Prostaglandin biosynthesis by fat body from the tobacco hornworm, Manduca sexta

We describe prostaglandin (PG) biosynthesis by microsomal-enriched preparations of fat body from larvae of the tobacco hornworm Manduca sexta. Four major PGs were synthesized under most experimental conditions, PGA 2, PGE 2, PGD 2 and PGF 2α. PGA 2, was the predominant product under most conditions....

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Veröffentlicht in:Insect biochemistry and molecular biology 1994-05, Vol.24 (5), p.481-491
Hauptverfasser: Stanley-Samuelson, David W., Ogg, Clyde L.
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Ogg, Clyde L.
description We describe prostaglandin (PG) biosynthesis by microsomal-enriched preparations of fat body from larvae of the tobacco hornworm Manduca sexta. Four major PGs were synthesized under most experimental conditions, PGA 2, PGE 2, PGD 2 and PGF 2α. PGA 2, was the predominant product under most conditions. Unlike mammals, in which PGA 2, is generally thought to arise from non-enzymatic rearrangemets of PGE 2, the fat body preparations did not convert exogenous PGE 2 into PGA 2. These findings suggest that PGA 2 is an important fat body product that is synthesized by a route that does not involve PGE 2. The PG synthase activity and the overall profile of PG synthesis were sensitive to experimental conditions, including incubation time, temperature, and protein concentration. Optimal PG biosynthesis was observed with 1 mg of microsomal-rich protein, incubated at 30°C for 1–2 min. The fat body preparation is sensitive to two non-steroidal anti-inflammatory drugs, indomethacin and naproxen, both of which inhibited PG synthesis at low dosages.
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Four major PGs were synthesized under most experimental conditions, PGA 2, PGE 2, PGD 2 and PGF 2α. PGA 2, was the predominant product under most conditions. Unlike mammals, in which PGA 2, is generally thought to arise from non-enzymatic rearrangemets of PGE 2, the fat body preparations did not convert exogenous PGE 2 into PGA 2. These findings suggest that PGA 2 is an important fat body product that is synthesized by a route that does not involve PGE 2. The PG synthase activity and the overall profile of PG synthesis were sensitive to experimental conditions, including incubation time, temperature, and protein concentration. Optimal PG biosynthesis was observed with 1 mg of microsomal-rich protein, incubated at 30°C for 1–2 min. 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Four major PGs were synthesized under most experimental conditions, PGA 2, PGE 2, PGD 2 and PGF 2α. PGA 2, was the predominant product under most conditions. Unlike mammals, in which PGA 2, is generally thought to arise from non-enzymatic rearrangemets of PGE 2, the fat body preparations did not convert exogenous PGE 2 into PGA 2. These findings suggest that PGA 2 is an important fat body product that is synthesized by a route that does not involve PGE 2. The PG synthase activity and the overall profile of PG synthesis were sensitive to experimental conditions, including incubation time, temperature, and protein concentration. Optimal PG biosynthesis was observed with 1 mg of microsomal-rich protein, incubated at 30°C for 1–2 min. 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subjects Animals
Arachidonic Acid - metabolism
Biochemistry. Physiology. Immunology
Biological and medical sciences
Fat Body - metabolism
Fundamental and applied biological sciences. Psychology
Hydroxyeicosatetraenoic Acids - metabolism
Indomethacin - pharmacology
Insect immunity
Insecta
Invertebrates
Larva - metabolism
Lepidoptera
Manduca sexta
Microsomes - metabolism
Moths - metabolism
Naproxen - pharmacology
Physiology. Development
Prostaglandin
Prostaglandin-Endoperoxide Synthases - metabolism
Prostaglandins - biosynthesis
Prostaglandins A - biosynthesis
Sphingidae
Temperature
title Prostaglandin biosynthesis by fat body from the tobacco hornworm, Manduca sexta
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