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Published on: July 3, 2014
Matrix metalloproteinases in human spontaneous intracerebral hemorrhage: an update
M Florczak-Rzepka1, C Grond-Ginsbach, J Montaner
1Department of Neurology, Medical University of Warsaw, PL–02-097Warsaw, Poland. malgorzata.florczak @ gmail.com
Background:
In default of a plausible and satisfactory causal treatment for hemorrhagic stroke, a role of matrix metalloproteinases (MMPs) in the pathogenesis of cerebrovascular diseases has recently been widely discussed. The well-known impact of MMPs on extracellular matrix destruction triggered by inflammation as a foundation for several diseases, including stroke, is very much in evidence. Newly, some additional aspects of MMP function considering their intracellular activity crucial for neuronal death following ischemic brain damage have emerged. The effect of blood-brain barrier disruption caused by MMPs on the prognosis in patients suffering from spontaneous intracerebral hemorrhage (ICH) has been of interest since it throws a new light upon the pathogenesis, course and possible therapeutic approaches for this least treatable and at the same time most life-threatening form of stroke. Hence, we primarily aimed to review the current clinical knowledge on the significance of metalloproteinase activation in the course of spontaneous intracranial hemorrhage in humans. We also provide a brief characterization of the MMP enzyme family and report on the latest findings on issues arising from experimental studies.
Methods:
A Medline search using the following key words was performed: matrix metalloproteinases + spontaneous intracerebral hemorrhage/intracranial hemorrhage/bleeding/hemorrhagic stroke. We accepted studies reporting on MMP expression in adult patients with spontaneous ICH, as well as its relation to radiological and clinical features and patients' outcome. For the final review, 18 clinical studies were considered. MMP inhibition was reviewed on the basis of 11 relevant experimental studies. Also, some relevant reports on the biology of MMPs and their pathophysiology in ICH were reviewed.
Results And Conclusions:
Many studies provide convincing evidence of a detrimental role of MMPs in ICH, stressing their association with neuroinflammation. The role of MMPs in hemorrhagic stroke appears critical for hematoma and brain edema growth as well as for neuronal death, which are understood as secondary brain injury and may have a considerable clinical impact. Although data on human spontaneous ICH are scarce and mostly based on small populations, they reveal the apparent correlation between MMPs and clinical and radiological ICH features as well as the functional outcome, which might rationalize future therapeutic strategies. However, attempts at MMP inhibition in spontaneous ICH have solely been made under experimental conditions and were associated with a wide range of possible side effects. Therefore, further comprehensive, elucidating investigations in this field are vital before any conclusions could be translated to humans.
Insights
Matrix metalloproteinases (MMPs) play a detrimental role in intracerebral hemorrhage (ICH) by worsening brain injury and impacting patient outcomes. Further research is needed before therapeutic inhibition can be considered in humans.
Area of Science:
- Neurology
- Biochemistry
Background:
- Matrix metalloproteinases (MMPs) are increasingly implicated in the pathogenesis of cerebrovascular diseases, including stroke.
- MMPs contribute to extracellular matrix destruction and inflammation, and emerging evidence highlights their intracellular role in neuronal death after ischemic brain damage.
- The impact of MMPs on blood-brain barrier disruption in spontaneous intracerebral hemorrhage (ICH) is of significant interest for understanding disease progression and potential therapies.
Purpose of the Study:
- To review current clinical knowledge on the significance of metalloproteinase activation in spontaneous ICH.
- To characterize the MMP enzyme family and summarize recent findings from experimental studies on MMPs in ICH.
Main Methods:
- A systematic Medline search was conducted using keywords related to matrix metalloproteinases and spontaneous intracerebral hemorrhage.
- Included studies focused on MMP expression in adult ICH patients, its correlation with clinical/radiological features and outcomes.
- 18 clinical studies and 11 experimental studies on MMP inhibition were reviewed, alongside relevant reports on MMP biology and pathophysiology in ICH.
Main Results:
- Convincing evidence indicates a detrimental role of MMPs in ICH, associated with neuroinflammation.
- MMPs are critical for hematoma and brain edema expansion and neuronal death, contributing to secondary brain injury.
- While human ICH data are limited, they show correlations between MMPs and clinical/radiological features, and functional outcomes.
Conclusions:
- MMPs play a critical role in the secondary injury mechanisms of ICH, impacting hematoma expansion, edema, and neuronal death.
- Existing human data, though scarce, suggest a link between MMPs and ICH severity and outcomes, warranting further investigation.
- Experimental MMP inhibition shows potential but is associated with side effects; comprehensive human studies are essential before clinical translation.
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