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1.
Chinese Journal of Integrated Traditional and Western Medicine ; (12): 1216-1220, 2013.
Artigo em Chinês | WPRIM | ID: wpr-359282

RESUMO

<p><b>OBJECTIVE</b>To observe the effect of Qingchang Huashi Recipe (QHR) on the activation and expressions of nuclear factor kappaB (NF-kappaB), Toll-like receptors (TLRs), and contents of interleukin-8 (IL-8), thus exploring its possible mechanisms for treating ulcerative colitis (UC).</p><p><b>METHODS</b>The HT-29 cells were induced to inflammation model by tumor necrosis factor-alpha (TNF-alpha) and lipopolysaccharides (LPS). HT-29 cells were divided into 6 groups, i.e., the vehicle control group, the model control group, the sulfasalazine (SASP) group, the high dose QHR group, the middle dose QHR group, the low dose QHR group. Effects on the cell growth were detected by MTT. The chemoattractant of macrophages was observed using Transwell. The expressions of NF-kappaB and TLR4 protein were detected using immune cell fluorescence method. The content of IL-8 was detected by ELISA.</p><p><b>RESULTS</b>The growth of cells were not inhibited in each group. Statistical difference existed in each dose QHR group in inhibiting the chemoattractant of macrophages, reducing activation of NF-kappaB, lowing expressions of TLR4 protein, and decreasing the secretion of IL-8, when compared with the model control group (P < 0.05). No statistical difference existed in inhibiting the chemoattractant of macrophages between the high dose QHR group and the vehicle control group (P > 0.05). But its inhibition on NF-kappaB activation was higher in the high dose QHR group than in the SASP group (P < 0.05).</p><p><b>CONCLUSION</b>QHR could obviously attenuate the inflammatory reaction of HT-29 cells, inhibit the chemoattractant of macrophages, reduce the activation of NF-kappaB, lower expressions of TLR-4, and attenuate the secretion of IL-8, which might be one of its mechanisms for treating UC.</p>


Assuntos
Humanos , Colite Ulcerativa , Metabolismo , Patologia , Medicamentos de Ervas Chinesas , Farmacologia , Células HT29 , Inflamação , Interleucina-8 , Metabolismo , NF-kappa B , Metabolismo , Transdução de Sinais , Receptor 4 Toll-Like , Metabolismo
2.
Chinese Journal of Contemporary Pediatrics ; (12): 888-891, 2009.
Artigo em Chinês | WPRIM | ID: wpr-305091

RESUMO

<p><b>OBJECTIVE</b>Recent studies have shown that integrin linked kinase (ILK) plays an important role in the pathogenesis and development of some kidney diseases. This study aimed to investigate the relationship between ILK and renal glomerular damage in children with Henoch schonlein purpura nephritis (HSPN).</p><p><b>METHODS</b>One hundred and eighty eight HSPN children (aged 3 to 17 years) were assigned to five groups according to the classification of the International Study of Kidney Disease in Children (ISKDC): grade < or = IIa (n = 62), grade IIb (n = 42), grade IIIa (n = 29), grade IIIb (n = 40) and grade > or = IV (n = 15). Fifteen children with basement membrane nephropathy served as the control group. ILK expression on glomeruli was ascertained by immunohistochemical staining. The relationships of ILK expression on glomeruli with glomerular histopathologic lesions and urinary protein excretions were examined.</p><p><b>RESULTS</b>The positive areas of ILK expression on glomeruli in the control, grade < or = IIa, grade IIb, grade IIIa, grade IIIb and grade > or = IV groups were (3.35 + or - 1.01)%, (4.88 + or - 1.13)%, (9.64 + or - 1.36)%, (11.27 + or - 1.68)%, (17.42 + or -3.0)% and (20.62 + or - 2.32%), respectively. There were significant differences in the ILK expression between groups (p<0.01). ILK expression on glomeruli increased with increased urinary protein excretions. There were significant differences in the ILK expression in children with different urinary protein excretions (p<0.01).</p><p><b>CONCLUSIONS</b>ILK might be involved in the process of renal glomerular histopathologic damage and the production of proteinuria in children with HSPN.</p>


Assuntos
Criança , Pré-Escolar , Feminino , Humanos , Masculino , Imuno-Histoquímica , Glomérulos Renais , Patologia , Nefrite , Patologia , Proteínas Serina-Treonina Quinases , Vasculite por IgA , Patologia
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