1975
DOI: 10.1111/j.1476-5381.1975.tb07634.x
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PROCEEDINGS OF THE British Pharmacological Society

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Cited by 2 publications
(2 citation statements)
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“…Interestingly, none of the other products of COX metabolism were found to be elevated in the WM group. PGD1 has been shown to reduce vascular permeability induced by other prostaglandins [26] and have anti-inflammatory effects in atopic dermatitis [27]. Further, PGD1 has been shown to be generated by murine macrophages when incubated with DGLA and stimulated with lipopolysaccharide [25].…”
Section: Discussionmentioning
confidence: 99%
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“…Interestingly, none of the other products of COX metabolism were found to be elevated in the WM group. PGD1 has been shown to reduce vascular permeability induced by other prostaglandins [26] and have anti-inflammatory effects in atopic dermatitis [27]. Further, PGD1 has been shown to be generated by murine macrophages when incubated with DGLA and stimulated with lipopolysaccharide [25].…”
Section: Discussionmentioning
confidence: 99%
“…We were unable to find much information on PGD1 in the literature, particularly its role in the brain. However, at least in relation to atopic dermatitis, it appears that it may be an anti-inflammatory mediator which is induced by inflammatory stimuli as a potential feedback mechanism [25,26,27]. The cytochrome p450 epoxygenases can epoxidize any of the four double bonds of arachidonic acid (AA) producing one of the following: 5,6-EpETrE, 8,9-EpETrE, 11,12-EpETrE, or 14,15-EpETrE [28].…”
Section: Discussionmentioning
confidence: 99%