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1.
Insect Biochem Mol Biol ; 24(5): 481-91, 1994 May.
Article in English | MEDLINE | ID: mdl-8205144

ABSTRACT

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, PGA2, PGE2, PGD2 and PGF2 alpha. PGA2, was the predominant product under most conditions. Unlike mammals, in which PGA2, is generally thought to arise from non-enzymatic rearrangements of PGE2, the fat body preparations did not convert exogenous PGE2 into PGA2. These findings suggest that PGA2 is an important fat body product that is synthesized by a route that does not involve PGE2. 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 degrees C for 1-2 min. The fat body preparations is sensitive to two non-steroidal anti-inflammatory drugs, indomethacin and naproxen, both of which inhibited PG synthesis at low dosages.


Subject(s)
Fat Body/metabolism , Moths/metabolism , Prostaglandins/biosynthesis , Animals , Arachidonic Acid/metabolism , Hydroxyeicosatetraenoic Acids/metabolism , Indomethacin/pharmacology , Larva/metabolism , Microsomes/metabolism , Naproxen/pharmacology , Prostaglandin-Endoperoxide Synthases/metabolism , Prostaglandins A/biosynthesis , Temperature
2.
Insect Biochem Mol Biol ; 23(4): 431-7, 1993 Jun.
Article in English | MEDLINE | ID: mdl-8508185

ABSTRACT

The fatty acid compositions of Malpighian tubules from adult females of the mosquito Aedes aegypti were determined for total lipids, phospholipids, triacylglycerols and three phospholipid fractions, namely phosphatidylcholine (PC), phosphatidylethanolamine (PE) and phosphatidylinositol/phosphatidylserine (PI/PS). The prostaglandin precursor arachidonic acid (20:4n-6) occurred in total lipids and phospholipids, but not triacylglycerols. Within phospholipids, nearly all of the 20:4n-6 was detected in PC, with only traces in PE, and none was detected in PI/PS. Isolated Malpighian tubules incorporated exogenous radioactive 20:4n-6 into tissue phospholipids and diacylglycerols, with most of the radioactivity recovered in diacylglycerol. These data indicate selective incorporation of 20:4n-6 into tissue lipids. PGE2 was detected in Malpighian tubule whole mounts by immunohistochemical staining. These findings support the idea that prostaglandins are physiologically active in mosquito Malpighian tubules.


Subject(s)
Aedes/chemistry , Arachidonic Acid/analysis , Dinoprostone/analysis , Malpighian Tubules/chemistry , Animals , Arachidonic Acid/metabolism , Fatty Acids/analysis , Female , Immunohistochemistry , Insect Vectors , Lipid Metabolism
3.
J Econ Entomol ; 85(3): 974-80, 1992 Jun.
Article in English | MEDLINE | ID: mdl-1619108

ABSTRACT

Field workers were monitored for dermal and respiratory exposure to chlorpyrifos (with and without crop oil), carbaryl, and permethrin at reentry intervals of 2, 4, 8, 24, and 48 h after application. Insecticides were applied to R3 stage corn through an overhead center-pivot irrigation system. Dermal exposure was measured by analyzing 18 gauze pads attached to the clothing of workers to represent human body regions. Hand exposure was determined using cotton gloves. Respiratory exposure was determined using portable air samplers equipped with polyurethane foam plugs to trap ambient insecticide residues. Gas liquid chromatography was used to quantify residues of chlorpyrifos and permethrin in gauze pads, gloves, and foam plugs. Carbaryl residues in pads, gloves, and foam plugs were analyzed using high-performance liquid chromatography. Highest dermal and respiratory exposures were found at the 2-h reentry interval. Exposures decreased as reentry interval increased. Dermal exposure was primarily confined to the hands. Residues detected by air samplers ranged from 0 to 0.03 micrograms/liter. Based on the estimated percentages of acute toxic dose (all less than 0.00038%), the risk of acute toxicity to workers at the intervals studied was low.


Subject(s)
Agricultural Workers' Diseases/chemically induced , Insecticides/adverse effects , Occupational Exposure , Pesticide Residues/adverse effects , Hand Dermatoses/chemically induced , Humans , Respiratory Tract Diseases/chemically induced , Skin Diseases/chemically induced , Zea mays
4.
Arch Environ Contam Toxicol ; 22(3): 253-9, 1992 Apr.
Article in English | MEDLINE | ID: mdl-1616308

ABSTRACT

Research was conducted to assess dermal and respiratory exposure to applicators from chlordane and heptachlor used for subterranean termite control and exposure to residents of treated homes. Dermal exposure of 29 applicators was evaluated by using gauze pads attached to outer and inner clothing at selected body regions. Respiratory exposure of applicators was monitored with personnel-type air samplers worn during application periods. Air samplers were equipped with polyurethane foam plugs to trap airborne chlordane and heptachlor. Exposure of residents was measured by sampling ambient air of 19 homes treated with the termiticides. Electric air samplers equipped with foam plugs were used to monitor ambient air from the basement, the kitchen, and one bedroom at: 24 h prior to termiticide application, during application, and post-application at 24 h, 1 wk, and monthly for 6 mo. Applicator dermal exposure was estimated based on exposure rates to each body region. Respiratory exposure was estimated based on termiticide concentrations in the air and on the ventilation rate of a person doing light work. Residents' exposure was estimated based on the amount of termiticide present in ambient air. Results indicated that applicator exposure rates to chlordane and heptachlor were 2.54 and 1.88 micrograms/kg/h, respectively. Residents were exposed to less than 0.69 and 2.86 micrograms/m3 of chlordane and heptachlor, respectively. During this research, the application of termiticide containing chlordane and heptachlor posed minimal risk in terms of acute exposure to either the applicators or the residents of the treated homes.


Subject(s)
Air Pollution, Indoor/analysis , Chlordan/analysis , Heptachlor/analysis , Insect Control/methods , Chlordan/administration & dosage , Heptachlor/administration & dosage , Humans , Skin Absorption
5.
Proc Natl Acad Sci U S A ; 88(3): 1064-8, 1991 Feb 01.
Article in English | MEDLINE | ID: mdl-1899480

ABSTRACT

Inhibition of eicosanoid formation in larvae of the tobacco hornworm Manduca sexta, using specific inhibitors of phospholipase A2, cyclooxygenase, and lipoxygenase, severely weakened the ability of larvae to clear the bacterium Serratia marscescens from their hemolymph. The reduced capability to remove bacteria is associated with increased mortality due to these bacteria. There is a dose-dependent relationship between the phospholipase A2 inhibitor dexamethasone and both the reduced bacterial clearance and increased larval mortality. The dexamethasone effects on larval survival were reversed by treatment with arachidonic acid. Maleic acid, a nonspecific antioxidant, did not interfere with the insects' ability to remove bacterial cells from hemolymph. The larvae were shown to contain all of the C20 polyunsaturated fatty acids necessary for eicosanoid biosynthesis and to be capable of converting radioactive arachidonic acid into several primary prostaglandins. These results strongly suggest that eicosanoids mediate transduction of bacterial infection signals into the complex of cellular and humoral responses that comprise invertebrate immunity.


Subject(s)
Arachidonic Acids/pharmacology , Cyclooxygenase Inhibitors , Dexamethasone/pharmacology , Eicosanoids/biosynthesis , Indomethacin/pharmacology , Moths/immunology , Phospholipases A/antagonists & inhibitors , Serratia marcescens/growth & development , Animals , Arachidonic Acid , Eicosanoids/antagonists & inhibitors , Larva , Moths/microbiology , Phospholipases A2 , Serratia marcescens/drug effects , Serratia marcescens/pathogenicity
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