance (ESR) spectroscopy using MC-PROXYL spin probe vs. Carbamoyl-PROXYL spin probe and Wistar-Kyoto control rats (WKYs) was evaluated on Distribution and decay rate of MC-PROXYL in the brain/head region on 2D ESR imaging. In vivo ESR spectroscopy with MC-PROXYL showed a faster spin-probe decay rate in the brain of stroke-prone spontaneously hypertensive rats vs Wistar-Kyoto controls, indicating higher oxidative stress.
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