Intravenous infusion of mesenchymal stem cells inhibits intracranial hemorrhage after recombinant tissue plasminogen activator therapy for transient middle cerebral artery occlusion in rats

Author:

Nakazaki Masahito1,Sasaki Masanori123,Kataoka-Sasaki Yuko1,Oka Shinichi1,Namioka Takahiro1,Namioka Ai1,Onodera Rie1,Suzuki Junpei1,Sasaki Yuichi1,Nagahama Hiroshi1,Mikami Takeshi4,Wanibuchi Masahiko4,Kocsis Jeffery D.23,Honmou Osamu123

Affiliation:

1. Department of Neural Regenerative Medicine, Research Institute for Frontier Medicine, and

2. Department of Neurology, Yale University School of Medicine, New Haven, Connecticut; and

3. Center for Neuroscience and Regeneration Research, VA Connecticut Healthcare System, West Haven, Connecticut

4. Department of Neurosurgery, Sapporo Medical University School of Medicine, Sapporo, Japan;

Abstract

OBJECTIVEReperfusion therapy with intravenous recombinant tissue plasminogen activator (rtPA) is the standard of care for acute ischemic stroke. However, hemorrhagic complications can result. Intravenous infusion of mesenchymal stem cells (MSCs) reduces stroke volume and improves behavioral function in experimental stroke models. One suggested therapeutic mechanism is inhibition of vascular endothelial dysfunction. The objective of this study was to determine whether MSCs suppress hemorrhagic events after rtPA therapy in the acute phase of transient middle cerebral artery occlusion (tMCAO) in rats.METHODSAfter induction of tMCAO, 4 groups were studied: 1) normal saline [NS]+vehicle, 2) rtPA+vehicle, 3) NS+MSCs, and 4) rtPA+MSCs. The incidence rate of intracerebral hemorrhage, both hemorrhagic and ischemic volume, and behavioral performance were examined. Matrix metalloproteinase–9 (MMP-9) levels in the brain were assessed with zymography. Quantitative analysis of regional cerebral blood flow (rCBF) was performed to assess hemodynamic change in the ischemic lesion.RESULTSThe MSC-treated groups (Groups 3 and 4) experienced a greater reduction in the incidence rate of intracerebral hemorrhage and hemorrhagic volume 1 day after tMCAO even if rtPA was received. The application of rtPA enhanced activation of MMP-9, but MSCs inhibited MMP-9 activation. Behavioral testing indicated that both MSC-infused groups had greater improvement than non-MSC groups had, but rtPA+MSCs provided greater improvement than MSCs alone. The rCBF ratio of rtPA groups (Groups 2 and 4) was similar at 2 hours after reperfusion of tMCAO, but both were greater than that in non-rtPA groups.CONCLUSIONSInfused MSCs may inhibit endothelial dysfunction to suppress hemorrhagic events and facilitate functional outcome. Combined therapy of infused MSCs after rtPA therapy facilitated early behavioral recovery.

Publisher

Journal of Neurosurgery Publishing Group (JNSPG)

Subject

Genetics,Animal Science and Zoology

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