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Receptor Autoradiography Protocol for the Localized Visualization of Angiotensin II Receptors
Published on: June 7, 2016
Cerebroprotective effects of angiotensin II (AT 1) receptor antagonists?
Insights
Angiotensin receptor blockers (ARBs) administered during acute stroke phases improve survival and reduce cardiovascular issues. ARBs also demonstrate stroke prevention benefits, potentially through AT2 receptor stimulation, independent of blood pressure reduction.
Area of Science:
- Cardiology
- Neurology
- Pharmacology
Background:
- The Acute Candesartan Cilexetil Therapy in Stroke Survivors (ACCESS) study investigated the effects of angiotensin receptor blockers (ARBs) in acute stroke.
- Antihypertensive trials indicate ARBs possess stroke-preventive properties.
- Animal studies suggest AT2 receptor stimulation by ARBs may reduce cerebral infarct size and mortality.
Approach:
- This report reviews pathophysiological mechanisms and clinical data.
- Evidence for cerebroprotective effects of ARBs is examined.
- The review focuses on effects independent of blood pressure modulation.
Key Points:
- Treatment with ARBs in the acute phase of stroke is associated with improved outcomes.
- ARBs have demonstrated efficacy in preventing stroke in comparative trials.
- AT2 receptor activation by ARBs shows promise in reducing stroke-related brain damage and mortality.
Conclusions:
- ARBs may offer cerebroprotective benefits beyond their antihypertensive actions.
- Further research into ARBs' role in stroke management and prevention is warranted.
- The findings support considering ARBs for neuroprotection in stroke survivors.
Abstract:
The results of the Acute Candesartan Cilexetil Therapy in Stroke Survivors (ACCESS) study show that treatment with an angiotensin receptor blocker (ARB) in the acute phase of a stroke improves mortality and cardiovascular morbidity. In addition, direct comparative antihypertensive trials have demonstrated beneficial effects of ARBs in preventing stroke. These possible cerebro-protective effects of ARBs are supported by animal studies, demonstrating that stimulation of the AT2 receptor was related to a reduction in both cerebral infarct size and mortality. In the present report, we review both pathophysiological and clinical evidence for possible cerebroprotective effects of ARBs, independent of their effect on blood pressure.
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