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1.
Biomedical and Environmental Sciences ; (12): 192-202, 2021.
Article in English | WPRIM | ID: wpr-878337

ABSTRACT

Objective@#To investigate involvement of the aryl hydrocarbon receptor (AhR) in the immunomodulatory effects of cadmium (Cd).@*Methods@#The effect of Cd on AhR activation ( @*Results@#Cd increased @*Conclusion@#AhR signaling is involved in the lung leukocyte proinflammatory cytokine response to Cd. The relevance of the AhR to the cytokine response to Cd provides new insight into the mechanisms of Cd immunotoxicity.


Subject(s)
Animals , Male , Rats , Basic Helix-Loop-Helix Transcription Factors/immunology , Cadmium/toxicity , Cytochrome P-450 CYP1A1/immunology , Cytochrome P-450 CYP1B1/immunology , Cytokines/immunology , Environmental Pollutants/toxicity , Receptors, Aryl Hydrocarbon/immunology
2.
Biomedical and Environmental Sciences ; (12): 508-519, 2019.
Article in English | WPRIM | ID: wpr-773377

ABSTRACT

OBJECTIVE@#The aim of this study is to investigate the effects of oral cadmium (Cd) ingestion on the pulmonary immune response.@*METHODS@#Determination of Cd content in lungs and histopathological evaluation of the tissue was performed in rats following 30-day oral Cd administration (5 and 50 mg/L). Antioxidant enzyme defense (superoxide dismutase and catalase), cell infiltration, and production of tumor necrosis factor (TNF) and interferon (IFN)-γ, as well as the activity of myeloperoxidase (MPO), nitric oxide (NO), and various cytokines [interleukin (IL)-1β, IL-6, IL-10, and IL-17] were investigated.@*RESULTS@#Cd caused tissue damage and cell infiltration in the lungs, and this damage was more pronounced at higher doses. Cd deposition resulted in lung inflammation characterized by a dose-dependent IL-1β increase in lung homogenates, increased TNF levels at both doses, and IL-6 stimulation at low doses with inhibition observed at higher doses. Cd exerted differential effects on lung leukocytes isolated by enzyme digestion, and these effects were characterized by a lack of change in the production of reactive oxygen and nitrogen species, an inhibition of IL-1β and TNF, and stimulation of MPO and IFN-γ. The higher capacity of Cd-exposed lung cells to respond to the opportunistic pathogen Staphylococcus epidermidis was demonstrated in vitro.@*CONCLUSION@#The potential of ingested Cd to exert both proinflammatory and immunosuppressive effects on pulmonary tissue inflammation and immune reactivity highlights the complex immunomodulatory actions of this metal.


Subject(s)
Animals , Male , Rats , Administration, Oral , Cadmium , Toxicity , Leukocytes , Metabolism , Lung , Allergy and Immunology , Pathology , Staphylococcus epidermidis , Toxicity Tests, Subchronic
3.
Biomedical and Environmental Sciences ; (12): 684-694, 2014.
Article in English | WPRIM | ID: wpr-270550

ABSTRACT

<p><b>OBJECTIVE</b>To evaluate immunologic mechanisms underlying Aspergillus fumigatus pulmonary infections in immunocompetent Dark Agouti (DA) and Albino Oxford (AO) rats recognized as being susceptible to some inflammatory diseases in different manners.</p><p><b>METHODS</b>Lung fungal burden (quantitative colony forming units, CFU, assay), leukocyte infiltration (histology, cell composition) and their function (phagocytosis, oxidative activity, CD11b adhesion molecule expression) and cytokine interferon-γ (IFN-γ) and interleukin-17 and -4 (IL-17 and IL-4) lung content were evaluated following infection (intratracheally, 1x10(7) conidia).</p><p><b>RESULTS</b>Slower reduction of fungal burden was observed in AO rats in comparison with that in DA rats, which was coincided with less intense histologically evident lung cell infiltration and leukocyte recovery as well as lower level of most of the their activities including intracellular myeloperoxidase activity, the capacity of nitroblue tetrazolium salt reduction and CD11b adhesion molecule expression (except for phagocytosis of conidia) in these rats. Differential patterns of changes in proinflammatory cytokine levels (unchanged levels of IFN-γ and transient increase of IL-17 in AO rats vs continuous increase of both cytokines in DA rats) and unchanged levels of IL-4 were observed.</p><p><b>CONCLUSION</b>Genetically-based differences in the pattern of antifungal lung leukocyte activities and cytokine milieu, associated with differential efficiency of fungal elimination might be useful in the future use of rat models in studies of pulmonary aspergillosis.</p>


Subject(s)
Animals , Male , Rats , Aspergillus fumigatus , Allergy and Immunology , Cytokines , Metabolism , Lung , Allergy and Immunology , Metabolism , Microbiology , Pathology , Pulmonary Aspergillosis , Allergy and Immunology
4.
Biomedical and Environmental Sciences ; (12): 180-189, 2011.
Article in English | WPRIM | ID: wpr-306874

