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1.
Chinese journal of integrative medicine ; (12): 432-438, 2013.
Artigo em Inglês | WPRIM | ID: wpr-347193

RESUMO

<p><b>OBJECTIVE</b>To investigate and compare the effects and mechanisms of three functional parts of Dahuang Zhechong Pill (DHZCP), including drugs with the function of removing blood stasis and promoting blood circulation (FP-I), drugs with the function of expelling heat and moistening dryness (FP-II), and drugs with the function of nourishing yin and replenishing blood (FP-III) of DHZCP, on platelet-derived growth factor (PDGF)-stimulated vascular smooth muscle cells (VSMCs) proliferation with the method of serum pharmacology.</p><p><b>METHODS</b>VSMCs proliferation of rat was assayed by measuring the cell viability with the 3-(4, 5-dimethylthiazol-2yl)-2, 5-diphenyltetrazolium bromide (MTT) method. DNA synthesis in VSMCs was examined by detecting 5'-bromo-2'-deoxyuridine incorporation with the immunocytochemical method. Cycle of VSMCs was evaluated with flow cytometry. Expression of cyclin D1, p27, PKCα, and phosphorylated extracellular signal regulated kinase 1/2 (ERK1/2) was quantified by the Western blotting method.</p><p><b>RESULTS</b>The FP-I and FP-III containing serum was capable of inhibiting PDGF-stimulated proliferation and DNA synthesis of VSMCs, arrested VSMCs in G phase, downregulated cyclin D1, and upregulated p27 expression (P <0.01 or P <0.05). The FP-I and FP-III containing serum also inhibited the PDGF-induced phosphorylation of tyrosine of ERK1/2 and PKCα expression (P <0.01 or P <0.05).</p><p><b>CONCLUSIONS</b>FP-I and FP-III of DHZCP are able to inhibit VSMCs proliferation via interrupting PKCα-ERK1/2 signaling, modulating the expression of cell cycle proteins to result in arresting the cells in G phase. The inhibitory effect is mainly related to the function of removing blood stasis and promoting blood circulation, slightly to the function of nourishing yin and replenishing blood, but not to the function of expelling heat and moistening dryness.</p>


Assuntos
Animais , Masculino , Ratos , Ciclo Celular , Proliferação de Células , Ciclina D1 , Metabolismo , Inibidor de Quinase Dependente de Ciclina p27 , Metabolismo , DNA , Medicamentos de Ervas Chinesas , Farmacologia , Ativação Enzimática , MAP Quinases Reguladas por Sinal Extracelular , Metabolismo , Sistema de Sinalização das MAP Quinases , Músculo Liso Vascular , Biologia Celular , Miócitos de Músculo Liso , Biologia Celular , Fator de Crescimento Derivado de Plaquetas , Farmacologia , Proteína Quinase C-alfa , Metabolismo , Ratos Sprague-Dawley , Soro , Metabolismo
2.
Chinese journal of integrative medicine ; (12): 371-377, 2012.
Artigo em Inglês | WPRIM | ID: wpr-328506

RESUMO

<p><b>OBJECTIVE</b>To investigate effects of dahuang zhechong pill ( DHZCP) on the cell cycle and the related signal pathways in vascular smooth muscle cells (VSMCs) stimulated by platelet-derived growth factor (PDGF) with the method of serum pharmacology.</p><p><b>METHODS</b>DNA synthesis in VSMCs was examined by detecting 5'-bromo-2'-deoxyuridine incorporation with the immunocytochemical method. The cycle of VSMCs was evaluated with flow cytometry. Expressions of cyclin D1, p27, protein kinase Cα (PKCα), and phosphorylated extracellular signal regulated kinase 1/2 (ERK1/2) were quantified by Western blot method.</p><p><b>RESULTS</b>DHZCP containing serum significantly inhibited DNA synthesis of PDGF-stimulated VSMCs, arrested the cells in G G(1) phase, modulated the protein expressions of cyclin D D(1) and p27, and suppressed the activation of PKCα and ERK1/2.</p><p><b>CONCLUSION</b>DHZCP containing serum inhibits VSMCs proliferation via modulating the expressions of cell cycle proteins to arrest the cell in G G(1) phase, which is attributed to, at least in part, suppressing PKCα-ERK1/2 signaling in VSMCs.</p>


Assuntos
Animais , Masculino , Ratos , Aorta Torácica , Biologia Celular , Proteínas Sanguíneas , Farmacologia , Proliferação de Células , Células Cultivadas , Ciclina D1 , Metabolismo , Inibidor de Quinase Dependente de Ciclina p27 , Metabolismo , DNA , Medicamentos de Ervas Chinesas , Farmacologia , Fase G1 , Fisiologia , Sistema de Sinalização das MAP Quinases , Fisiologia , Músculo Liso Vascular , Biologia Celular , Fator de Crescimento Derivado de Plaquetas , Farmacologia , Proteína Quinase C-alfa , Metabolismo , Ratos Sprague-Dawley
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