长白瑞香的化学成 分

长白瑞香的化学成分冀春茹,丁岗,冯卫生,刘延泽（河南中医学院,郑州,４５０００３）ＣＨＥＭＩＣＡＬＣＯＮＳＴＩＴＵＥＮＴＳＯＦＤＡＰＨＮＥＫＯＲＥＡＮＡ￥ＪｉＣｈｕｎ－ｒｕ;ＤｉｎｇＧａｎｇ;ＦｅｎｇＷｅｉ－ｓｈｅｎｇ;ＬｉｕＹａｎ－ｚｅ（Ｈｅｎａｎ...     

河南紫荆属订正

河南紫荆属订正朱长山，李学德（河南农业大学，郑州４５０００２）（郑州师范学校，郑州４５００５２）ＡＲＥＶＩＳＩＯＮＯＦＣＥＲＣＩＳＦＲＯＭＨＥＮＡＮ￥ＺＨＵＣｈａｎｇ－Ｓｈａｎ；ＬＩＸｕｅ－Ｄｅ（ＨｅｎａｎＡｇｒｉｃｕｌｔｕｒａｌＵｎｉｖｅｒｓｉｔｙ...     

不同生态条件下苹果叶面附生物种群演替的初步研究

不同生态条件下苹果叶面附生物种群演替的初步研究陈功友,郑铁民,任国兰,时向阳（河南农业大学,郑州４５０００２）郭艳春,宋爱仙（河南省植保总站,郑州４５０００２）（郑州市园艺场,４５０００２）ＳｕｃｃｅｓｓｉｏｎｏｆＥｐｉｐｈｙｔｉｃＭｉｃｒｏｆｌｏｒａＰｏｐｕｌａｔｉｏｎｓｏｎＡｐｐｌｅＰｈｙｌｌｏｐｌａｎｅｕｎｄｅｒＤｉｆｆｃｒｅｎｔＥｃｏｌｏｇｉｃａｌＣｏｎｄｉ－ｔｉｏｎｓ￥．ＣｈｅｎＧｏｎｇｙｏｕ,ＺｈｅｎｇＴｉｅｍｉｎ,ＲｅｎＧｕｏｌａｎ,ＳｈｉＸｉａｎｇｙａｎｇ（Ｈｅｎａｎ,ＡｇｒｉｃｕｌｔｕｒａｌＵｎｉｕｅｒｓｉｔｙ,Ｚｈｅｎｇｚｈｏｕ４５０００２）,ＧｕｏＹａｎｃｈｕｎ（ＨｅｎａｎＧｅｎｅｒａｌＳｔａｔｉｏｎｏｆｐｌａｎｔｐｒｏｔｅｃｔｉｏｎ,Ｚｈｅｎｇｚｈｏｕ４５０００２）,ＳｏｎｇＡｉｘｉａｎ（ＨｏｒｌｉｃｕｌｔｕｒａｌＦａｒｍｏｆＺｈｅｎｇｚｈｏｕＭｕｎｉｃｉｐａｌｉｔｙ,Ｚｈｅｎｇｚｈｏｕ４５０００２）．（ＣｈｉｎｅｓｅＪｏｕｒｎａｌｏｆＥｃｏｌｏｇｙ,１９９３,１２（４）：７－１３．Ｓｅａｓｏｎａｌｖａｒｉａｔｉｏｎｓｏｆｅｐｉｐｈｙｔｉｃｍｉｃｒｏｆｌｏｒａｏｎａｐｐｌｅｐｈｙｌｌ     

凹叶瑞香中的香豆素类化合物

凹叶瑞香中的香豆素类化合物刘延泽，冀春茹，杨林莎，冯卫生（河南中医学院，郑州，４５０００３）谢晶曦，谢蓝（中国医学科学院药物研究所，北京，１０００５０）ＣＯＵＭＡＲＩＮＳＦＲＯＭＤＡＰＨＮＥＮＥＲＥＴＵＳＡ￥ＬｉｎＹａｎ－ｚｅ；ＪｉＣｈｕｎ－ｒｕ；Ｙ...     

Detection and Analysis of an Estrous－associated Oviductal Glycoprotein DNA Fragment from Primates by PCR

ＤｅｔｅｃｔｉｏｎａｎｄＡｎａｌｙｓｉｓｏｆａｎＥｓｔｒｏｕｓ－ａｓｓｏｃｉａｔｅｄＯｖｉｄｕｃｔａｌＧｌｙｃｏｐｒｏｔｅｉｎＤＮＡＦｒａｇｍｅｎｔｆｒｏｍＰｒｉｍａｔｅｓｂｙＰＣＲ￥ＣＨＥＮＱｉｎｇ－ｘｕａｎ（陈清轩）;ＣｌａｙｔｏｎＥ．Ｗａｌｔｏ...     

