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In This Article

  • Summary
  • Abstract
  • Introduction
  • Protocol
  • Representative Results
  • Discussion
  • Disclosures
  • Acknowledgements
  • Materials
  • References
  • Reprints and Permissions

Summary

A mouse model of cerebral ischemia-reperfusion is established to investigate the pathophysiology of stroke. We distally ligate the right middle cerebral artery and right common carotid artery and restore blood flow after 10 or 40 min of ischemia.

Abstract

In this study, a middle cerebral artery (MCA) occlusion mouse model is employed to study cerebral ischemia-reperfusion. A reproducible and reliable mouse model is useful for investigating the pathophysiology of cerebral ischemia-reperfusion and determining potential therapeutic strategies for patients with stroke. Variations in the anatomy of the circle of Willis of C57BL/6 mice affects their infarct volume after cerebral-ischemia-induced injury. Studies have indicated that distal MCA occlusion (MCAO) can overcome this problem and result in a stable infarct size. In this study, we establish a two-vessel occlusion mouse model of cerebral ischemia-reperfusion through the interruption of the blood flow to the right MCA. We distally ligate the right MCA and right common carotid artery (CCA) and restore blood flow after a certain period of ischemia. This ischemia-reperfusion injury induces an infarct of stable size and a behavioral deficit. Peripheral immune cells infiltrate the ischemic brain within the 24 h infiltration period. Additionally, the neuronal loss in the cortical area is less for a longer reperfusion duration. Therefore, this two-vessel occlusion model is suitable for investigating the immune response and neuronal recovery during the reperfusion period after cerebral ischemia.

Introduction

The cerebral ischemia-reperfusion mouse model is one of the most widely used experimental approaches for investigating the pathophysiology of ischemia-induced brain injury1. Because cerebral ischemia-reperfusion activates the peripheral immune system, peripheral immune cells infiltrate into the ischemic brain and cause neuronal damage2. Thus, a reliable and reproducible mouse model that mimics cerebral ischemia-reperfusion is required to understand the pathophysiology of stroke.

C57BL/6J (B6) mice are the most commonly used strain in stroke experiments because they can easily be genetically ma....

Protocol

The institutional animal care and use committees of Academia Sinica and Taipei Medical University approved this protocol for the use of experimental animals.

1. MCAO/reperfusion model

  1. Provide the mice with free access to water and chow until the surgery.
  2. Autoclave the surgical tools and sanitize the surgery table and equipment using 70% ethanol. Wear a surgical mask and sterile gloves. Use a dry bead sterilizer to resterilize the surgical tools if multiple mouse surgeries will be conducted in one experiment.
  3. Anesthetize an 8- to 12-week-old mouse (mass: 25–30 g) by using 0.8% chloral hydrate, via an int....

Representative Results

This MCAO/reperfusion procedure produced a cortical infarct in the vicinity of the right MCA and caused a behavioral deficit. Different degrees of ischemia-induced infarct volume (Figure 1A,B) and neuronal loss (Figure 1C,D) were created in the cerebral cortex of the right MCA area through an increase in ligation duration. This MCAO/reperfusion injury decreased the animal's locomotor activity.......

Discussion

The MCAO/reperfusion mouse model is an animal model commonly employed to mimic transient ischemia in humans. This animal model can be applied to transgenic and knockout mice strains to investigate the pathophysiology of stroke. Several steps in the protocol are especially critical. (1) The microdrill must be carefully used when creating a hole in the skull, with inappropriate action easily causing bleeding from the MCA. (2) The MCA should not be damaged, and bleeding must be avoided before and after the ligation procedur.......

Disclosures

The authors have nothing to disclose.

Acknowledgements

This work was supported by the Ministry of Science and Technology, Taiwan (MOST 106-2320-B-038-024, MOST 105-2221-E-038-007-MY3, and MOST 104-2320-B-424-001) and Taipei Medical University Hospital (107TMUH-SP-01). This manuscript was edited by Wallace Academic Editing.

....

Materials

NameCompanyCatalog NumberComments
Bone rongeurDienerFriedman
BuprenorphineSigmaB-044
CefazolinSigma1097603
Chloral hydrateSigmaC8383
Dissection microscopeNikonSMZ-745
Electric clippersPetpro
10% formalinSigmaF5304
Germinator dry bead sterilizerBraintree Scientific
Iris ForcepsKarl Klappenecker10 cm
Iris ScissorsDiener9 cm
Iris Scissors STRKarl Klappenecker11 cm
MicrodrillStoeltingFOREEDOM K.1070
Micro-scissors-VannasHEISSH-4240blade 7mm, 8 cm
Mouse brain matrixWorld Precision Instruments
Non-invasive blood pressure systemMuromachiMK-2000ST
Operating Scissors STRKarl Klappenecker14 cm
Physiological Monitoring SystemHarvard Apparatus
Razor bladesEver-Ready
Stoelting Rodent WarmersStoelting53810Heating pad
Suture clipStoelting
TweezersIDEALTEKNo.3
Vetbond3M15672Surgical glue
10-0 sutureUNIKNT0410
2,3,5-Triphenyltetrazolium chlorideSigmaT8877

References

  1. Woodruff, T. M., et al. Pathophysiology, treatment, and animal and cellular models of human ischemic stroke. Molecular Neurodegeneration. 6 (1), 11 (2011).
  2. Chamorro, A., et al. The immunology of acute stroke.

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