Abstract

Circulation through cerebral collaterals can maintain tissue viability until reperfusion is achieved. However, collateral circulation is time limited, and failure of collaterals is accelerated in the aged. Remote ischemic perconditioning (RIPerC), which involves inducing a series of repetitive, transient peripheral cycles of ischemia and reperfusion at a site remote to the brain during cerebral ischemia, may be neuroprotective and can prevent collateral failure in young adult rats. Here, we demonstrate the efficacy of RIPerC to improve blood flow through collaterals in aged (16–18 months of age) Sprague Dawley rats during a distal middle cerebral artery occlusion. Laser speckle contrast imaging and two-photon laser scanning microscopy were used to directly measure flow through collateral connections to ischemic tissue. Consistent with studies in young adult rats, RIPerC enhanced collateral flow by preventing the stroke-induced narrowing of pial arterioles during ischemia. This improved flow was associated with reduced early ischemic damage in RIPerC treated aged rats relative to controls. Thus, RIPerC is an easily administered, non-invasive neuroprotective strategy that can improve penumbral blood flow via collaterals. Enhanced collateral flow supports further investigation as an adjuvant therapy to recanalization therapy and a protective treatment to maintain tissue viability prior to reperfusion.

Highlights

  • Circulation through cerebral collaterals can maintain tissue viability until reperfusion is achieved

  • Our findings demonstrated that Remote ischemic perconditioning (RIPerC) induced by bilateral femoral occlusion (BFO) 1 h after distal middle cerebral artery occlusion is effective in reducing early ischemic damage and improves collateral blood flow by preventing collateral narrowing in aged animals

  • Previous studies suggest that pial collateral blood flow fails over time in aged rats after distal middle cerebral artery occlusion (dMCAO), exacerbating the insufficient perfusion of the penumbra and leading to greater ischemic d­ amage[16]

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Summary

Introduction

Circulation through cerebral collaterals can maintain tissue viability until reperfusion is achieved. Consistent with studies in young adult rats, RIPerC enhanced collateral flow by preventing the stroke-induced narrowing of pial arterioles during ischemia. This improved flow was associated with reduced early ischemic damage in RIPerC treated aged rats relative to controls. Strategies that can augment collateral blood flow to reduce expansion of the infarct core before recanalization treatment may extend the time window for reperfusion interventions and allow more patients to ­benefit[3]. Our findings demonstrated that RIPerC induced by BFO 1 h after distal middle cerebral artery occlusion (dMCAO) is effective in reducing early ischemic damage and improves collateral blood flow by preventing collateral narrowing in aged animals

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