Menthol attenuates respiratory irritation and elevates blood cotinine in cigarette smoke exposed mice.

dc.contributor.author

Ha, Michael A

dc.contributor.author

Smith, Gregory J

dc.contributor.author

Cichocki, Joseph A

dc.contributor.author

Fan, Lu

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Liu, Yi-Shiuan

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Caceres, Ana I

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Jordt, Sven Eric

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Morris, John B

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McKemy, David D

dc.coverage.spatial

United States

dc.date.accessioned

2015-10-22T13:21:57Z

dc.date.issued

2015

dc.description.abstract

Addition of menthol to cigarettes may be associated with increased initiation of smoking. The potential mechanisms underlying this association are not known. Menthol, likely due to its effects on cold-sensing peripheral sensory neurons, is known to inhibit the sensation of irritation elicited by respiratory irritants. However, it remains unclear whether menthol modulates cigarette smoke irritancy and nicotine absorption during initial exposures to cigarettes, thereby facilitating smoking initiation. Using plethysmography in a C57Bl/6J mouse model, we examined the effects of L-menthol, the menthol isomer added to cigarettes, on the respiratory sensory irritation response to primary smoke irritants (acrolein and cyclohexanone) and smoke of Kentucky reference 2R4 cigarettes. We also studied L-menthol's effect on blood levels of the nicotine metabolite, cotinine, immediately after exposure to cigarette smoke. L-menthol suppressed the irritation response to acrolein with an apparent IC₅₀ of 4 ppm. Suppression was observed even at acrolein levels well above those necessary to produce a maximal response. Cigarette smoke, at exposure levels of 10 mg/m³ or higher, caused an immediate and marked sensory irritation response in mice. This response was significantly suppressed by L-menthol even at smoke concentrations as high as 300 mg/m³. Counterirritation by L-menthol was abolished by treatment with a selective inhibitor of Transient Receptor Potential Melastatin 8 (TRPM8), the neuronal cold/menthol receptor. Inclusion of menthol in the cigarette smoke resulted in roughly a 1.5-fold increase in plasma cotinine levels over those observed in mice exposed to smoke without added menthol. These findings document that, L-menthol, through TRPM8, is a strong suppressor of respiratory irritation responses, even during highly noxious exposures to cigarette smoke or smoke irritants, and increases blood cotinine. Therefore, L-menthol, as a cigarette additive, may promote smoking initiation and nicotine addiction.

dc.identifier

http://www.ncbi.nlm.nih.gov/pubmed/25679525

dc.identifier

PONE-D-14-33880

dc.identifier.eissn

1932-6203

dc.identifier.uri

https://hdl.handle.net/10161/10771

dc.language

eng

dc.publisher

Public Library of Science (PLoS)

dc.relation.ispartof

PLoS One

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10.1371/journal.pone.0117128

dc.subject

Acrolein

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Animals

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Cotinine

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Female

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Irritants

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Menthol

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Mice

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Respiration

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Smoking

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TRPM Cation Channels

dc.title

Menthol attenuates respiratory irritation and elevates blood cotinine in cigarette smoke exposed mice.

dc.type

Journal article

duke.contributor.orcid

Jordt, Sven Eric|0000-0001-6171-5622

pubs.author-url

http://www.ncbi.nlm.nih.gov/pubmed/25679525

pubs.begin-page

e0117128

pubs.issue

2

pubs.organisational-group

Anesthesiology

pubs.organisational-group

Clinical Science Departments

pubs.organisational-group

Duke

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School of Medicine

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Staff

pubs.publication-status

Published online

pubs.volume

10

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