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1.
Berbamine induces apoptosis in human hepatoma cell line SMMC7721 by loss in mitochondrial transmembrane potential and caspase activation 总被引：14，自引：2，他引：12
Objective： To investigate the effect ofberbamine on human hepatoma cell line SMMC7721. Methods： The effects of 24 h and 48 h incubation with different concentrations （0-64 μg/ml） of the berbamine on SMMC7721 cells were evaluated using 3-4,5-dimethylthiazol-2-yl-2,5-diphenyltetrazolium bromide （MTT） assay. Hoechst 33258 staining was conducted to distinguish the apoptotic cell, and the appearance of sub-G1 stage was determined by PI （propidium iodide） staining, the percentage of apoptotic cell was determined by flow cytometry following annexin V/PI staining. Flow cytometry was performed to analyze the cell cycle distribution and the mitochondrial membrane potential （△ψm）, the expression of activated caspase3 and caspase9 was analyzed by Western-blot. Results： The proliferation of SMMC7721 was decreased after treatment with berbamine in a dose- and time-dependent manner. Berbamine could induce apoptosis in SMMC7721 cells and could cause cell cycle arrest in G0/G1 phase, to induce loss of mitochondrial membrane potential （AVm） and activate caspase3 and caspase9. Berbamine-induced apoptosis could be blocked by the broad caspase inhibitor z-VAD-fmk. Conclusion： Berbamine exerts antiproliferative effects on human hepatocellular carcinoma SMMC7721 cells. The anticancer activity of berbamine could be attributed partly to its inhibition of cell proliferation and induction of apoptosis in cancer cells through loss in mitochondrial transmembrane potential and caspase activation. 相似文献
2.
目的：研究峨眉岩白菜提取物体内外抗肝肿瘤作用。方法：应用MTT法和移植性S180实体荷瘤小鼠。研究不同剂量提取物的体内体外抗肿瘤作用。结果：峨眉岩白菜提取物对体外培养的人肺癌A549细胞增殖有显著的抑制作用。抑制作用与浓度有明显的依赖关系,且随提取浓度的增大,抑制效果越好;荷瘤小鼠模型研究表明,提取物对S180有显著的抑制作用,当剂量为400mg/kg时对肿瘤的抑制效果最好,抑瘤率达52.11％。 相似文献
3.
从关白附（Aconitum Coreanum（Levl.）Rapaics）中分离出内生菌共29株,通过TLC检测筛选出2株可能产生生物碱类成分的内生菌.对筛选出的2株内生菌株的发酵培养物分别以纸片法和MTT法进行抑菌和细胞毒活性测定.实验结果显示,2个内生菌株发酵产物对金黄色葡萄球菌、大肠杆菌具有良好的抑菌作用,对肝癌细胞SMMC-7721、胃癌细胞SGC-7901具有良好的细胞毒活性.通过16S rDNA基因序列分析,2株内生菌分别被鉴定为类芽孢杆菌属和芽孢杆菌属细菌. 相似文献
4.
目的探讨银杏叶总黄酮对体外培养的人肝癌细胞HepG2增殖与凋亡的影响。方法将银杏叶总黄酮作用于体外培养的人肝癌细胞HepG2,MTT法检测其对HepG2细胞增殖的影响,缺口末端核苷标记（TUNNEL）法检测其对HepG2细胞凋亡的影响。结果银杏叶总黄酮对体外培养的人肝癌细胞HepG2的增殖效率下降,使凋亡细胞数增加（P〈0．01）,且呈剂量依赖效应。结论银杏叶总黄酮对体外培养的人HepG2细胞增殖有抑制作用,并能诱导细胞凋亡。 相似文献
5.
目的探讨银杏叶黄酮单体成分槲皮素体外对人肝癌细胞HepG2增殖与凋亡的影响。方法将银杏叶黄酮单体成分槲皮素作用于体外培养的人肝癌细胞HepG2,MTT法检测其对HepG2细胞增殖的影响,缺口末端核苷标记（TUNNEL）法检测其对HepG2细胞凋亡的影响。结果银杏叶黄酮单体成分槲皮素使体外培养的人肝癌细胞HepG2的增殖效率下降,使凋亡细胞数增加（P〈0.01）,两者均呈剂量依赖效应。结论银杏叶黄酮单体成分槲皮素具有与银杏叶总黄酮相似的作用,对体外培养的人HepG2细胞增殖有抑制作用,并能诱导细胞凋亡。 相似文献
6.
