Effects of sulfur oxides on eicosanoids
- 31 August 1989
- journal article
- research article
- Published by Taylor & Francis in Journal of Toxicology and Environmental Health
- Vol. 28 (1), 99-109
- https://doi.org/10.1080/15287398909531331
Abstract
Ultrafine metal oxides and SO2 react during coal combustion or smelting operations to form primary emissions coated with an acidic SOx layer. Ongoing work in this laboratory has examined the effects of sulfur oxides on pulmonary functions of guinea pigs. We have previously reported that 20 μg/m3 acidic sulfur oxide as a surface layer on ultrafine ZnO particles decreases lung volumes, decreases carbon monoxide diffusing capacity, and causes lung inflammation in guinea pigs after 4 daily 3‐h exposures. It also produces bronchial hypersensitivity following a single 1‐h exposure. The importance of this surface layer is demonstrated by our observation that 200 μg/m3 of sulfuric acid droplets of equivalent size are needed to produce the same degree of hypersensitivity. This study characterized the concentration‐dependent effects of in vivo exposures to sulfur oxides on arachidonic acid metabolism in the guinea pig lung, and investigated the time course and the relation between eicosanoid composition and pulmonary functions. We focused specifically on four cyclooxygenase metabolites of arachidonic acid, that is, prostaglandins (PC) E1, F2α, 6‐keto prostaglandin F1α, and thromboxane (Tx) B2, and two groups of sulfidopeptide leukotrienes (C4, D4, E4, and F4). Guinea pigs were exposed to ultrafine ZnO aerosol (count median diameter — 0.05 μm, σg = 1.80) with a layer of acidic sulfur oxide on the surface of the particles. Lung lavage was collected after exposures, and the levels of arachidonic acid metabolites were determined using radioimmunoassay (RIA). Concentration‐dependent promotion of PGF2α and concentration‐dependent suppression of LtB4 were observed. The increased PGF2α was associated with depressed vital capacity and diffusing capacity of the lungs measured in guinea pigs exposed to the same atmosphere described in a previous study. There is no causal relationship between the levels of other arachidonic acid metabolites and the pulmonary functional changes after exposures to these aerosols.Keywords
This publication has 34 references indexed in Scilit:
- Furnace-Generated Acid Aerosols: Speciation and Pulmonary EffectsEnvironmental Health Perspectives, 1989
- Changes in pulmonary lavage fluid of guinea pigs exposed to ultrafine zinc oxide with adsorbed sulfuric acidJournal of Toxicology and Environmental Health, 1989
- Speciation and pulmonary effects of acidic SOx formed on the surface of ultrafine zinc oxide aerosolsAtmospheric Environment (1967), 1988
- Effect of ozone exposure on lung functions and plasma prostaglandin and thromboxane concentrations in guinea pigsToxicology and Applied Pharmacology, 1987
- Coal combustion aerosols and sulfur dioxide: an interdisciplinary analysisEnvironmental Science & Technology, 1986
- Functional and morphologic changes in the lungs of guinea pigs exposed to freshly generated ultrafine zinc oxideToxicology and Applied Pharmacology, 1985
- Changes in lung volumes and diffusing capacity in guinea pigs exposed to a combination of sulfur dioxide and submicron zinc oxide mixed in a humidified furnaceToxicology and Applied Pharmacology, 1982
- Normobaric Oxygen Toxicity of the LungNew England Journal of Medicine, 1980
- Leukotriene B, a potent chemokinetic and aggregating substance released from polymorphonuclear leukocytesNature, 1980
- The effects of ozone and paraquat on PGF2α and PGE2 levels in plasma and combined pleural effusion and lung lavage of ratsEnvironmental Research, 1980