Key result
Hydrochlorothiazide prevents blood pressure increases and normalizes infarct size after ischemia-reperfusion injury in obese rats.
Why the study?
The determinants of increased stroke risk in obesity, particularly the role of hypertension in cerebral vascular remodeling and stroke severity, are unknown.
Does preventing increased blood pressure with hydrochlorothiazide or a low-sodium diet reduce infarct size and improve cerebral vascular remodeling in obese Zucker rats?
Does preventing increased blood pressure with hydrochlorothiazide or a low-sodium diet reduce infarct size and improve cerebral vascular remodeling in obese Zucker rats?
Preventing hypertension with hydrochlorothiazide normalizes stroke infarct size and improves cerebral vascular remodeling in obese Zucker rats.
Preventing hypertension normalizes infarct size and MCA remodeling in obese rats; leaves open whether BP control alone reduces stroke risk in human obesity.
Obesity is a risk factor for stroke, but the determinants of increased stroke risk in obesity are unknown. We have previously reported that obese Zucker rats (OZRs) have a worse stroke outcome and display evidence of remodeling of the middle cerebral artery (MCA), in parallel with hypertension, compared with lean controls. This study tested the hypothesis that hypertension is an essential determinant of cerebral vascular remodeling and increased stroke damage in OZRs. Blood pressure was measured by telemetry in lean and obese rats with and without hydrochlorthiazide (HCT; 2 mg.kg(-1).day(-1)) from 8 to 15 wk of age. A separate group of rats was also chronically fed a low-sodium (LS) diet. Vessel structure was assessed in isolated, pressurized MCAs. Cerebral ischemia was induced for 60 min using an intralumenal suture technique, followed by 24 h of reperfusion. HCT treatment effectively prevented the increase in blood pressure in obese rats; however, the LS diet did not lower pressure. Importantly, infarct size was normalized by HCT after ischemia-reperfusion injury. Additionally, HCT improved the changes in MCA structure observed in untreated OZRs. There were no benefits of the LS diet on stroke injury or vessel structure. These results indicate that increased pressure is essential for driving the changes in infarct size in OZRs.
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Osmond et al. (2010) studied Obesity, hypertension, and stroke. Hydrochlorothiazide (HCT) vs. Untreated obese Zucker rats and lean controls was evaluated on Infarct size and middle cerebral artery structure after cerebral ischemia-reperfusion injury. Hydrochlorothiazide treatment prevented the increase in blood pressure and normalized infarct size and middle cerebral artery structure in obese Zucker rats after ischemia-reperfusion injury.
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