Emey Suhana MOHD AZAMAI Suhaniza SULAIMAN Shafina Hanim MOHD HABIB Mee Lee LOOI Srijit DAS Nor Aini ABDUL HAMID Wan Zurinah WANG NGAH Yasmin Anum MOHD YUSOF 《Journal of Zhejiang University. Science. B》2009,10(1)
Chlorella vulgaris (CV) has been reported to have antioxidant and anticancer properties. We evaluated the effect of CV on apoptotic regulator protein expression in liver cancer-induced rats. Male Wistar rats (200-250 g) were divided into eight groups: control group (normal diet), CDE group (choline deficient diet supplemented with ethionine in drinking water to induce hepatocarcinogenesis), CV groups with three different doses of CV (50, 150, and 300 mg/kg body weight), and CDE groups treated with different doses of CV (50, 150, and 300 mg/kg body weight). Rats were sacrificed at various weeks and liver tissues were embedded in paraffin blocks for immunohistochemistry studies. CV, at increasing doses, decreased the expression of anti-apoptotic protein, Bcl-2, but increased the expression of pro-apoptotic protein, caspase 8, in CDE rats, which was correlated with decreased hepatoctyes proliferation and increased apoptosis as determined by bromodeoxy-uridine (BrdU) labeling and terminal deoxynucleotidyl transferase mediated dUTP nick-end labeling (TUNEL) assay, respectively. Our study shows that CV has definite chemopreventive effect by inducing apoptosis via decreasing the expression of Bcl-2 and increasing the expression of caspase 8 in hepatocarcinogenesis-induced rats. 相似文献
7.
日粮中添加茶多酚对肉仔鸡脂肪沉积的影响 总被引：3，自引：0，他引：3
为研究日粮中添加茶多酚对肉仔鸡脂肪沉积及色泽的影响,试验选用1日龄AA鸡200只随机分成4组,每组50只,对照组饲喂基础日粮,试验组日粮为在基础日粮中分别添加100 mg/kg、250 mg/kg、500 mg/kg的茶多酚,于14、28、42日龄每组随机抽取5只进行屠宰,测定腹脂重、腹脂色泽。结果日粮中添加不同水平茶多酚,肉鸡的腹脂重、腹脂率均有明显的降低,且随茶多酚添加剂量增加而降低,当剂量增加到500 mg/kg时,差异极显著(P<0.01);腹脂的L值(亮度)和a值(红度)随剂量增加而降低,b值(黄度)随剂量增加而升高,以添加250 mg/kg时,茶多酚对脂肪色泽改变效果最佳。结果表明日粮中添加不同剂量的茶多酚可以降低腹脂沉积,加深脂肪色泽,改善肉仔鸡的胴体品质。 相似文献
8.
检测地塞米松对体外培养的人视网膜色素上皮细胞生长的影响．对hRPE细胞进行常规培养,取3-4代生长良好的细胞用于实验,采用MTT法研究不同浓度、不同作用时间．地塞米松对hRPE细胞增殖的影响．用免疫细胞化学染色法检测添加不同浓度、不同作用时间地塞米松对hRPE细胞核内细胞增殖核抗原表达的影响．MTT法发现小剂量地塞米松促进hRPE细胞的增殖．50-200mg／L浓度组随着浓度的增高。hRPE细胞的增殖更加明显．大剂量地塞米松抑制hRPE细胞的增殖,且随着浓度的增高,对hRPE细胞的增殖的抑制更加明显．免疫细胞化学染色法发现．在50-200mg／L浓度组,随着浓度的增高,hRPE细胞核内PCNA表达增强。光密度值增大．在400-800mg／L浓度组。随着浓度的增高。hRPE细胞核内PCNA表达减弱．光密度值减少．小剂量地塞米松促进体外培养的hRPE细胞的增殖及细胞核内PCNA的表达,大剂量地塞米松抑制体外培养的hRPE细胞的增殖及细胞核内PCNA的表达． 相似文献
9.
