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1.
Journal of Zhejiang University. Medical sciences ; (6): 521-527, 2014.
Artigo em Chinês | WPRIM | ID: wpr-251671

RESUMO

<p><b>OBJECTIVE</b>To investigate the effect of inositol hexaphosphate (IP6) on proliferation of human prostate carcinoma LNCaP cells and its relation to insulin-like growth factors binding protein-3 (IGFBP-3) expression.</p><p><b>METHODS</b>The siRNA technology was used to silence the IGFBP-3 gene in LNCaP cells. LNCaP cells and IGFBP-3 gene silenced LNCaP cells were exposed to IP6 for 24 h. Cell viability was measured by MTT assay; cell cycle arrest and cell apoptosis were detected by flow cytometry. The expression levels of IGFBP-3 and Bcl-2 mRNA and protein were analyzed by real-time quantitative RT-PCR and Western blotting, respectively.</p><p><b>RESULTS</b>The proliferation of LNCaP cells was be inhibited by IP6 in a dose dependent manner. After exposure to IP6 for 24 h, the cell viability in LNCaP cells and siRNA-treated LNCaP cells was 53.2%±11.6% and 82.3%±10.9%, respectively (P<0.05). After treatment of 1.5 mmol IP6,the apoptosis rate of LNCAP cells and siRNA-treated LNCAP cells was 40.48%±13.21% and 30.43%±10.65%, respectively (P<0.05). The proportion of G1 and G2 phase in LNCAP cells was 70.58%±8.25% and 5.64%±1.23%,after IP6 treatment the percentage of G1 phase cells decreased to 48.66%±11.23% and G2 phase cells increased to 31.11%±9.68%. However, for siRNA treated LNCAP cells, the proportion of G1 phase cells was 58.25%±12.36% and G2 phase cells was 23.85%±12.45%. Higher expression of IGFBP-3 and lower expression of Bcl-2 in LNCaP cells treated with IP6 were found at both mRNA and protein levels. IP6 treatment enhanced IGFBP-3 mRNA expression by 2.21±0.15 folds. In the contrast, expression of Bcl-2 mRNA decreased by 0.69±0.03 folds. Meanwhile, after IGFBP- gene silence Bcl-2 expression was not decreased.</p><p><b>CONCLUSION</b>IP6 can inhibit the proliferation of LNCaP cells, which may be associated with the changes of IGFBP-3 level through Bcl-2 expression.</p>


Assuntos
Humanos , Masculino , Apoptose , Linhagem Celular Tumoral , Proliferação de Células , Inativação Gênica , Proteína 3 de Ligação a Fator de Crescimento Semelhante à Insulina , Metabolismo , Ácido Fítico , Farmacologia , Neoplasias da Próstata , Metabolismo , Proteínas Proto-Oncogênicas c-bcl-2 , Metabolismo , RNA Interferente Pequeno
2.
China Journal of Chinese Materia Medica ; (24): 718-721, 2007.
Artigo em Chinês | WPRIM | ID: wpr-283398

RESUMO

<p><b>OBJECTIVE</b>To investigate the effect of Suanzao nacute hepatic failure in mice.</p><p><b>METHOD</b>Acute liver failure was induced in male Kunming strain mice by enterocoelia injecting the animals with D-Gal-N and LPS. The mice in treatment groups were given corresponding drug 2 h before administration of D-Ga1-N and LPS, and the mice in control group were given the same dose of distilled water. The 24 h survival rate, serum alanine aminotransferase (ALT), aspartate aminotransferase (AST) levels were compared. Serum the levels of TNF-alpha and IL-1 and the levels of SOD, MDA, GR, GSH, NO and NOS in the liver were determined.</p><p><b>RESULT</b>Treatment with suanzaoren decoction could increase the survival rate and improve the liver histological feather. Suanzaoren decoction inhibited the serum the levels of ALT, AST, TNF-alpha and IL-1, and reduced the levels of MDA, NO and NOS and increased the levels of GR and SOD in the liver.</p><p><b>CONCLUSION</b>Treatment with Suanzaoren decoction can suppress the D-Gal-N/LPS-induced acute hepatic failure. It may be the mechanism that Suanzaoren decocotion regulate the production of inflammatory cytokines and free radicals.</p>


