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What have Genetically Engineered Mice Taught Us About Ischemic Injury?
Abstract
Stroke, is the third leading cause of death and disability in the Western world. Stroke refers to set of ischemic conditions resulting from the occlusion or hemorrhage of blood vessels supplying the brain. Loss of blood flow to the brain results in neuronal injury due to both oxygen and nutrient deprivation and the activation of injurious signal cascades. Ultimately cerebral ischemia results in death and dysfunction of brain cells, and neurological deficits that reflect the location and size of the compromised brain area. Injury due to ischemic stroke occurs by a highly choreographed series of complex spatial and temporal events that evolve over hours to days. These events involve complex interactions between fundamental cell injury mechanisms including excitotoxicity and ionic imbalance, oxidative and nitrosative stress, apoptotic-like cell death and inflammatory responses. Genetically engineered mice have been valuable tools to probe putative mechanisms of neuronal death and uncover potential strategies that might render neurons resistant to ischemic injury. Findings from experimental stroke studies in genetically engineered animals are discussed.
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Pronounced loss and gradual degeneration of dendritic structure and spines at longer time points (>7 h) are consistent with ischemia activating signal transduction cascades that lead to apoptosis or necrosis.
“However, the pronounced loss and gradual degeneration of dendritic structure and spines at longer time points (Ͼ7 h) (supplemental Fig. 1a, available at www.jneurosci.org as supplemental material) are consistent with ischemia, activating signal transduction cascades that lead to apoptosis or necrosis (Liang et al., 2004).”
From Rapid Reversible Changes in Dendritic Spine Structure In Vivo Gated by the Degree of Ischemia (2005) · cites this paper as Liang et al., 2004
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Rapid Reversible Changes in Dendritic Spine Structure In Vivo Gated by the Degree of Ischemia
Zhang, S., Boyd, J., Delaney, K., & Murphy, T. H. (2005) · The Journal of Neuroscience · doi:10.1523/jneurosci.1085-05.2005 · Cited by 267
“that lead to apoptosis or necrosis (Liang et al., 2004).”
Metadata
- Authors
- Liang, D., Dawson, T., & Dawson, V.
- Affiliations
- Johns Hopkins University (US)
- Venue
- Current Molecular Medicine
- Publisher
- Bentham Science Publishers Ltd.
- Published
- 2004-03-01
- Volume
- 4
- Issue
- 2
- Pages
- 207-225
- ISSN
- 1566-5240 (ISSN-L)
- OpenAlex
- W2120151830
- Cited by
- 18
- References
- 0
- Citations by year
- 2021: 2 · 2017: 1 · 2013: 1 · 2012: 1
- FWCI
- 1.95
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Current Molecular Medicine (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Institute of Neurological Disorders and Stroke (NS 39148, P01NS039148)
- Topics
- Health Sciences › Medicine › Clinical Neurology › Acute Ischemic Stroke Management
- Life Sciences › Neuroscience › Neurology › Neuroprotection in Cerebral Ischemia
- Life Sciences › Neuroscience › Neurology › Neurological Disease Mechanisms and Treatments
- Keywords
- ischemic stroke, cerebral ischemia, genetically modified mice, neuronal injury, excitotoxicity, ionic imbalance, oxidative stress, nitrosative stress, apoptosis, neuroinflammation, neuroprotection
- MeSH terms
- Animals, Brain Injuries, Cell Membrane, Cell Nucleus, Brain Ischemia, Cloning, Molecular, Disease Models, Animal, Growth Substances, Humans, Inflammation, Mice, Transgenic, Nitrogen, Signal Transduction, Apoptosis, Oxidative Stress, Mice
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