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1.
China Journal of Chinese Materia Medica ; (24): 936-939, 2008.
Artigo em Chinês | WPRIM | ID: wpr-295435

RESUMO

<p><b>OBJECTIVE</b>To investigate the changes of proto-oncogene c-fos, c-jun mRNA expression in angiotensin II (Ang II)-induced hypertrophy and effects of tanshinone II A (Tan) in the primary culture of neonatal rat cardiomyocytes.</p><p><b>METHOD</b>Twelve neonatal Wistar rats aged one day old of clean grade and both sexes were selected to isolate and culture cardiomyocytes. The cardiomyocytes were divided into: normal control group, Ang II (10(-6) mol x L(-1)) group, Ang II (10(-6) mol x L(-1)) +Tan (10(-8) g x L(-1)) group, Ang II (10(-6) mol x L(-1)) + valsartan (10(-6) mol x L(-1)) group, Tan (10(-8) g x L(-1)) group, valsartan (10(-6) mol x L(-1)) group. The cardiomyocyte size was determined by phase contrast microscope, the rate of protein synthesis in cardiomyocytes was measured by 3H-leucine incorporation. The c-fos, c-jun mRNA expression of cardiomyocytes were assessed using reverse transcription polymerase chain reaction (RT-PCR).</p><p><b>RESULT</b>Ang II was added to the culture medium and 30 min later, the c-fos, c-jun mRNA expression of cardiomyocytes increased significantly (P < 0. 01). After Ang II took effect for 24 h, the rate of protein synthesis in Ang II group increased more prominently than that in normal control group (P < 0.01). After Ang II took effect for 7 days, the size of cardiomyocyte in Ang II group increased obviously (P < 0. 05). If tanshinone II or valsartan was added to the culture medium before Ang II, both of them could inhibit the increase of c-fos, c-jun mRNA expression (P < 0.01), cardiomyocyte protein synthesis rate (P < 0.01), and cardiomyocyte size (P < 0.05) induced by Ang II.</p><p><b>CONCLUSION</b>Tanshinone II could ameliorate Ang II-induced cardiomyocytes hypertrophy by inhabiting c-fos, c-jun mRNA expression.</p>


Assuntos
Animais , Ratos , Angiotensina II , Farmacologia , Cardiomegalia , Metabolismo , Patologia , Abietanos , Regulação da Expressão Gênica , Genes fos , Genética , Genes jun , Genética , Miócitos Cardíacos , Metabolismo , Patologia , Fenantrenos , Farmacologia , Proteínas Proto-Oncogênicas c-fos , Genética , Proteínas Proto-Oncogênicas c-jun , Genética , RNA Mensageiro , Genética , Metabolismo , Ratos Wistar , Tetrazóis , Farmacologia , Valina , Farmacologia , Valsartana
2.
China Journal of Chinese Materia Medica ; (24): 1921-1924, 2007.
Artigo em Chinês | WPRIM | ID: wpr-307558

RESUMO

<p><b>OBJECTIVE</b>To observe effects of tetrandrine (Tet) on angiotensin II (Ang II)-induced cardiomyocyte hypertrophy and the activity and expression of phosphorylated ERK1/2 (p-ERK1/2).</p><p><b>METHOD</b>In the primary culture of neonatal rat cardiomyocytes, as indexes of cardiomyocyte hypertrophy, pulsation rate was measured under phase contrast microscope. Cell size was determined by cell morphology analytical system. The total protein was determined by coomassie brilliant blue and protein synthesis rate was measured by [3H]-Leucine incorporation. ERK activity was measured by immuno-precipitation. The expression of p-ERK1/2 was assessed using Western blot.</p><p><b>RESULT</b>Tet can decrease Ang II-induced elevations of the pulsation rate, cell size, total protein and protein synthesis rate; inhibit the activity and expression of p-ERK1/2.</p><p><b>CONCLUSION</b>The anti-hypertrophic effect of Tet on Ang II-induced cardiomyocyte hypertrophy was associated with inhibition of ERK1/2 signaling pathway.</p>


Assuntos
Animais , Ratos , Angiotensina II , Toxicidade , Animais Recém-Nascidos , Benzilisoquinolinas , Farmacologia , Western Blotting , Tamanho Celular , Células Cultivadas , Medicamentos de Ervas Chinesas , Farmacologia , Hipertrofia , Imunoprecipitação , Microscopia de Contraste de Fase , Proteína Quinase 1 Ativada por Mitógeno , Metabolismo , Proteína Quinase 3 Ativada por Mitógeno , Metabolismo , Miócitos Cardíacos , Metabolismo , Patologia , Fosforilação , Plantas Medicinais , Química , Biossíntese de Proteínas , Ratos Sprague-Dawley , Transdução de Sinais , Stephania tetrandra , Química
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