86. Eicosanoids Flashcards
Autacoids
Every cell releases chemical signals. Mainly those of the diffuse endocrine system (Diffuse Neuro- Endocrine System, DNES) function like this. Their products (signals) were named as autacoids.
They can be chemically divided into two groups: peptides and fatty acid-like substances.
Site of eicosanoid production
It is produced everywhere in the body
Every cell is able to produce
Eicosanoid synthesis
20-C FA’s. Controlled synth. from phospholipids via enzymatic steps
Mediated by G protein → activates PLA2 enzyme
MPL (membrane phospholipids) = PLA2 substrates
HPETE (hydroxy-peroxy-eicosa-tetraenoic acid), Lipoxins, HETE (Hydroxy-eicosa-tetranenoic acid), leukotrienes
common feature
- Their common feature is that they are quickly degraded after entering the plasma.
- Their plasma concentration is fairly low. They mostly act locally or through a paracrine way.
- Although they are lipid soluble, they bind to surface membrane receptors and elicit G protein dependent transduction.
Effects – increasing inflammation
Prostaglandins and leukotrienes are both involved in initiation of inflammation.
Effects – insulin release
- still not entirely elucidated eicosanoid action-mechanism is the effect on insulin release of B cells. HPETE (lipoxygenase pathway) stimulates, PGE2 (cyclooxygenase pathway) inhibits insulin release.
Effects – bone resorption
PGE2, produced by the osteoblast cellular line, has a parathyroid hormone-like effect on calcium mobilization from the bone: it increases calcium permeability in the osseous interstitial side, making possible the entry of calcium into the plasma.
Effects – reproduction
Precondition of luteolysis is PGF2-alpha prod.
Effects – thrombocyte
Enothelial cells (in mouse) release PGI & NO → induce G protein mediated incr. of cAMP. IC cAMP inhibits PLA2 enzyme → no thromboxane → no platelet aggregation. TXA2 synth in platelets increases → increase aggregation.
Effects – kidney
Prostatcyclin synthesis in renal tubule cells enhances renin secretion, increases RPF, and antagonizes the effect of ADH.
Regulation
- Corticosteroids, Mepacrine inhibit the entire eicosanoid synthesis. This is one cause of the anti-inflammatory effect of glucocorticoids.
- Salicylic acid, Indomethacin, Ibuprofen specifically inhibits cyclooxygenase enzyme. Since it does not inhibit lipoxygenase pathway, it does not have any influence on the communication between leukocytes (LT, LX, etc.).
- Benzidamine, Imidazol specifically inhibit thromboxane synthase enzyme. By applying it, normal production of prostaglandins (reproductive processes) is not blocked, but the synthesis of thromboxane decreases. (E.g., the aggregation of platelets can be effectively decreased this way!)