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12(R)-hydroxy-5,8,10,14-eicosatetraenoic acid is a chemoattractant fo human polymorphonuclear leucocytes in vitro
- Source :
- Prostaglandins. 34:71-78
- Publication Year :
- 1987
- Publisher :
- Elsevier BV, 1987.
-
Abstract
- Increased amounts of 12-hydroxy - 5,8,10,14-eicosatetraenoic acid (12-HETE) are found in the lesional skin of patients with the skin disease psoriasis when compared to clinically normal skin. Stereochemical analysis has recently shown that the 12-HETE present in lesional psoriatic scale is the (R), and not the (S) hydroxyl enantiomer, produced by platelets. Since the chemoattractant activity of 12(R)-HETE has not previously been described, the (R) and (S) hydroxyl enantiomers of 12-HETE have now been synthesised and their chemokinetic activity compared in vitro. 12(R)-HETE, was more potent than 12(S)-HETE as a chemokinetic agent for human polymorphonuclear leucocytes but 2000 times less potent than leukotriene B4. In contrast to results obtained with the 12-HETE enantiomers, the chemoattractant compound 5(S)-HETE was found to be more potent than the 5(R) hydroxyl enantiomer. Thus, the configuration of the hydroxyl group appears to be of importance to the chemokinetic activity of the HETEs, and the increased potency of the 12(R) enantiomer may enhance its significance as a mediator of inflammation in psoriasis.
- Subjects :
- Neutrophils
Leukotriene B4
Eicosatetraenoic acid
In Vitro Techniques
Granulocyte
Pharmacology
Biochemistry
chemistry.chemical_compound
Endocrinology
Hydroxyeicosatetraenoic Acids
medicine
Humans
Psoriasis
12-Hydroxy-5,8,10,14-eicosatetraenoic Acid
Interleukin 8
Chemoattractant activity
Chemotactic Factors
Interleukin-8
Stereoisomerism
hemic and immune systems
In vitro
Kinetics
medicine.anatomical_structure
chemistry
cardiovascular system
lipids (amino acids, peptides, and proteins)
Arachidonic acid
Enantiomer
circulatory and respiratory physiology
Subjects
Details
- ISSN :
- 00906980
- Volume :
- 34
- Database :
- OpenAIRE
- Journal :
- Prostaglandins
- Accession number :
- edsair.doi.dedup.....c1cddced954a957b083e716f6430e9b2