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1.
Chinese Pharmacological Bulletin ; (12): 455-461, 2024.
Artículo en Chino | WPRIM | ID: wpr-1013637

RESUMEN

Aim To investigate the mechanism of ligu aged 2 months of the same strain were used as the constilide (LIG) in delaying the senescence of auditory trol (Ctrl) group. Auditory brainstem response test was cortex and treating central presbycusis. Methods used to detect the auditory threshold of mice before and Forty C57BL/6J mice aged 13 months were randomly di after treatment. Levels of serum MDA and activity of vided into ligustilide low-dose(L-LIG) group, ligustil serum SOD were detected to display the level of oxidative ide medium-dose (M-LIG) group, ligustilide high-dose stress. The pathological changes of auditory cortex were (H-LIG) group and aging (Age) group, and 10 mice observed by HE staining. Ferroptosis was observed by

2.
Tumor ; (12): 378-381, 2008.
Artículo en Chino | WPRIM | ID: wpr-849363

RESUMEN

Objective: To study the inhibitory effect of chemokine receptor CXCR4-targeted small interference RNA (siRNA) on invasion capability of human lung cancer cell line (A549) in vitro. Methods: siRNA for specifically targeting chemokine receptor CXCR4 was designed using T7 RNA polymerase. A549 cell was cultured in a standard condition and was transfected with siRNA via lipofectamin AMINE 2000 mediation. The mRNA level of CXCR4 was detected by RT-PCR at 72 h after transfection. The expression of CXCR4 protein was detected by Western blotting. Invasion capability of A549 cells in vitro was evaluated by using Boyden chamber model. The cell cycle distribution was measured by flow cytometry and the proliferation capability was determined by MTT assay. Results: At 72 h after transfection of CXCR4 siRNA, the expression of CXCR4 mRNA and protein was down-regulated significantly. The invasion and proliferation capabilities of A549 cells decreased substantially. But CXCR4 siRNA transfection had no significant effect on the distribution of cell cycle. Conclusion: CXCR4 siRNA effectively down-regulates the expression of CXCR4 gene and decreased invasion capability of A549 cells in vitro.

3.
Chinese Journal of Oncology ; (12): 325-329, 2008.
Artículo en Chino | WPRIM | ID: wpr-348101

RESUMEN

<p><b>OBJECTIVE</b>To construct a CXCR4 specific recombinant plasmid vector and study its inhibiting effect on invasion capacity in vitro of human breast cancer MDA-MB-231 cell line and its metastatic potential to the lung in nude mice.</p><p><b>METHODS</b>A CXCR4 specific recombinant plasmid vector was constructed and transfected into the cultured MDA-MB-231 cell line with lipofectamine 2000. RT-PCR and Western blot were used to detect the mRNA and protein expression of CXCR4, respectively. Invasion capability in vitro of the cells was evaluated by Boyden chamber. The cell proliferation capacity was detected by MTT method. The nude mouse model of lung metastasis was established by injection of MDA-MB-231 cells into the tail vein. The animals were sacrificed at 6 weeks after the tumor cells injection. Whole lung tissues were harvested, embedded in paraffin, sectioned serially, and the HE-stained paraffin sections were examined pathologically to evaluate the presence and number of metastatic tumors.</p><p><b>RESULTS</b>The CXCR4 mRNA expression rate was 29.5% +/- 3.8% in the CXCR4-shRNA group, significantly lower than that of the control group (69.7% +/- 2.6%, P < 0.01) and mock-control group (67.8% +/- 3.5%, P < 0.01). The CXCR4 protein expression rate was 15.4% +/- 1.1% in the CXCR4-shRNA group, significantly lower than that of the control group (39.0% +/- 2.4%, P < 0.01) and mock-control group (35.9% +/- 3.9%, P < 0.01). Silencing of CXCR4 by shRNA lead to a significant decrease in breast cancer cell invasion and proliferation capacity in vitro. Furthermore, tumor cells with CXCR4 shRNA permanent transfcetion had a much lower lung metastatic potential in nude mice than control cells and mock control cells in vivo.</p><p><b>CONCLUSION</b>CXCR4 shRNA can inhibit the expression of CXCR4 and decrease the invasion and lung metastatic potential of human breast cancer cells.</p>


