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Updated: May 30, 2026

The Application Of Permanent Middle Cerebral Artery Ligation in the Mouse
Published on: July 25, 2011
The application of permanent middle cerebral artery ligation in the mouse
Gozde Colak1, Anthony J Filiano, Gail V W Johnson
1Department of Pharmacology and Physiology, University of Rochester, USA.
Abstract:
Focal cerebral ischemia is among the most common type of stroke seen in patients. Due to the clinical significance there has been a prolonged effort to develop suitable animal models to study the events that unfold during ischemic insult. These techniques include transient or permanent, focal or global ischemia models using many different animal models, with the most common being rodents. The permanent MCA ligation method which is also referred as pMCAo in the literature is used extensively as a focal ischemia model in rodents. This method was originally described for rats by Tamura et al. in 1981. In this protocol a craniotomy was used to access the MCA and the proximal regions were occluded by electrocoagulation. The infarcts involve mostly cortical and sometimes striatal regions depending on the location of the occlusion. This technique is now well established and used in many laboratories. Early use of this technique led to the definition and description of "infarct core" and "penumbra", and it is often used to evaluate potential neuroprotective compounds. Although the initial studies were performed in rats, permanent MCA ligation has been used successfully in mice with slight modifications. This model yields reproducible infarcts and increased post-survival rates. Approximately 80% of the ischemic strokes in humans happen in the MCA area and thus this is a very relevant model for stroke studies. Currently, there is a paucity of effective treatments available to stroke patients, and thus there is a need for good models to test potential pharmacological compounds and evaluate physiological outcomes. This method can also be used for studying intracellular hypoxia response mechanisms in vivo. Here, we present the MCA ligation surgery in a C57/BL6 mouse. We describe the pre-surgical preparation, MCA ligation surgery and 2,3,5 Triphenyltetrazolium chloride (TTC) staining for quantification of infarct volumes.
Insights
This study details a permanent middle cerebral artery (MCA) ligation method in mice, a key model for studying focal cerebral ischemia and stroke. The technique provides reproducible infarcts for evaluating neuroprotective compounds and understanding stroke mechanisms.
Area of Science:
- Neuroscience
- Cerebrovascular Research
- Animal Models of Stroke
Background:
- Focal cerebral ischemia, a common stroke type, necessitates reliable animal models for research.
- Rodent models, particularly those mimicking middle cerebral artery (MCA) occlusion, are crucial for studying ischemic events.
- The permanent MCA ligation (pMCAo) method is a well-established technique for inducing focal cerebral ischemia in rodents.
Purpose of the Study:
- To present a detailed protocol for performing permanent MCA ligation surgery in C57/BL6 mice.
- To establish a reproducible animal model for studying focal cerebral ischemia and evaluating neuroprotective agents.
- To facilitate research into intracellular hypoxia response mechanisms in vivo.
Main Methods:
- Detailed surgical procedure for permanent MCA ligation in mice, including pre-surgical preparation.
- Occlusion of the MCA via electrocoagulation after craniotomy.
- Quantification of infarct volumes using 2,3,5 Triphenyltetrazolium chloride (TTC) staining.
Main Results:
- The permanent MCA ligation model in mice yields reproducible infarcts.
- This model demonstrates increased post-survival rates.
- The induced infarcts primarily affect cortical and sometimes striatal regions, relevant to human stroke.
Conclusions:
- Permanent MCA ligation in mice is a highly relevant and reproducible model for stroke research.
- This model is suitable for testing potential neuroprotective compounds and evaluating physiological outcomes.
- The technique aids in understanding stroke pathophysiology and hypoxia response mechanisms.