ABSTRACT

<p><b>OBJECTIVE</b>To evaluate the effects of epicutaneous application of anticoagulant warfarin, by examining the presence of tissue injury and immune/inflammatory activity in exposed skin.</p><p><b>METHODS</b>Rats were exposed to warfarin by applying 10 μg of warfarin-sodium to 10-12 cm(2) skin (range 0.8-1 μg per 1 cm(2)) for 3 consecutive days. Tissue injury was evaluated by lipid peroxidation, histomorphological changes and signs of reparative activity in skin. T cell infiltration and selected aspects of epidermal cell activity were examined as indicators of immune/inflammatory skin response to warfarin application.</p><p><b>RESULTS</b>Repeated warfarin application exerted no effect on skin metabolic viability, but resulted in tissue injury (increased malondialdehyde, MDA, production, evident histo-morphological changes in epidermis and dermis depicting cell injury and death). Increased numbers of proliferating cell nuclear antigen (PCNA(+)) cells indicated reparative processes in injured skin. Infiltration of CD3(+) cells (T lymphocytes) along with the increased production of tumor necrosis factor-a (TNF-a) by epidermal cells from warfarin-treated skin and their co-stimulatory effect in an in vitro T-cell activation assay demonstrated immunomodulatory effects of epicutaneous warfarin.</p><p><b>CONCLUSION</b>Presented data have documented tissue damage associated with immune/inflammatory activity in skin exposed to warfarin. Observed effects are relevant to immunotoxic potential of this anticoagulant in settings of external exposure.</p>


Subject(s)
Animals , Male , Rats , CD3 Complex , Genetics , Metabolism , Dermatitis, Contact , Pathology , Epidermis , Cell Biology , Gene Expression Regulation , Physiology , Inflammation , Metabolism , Lipid Peroxidation , Proliferating Cell Nuclear Antigen , Genetics , Metabolism , Rodenticides , Pharmacology , Skin , Cell Biology , Metabolism , T-Lymphocytes , Physiology , Warfarin , Pharmacology
5.
Biomedical and Environmental Sciences ; (12): 293-299, 2010.
Article in English | WPRIM | ID: wpr-306926

ABSTRACT

<p><b>OBJECTIVE</b>To examine the presence of gender differences in pulmonary inflammation evoked by acute systemic cadmium administration in rats.</p><p><b>METHODS</b>Presence of basic indicators of lung inflammation (inflammatory cytokine lung content, leukocyte infiltration and activity of cells recovered from lungs by enzyme digestion) was analyzed and compared in animals of the two sexes.</p><p><b>RESULTS</b>Intraperitoneal administration of cadmium (1.0 mg/kg) resulted in higher cadmium content in lungs of female rats. Higher tumor necrosis factor (TNF) content was noted in lung homogenates of male rats, while interleukin-6 (IL-6) content was slightly, but significantly greater in lungs of female rats. Increased leukocyte infiltration was observed in lungs of male rats, mainly due to neutrophils. Increased responsiveness to phorbol myristate acetate (PMA) stimulation was noted in cells recovered from lungs of male rats. Rise in intracellular content of myeloperoxidase (MPO) was noted in lung cells from cadmium-treated rats of both sexes, but higher in cells from male rats.</p><p><b>CONCLUSIONS</b>Presented data documented a more intense pulmonary inflammatory response to systemic cadmium administration in males, with higher IL-6 levels in lungs of female individuals. These sex differences in proinflamatory activity of cadmium in lungs should be taken into consideration in studying the remote toxicity of this heavy metal.</p>


Subject(s)
Animals , Female , Male , Rats , Cadmium Chloride , Pharmacokinetics , Toxicity , Cytokines , Allergy and Immunology , Environmental Pollutants , Pharmacokinetics , Toxicity , Enzyme-Linked Immunosorbent Assay , Leukocyte Count , Leukocytes , Cell Biology , Allergy and Immunology , Lung , Allergy and Immunology , Metabolism , Neutrophil Infiltration , Allergy and Immunology , Peroxidase , Metabolism , Pneumonia , Allergy and Immunology , Metabolism , Rats, Inbred Strains , Sex Characteristics
6.
Biomedical and Environmental Sciences ; (12): 1-7, 2009.
Article in English | WPRIM | ID: wpr-296012

ABSTRACT

<p><b>OBJECTIVE</b>To examine the presence of gender differences in pro-inflammatory potential of cadmium in rats by comparing systemic inflammatory response to acute cadmium intoxication in animals of the two sexes.</p><p><b>METHODS</b>Basic aspects of this response were evaluated, including plasma levels of inflammatory cytokines tumor necrosis factor (TNF) and interleukin-6 (IL-6) and of major rat acute phase protein alpha 2-macroglobulin (alpha2-M), as soluble indicators of inflammation, and the number and activity of peripheral blood leukocytes, as cellular indicators of inflammation.</p><p><b>RESULTS</b>Differential increases of IL-6 and alpha2-M (higher in males than in females) in peripheral blood cell counts and types (leukocytosis and shift in the ratio of granulocytes to lymphocytes more pronounced in males vs females) and in levels of neutrophil priming (higher in males vs females) were noted.</p><p><b>CONCLUSION</b>The data document a more intense inflammatory response to cadmium administration in males. The sex differences in inflammatory effects of cadmium might be taken into consideration in studying the toxicity of this heavy metal.</p>


Subject(s)
Animals , Female , Male , Rats , Cadmium , Toxicity , Inflammation , Interleukin-6 , Blood , Leukocyte Count , Neutrophils , Rats, Inbred Strains , Sex Factors , Tumor Necrosis Factor-alpha , Blood , alpha-Macroglobulins
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