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Mechanisms of Acute Inhalation Effects of (+) and(−)‐α‐Pinene in BALB/c Mice
Author(s) -
Nielsen Gunnar Damgård,
Larsen Søren Thor,
Hougaard Karin Sørig,
Hammer Maria,
Wolkoff Peder,
Clausen Per Axel,
Wilkins Cornelius Kendall,
Alarie Yves
Publication year - 2005
Publication title -
basic and clinical pharmacology and toxicology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.805
H-Index - 90
eISSN - 1742-7843
pISSN - 1742-7835
DOI - 10.1111/j.1742-7843.2005.pto_96604.x
Subject(s) - irritation , chemistry , inhalation , respiratory system , enantiomer , inhalation exposure , anesthesia , toxicity , respiratory tract , pharmacology , vapours , medicine , stereochemistry , immunology , organic chemistry , psychiatry
The effects of (+)‐α‐pinene and (−)‐α‐pinene vapours were studied for respiratory effects in BALB/c mice. The (+) enantiomer showed persistent sensory irritation effect on the upper respiratory tract during exposures in the range of 100 to 3691 ppm. The threshold concentration for this effect was calculated to be about 70 ppm, which is close to the no‐effect level of about 40 ppm in humans. A significant airflow limitation occurred from exposure concentrations of 200 ppm and higher. No irritating effect was observed at the alveolar level and no central nervous system effect was obvious. In the exposure range from 218 to 5213 ppm, the (−) enantiomer produced only a short‐lasting sensory irritation effect during the first 10 min. of exposure and only at concentrations above 2900 ppm. The tidal volume decreased significantly from ∼400 ppm, but it was first conspicuous above 1000 ppm. Airflow limitation appeared consistently from ∼2000 ppm. The (−) enantiomer also induced anesthesia/and or pulmonary irritation as well as sudden death at concentrations above 2600 ppm. Overall, the enantiomers showed different time‐dependent and stereoselective effects. The lower sensory irritation effect of the (−) enantiomer probably being due to less of the molecule being adsorbed to a sensory irritant receptor.