Last modified on 12 July 2012, at 21:03

Structural Biochemistry/Lipids/Fatty Acids/Eicosanoids

Arachidonate, a 20:4 fatty acid derived from linoleate, is the dominant precursor of several eicosanoid hormones. There are four families of eicosanoids—the prostaglandins, prostacyclins, the thromboxanes and the leukotrienes. These molecules react with cell receptors to produce signal transduction responses. Also, anti-inflammatory drugs and aspirin are known to reduce effects of these molecules.

Eicosanoids are molecules which affect the synthesis of other molecules in cellular reactions. They take part in complex checks and balances systems in many parts of the human body such as during the inflammatory response or relaying messages in the central nervous system. They are derived from oxidation of essential fatty acids, generally Omega-3 or Omega-6 polyunsaturated fatty acids. The name is derived from "eicosa" which means twenty in Greek. This is because eicosanoids are made of 20 carbon fatty acids called eicosatetraenoïc acid.

they are local hormones because they exist only for a short amount of time. they change the cell activities which they are sunthesized and of adjoining cells by binding to 7TM receptors. however, their effects are not uniformed and varies from cell to cell.

BiosynthesisEdit

Biosynthesis of eicosanoids involves two steps: arachidonic acid release and its transformation into active products. Eicosanoids are not stored anywhere but rather created whenever required by the body. When a stimuli is triggered, such as cytokines, or growth factors, a phospholipase is released at the cell membrane and travels to the nuclear membrane. Here, the phoshpolipase catalyzes the break down of either a phospholipid or a diacyglycerol. This step releases a 20-carbon fatty acid. This fatty acid is a precursor to the different eicosanoids.

Two key enzymes starts the eicosanoid routes: cyclo-oxygenases lead to the formation of prostaglandins, while lipoxygenase produces hydroperoxides of arachidonic acid or catalyze the first step of leukotriene synthesis.

Arachidonic acid metabolism: cyclooxygenase pathwayEdit

catalyzes fatty acids to prostanoids by a 2 step process. two Oxygen molecules are added as two peroxide linkages, this leads to the formation of short lived, active intermediate PGG when a 5 member ring is forged in the middle of the fatty acid chain. secondly, one of the peroxide loses H and sheds a single oxygen, forming PGH.

Arachidonic acid metabolism: lipoxygenase pathwayEdit

Catabolism (inactivation) of eicosanoidsEdit

All arachidonic acid derivatives are quickly, in less than a few minutes, inactivated in the body by several complex reactions

Functions in the Human BodyEdit

Different Eicosanoids have different medical applications. Within the body, they are mostly paracrine and autocrine agents acting on cells close by and then are quickly used up. Each eicosanoid has its own specific receptor so they have highly unique functions. Some Eicosanoids have been isolated and have been identified. Some prostanoids have been identified to help sleep, smoothen muscle contraction like bronchoconstriction, uterine constraction, and platelet aggregation. Some leukotrienes have similar uses. Some stimulate platelet aggregation as well, vasoconstriction, leukocyte chemotaxis, and muscle contraction.

prostagladins stimulate inflammation, regulate blood flow to particular organs. control ion transport across membranes, modulate synaptic transmission, and induce sleep.

ReferencesEdit

http://eurheartjsupp.oxfordjournals.org/cgi/reprint/3/suppl_D/D42.pdf

http://www.jci.org/articles/view/18338/version/1