Androgens augment pulmonary responses to ozone in mice

Autor: Ross S. Osgood, Stephanie A. Shore, David I. Kasahara, Youngji Cho, Hiroki Tashiro
Rok vydání: 2019
Předmět:
Male
Physiology
IL‐1α
Reproductive Hormones
030204 cardiovascular system & hematology
lcsh:Physiology
Flutamide
chemistry.chemical_compound
0302 clinical medicine
Interleukin-1alpha
Lung
Methacholine Chloride
Original Research
Sex Characteristics
lcsh:QP1-981
medicine.diagnostic_test
respiratory system
Neutrophil Infiltration
Androgens
Cytokines
medicine.symptom
Bronchoalveolar Lavage Fluid
Toxins
Pollutants and Chemical Agents

medicine.drug
medicine.medical_specialty
Immunology
Inflammation
03 medical and health sciences
Ozone
Airway hyperresponsiveness
Physiology (medical)
Internal medicine
medicine
Respiratory Hypersensitivity
Animals
Asthma
Respiratory Conditions Disorder and Diseases
business.industry
Interleukin-6
Androgen Antagonists
Pneumonia
castration
medicine.disease
respiratory tract diseases
Androgen receptor
Mice
Inbred C57BL

Oxidative Stress
Bronchoalveolar lavage
Endocrinology
Castration
chemistry
Respiratory Mechanics
Methacholine
business
Corticosterone
Orchiectomy
030217 neurology & neurosurgery
Hormone
Zdroj: Physiological Reports
Physiological Reports, Vol 7, Iss 18, Pp n/a-n/a (2019)
ISSN: 2051-817X
Popis: Ozone causes airway hyperresponsiveness, a defining feature of asthma, and is an asthma trigger. In mice, ozone‐induced airway hyperresponsiveness is greater in males than in females, suggesting a role for sex hormones in the response to ozone. To examine the role of androgens in these sex differences, we castrated 4‐week‐old mice. Controls underwent sham surgery. At 8 weeks of age, mice were exposed to ozone (2ppm, 3 h) or room air. Twenty‐four hours later, mice were anesthetized and measurements of airway responsiveness to inhaled aerosolized methacholine were made. Mice were then euthanized and bronchoalveolar lavage was performed. Castration attenuated ozone‐induced airway hyperresponsiveness and reduced bronchoalveolar lavage cells. In intact males, flutamide, an androgen receptor inhibitor, had similar effects to castration. Bronchoalveolar lavage concentrations of several cytokines were reduced by either castration or flutamide treatment, but only IL‐1α was reduced by both castration and flutamide. Furthermore, an anti‐IL‐1α antibody reduced bronchoalveolar lavage neutrophils in intact males, although it did not alter ozone‐induced airway hyperresponsiveness. Our data indicate that androgens augment pulmonary responses to ozone and that IL‐1α may contribute to the effects of androgens on ozone‐induced cellular inflammation but not airway hyperresponsiveness.
Databáze: OpenAIRE
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