A C. elegans model of electronic cigarette use: Physiological effects of e-liquids in nematodes

Electronic cigarettes (e-cigs) have recently become very popular particularly among the younger generation. These nicotine delivery devices are viewed as a preferable alternative to more conventional forms of tobacco use and are thought to reduce the risk of chronic obstructive pulmonary disease, th...

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Veröffentlicht in:BMC pharmacology & toxicology 2015-12, Vol.16 (1), p.32-32, Article 32
Hauptverfasser: Panitz, Daniel, Swamy, Harsha, Nehrke, Keith
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description Electronic cigarettes (e-cigs) have recently become very popular particularly among the younger generation. These nicotine delivery devices are viewed as a preferable alternative to more conventional forms of tobacco use and are thought to reduce the risk of chronic obstructive pulmonary disease, the third leading cause of death worldwide. However, there is very little data available on the consequences of e-cig use, though recently nicotine-independent inflammatory responses have been reported. The genetic model organism Caenorhabditis elegans is a soil nematode whose cell biology is remarkably well conserved with mammals. Here, we used C. elegans to test the physiologic effects of e-liquids used to refill e-cigs. Larval worms were exposed from hatching onwards to low concentrations (0.2 %) of e-liquids, distilled e-liquid vapor, propylene glycol (PG), or M9 buffer as a negative control. E-liquids tested included grape, menthol, and V2 Red "classic tobacco" flavors. Nicotine (48 ppm) was tested as a second level variable. Stereotypical physiological outputs were then measured, including developmental rate, fecundity, locomotion, lifespan, and the induction of canonical stress signaling pathways. A small but significant impairment of developmental rate and brood size was observed for PG and V2 Red treated worms compared to the negative control. Worms treated with e-liquids containing nicotine fared significantly worse than those that did not, but vaporization did not increase toxicity. Finally, both PG and V2 Red e-liquid induced an oxidative stress response in the absence of nicotine. PG exposure is sufficient to induce an oxidative stress response in nematodes, while nicotine is not. Both PG and nicotine independently influence physiologic measures of health and viability. The e-liquid flavorings did not significantly impact outcomes and there was no evidence for vaporization altering toxicity. These data suggest that the major physiologically significant component of e-liquids besides nicotine is likely the common solvent PG. We conclude that C. elegans are an appropriate model to rapidly assess parameters that may contribute to the basic cell biological effects of e-cigs.
doi_str_mv 10.1186/s40360-015-0030-0
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These nicotine delivery devices are viewed as a preferable alternative to more conventional forms of tobacco use and are thought to reduce the risk of chronic obstructive pulmonary disease, the third leading cause of death worldwide. However, there is very little data available on the consequences of e-cig use, though recently nicotine-independent inflammatory responses have been reported. The genetic model organism Caenorhabditis elegans is a soil nematode whose cell biology is remarkably well conserved with mammals. Here, we used C. elegans to test the physiologic effects of e-liquids used to refill e-cigs. Larval worms were exposed from hatching onwards to low concentrations (0.2 %) of e-liquids, distilled e-liquid vapor, propylene glycol (PG), or M9 buffer as a negative control. E-liquids tested included grape, menthol, and V2 Red "classic tobacco" flavors. Nicotine (48 ppm) was tested as a second level variable. Stereotypical physiological outputs were then measured, including developmental rate, fecundity, locomotion, lifespan, and the induction of canonical stress signaling pathways. A small but significant impairment of developmental rate and brood size was observed for PG and V2 Red treated worms compared to the negative control. Worms treated with e-liquids containing nicotine fared significantly worse than those that did not, but vaporization did not increase toxicity. Finally, both PG and V2 Red e-liquid induced an oxidative stress response in the absence of nicotine. PG exposure is sufficient to induce an oxidative stress response in nematodes, while nicotine is not. Both PG and nicotine independently influence physiologic measures of health and viability. The e-liquid flavorings did not significantly impact outcomes and there was no evidence for vaporization altering toxicity. 