Effect of dibenz(b,f)-1,4-oxazepine aerosol on the breathing pattern and respiratory variables by continuous recording and analysis in unanaesthetised mice
| Autor: | Rajagopalan Vijayaraghavan, Pranav K. Gutch, Utsab Deb |
|---|---|
| Jazyk: | angličtina |
| Rok vydání: | 2020 |
| Předmět: |
Respiratory rate
Riot control agent Health Toxicology and Mutagenesis Sensory system 010501 environmental sciences Lung injury Toxicology medicine.disease_cause 01 natural sciences Mice 03 medical and health sciences 0302 clinical medicine Breathing pattern TRPA1 receptor lcsh:RA1190-1270 medicine Respiratory system Dibenz(b.f)-1 4-oxazepine ComputingMethodologies_COMPUTERGRAPHICS 0105 earth and related environmental sciences lcsh:Toxicology. Poisons Inhalation business.industry Regular Article Sensory irritation RD50 medicine.anatomical_structure Anesthesia Irritation business 030217 neurology & neurosurgery Respiratory tract |
| Zdroj: | Toxicology Reports, Vol 7, Iss, Pp 1121-1126 (2020) Toxicology Reports |
| ISSN: | 2214-7500 |
| Popis: | Graphical abstract Highlights • Dibenz (b,f)-1,4-oxazepine (CR) is a riot control agent. • Respiratory variables and breathing pattern were recorded continuously in mice. • CR produced concentration dependent sensory irritation without pulmonary irritation. • Concentrations below 158.2 mg/m3 showed recovery to normal breathing. • Study shows CR causes sensory irritation only and may not cause lung injury. A riot control agent has to be a sensory irritant of a reversible type without pulmonary irritation as the later can cause lung injury. The aim of the present study is to continuously record and analyse breathing pattern and respiratory variables of dibenz (b,f)-1,4-oxazepine (CR) in unanaesthetised mice during and after exposure. The lowest concentration of 0.65 mg/m3 did not produce any effect on the breathing pattern. As high as 500 fold increase (315.9 mg/m3) in the concentration was used and no mortality was observed. CR produced a concentration dependent sensory irritation, without pulmonary irritation or airflow obstruction, showing that it may not cause any lung injury. The sensory irritation was initiated within 5 min of exposure due to the activation of TRPA1 receptors of the upper respiratory tract. Immediate recovery of normal breath without sensory irritation was observed in all the concentrations except the highest concentration of 315.9 mg/m3. Corresponding to the sensory irritation there was concentration dependent respiratory depression. The 50 percent respiratory depression (RD50) in this experiment was 152 mg/m3 and the estimated threshold limit value for occupational exposure was 4.56 mg/m3. The present study shows that CR causes sensory irritation only which is completely recoverable. |
| Databáze: | OpenAIRE |
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