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Am J Physiol Heart Circ Physiol ; 320(4): H1510-H1525, 2021 04 01.
Artículo en Inglés | MEDLINE | ID: mdl-33543686

RESUMEN

After more than a decade of electronic cigarette (E-cig) use in the United States, uncertainty persists regarding E-cig use and long-term cardiopulmonary disease risk. As all E-cigs use propylene glycol and vegetable glycerin (PG-VG) and generate abundant saturated aldehydes, mice were exposed by inhalation to PG-VG-derived aerosol, formaldehyde (FA), acetaldehyde (AA), or filtered air. Biomarkers of exposure and cardiopulmonary injury were monitored by mass spectrometry (urine metabolites), radiotelemetry (respiratory reflexes), isometric myography (aorta), and flow cytometry (blood markers). Acute PG-VG exposure significantly affected multiple biomarkers including pulmonary reflex (decreased respiratory rate, -50%), endothelium-dependent relaxation (-61.8 ± 4.2%), decreased WBC (-47 ± 7%), and, increased RBC (+6 ± 1%) and hemoglobin (+4 ± 1%) versus air control group. Notably, FA exposure recapitulated the prominent effects of PG-VG aerosol on pulmonary irritant reflex and endothelial dysfunction, whereas AA exposure did not. To attempt to link PG-VG exposure with FA or AA exposure, urinary formate and acetate levels were measured by GC-MS. Although neither FA nor AA exposure altered excretion of their primary metabolite, formate or acetate, respectively, compared with air-exposed controls, PG-VG aerosol exposure significantly increased post-exposure urinary acetate but not formate. These data suggest that E-cig use may increase cardiopulmonary disease risk independent of the presence of nicotine and/or flavorings. This study indicates that FA levels in tobacco product-derived aerosols should be regulated to levels that do not induce biomarkers of cardiopulmonary harm. There remains a need for reliable biomarkers of exposure to inhaled FA and AA.NEW & NOTEWORTHY Use of electronic cigarettes (E-cig) induces endothelial dysfunction (ED) in healthy humans, yet the specific constituents in E-cig aerosols that contribute to ED are unknown. Our study implicates formaldehyde that is formed in heating of E-cig solvents (propylene glycol, PG; vegetable glycerin, VG). Exposure to formaldehyde or PG-VG-derived aerosol alone stimulated ED in female mice. As ED was independent of nicotine and flavorants, these data reflect a "universal flaw" of E-cigs that use PG-VG.Listen to this article's corresponding podcast at https://ajpheart.podbean.com/e/e-cigarettes-aldehydes-and-endothelial-dysfunction/.


Asunto(s)
Acetaldehído/toxicidad , Aorta Torácica/efectos de los fármacos , Cigarrillo Electrónico a Vapor/toxicidad , Endotelio Vascular/efectos de los fármacos , Formaldehído/toxicidad , Glicerol/toxicidad , Pulmón/efectos de los fármacos , Propilenglicol/toxicidad , Solventes/toxicidad , Acetaldehído/orina , Aerosoles , Animales , Aorta Torácica/metabolismo , Aorta Torácica/fisiopatología , Biomarcadores/sangre , Biomarcadores/orina , Cigarrillo Electrónico a Vapor/orina , Endotelio Vascular/metabolismo , Endotelio Vascular/fisiopatología , Femenino , Formaldehído/orina , Exposición por Inhalación , Pulmón/metabolismo , Pulmón/fisiopatología , Masculino , Ratones Endogámicos C57BL , Respiración/efectos de los fármacos , Medición de Riesgo , Vasoconstricción/efectos de los fármacos , Vasodilatación/efectos de los fármacos
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