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1.
Laboratory Animal Research ; : 92-100, 2018.
Article Dans Anglais | WPRIM | ID: wpr-717162

Résumé

Water extract of guibi-tang (GB), a traditional Chinese, Japanese, and Korean herbal medicine, is used to treat memory impairment, insomnia, and peptic ulcers. The aim of this study was to investigate the protective effects of GB on pulmonary inflammation induced by cigarette smoke (CS) and lipopolysaccharide (LPS). C57BL/6 mice were used to develop a pulmonary inflammation model by exposing them to CS for 1 h per day for 7 days. LPS was intranasally administered to mice under mild anesthesia on day 5. GB was administered 1 h before CS exposure at doses of 50 or 100 mg/kg for 7 days. Our results showed that GB suppressed the CS and LPS induced elevation in inflammatory cell counts in the bronchoalveolar lavage fluid (BALF), with significant reductions in protein, tumor necrosis factor (TNF)-α, and interleukin (IL)-6 levels. Histological studies revealed that GB decreased the inflammatory cell infiltration into lung tissue caused by CS- and LPS-exposure. GB also significantly decreased the CS and LPS-induced expression of inducible nitric oxide synthase (iNOS) in the lung tissue. Taken together, GB effectively attenuated airway inflammation caused by CS and LPS. These results indicate that GB is a potential therapeutic herbal formula for pulmonary inflammatory disease.


Sujets)
Animaux , Humains , Souris , Anesthésie , Asiatiques , Liquide de lavage bronchoalvéolaire , Numération cellulaire , Science des plantes médicinales , Inflammation , Interleukines , Poumon , Mémoire , Nitric oxide synthase type II , Ulcère peptique , Pneumopathie infectieuse , Troubles de l'endormissement et du maintien du sommeil , Fumée , Produits du tabac , Facteur de nécrose tumorale alpha , Eau
2.
Journal of Rheumatic Diseases ; : 55-59, 2017.
Article Dans Anglais | WPRIM | ID: wpr-160549

Résumé

Takayasu arteritis (TA) and ulcerative colitis (UC), both immune-mediated inflammatory diseases, rarely occur together. This report describes TA in a 29-year old female patient who was being treated for UC for three years. As she had left-side neck pain and headache, she was diagnosed with TA and her response to tumor necrosis factor (TNF) inhibitor was assessed by fluorine-18-fluorodeoxyglucose (¹⁸F-FDG) positron emission tomography (PET)/computed tomography (CT). Positive responses to the TNF inhibitor were seen by PET/CT for the TA and by endoscopy for the UC. We conclude that TNF inhibitors are effective treatments for both TA and UC. We found that PET/CT is a useful for diagnosing and assessing TA.


Sujets)
Femelle , Humains , Rectocolite hémorragique , Diagnostic , Électrons , Endoscopie , Fluorodésoxyglucose F18 , Céphalée , Cervicalgie , Tomographie par émission de positons , Tomographie par émission de positons couplée à la tomodensitométrie , Maladie de Takayashu , Facteur de nécrose tumorale alpha , Ulcère
3.
Laboratory Animal Research ; : 200-207, 2016.
Article Dans Anglais | WPRIM | ID: wpr-221837

Résumé

This study investigated the protective effects of diallyl disulfide (DADS) against acetaminophen (AAP)-induced acute renal injury in male rats. We also investigated the effects of DADS on kidney injury molecule-1 (KIM-1) and neutrophil gelatinase-associated lipocalin (NGAL), which are novel biomarkers of nephrotoxicity in renal tissues, in response to AAP treatment. The following four experimental groups were evaluated: (1) vehicle control, (2) AAP (1,000 mg/kg), (3) AAP&DADS, and (4) DADS (50 mg/kg/day). AAP treatment caused acute kidney injury evidenced by increased serum blood urea nitrogen (BUN) levels and histopathological alterations. Additionally, Western blot and immunohistochemistry analysis showed increased expression of KIM-1 and NGAL proteins in renal tissues of AAP-treated rats. In contrast, DADS pretreatment significantly attenuated the AAP-induced nephrotoxic effects, including serum BUN level and expression of KIM-1 and NGAL proteins. Histopathological studies confirmed the renoprotective effect of DADS. The results suggest that DADS prevents AAP-induced acute nephrotoxicity, and that KIM-1 and NGAL may be useful biomarkers for the detection and monitoring of acute kidney injury associated with AAP exposure.


Sujets)
Animaux , Humains , Mâle , Rats , Acétaminophène , Atteinte rénale aigüe , Marqueurs biologiques , Azote uréique sanguin , Technique de Western , Immunohistochimie , Rein , Lipocalines , Granulocytes neutrophiles
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