Assuntos
Animais , Masculino , Camundongos , Alanina Transaminase , Sangue , Aspartato Aminotransferases , Sangue , Citocinas , Metabolismo , Combinação de Medicamentos , Medicamentos de Ervas Chinesas , Farmacologia , Radicais Livres , Metabolismo , Galactosamina , Glutationa , Metabolismo , Lipopolissacarídeos , Fígado , Metabolismo , Patologia , Falência Hepática Aguda , Sangue , Malondialdeído , Metabolismo , Óxido Nítrico , Metabolismo , Óxido Nítrico Sintase , Metabolismo , Distribuição Aleatória , Superóxido Dismutase , Metabolismo
3.
Chinese Journal of Integrated Traditional and Western Medicine ; (12): 303-305, 2007.
Artigo em Chinês | WPRIM | ID: wpr-269074

RESUMO

<p><b>OBJECTIVE</b>To investigate the curative effect and safety of auxiliary treatment with Suanzaoren Decoction (SZRD) on patients with chronic severe hepatitis (CSH).</p><p><b>METHODS</b>Sixty patients, with the diagnosis in accordance with the diagnostic criterion of CSH, were assigned to the treated group and the control group, 30 in each group. Patients in the control group were treated with comprehensive therapy including symptomatic supportive treatment, anti-infective therapy and artificial liver plasmapheresis etc., while those in the treated group were orally taken SZRD additionally. Patients' condition of sleeping and changes of total bilirubin (TBIL), prothrombin activity (PTA), tumor necrosis factor-alpha (TNF-alpha) and interleukin-1 (IL-1) were observed before and after treatment, and the adverse reactions were observed as well.</p><p><b>RESULTS</b>The sleeping status were significantly improved in the treated group after treatment, and the serum levels of TBIL, TNF-alpha and IL-1 were significantly decreased. The improvement rate was 66.7% (20/30) and significantly higher than that (40.0%, 12/30) in the control group.</p><p><b>CONCLUSION</b>SZRD can significantly improve the sleeping status of CSH patients, alleviate the hepato-cellular injury by inflammatory cytokines and without obvious adverse reaction.</p>


Assuntos
Adulto , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Adulto Jovem , Bilirrubina , Sangue , Medicamentos de Ervas Chinesas , Usos Terapêuticos , Hepatite Crônica , Tratamento Farmacológico , Patologia , Interleucina-1 , Sangue , Fitoterapia , Fator de Necrose Tumoral alfa , Sangue
4.
Journal of Central South University(Medical Sciences) ; (12): 344-348, 2005.
Artigo em Chinês | WPRIM | ID: wpr-813365

RESUMO

OBJECTIVE@#To investigate the effect of diazepam and modafinil on acute hepatic failure in mice.@*METHODS@#Acute liver failure was induced in male Kunming strain mice by enterocoelia injecting the mice with D-GalN and LPS . The mice in the treatment groups were given corresponding drug 2 h before the administration of D-GalN and LPS, and the mice in the control group were given the same dose of distilled water. The 24-hour survival rate, serum alanine aminotransferase (ALT), and aspartate aminotransferase (AST) levels were compared. Serum levels of TNF-alpha and IL-1 and the levels of SOD, MDA, GR, GSH, NO and NOS in the liver were determined.@*RESULTS@#Treatment with diazepam increased the survival rate and improved liver histological feature. Diazepam inhibited the serum levels of ALT, AST, TNF-alpha and IL-1, and reduced levels of MDA, NO and NOS and increased levels of GR and SOD in the liver. Modafinil decreased liver histological feature, increased the serum levels of ALT, AST, TNF-alpha and IL-1, increased level of MDA, and inhabited levels of SOD and GR in the liver.@*CONCLUSION@#Treatment with diazepam may suppress the D-GalN/LPS-induced acute hepatic failure and modafinil may facilitate the acute hepatic failure.


Assuntos
Animais , Masculino , Camundongos , Compostos Benzidrílicos , Usos Terapêuticos , Diazepam , Usos Terapêuticos , Galactosamina , Lipopolissacarídeos , Fígado , Patologia , Falência Hepática Aguda , Tratamento Farmacológico , Patologia , Modafinila , Distribuição Aleatória
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