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Tytuł pozycji:

Biological changes in C57BL/6 mice following 3 weeks of inhalation exposure to cigarette smoke or e-vapor aerosols.

Tytuł:
Biological changes in C57BL/6 mice following 3 weeks of inhalation exposure to cigarette smoke or e-vapor aerosols.
Autorzy:
Lee KM; a Altria Client Services LLC , Richmond , VA , USA.
Hoeng J; b PMI R&D, Philip Morris Products S.A , Neuchâtel , Switzerland.
Harbo S; c Battelle , Columbus , OH , USA.
Kogel U; b PMI R&D, Philip Morris Products S.A , Neuchâtel , Switzerland.
Gardner W; a Altria Client Services LLC , Richmond , VA , USA.
Oldham M; a Altria Client Services LLC , Richmond , VA , USA.
Benson E; c Battelle , Columbus , OH , USA.
Talikka M; b PMI R&D, Philip Morris Products S.A , Neuchâtel , Switzerland.
Kondylis A; b PMI R&D, Philip Morris Products S.A , Neuchâtel , Switzerland.
Martin F; b PMI R&D, Philip Morris Products S.A , Neuchâtel , Switzerland.
Titz B; b PMI R&D, Philip Morris Products S.A , Neuchâtel , Switzerland.
Ansari S; b PMI R&D, Philip Morris Products S.A , Neuchâtel , Switzerland.
Trivedi K; b PMI R&D, Philip Morris Products S.A , Neuchâtel , Switzerland.
Guedj E; b PMI R&D, Philip Morris Products S.A , Neuchâtel , Switzerland.
Elamin A; b PMI R&D, Philip Morris Products S.A , Neuchâtel , Switzerland.
Ivanov NV; b PMI R&D, Philip Morris Products S.A , Neuchâtel , Switzerland.
Vanscheeuwijck P; b PMI R&D, Philip Morris Products S.A , Neuchâtel , Switzerland.
Peitsch MC; b PMI R&D, Philip Morris Products S.A , Neuchâtel , Switzerland.
McKinney WJ Jr; a Altria Client Services LLC , Richmond , VA , USA.
Źródło:
Inhalation toxicology [Inhal Toxicol] 2018 Nov - Dec; Vol. 30 (13-14), pp. 553-567. Date of Electronic Publication: 2019 Mar 08.
Typ publikacji:
Comparative Study; Journal Article; Research Support, Non-U.S. Gov't
Język:
English
Imprint Name(s):
Publication: London : Informa Healthcare
Original Publication: New York, N.Y. : Hemisphere Pub. Corp., c1989-
MeSH Terms:
Electronic Nicotine Delivery Systems*
Respiratory System/*drug effects
Smoke/*adverse effects
Tobacco Products/*adverse effects
Administration, Inhalation ; Aerosols ; Animals ; Bronchoalveolar Lavage Fluid/chemistry ; Bronchoalveolar Lavage Fluid/cytology ; Carboxyhemoglobin/analysis ; Female ; Gene Expression Profiling ; Mice, Inbred C57BL ; Respiratory Function Tests ; Respiratory Physiological Phenomena/drug effects ; Respiratory System/metabolism ; Respiratory System/pathology
Contributed Indexing:
Keywords: 3R4F; MarkTen®; aerosols; e-cigarette; e-vapor; inhalation; mice; proteomics; transcriptomics
Substance Nomenclature:
0 (Aerosols)
0 (Smoke)
9061-29-4 (Carboxyhemoglobin)
Entry Date(s):
Date Created: 20190309 Date Completed: 20190903 Latest Revision: 20190903
Update Code:
20240105
DOI:
10.1080/08958378.2019.1576807
PMID:
30849254
Czasopismo naukowe
We compared early biological changes in mice after inhalation exposures to cigarette smoke or e-vapor aerosols (MarkTen ® cartridge with Carrier, Test-1, or Test-2 formulations; 4% nicotine). Female C57BL/6 mice were exposed to 3R4F cigarette smoke or e-vapor aerosols by nose-only inhalation for up to 4 hours/day, 5 days/week, for 3 weeks. The 3R4F and e-vapor exposures were set to match the target nose port aerosol nicotine concentration (∼41 µg/L). Only the 3R4F group showed postexposure clinical signs such as tremors and lethargy. At necropsy, the 3R4F group had significant increases in lung weight and changes in bronchoalveolar lavage parameters, as well as microscopic findings in the respiratory tract. The e-vapor groups had minimal microscopic changes, including squamous metaplasia in laryngeal epiglottis, and histiocytic infiltrates in the lung (Test-2 group only). The 3R4F group had a higher incidence and severity of microscopic findings compared to any e-vapor group. Transcriptomic analysis also showed that the 3R4F group had the highest number of differentially expressed genes compared to Sham Control. Among e-vapor groups, Test-2 group had more differentially expressed genes but the magnitude of gene expression-based network perturbations in all e-vapor groups was ∼94% less than the 3R4F group. On proteome analysis in the lung, differentially regulated proteins were detected in the 3R4F group only. In conclusion, 3-weeks of 3R4F exposure induced molecular and microscopic changes associated with smoking-related diseases in the respiratory tract, while e-vapor exposures showed substantially reduced biological activities.
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