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Nicos A. Petasis

Researcher at University of Southern California

Publications -  272
Citations -  21078

Nicos A. Petasis is an academic researcher from University of Southern California. The author has contributed to research in topics: Lipoxin & Inflammation. The author has an hindex of 76, co-authored 268 publications receiving 19503 citations. Previous affiliations of Nicos A. Petasis include Université de Montréal & University of Pennsylvania.

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Stereochemical assignment, antiinflammatory properties, and receptor for the omega-3 lipid mediator resolvin E1

TL;DR: Novel counterregulatory responses in inflammation initiated via RvE1 receptor activation that provide the first evidence for EPA-derived potent endogenous agonists of antiinflammation are demonstrated.
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Resolvins and Protectins in Inflammation-Resolution

TL;DR: This review summarizes efforts on the resolvins and protectins with an emphasis on the corresponding biochemical pathways and the key role of a number of lipid mediators in the initiation of the inflammatory response and the subsequent progression towards resolution.
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Resolvin D1 binds human phagocytes with evidence for proresolving receptors

TL;DR: It is demonstrated that RvD1 actions on human polymorphonuclear leukocytes (PMNs) are pertussis toxin sensitive, decrease actin polymerization, and block LTB4-regulated adhesion molecules (β2 integrins).
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Cutting edge: lipoxins rapidly stimulate nonphlogistic phagocytosis of apoptotic neutrophils by monocyte-derived macrophages.

TL;DR: It is suggested that LXA4 is an endogenous stimulus for PMN clearance during inflammation and provide a novel rationale for using stable synthetic analogues as anti-inflammatory compounds in vivo.
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Resolvin D2 is a potent regulator of leukocytes and controls microbial sepsis

TL;DR: This work identifies RvD2 as a potent endogenous regulator of excessive inflammatory responses that acts via multiple cellular targets to stimulate resolution and preserve immune vigilance in mice with microbial sepsis induced by caecal ligation and puncture and surgery.