2011
DOI: 10.1016/j.neurobiolaging.2010.04.001
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The polyunsaturated fatty acids, EPA and DPA exert a protective effect in the hippocampus of the aged rat

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Cited by 117 publications
(98 citation statements)
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“…[41][42][43] The mechanism of the protective effect of DPA on prostate cancer may be explained by biochemical processes involving: reduced prostacyclin production, expression of inflammatory genes and TNF-induced necrotic cell death; competition with cycloxygenase 2 (COX2) enzymes resulting to anti-neoplastic activity via proapoptotic pathway; and inhibition of angiogenesis. [44][45][46][47][48][49] Detection of such association may suggest that serum level DPA implicates individual genetic difference in biochemical characteristics of enzymatic activities, which may be further investigated as a probable new serum biomarker for prostate cancer risk assessment in the future.…”
Section: Discussionmentioning
confidence: 99%
“…[41][42][43] The mechanism of the protective effect of DPA on prostate cancer may be explained by biochemical processes involving: reduced prostacyclin production, expression of inflammatory genes and TNF-induced necrotic cell death; competition with cycloxygenase 2 (COX2) enzymes resulting to anti-neoplastic activity via proapoptotic pathway; and inhibition of angiogenesis. [44][45][46][47][48][49] Detection of such association may suggest that serum level DPA implicates individual genetic difference in biochemical characteristics of enzymatic activities, which may be further investigated as a probable new serum biomarker for prostate cancer risk assessment in the future.…”
Section: Discussionmentioning
confidence: 99%
“…The increases in MTT and CTT are probably due to a combination of decreased blood flow and altered perfusion coefficient of the tissue (Kelly et al, 2009). MTT has been shown to correlate with accumulation of lactate following stroke suggesting that it may provide a marker of ischemia (Cvoro et al, 2009) and, in this context, it is interesting that there is evidence of oxidative changes in the brain of aged rats (Kelly et al, 2011;O'Donnell et al, 2000). These changes cannot be attributed to any age-related difference in hippocampal volume because, although a decrease in cortical thickness was observed, we found no evidence of any difference in hippocampal volume in aged, compared with young, rats.…”
Section: Discussionmentioning
confidence: 99%
“…Of particular interest, the lipid species showing the greatest change was DPAn-3. There have been many studies, both in vitro and in vivo, demonstrating the neuroprotective effects of DHA (Belayev et al, 2009;Ménard et al, 2009;Ward et al, 2010), but little work has been done on the role DPAn-3 can play in injury and disease (Kelly et al, 2011).…”
Section: Discussionmentioning
confidence: 99%