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1.
Biomed Environ Sci ; 35(11): 1038-1050, 2022 Nov 20.
Artigo em Inglês | MEDLINE | ID: mdl-36443256

RESUMO

Objective: The effect of oral cadmium (Cd) intake to influence contact skin allergies was examined, since it is known that Cd is a heavy metal that affects many tissues, including the skin, in which it disturbs homeostasis, thus resulting in inflammation and injury. Methods: Male rats were evoked with experimental contact hypersensitivity reaction (CHS) to hapten dinitrochlorobenzene (DNCB), after prolonged (30 day) oral exposure to an environmentally relevant Cd dose (5 ppm). The ear cell population was analyzed with flow cytometry. Cytokine production by ear skin cells and the activity of skin-draining lymph node (DLN) cells were measured using enzyme-linked immunosorbent assay (ELISA). Results: Orally acquired Cd (5 ppm) increased CHS intensity only in Dark Agouti (DA) rats by affecting inflammatory responses in both the sensitization (an increase of IFN-γ and IL-17 cytokine production) and challenge (an increase of CD8 + and CD4 + cell number and TNF, IFN-γ and IL-17 cytokine production) phases. An increased CHS reaction was seen in Albino Oxford (AO) rats only at a high Cd dose (50 ppm), during the challenge phase (an increase of CD8 + and CD4 + cell number and TNF, IFN-γ and IL-17 cytokine production). Conclusion: These novel data indicate that oral Cd intensifies the skin response to sensitizing chemicals such as DNCB.


Assuntos
Alérgenos , Cádmio , Masculino , Ratos , Animais , Alérgenos/toxicidade , Cádmio/toxicidade , Dinitroclorobenzeno/toxicidade , Interleucina-17 , Citocinas
2.
Artigo em Inglês | WPRIM (Pacífico Ocidental) | ID: wpr-878337

RESUMO

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.


Assuntos
Animais , Masculino , Ratos , Fatores de Transcrição Hélice-Alça-Hélice Básicos/imunologia , Cádmio/toxicidade , Citocromo P-450 CYP1A1/imunologia , Citocromo P-450 CYP1B1/imunologia , Citocinas/imunologia , Poluentes Ambientais/toxicidade , Receptores de Hidrocarboneto Arílico/imunologia
3.
Artigo em Inglês | WPRIM (Pacífico Ocidental) | ID: wpr-773377

RESUMO

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.


Assuntos
Animais , Masculino , Ratos , Administração Oral , Cádmio , Toxicidade , Leucócitos , Metabolismo , Pulmão , Alergia e Imunologia , Patologia , Staphylococcus epidermidis , Testes de Toxicidade Subcrônica
4.
Artigo em Inglês | WPRIM (Pacífico Ocidental) | ID: wpr-270550

RESUMO

<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>


Assuntos
Animais , Masculino , Ratos , Aspergillus fumigatus , Alergia e Imunologia , Citocinas , Metabolismo , Pulmão , Alergia e Imunologia , Metabolismo , Microbiologia , Patologia , Aspergilose Pulmonar , Alergia e Imunologia
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