Also found in: Dictionary, Thesaurus, Medical, Financial, Acronyms, Wikipedia.
Related to prostaglandin: Prostaglandin analogue, prostaglandin E1, Prostaglandin E2


(prŏs'təglăn`dən), any of a group of about a dozen compounds synthesized from fatty acids in mammals as well as in lower animals. Prostaglandins are highly potent substances that are not stored but are produced as needed by cell membranes in virtually every body tissue. Different prostaglandins have been found to raise or lower blood pressure and regulate smooth muscle activity and glandular secretion. One such substance, which stimulates contraction of the uterus, is used clinically to induce labor; another has been in experimental use as a birth control agent. Prostaglandins also control the substances involved in the transmission of nerve impulses, participate in the body's defenses against infection, and regulate the rate of metabolism in various tissues. Several prostaglandins have been shown to induce fever, possibly by participating in the temperature-regulating mechanisms in the hypothalamus; they also play a part in causing inflammation. The fact that aspirin and other nonsteroidal anti-inflammatory drugs have been shown to inhibit prostaglandin synthesis may account for their usefulness in reducing fever and inflammation. Many naturally occurring prostaglandins as well as many artificial forms have been synthesized in the laboratory.



in mammals, a hormone that has a broad spectrum of physiological action. Prostaglandins were discovered in human semen by the Swedish scientist U. Euler in 1936. Initially, they were thought to be secretions of the prostate gland (hence the name). They were obtained in a pure form in 1956–65 by Swedish and American scientists.

About 20 natural prostaglandins are known, including thick liquids and low-melting crystalline substances. All prostaglandins are unsaturated hydroxy fatty acids that have a skeleton of 20 carbon atoms. According to their chemical structure, prostaglandins are divided into four groups—A, B, E, and F—E and F prostaglandins being the most important biologically. The subscripts in the formula below indicate the number of double bonds in the lateral chains of the molecule.

Prostaglandins are found in low concentrations (about 1 μg/g) in almost all organs, tissues, and biological fluids of higher animals. The most important physiological effect that is stimulated by prostaglandins is the ability to contract smooth muscles, especially the muscles of the uterus and fallopian tubes; at childbirth and during menstruation, the concentration of prostaglandins in uterine tissues increases substantially. For this reason, they are used in obstetrics and gynecology to facilitate normal labor and to artificially terminate pregnancy in its early stage.

Prostaglandins are also cardiotonics and bronchodilators. Arterial pressure is lowered by A and E prostaglandins and raised by F prostaglandin. A, E, and F prostaglandins intensify coronary and renal blood flow, inhibit gastric secretion, and affect the endocrine glands, including the thyroid gland; they also affect water-salt metabolism by altering the ratio Na+: K+ and blood coagulation by inhibiting the aggregation of thrombocytes.

The biosynthesis of prostaglandins occurs in the cells of different tissues. The precursors of prostaglandins are phospholipids; polyunsaturated fatty acids with a linear chain of 20 carbon atoms are released from phospholipids by the enzyme phospholipase. The oxidative cyclization of the carbon atoms, which occurs with the participation of prostaglandin synthetases (a special system of enzymes), results in the synthesis of E and F prostaglandins.

The classification of prostaglandins as local, or cellular, hormones is justified by their varied functions and the absence of a special organ for their biosynthesis. Their mechanism of action is still unclear. It has been established that prostaglandins affect the activity of the enzyme adenyl cyclase, which regulates the concentration of cyclic adenosine 3’: 5’-monophosphate (cyclic AMP) in the cell. Since prostaglandins influence the biosynthesis of cyclic AMP and since cyclic AMP participates in hormonal regulation, a possible mechanism of action of prostaglandins could consist in correcting (intensifying or weakening) the action of other hormones.

Clinical tests have shown prostaglandins to be promising in the treatment of such conditions as gastric ulcer, asthma, hypertonia, thromboses, arthritides, and inflammations of the nasopharynx. For medical and research purposes, prostaglandins are produced: (1) by enzymatic synthesis based on polyunsaturated fatty acids that are produced in the food-processing industry, (2) by complete chemical synthesis in nine to 13 stages chiefly based on cyclopentadiene, and (3) by partial synthesis in three to five stages based on prostaglandin A2 and E2 derivatives that are present in high concentrations (reaching 1.4 percent of the raw mass) in several varieties of the soft marine coral Plexaura homomalla.


Markov, Kh. M. “Prostaglandiny.” Uspekhi fiziologicheskikh nauk, 1970, vol. 1, no. 4.
Prostaglandins. New York, 1971. (Annals of the New York Academy of Sciences, vol. 180.)
The Prostaglandins: Progress in Research. Edited by M. M. Karim. Oxford-Lancaster, 1972.



Any of various physiologically active compounds containing 20 carbon atoms and formed from essential fatty acids; found in highest concentrations in normal human semen; activities affect the nervous system, circulation, female reproductive organs, and metabolism.
References in periodicals archive ?
Samuelsson, who was awarded the 1982 Nobel Prize in medicine for his prostaglandin research, is a member of the National Academy of Sciences and The Liposome Company board of directors.
In the absence of barrier contraceptives, our research has highlighted the potential advantages of using prostaglandin receptor antagonists to prevent the activation and signalling of prostaglandin receptors by [PGE.
Prostaglandins are well characterized for their role in many bodily functions - controlling cell growth, constricting and dilating smooth muscle tissue - and a different prostaglandin (F2alpha) is known to increase hair growth.
Two serious maternal adverse events occurred, both in the prostaglandin group.
The drug may be used up to 63 days LMP; the dosage of expensive RU486 pills (about $90 each) is reduced from three pills to one; the dose of the prostaglandin is doubled; and women administer that drug to themselves at home, vaginally, rather than taking it orally in the doctor's office.
There was no association with use of acetaminophen, which does not inhibit prostaglandin synthesis.
1) In a randomized controlled real, the average time from the start of the procedure to delivery of the placenta was 3-13 hours longer for those given misoprostol orally than for those who received it vaginally or who received intra-amniotic prostaglandin.
The half life of this drug is much longer than other prostaglandin drugs now used.
Teather, Richard Wurtman, director of MIT's Clinical Research Center, and Jane Magnusson of Canada's University of Calgary found that drugs which interfere with PAF's action block prostaglandin production and diminish pain and inflammation.
It said it expected to see growth in the coming years as new prostaglandin drugs are brought out and existing drugs come off patent.
Despite the growing interest in this prostaglandin metabolite, no reliable assay has been reported, especially by gas chromatography-mass spectrometry (GC-MS), a reference method for prostanoids (13).
Evidence for elevated levels of histamine, prostaglandin [D.