Suo-fu Ye Yong Yang Lin Wu Wei-wei Ma Hui-Hui Zeng 《Journal of Zhejiang University. Science. B》2017,18(5):373-382
It has been reported that Ethaselen shows inhibitory effects on thioredoxin reductase (TrxR) activity and human tumor cell growth. In order to find an efficient way to reverse cisplatin resistance, we investigated the reversal effects of Ethaselen on cisplatin resistance in K562/cisplatin (CDDP) cells that were established by pulse-inducing human erythrocyte leukemic cell line K562, which are fivefold more resistant to cisplatin compared to K562 cells. The morphology and growth showed that the adhesion of K562/CDDP further decreased while the cell volume increased. The proliferation of K562/CDDP is strengthened. The antitumor activities in vitro were assessed by MTT (3-(4,5- dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide) assay and combination index (CI), showing the significant synergic effects of cisplatin and Ethaselen. Focusing on apoptosis, a series of comparisons was made between K562 and K562/CDDP. Cisplatin induced higher reactive oxygen species (ROS) generation in K562 and subsequently induced the formation of mitochondrial permeability transition pores (PTPs). In addition, cisplatin increased the ratio of Bax to Bcl-2 in K562, which can influence the mitochondrial membrane permeability. PTP formation and mitochondrial membrane permeabilization eventually resulted in the release of cytochrome c and activation of the Caspase pathway. However, these effects were not clearly seen in K562/CDDP, which may be the reason for the acquired CDDP resistance. However, Ethaselen can induce a high level of ROS in K562/CDDP by TrxR activity inhibition and increased ratio of Bax to Bcl-2 in K562/CDDP by nuclear factor κB (NF-κB) suppression, which subsequently induces the release of cytochrome c in K562/CDDP. This response is partly responsible for the reversal of the cisplatin resistance in K562/CDDP cells. 相似文献
10.
Objective: To investigate the in-vitro antitumor immune responses of dendritoma formed by mouse hepatocellular carcinoma (HCC) cells and lymphotactin (Lptn) gene modified dendritic cells (DCs). Method: DCs prepared from mouse bone marrow were genetically modified by lymphotactin adenovirus, and fused with H22 cells by polyethylene glycol (PEG). RT-PCR and ELISA were employed to identify lymphotactin expression at mRNA and protein level. Cell phenotypes and fusion efficiency was detected by FACS. The stimulatory effect of DC on T cells was detected by mixed lymphocyte reaction. The cytotoxicity activity against H22 cells was assayed by LDH method. Results: Lymphotactin could be efficiently expressed by DCLptn/H22 hybridoma. DCLptn/H22 cells could induce potent T cell proliferation effect and generate strong cytotoxic T lymphocyte (CTL) reaction against allogenic H22 cells. Conclusion: Lymphotactin genetic modification could enhance the in vitro immune activity of the dendritoma. 相似文献
11.
盐生隐杆藻胞外多糖(EPAH)抗肿瘤作用的实验研究 总被引：1，自引：0，他引：1
目的:探讨盐生隐杆藻胞外多糖对小鼠抗肿瘤作用的影响.方法:建立小鼠移植性S180实体瘤模型,观察EPAH对S180荷瘤小鼠的抑瘤作用、对白细胞的数量、对免疫器官及红细胞粘附肿瘤细胞能力的影响;另建立小鼠移植性S180腹水瘤模型,观察EPAH对小鼠存活时间的影响;同时,通过体外培养检测EPAH对SMMC7721细胞增殖的影响.结果:EPAH能明显抑制S180、SMMC7721细胞生长、促进红细胞粘附肿瘤细胞能力、增强免疫力并能有效提升减少的白细胞数量.结论:EPAH能显著增强小鼠抗肿瘤活性. 相似文献
12.
研究旨在通过MTT法从萘酰亚胺为母体合成的一系列化合物中,筛选出能够高效诱导肿瘤细胞凋亡的化合物C8。研究方法为选用不同组织来源的肿瘤细胞系MCF-7、Hela、U-251和SMMC-7721通过MTT比色法测定不同浓度的萘酰亚胺类化合物作用不同时间后对细胞体外培养的抑制影响。实验结果显示若干种亚胺类化合物中,只有化合物C8对上述肿瘤细胞的生长都具有明显的抑制作用,并随时间延长更为显著,其他化合物无显著性,进而推测化合物C8能够明显抑制不同组织来源的肿瘤细胞生长,并与剂量和时间呈正相关关系,具有高效诱导肿瘤细胞凋亡的作用。 相似文献
13.
