Neuroinflammation and MMPs: potential therapeutic targets in neonatal hypoxic-ischemic injury

<p>Abstract</p> <p>Exposure to hypoxic-ischemic insults during the neonatal or perinatal developmental periods produces various forms of pathology. Injuries that occur in response to these events often manifest as severe cognitive and/or motor disturbances over time. Due to difficu...

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Main Authors: Pennypacker Keith R, Leonardo Christopher C
Format: Article
Language:English
Published: BMC 2009-04-01
Series:Journal of Neuroinflammation
Online Access:http://www.jneuroinflammation.com/content/6/1/13
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spelling doaj-788b9ff7632b45e097ca44e04ddd65c72020-11-25T00:03:10ZengBMCJournal of Neuroinflammation1742-20942009-04-01611310.1186/1742-2094-6-13Neuroinflammation and MMPs: potential therapeutic targets in neonatal hypoxic-ischemic injuryPennypacker Keith RLeonardo Christopher C<p>Abstract</p> <p>Exposure to hypoxic-ischemic insults during the neonatal or perinatal developmental periods produces various forms of pathology. Injuries that occur in response to these events often manifest as severe cognitive and/or motor disturbances over time. Due to difficulties regarding the early diagnosis and treatment of hypoxic-ischemic injury, there is a growing need for effective therapies that can be delivered at delayed time points. Much of the research into mechanisms of neural injury has focused on molecular targets associated with excitotoxicity and free oxygen radicals. Despite repeated success in animal models, these compounds have failed to show efficacy in clinical trials. Increasing evidence indicates that hypoxic-ischemic injury in the neonate is progressive, and the resulting neuropathies are linked to the activation of neuroinflammatory processes that occur in response to the initial wave of cell death. Understanding this latter response, therefore, will be critical in the development of novel therapies to block the progression of the injury. In this review, we summarize emerging concepts from rodent models concerning the regulation of various cytokines, chemokines, and matrix metalloproteinases in response to ischemia, and the various ways in which the delayed neuroinflammatory response may contribute to the progressive nature of neonatal hypoxic-ischemic injury in rat. Finally, we discuss data that supports the potential to target these neuroinflammatory signals at clinically relevant time points.</p> http://www.jneuroinflammation.com/content/6/1/13
collection DOAJ
language English
format Article
sources DOAJ
author Pennypacker Keith R
Leonardo Christopher C
spellingShingle Pennypacker Keith R
Leonardo Christopher C
Neuroinflammation and MMPs: potential therapeutic targets in neonatal hypoxic-ischemic injury
Journal of Neuroinflammation
author_facet Pennypacker Keith R
Leonardo Christopher C
author_sort Pennypacker Keith R
title Neuroinflammation and MMPs: potential therapeutic targets in neonatal hypoxic-ischemic injury
title_short Neuroinflammation and MMPs: potential therapeutic targets in neonatal hypoxic-ischemic injury
title_full Neuroinflammation and MMPs: potential therapeutic targets in neonatal hypoxic-ischemic injury
title_fullStr Neuroinflammation and MMPs: potential therapeutic targets in neonatal hypoxic-ischemic injury
title_full_unstemmed Neuroinflammation and MMPs: potential therapeutic targets in neonatal hypoxic-ischemic injury
title_sort neuroinflammation and mmps: potential therapeutic targets in neonatal hypoxic-ischemic injury
publisher BMC
series Journal of Neuroinflammation
issn 1742-2094
publishDate 2009-04-01
description <p>Abstract</p> <p>Exposure to hypoxic-ischemic insults during the neonatal or perinatal developmental periods produces various forms of pathology. Injuries that occur in response to these events often manifest as severe cognitive and/or motor disturbances over time. Due to difficulties regarding the early diagnosis and treatment of hypoxic-ischemic injury, there is a growing need for effective therapies that can be delivered at delayed time points. Much of the research into mechanisms of neural injury has focused on molecular targets associated with excitotoxicity and free oxygen radicals. Despite repeated success in animal models, these compounds have failed to show efficacy in clinical trials. Increasing evidence indicates that hypoxic-ischemic injury in the neonate is progressive, and the resulting neuropathies are linked to the activation of neuroinflammatory processes that occur in response to the initial wave of cell death. Understanding this latter response, therefore, will be critical in the development of novel therapies to block the progression of the injury. In this review, we summarize emerging concepts from rodent models concerning the regulation of various cytokines, chemokines, and matrix metalloproteinases in response to ischemia, and the various ways in which the delayed neuroinflammatory response may contribute to the progressive nature of neonatal hypoxic-ischemic injury in rat. Finally, we discuss data that supports the potential to target these neuroinflammatory signals at clinically relevant time points.</p>
url http://www.jneuroinflammation.com/content/6/1/13
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