The effects of parenteral or dietary omega-3 polyunsaturated fatty acids in rat models of spinal cord injury

There is currently no effective treatment for spinal cord injury (SCI). Long chain omega-3 polyunsaturated fatty acids (PUFA) such as docosahexaenoic acid (DHA) and eicosapentaenoic acid (EPA) have beneficial effects in various neurological disorders. DHA and EPA have neuroprotective effects when gi...

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Main Author: Hall, Jodie Christine Elizabeth
Published: Queen Mary, University of London 2010
Subjects:
Online Access:https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.528429
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spelling ndltd-bl.uk-oai-ethos.bl.uk-5284292019-02-27T03:16:53ZThe effects of parenteral or dietary omega-3 polyunsaturated fatty acids in rat models of spinal cord injuryHall, Jodie Christine Elizabeth2010There is currently no effective treatment for spinal cord injury (SCI). Long chain omega-3 polyunsaturated fatty acids (PUFA) such as docosahexaenoic acid (DHA) and eicosapentaenoic acid (EPA) have beneficial effects in various neurological disorders. DHA and EPA have neuroprotective effects when given intravenously (i.v.) after SCI, but dietary enrichment with these fatty acids is less well-characterized. It is important to characterize the effect of these compounds after parenteral and oral administration, as both regimes could be used clinically. The aims of this thesis were to: i) characterize the inflammatory response in the rat after T12 compression SCI, ii) characterize the effects of acute i.v. injection of DHA or EPA on inflammation after SCI, iii) explore the effects of i.v. DHA in a rat contusion model of SCI, iv) assess the effects of dietary enrichment with DHA or EPA before and/or after SCI. Compression SCI led to acute infiltration of neutrophils and delayed accumulation of macrophages/microglia in the spinal cord, and a systemic inflammatory response in plasma and liver. DHA i.v. injection reduced neutrophil infiltration to the epicentre and C-reactive protein in the plasma, whereas EPA had no significant effect. There was no effect of i.v. EPA or DHA on the increase in cytokines/chemokines following injury. Acute DHA restored stepping ability after contusion SCI, but there was no effect on histological markers. Dietary enrichment with EPA after compression SCI had a detrimental effect on recovery, but this was not correlated with changes in neurones, oligodendrocytes or macrophages/microglia. Dietary pre-treatment with DHA had no effect on locomotor outcome after compression SCI. Therefore, the inflammatory response after SCI is not changed significantly by acute administration of EPA and DHA. The study did not reveal a beneficial prophylactic effect of dietary DHA, but highlighted a possible risk associated with dietary EPA after SCI.612.3MedicineQueen Mary, University of Londonhttps://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.528429http://qmro.qmul.ac.uk/xmlui/handle/123456789/517Electronic Thesis or Dissertation
collection NDLTD
sources NDLTD
topic 612.3
Medicine
spellingShingle 612.3
Medicine
Hall, Jodie Christine Elizabeth
The effects of parenteral or dietary omega-3 polyunsaturated fatty acids in rat models of spinal cord injury
description There is currently no effective treatment for spinal cord injury (SCI). Long chain omega-3 polyunsaturated fatty acids (PUFA) such as docosahexaenoic acid (DHA) and eicosapentaenoic acid (EPA) have beneficial effects in various neurological disorders. DHA and EPA have neuroprotective effects when given intravenously (i.v.) after SCI, but dietary enrichment with these fatty acids is less well-characterized. It is important to characterize the effect of these compounds after parenteral and oral administration, as both regimes could be used clinically. The aims of this thesis were to: i) characterize the inflammatory response in the rat after T12 compression SCI, ii) characterize the effects of acute i.v. injection of DHA or EPA on inflammation after SCI, iii) explore the effects of i.v. DHA in a rat contusion model of SCI, iv) assess the effects of dietary enrichment with DHA or EPA before and/or after SCI. Compression SCI led to acute infiltration of neutrophils and delayed accumulation of macrophages/microglia in the spinal cord, and a systemic inflammatory response in plasma and liver. DHA i.v. injection reduced neutrophil infiltration to the epicentre and C-reactive protein in the plasma, whereas EPA had no significant effect. There was no effect of i.v. EPA or DHA on the increase in cytokines/chemokines following injury. Acute DHA restored stepping ability after contusion SCI, but there was no effect on histological markers. Dietary enrichment with EPA after compression SCI had a detrimental effect on recovery, but this was not correlated with changes in neurones, oligodendrocytes or macrophages/microglia. Dietary pre-treatment with DHA had no effect on locomotor outcome after compression SCI. Therefore, the inflammatory response after SCI is not changed significantly by acute administration of EPA and DHA. The study did not reveal a beneficial prophylactic effect of dietary DHA, but highlighted a possible risk associated with dietary EPA after SCI.
author Hall, Jodie Christine Elizabeth
author_facet Hall, Jodie Christine Elizabeth
author_sort Hall, Jodie Christine Elizabeth
title The effects of parenteral or dietary omega-3 polyunsaturated fatty acids in rat models of spinal cord injury
title_short The effects of parenteral or dietary omega-3 polyunsaturated fatty acids in rat models of spinal cord injury
title_full The effects of parenteral or dietary omega-3 polyunsaturated fatty acids in rat models of spinal cord injury
title_fullStr The effects of parenteral or dietary omega-3 polyunsaturated fatty acids in rat models of spinal cord injury
title_full_unstemmed The effects of parenteral or dietary omega-3 polyunsaturated fatty acids in rat models of spinal cord injury
title_sort effects of parenteral or dietary omega-3 polyunsaturated fatty acids in rat models of spinal cord injury
publisher Queen Mary, University of London
publishDate 2010
url https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.528429
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