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These nicotine delivery devices are viewed as a preferable alternative to more conventional forms of tobacco use and are thought to reduce the risk of chronic obstructive pulmonary disease, the third leading cause of death worldwide. However, there is very little data available on the consequences of e-cig use, though recently nicotine-independent inflammatory responses have been reported. The genetic model organism Caenorhabditis elegans is a soil nematode whose cell biology is remarkably well conserved with mammals. Here, we used C. elegans to test the physiologic effects of e-liquids used to refill e-cigs. Larval worms were exposed from hatching onwards to low concentrations (0.2 %) of e-liquids, distilled e-liquid vapor, propylene glycol (PG), or M9 buffer as a negative control. E-liquids tested included grape, menthol, and V2 Red "classic tobacco" flavors. Nicotine (48 ppm) was tested as a second level variable. Stereotypical physiological outputs were then measured, including developmental rate, fecundity, locomotion, lifespan, and the induction of canonical stress signaling pathways. A small but significant impairment of developmental rate and brood size was observed for PG and V2 Red treated worms compared to the negative control. Worms treated with e-liquids containing nicotine fared significantly worse than those that did not, but vaporization did not increase toxicity. Finally, both PG and V2 Red e-liquid induced an oxidative stress response in the absence of nicotine. PG exposure is sufficient to induce an oxidative stress response in nematodes, while nicotine is not. Both PG and nicotine independently influence physiologic measures of health and viability. The e-liquid flavorings did not significantly impact outcomes and there was no evidence for vaporization altering toxicity. 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We conclude that C. elegans are an appropriate model to rapidly assess parameters that may contribute to the basic cell biological effects of e-cigs.</description><subject>Animals</subject><subject>Animals, Genetically Modified</subject><subject>Biological effects</subject><subject>Caenorhabditis elegans - drug effects</subject><subject>Caenorhabditis elegans - genetics</subject><subject>Caenorhabditis elegans - physiology</subject><subject>Cells</subject><subject>Chronic obstructive pulmonary disease</subject><subject>Cigarettes</subject><subject>Electronic cigarettes</subject><subject>Electronic Nicotine Delivery Systems - methods</subject><subject>Fecundity</subject><subject>Flavorings</subject><subject>Gravitational physiology</subject><subject>Green Fluorescent Proteins - genetics</subject><subject>Green Fluorescent Proteins - metabolism</subject><subject>Hatching</subject><subject>Humans</subject><subject>Inflammation</subject><subject>Life span</subject><subject>Liquids</subject><subject>Locomotion</subject><subject>Low concentrations</subject><subject>Lung diseases</subject><subject>Lung diseases, Obstructive</subject><subject>Mammals</subject><subject>Menthol</subject><subject>Menthol - administration &amp; dosage</subject><subject>Menthol - pharmacology</subject><subject>Microscopy, Confocal</subject><subject>Models, Animal</subject><subject>Nematoda</subject><subject>Nematodes</subject><subject>Nicotiana - chemistry</subject><subject>Nicotine</subject><subject>Nicotine - administration &amp; dosage</subject><subject>Nicotine - pharmacology</subject><subject>Obstructive lung disease</subject><subject>Oxidative stress</subject><subject>Oxidative Stress - drug effects</subject><subject>Physiological aspects</subject><subject>Physiological effects</subject><subject>Physiology</subject><subject>Propylene</subject><subject>Propylene glycol</subject><subject>Propylene Glycol - administration &amp; dosage</subject><subject>Propylene Glycol - pharmacology</subject><subject>Risk reduction</subject><subject>Smoking</subject><subject>Smoking cessation</subject><subject>Stress response</subject><subject>Studies</subject><subject>Tobacco</subject><subject>Toxicity</subject><subject>Vaping</subject><subject>Vaporization</subject><subject>Volatilization</subject><subject>Worms</subject><subject>Young