Ozone-Induced Vascular Contractility and Pulmonary Injury Are Differentially Impacted by Diets Enriched With Coconut Oil, Fish Oil, and Olive Oil

Author:

Snow Samantha J1ORCID,Cheng Wan-Yun1,Henriquez Andres2,Hodge Myles3,Bass Virgina4,Nelson Gail M5,Carswell Gleta5,Richards Judy E1,Schladweiler Mette C1,Ledbetter Allen D1,Chorley Brian5ORCID,Gowdy Kymberly M3,Tong Haiyan1,Kodavanti Urmila P12

Affiliation:

1. Environmental Public Health Division, NHEERL, U.S. Environmental Protection Agency, Research Triangle Park, North Carolina 27711

2. Curriculum in Toxicology, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina 27514

3. Department of Pharmacology and Toxicology, East Carolina University, Greenville, North Carolina 27834

4. School of Public Health, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina 27514

5. Integrated Systems Toxicology Division, NHEERL, U.S. Environmental Protection Agency, Research Triangle Park, North Carolina 27711

Abstract

Abstract Fish, olive, and coconut oil dietary supplementation have several cardioprotective benefits, but it is not established if they protect against air pollution-induced adverse effects. We hypothesized that these dietary supplements would attenuate ozone-induced systemic and pulmonary effects. Male Wistar Kyoto rats were fed either a normal diet, or a diet supplemented with fish, olive, or coconut oil for 8 weeks. Animals were then exposed to air or ozone (0.8 ppm), 4 h/day for 2 days. Ozone exposure increased phenylephrine-induced aortic vasocontraction, which was completely abolished in rats fed the fish oil diet. Despite this cardioprotective effect, the fish oil diet increased baseline levels of bronchoalveolar lavage fluid (BALF) markers of lung injury and inflammation. Ozone-induced pulmonary injury/inflammation were comparable in rats on normal, coconut oil, and olive oil diets with altered expression of markers in animals fed the fish oil diet. Fish oil, regardless of exposure, led to enlarged, foamy macrophages in the BALF that coincided with decreased pulmonary mRNA expression of cholesterol transporters, cholesterol receptors, and nuclear receptors. Serum microRNA profile was assessed and demonstrated marked depletion of a variety of microRNAs in animals fed the fish oil diet, several of which were of splenic origin. No ozone-specific changes were noted. Collectively, these data indicate that although fish oil offered vascular protection from ozone exposure, it increased pulmonary injury/inflammation and impaired lipid transport mechanisms resulting in foamy macrophage accumulation, demonstrating the need to be cognizant of potential off-target pulmonary effects that might offset the overall benefit of this vasoprotective supplement.

Funder

U.S. EPA

Fulbright (CONICYT)

Environmental Protection Agency—University of North Carolina at Chapel Hill Cooperative Trainee Agreement

HEI Walter A. Rosenblith Award

Health Effects Institute

Publisher

Oxford University Press (OUP)

Subject

Toxicology

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