Effect of glycine site/NMDA receptor antagonist MRZ2/576 on the conditioned place preference and locomotor activity induced by morphine in mice 总被引：3，自引：0，他引：3
Objective： To study the effect of glycine site/NMDA （N-methyl-D-aspartate） receptor antagonist MRZ2/576 on the conditioned place preference （CPP） and locomotor activity induced by morphine in mice. Methods： Different doses （1.25, 2.5 and 5 mg/kg, i.p.） of MRZ2/576 were used to evaluate the effect of MRZ2/576 on the acquisition and expression of CPP induced by morphine （5 mg/kg） in mice. In addition, we examined the locomotor activity of mice in conditioning and testing phase of CPP paradigm. Results： MRZ2/576 alone could not establish place preference, but a 5 mg/kg dose of MRZ2/576 could block both acquisition and expression of morphine-induced CPP. In testing phase of CPP, there was no statistical difference for locomotor activity between the groups; injection of MRZ2/576 showed a dose-dependent decrease of locomotor activity on both control and morphine-treated mice, especially 5 mg/kg of MRZ2/576 significantly suppressed the locomotor activity of mice. Conclusion： Based on the present results, we assume that MRZ2/576 can antagonize the rewarding effect of morphine, suggesting that this glycine site/NMDA receptor antagonist could be used to treat addictions due to its light side effect profile. 相似文献
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15.
Xing CH Zhu MH Cai MZ Liu P Xu GD Wu SH 《Journal of Zhejiang University. Science. B》2008,9(3):261-264
To investigate the Fe2 effects on root tips in rice plant, experiments were carded out using border cells in vitro. The border cells were pre-planted in aeroponic culture and detached from root tips. Most border cells have a long elliptical shape. The number and the viability of border cells in situ reached the maxima of 1600 and 97.5%, respectively, at 20～25 mm root length. This mortality was more pronounced at the first 1～12 h exposure to 250 mg/L Fe2 than at the last 12～36 h. After 36 h, the cell viability exposed to 250 mg/L Fe2 decreased to nought, whereas it was 46.5% at 0 mg/L Fe2 . Increased Fe2 dosage stimulated the death of detached border cells from rice cultivars. After 4 h Fe2 treatment, the cell viabilities were≥80% at 0 and 50 mg/L Fe2 treatment and were <62% at 150, 250 and 350 mg/L Fe2 treatment; The viability of border cells decreased by 10% when the Fe2 concentration increased by 100 mg/L. After 24 h Fe2 treatment, the viabilities of border cells at all the Fe2 levels were <65%; The viability of border cells decreased by 20% when the Fe2 concentration increased by 100 mg/L. The decreased viabilities of border cells indicated that Fe2 dosage and treatment time would cause deadly effect on the border cells. The increased cell death could protect the root tips from toxic harm. Therefore, it may protect root from the damage caused by harmful iron toxicity. 相似文献
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Electromigration in porous media is enhanced by a new type of electrokinetic processing. Compared with a single-oriented electric field, a continuously reoriented electric field was proven to sharply enhance mass transport of several heavy metals in kaolin. The initial concentration of the metals was: Cd: 250 mg/kg; Cu: 250 mg/kg; Ni: 250 mg/kg; Zn: 900 mg/kg. Electric field reorientation was obtained by the use of a fixed anode and a cathode that rotated at different frequencies (0, 0.25, 1.00, 1.25, 2.00, 5.00 and 10.00 r/m). Mass transport evidently increased from 0 r/m to 1.25 r/m, and then decreased as the rotation speed reached 10 r/m. From 0 r/m to 1.25 r/m, mass transport increased 2.87 times for Cd, 3.17 times for Cu, 2.11 times for Ni, and 4.13 times for Zn. We suggest that continuous reorientation of the electric field facilitates the advance of ions through kaolin pores, minimizing the retardation effect caused by media tortuosity. 相似文献
18.
Siti Balkis Budin Seri Masran Siti Nor Ain Baharuddin Omar Izatus Shima Taib Othman Hidayatulfathi 《Journal of Zhejiang University. Science. B》2012,13(10):783-790
Litsea elliptica Blume has been traditionally used to treat headache, fever, and stomach ulcer, and has also been used as an insect repellent. The acute and subacute toxicities of L. elliptica essential oil were evaluated orally by gavage in female Sprague-Dawley rats. For the acute toxicity study, L. elliptica essential oil was administered in doses from 500 to 4 000 mg/kg (single dose), and in the subacute toxicity test, the following doses were used: 125, 250, and 500 mg/kg, for 28 consecutive days. In the acute toxicity study, L. elliptica essential oil caused dose-dependent adverse behaviours and mortality. The median lethal dose value was 3 488.86 mg/kg and the acute non-observed-adversed-effect level value was found to be 500 mg/kg. The subacute toxicity study of L. elliptica essential oil did not reveal alterations in body weight, and food and water consumptions. The haematological and biochemical analyses did not show significant differences between control and treated groups in most of the parameters examined, except for the hemoglobin, mean cell hemoglobin concentration, mean cell volume, mean cell hemoglobin, serum albumin, and serum sodium. However, these differences were still within the normal range. No abnormalities or histopathological changes were observed in the liver, pancreatic islet of Langerhans, and renal glomerulous and tubular cells of all treated groups. In conclusion, L. elliptica essential oil can be classified in the U group, which is defined as a group unlikely to present an acute hazard according to World Health Organization (WHO) classification. 相似文献
19.