Asunto(s)
Animales , Femenino , Humanos , Ratones , Neoplasias de la Mama , Genética , Metabolismo , Patología , Línea Celular Tumoral , Movimiento Celular , Proliferación Celular , Silenciador del Gen , Vectores Genéticos , Neoplasias Pulmonares , Ratones Endogámicos BALB C , Ratones Desnudos , Invasividad Neoplásica , Trasplante de Neoplasias , ARN Mensajero , Metabolismo , ARN Interferente Pequeño , Genética , Distribución Aleatoria , Receptores CXCR4 , Genética , Metabolismo , Fisiología , Transfección , Ensayos Antitumor por Modelo de Xenoinjerto
4.
Chinese Journal of Oncology ; (12): 297-299, 2004.
Artículo en Chino | WPRIM | ID: wpr-254349

RESUMEN

<p><b>OBJECTIVE</b>To study the thymidine phosphorylase (TP) expression in different types of cancer and its correlation with tumor microvessel density (MVD).</p><p><b>METHODS</b>The expression of TP and MVD was detected by immunohistochemistry method. In a series of 251 cancer patients there were 48 patients with gastric cancer, 53 with colorectal cancer, 47 with breast cancer, 56 with cervical cancer, 47 with lung cancer. Normal gastric (n = 25), colorectal (n = 25), cervical (n = 17) and lung (n = 25) tissues around the cancer were also examined.</p><p><b>RESULTS</b>The TP expression rate was 64.6% in gastric cancer, 67.9% in colorectal cancer, 80.9% in breast cancer, 82.1% in cervical cancer, and 63.8% in lung cancer, which was significantly higher than that in normal tissues (P = 0.0000). TP expression was positively correlated with MVD in gastric, colorectal, breast, and cervical cancers. The correlation was not statistically significant in lung cancer.</p><p><b>CONCLUSION</b>This study indicates that TP overexpression in cancer may be associated with tumor angiogenesis.</p>


Asunto(s)
Adulto , Anciano , Anciano de 80 o más Años , Femenino , Humanos , Masculino , Persona de Mediana Edad , Neoplasias de la Mama , Neoplasias Colorrectales , Neovascularización Patológica , Patología , Neoplasias Gástricas , Timidina Fosforilasa , Metabolismo , Neoplasias del Cuello Uterino
5.
Chinese Journal of Anesthesiology ; (12)1994.
Artículo en Chino | WPRIM | ID: wpr-674215

RESUMEN

Objective To determine if Shenfu injectio(SFI)has any analeptic action in patients emerging from general anesthesia.Methods Eighty-six ASAⅠorⅡadult patients undergoing elective abdominal surgery under general anesthesia were randomly divided into 2 groups(n=43 each):SFI group and control group.The patients were premedicated with intramuscular phenobarbital 0.1g and atropine 0.5mg.Anesthesia was induced with propofol 2 mg?kg~(-1),fentanyl 4-5?g?kg~(-1) and vecuronium 0.1 mg?kg~(-1) and maintained with propofol infusion(2-4 mg?kg~(-1)?h~(-1)),0.5%-1.0% isoflurane inhalation and intermittent i.v.boluses of fentanyl and vecuronium.The patients were intubated and mechanically ventilated.The propofol infusion and isoflurane inhalation were stopped during skin closure.The patients were still unconscious and on mechanical ventilation at the end of surgery and transferred to PACU with a tube in trachea.As soon as the patients reached the PACU,SFI 1 ml?kg~(-1) in Ringer's solution 100 ml was infused over 10 min.In control group the patients received Ringer's solution 100 ml without SFI.The following times were recorded:(1)the time when the patients opened their eyes on command;(2)the time when mechanical ventilation was stopped;(3)the time when oxygen inhalation was stopped;(4)the extubation time;(5)the time of staying in PACU.Venous blood samples were taken before(T_0) and 5,15 and 45 min(T_(1,2,3))after SFI infusion for determination of plasma?-endorphin concentration.Results The awakening time,the mechanical ventilation time,oxygen inhalation time,extubation time and duration of PACU stay were significantly shorter in SFI group than in control group.There were no significant differences in MAP and HR after SFI between the two groups.The plasma?-endorphin concentration was significantly higher in group SFI than in control group.Conclusion Shenfu injectio can make patients emerging from general anesthesia faster.

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