adults</subject><issn>2050-6511</issn><issn>2050-6511</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><recordid>eNptkl1rFDEUhoMottT-AG8kIIg3s-bMTD7GC2FZWhUKetH7kM2cmU3JJG0yI_Tfm3Vr2RWTixxOnvfNBy8hb4GtAJT4lFvWCFYx4BVjTSlekPOacVYJDvDyqD4jlznfsTKkVIrXr8lZLUQja9adE72mmxVFj6MJmU6xR0_jsG_YOcXgLLVuNAnnGemS8TP9uXvMLvo4Oms8xWEoYP4jqbx7WFyfqQs04GTmYpbfkFeD8Rkvn9YLcnt9dbv5Vt38-Pp9s76pLK_5XG1N15tyQd43tRysMKreQiklWtUKqbATXcc59NJgDzgIJnpkRvCWQQfQXJAvB9v7ZTthbzHMyXh9n9xk0qOOxunTneB2eoy_dCtEJ2pZDD4-GaT4sGCe9eSyRe9NwLhkDbIVSjKAuqDv_0Hv4pJCeV2hZLmlgvaIGo1H7cIQy7l2b6rXrehYA22jCrX6D1Vmj5OzMeDgSv9E8OFIsEPj512OfpldDPkUhANoU8w54fD8GcD0PkD6ECBdAqT3AdKsaN4d_-Kz4m9cmt87eb2_</recordid><startdate>20151204</startdate><enddate>20151204</enddate><creator>Panitz, Daniel</creator><creator>Swamy, Harsha</creator><creator>Nehrke, Keith</creator><general>BioMed Central Ltd</general><general>BioMed Central</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7U7</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20151204</creationdate><title>A C. elegans model of electronic cigarette use: Physiological effects of e-liquids in nematodes</title><author>Panitz, Daniel ; Swamy, Harsha ; Nehrke, Keith</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c525t-ba9da0075d327fc6a82b13277ec84678e9699551d7aed1ef606de0a654019113</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Animals</topic><topic>Animals, Genetically Modified</topic><topic>Biological effects</topic><topic>Caenorhabditis elegans - drug effects</topic><topic>Caenorhabditis elegans - genetics</topic><topic>Caenorhabditis elegans - physiology</topic><topic>Cells</topic><topic>Chronic obstructive pulmonary disease</topic><topic>Cigarettes</topic><topic>Electronic cigarettes</topic><topic>Electronic Nicotine Delivery Systems - methods</topic><topic>Fecundity</topic><topic>Flavorings</topic><topic>Gravitational physiology</topic><topic>Green Fluorescent Proteins - genetics</topic><topic>Green Fluorescent Proteins - metabolism</topic><topic>Hatching</topic><topic>Humans</topic><topic>Inflammation</topic><topic>Life span</topic><topic>Liquids</topic><topic>Locomotion</topic><topic>Low concentrations</topic><topic>Lung diseases</topic><topic>Lung diseases, Obstructive</topic><topic>Mammals</topic><topic>Menthol</topic><topic>Menthol - administration &amp; 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These nicotine delivery devices are viewed as a preferable alternative to more conventional forms of tobacco use and are thought to reduce the risk of chronic obstructive pulmonary disease, the third leading cause of death worldwide. However, there is very little data available on the consequences of e-cig use, though recently nicotine-independent inflammatory responses have been reported. The genetic model organism Caenorhabditis elegans is a soil nematode whose cell biology is remarkably well conserved with mammals. Here, we used C. elegans to test the physiologic effects of e-liquids used to refill e-cigs. Larval worms were exposed from hatching onwards to low concentrations (0.2 %) of e-liquids, distilled e-liquid vapor, propylene glycol (PG), or M9 buffer as a negative control. E-liquids tested included grape, menthol, and V2 Red "classic tobacco" flavors. Nicotine (48 ppm) was tested as a second level variable. 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subjects Animals
Animals, Genetically Modified
Biological effects
Caenorhabditis elegans - drug effects
Caenorhabditis elegans - genetics
Caenorhabditis elegans - physiology
Cells
Chronic obstructive pulmonary disease
Cigarettes
Electronic cigarettes
Electronic Nicotine Delivery Systems - methods
Fecundity
Flavorings
Gravitational physiology
Green Fluorescent Proteins - genetics
Green Fluorescent Proteins - metabolism
Hatching
Humans
Inflammation
Life span
Liquids
Locomotion
Low concentrations
Lung diseases
Lung diseases, Obstructive
Mammals
Menthol
Menthol - administration & dosage
Menthol - pharmacology
Microscopy, Confocal
Models, Animal
Nematoda
Nematodes
Nicotiana - chemistry
Nicotine
Nicotine - administration & dosage
Nicotine - pharmacology
Obstructive lung disease
Oxidative stress
Oxidative Stress - drug effects
Physiological aspects
Physiological effects
Physiology
Propylene
Propylene glycol
Propylene Glycol - administration & dosage
Propylene Glycol - pharmacology
Risk reduction
Smoking
Smoking cessation
Stress response
Studies
Tobacco
Toxicity
Vaping
Vaporization
Volatilization
Worms
Young adults
title A C. elegans model of electronic cigarette use: Physiological effects of e-liquids in nematodes
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