Emey Suhana Mohd Azamai Suhaniza Sulaiman Shafina Hanim Mohd Habib Mee Lee Looi Srijit Das Nor Aini Abdul Hamid Wan Zurinah Wan Ngah Yasmin Anum Mohd Yusof 《Journal of Zhejiang University. Science. B》2009,10(1):14-21
Chlorella vulgaris (CV) has been reported to have antioxidant and anticancer properties. We evaluated the effect of CV on apoptotic regulator
protein expression in liver cancer-induced rats. Male Wistar rats (200∼250 g) were divided into eight groups: control group
(normal diet), CDE group (choline deficient diet supplemented with ethionine in drinking water to induce hepatocarcinogenesis),
CV groups with three different doses of CV (50, 150, and 300 mg/kg body weight), and CDE groups treated with different doses
of CV (50, 150, and 300 mg/kg body weight). Rats were sacrificed at various weeks and liver tissues were embedded in paraffin
blocks for immunohistochemistry studies. CV, at increasing doses, decreased the expression of anti-apoptotic protein, Bcl-2,
but increased the expression of pro-apoptotic protein, caspase 8, in CDE rats, which was correlated with decreased hepatoctyes
proliferation and increased apoptosis as determined by bromodeoxy-uridine (BrdU) labeling and terminal deoxynucleotidyl transferase
mediated dUTP nick-end labeling (TUNEL) assay, respectively. Our study shows that CV has definite chemopreventive effect by
inducing apoptosis via decreasing the expression of Bcl-2 and increasing the expression of caspase 8 in hepatocarcinogenesis-induced
rats.
Project supported by Department of Biochemistry, Faculty of Medicine, UKM Medical Center, Universiti Kebangsaan Malaysia,
and the Malaysian Ministry of Science and Technological Innovation (MOSTI) 相似文献
20.
Sheng-hong ZHU ;Li-jia ZHOU ;Hong JIANG ;Rong-jun CHEN ;Chuan LIN ;Shi FENG ;Juan JIN ;Jiang-hua CHEN ;Jian-yong WU 《Journal of Zhejiang University. Science. B》2014,15(8):735-742
研究目的:在小鼠模型中利用吲哚美辛阻断COX-1/2通路,探讨非甾体类抗炎药对肾缺血再灌注损伤的保护作用。创新要点:非甾体类抗炎药被认为具有肾毒性,本研究首次在小鼠模型中探讨非甾体类抗炎药对肾缺血再灌注损伤的保护作用。研究方法:小鼠左侧肾蒂夹闭后,通过腹腔注射不同剂量的吲哚美辛,在肾缺血再灌注损伤24小时后,获取血液和肾脏标本。利用酶联免疫(ELISA)试剂盒测定血清肌酐和细胞因子浓度来评估肾功能,肾组织样本进行苏木精-伊红染色和免疫组化分析。重要结论:腹腔注射吲哚美辛5 mg/kg组的小鼠血清肌酐值与对照组相比显著降低,肾小管损伤也显著减轻(见图1和2);腹腔注射5和7 mg/kg吲哚美辛组的小鼠血清肾肿瘤坏死因子-α和白介素-6的浓度显著降低(见图3a和3b);腹腔注射3和5 mg/kg吲哚美辛组的小鼠血清血栓素B2与6-酮前列腺素F1α的比值明显降低(见图3c);腹腔注射5 mg/kg吲哚美辛组小鼠肾组织COX-1和COX-2染色较弱(见图4)。因此,吲哚美辛对小鼠肾缺血再灌注损伤的作用与其剂量相关,在某个特定的剂量范围内具有肾保护作用。吲哚美辛对小鼠肾缺血再灌注损伤的保护作用与阻断COX-1/2有关。 相似文献