用显微切割技术和催化信号扩增法检测何杰金病瘤细胞（H／RS）中的 …

为明确何杰金病（Ｈｏｄｇｋｉｎ’ｓ ｄｉｓｅａｓｅ,ＨＤ）瘤细胞中是否存在人巨细胞病毒（ｈｕｍａｎ ｃｙｔｏｍｅｇａｌｏｖｉｒｕｓ,ＨＣＭＶ）感染,采用显微切割技术结合ＰＣＲ方法检测ＨＤ组织及其瘤细胞Ｈｏｄｇｋｉｎ／Ｒｅｅｄ－Ｓｔｅｒｎｂｅｒｇ（Ｈ／ＲＳ）中的ＨＣＭＶ核酸;采用免疫组织化学催化信号扩增（ｃａｔａｌｙｓｅｄ ｓｉｇｎａｌ ａｍｐｌｉｆｉｃａｔｉｏｎ,ＣＳＡ）法检测ＨＤ中ＨＣＭＶ的立即     

部分裸子植物叶片总蛋白分析

采用ＳＤＳ－ ＰＡＧＥ 技术, 分析了红豆杉科（Ｔａｘａｃｅａｅ） 植物南方红豆杉（ Ｔａｘｕｓ ｃｈｉｎｅｎｓｉｓｖａｒ－ ｍａｉｒｅｉ （Ｌｅｍｅｅ ｅｔ Ｌｅｖｌ－） Ｃｈｅｎｇ ｅｔ Ｌ－Ｋ－Ｆｕ） 、穗花杉（ Ａｍｅｎｔｏｔａｘｕｓ ａｒｇｏｔａｅｎｉａ （Ｈａｎｃｅ） Ｐｉｌ ｇｅｒ） 、云南穗花杉（ Ａ－ ｙｕｎｎａｎｅｎｓｉｓ Ｌｉ） 、白豆杉（ Ｐｓｅｕｄｏｔａｘｕｓｃｈｉｅｎｉｉ（Ｃｈｅｎｇ） Ｃｈｅｎｇ） 以及三尖杉科（Ｃｅｐｈａｌｏｔａｘａｃｅａｅ） 、植物三尖杉（ Ｃｅｐｈａｌｏｔａｘｕｓ ｆｏｒｔｕｎｅｉ Ｈｏｏｋ－ｆ－） 、粗榧（ Ｃ－ｓｉｎｅｎｓｉｓ （Ｒｅｈｄ－ｅｔＷｉｌｓ－） Ｌｉ） 、海南粗榧（ Ｃ－ｈａｉｎａｎｅｎｓｉｓ Ｌｉ） 、篦子三尖杉（ Ｃ－ｏｌｉｖｅｒｉ Ｍａｓｔ－） 和罗汉松科（Ｐｏｄｏｃａｒｐａｃｅａｅ） 、植 物罗汉松 （ Ｐｏｄｏｃａｒｐｕｓ ｍａｃｒｏｐｈｙｌｌｕｓ （ Ｔｈｕｎｂ－ ） Ｄ－Ｄｏｎ） 、鸡毛 松（ Ｐ－ｉｍｂｒｉｃａｔｕｓ Ｂｌ－） 、竹柏（ Ｐ－ ｎａｇｉ（Ｔｈｕｎｂ－） Ｚｏｌｌ） 、陆均松（ Ｄａｃｒｙｄｉｕｍ ｐｉｅｒｒｅｉ Ｈｉｃｋｅｌ） 共１２ 种植物的叶片蛋白, 在蛋白质水平上采用     

蛇毒蛋白Echistatin的C端突变基因的构建，表达及其活性研究

通过ＰＣＲ定点突变的技术,将蛇毒蛋白Ｅｃｈｉｓｔａｔｉｎ基因的Ｃ端进行了突变（Ａｌａ４８→Ａｒｇ４８→,Ｔｈｒ４９→Ｖａｌ４９）,模拟纤维蛋白Ｎ端的四肽（Ｇｌｙ－Ｐｒｏ－Ａｒｇ－Ｖａｌ）,以期增加Ｅｃｓ（Ｅｃｈｉｓｔａｔｉｎ）的活性。突变的基因重组到表达质粒ｐＪＣ２６４上,经ＩＰＴＧ诱导,以ＣｈｅＹ－Ｅｃｓ融合蛋白方式进行了表达,表达量占菌体总蛋白的１５～２０％。ＳｅｐｈａｄｅｘＧ－７５初步纯化该融合蛋白,然后用ＣＮＢｒ裂解,透析,冻干,反相ＨＰＬＣ纯化Ｃ端突变体Ｅｃｓ蛇毒蛋白,Ｎ端十个氨基酸分析与天然的相符,在ＰＲＰ（ｐｌａｔｅｌｅｔ－ｒｉｃｈｐｌａｓｍａ）测活体系中,１０μｍｏｌ／Ｌ的ＡＤＰ诱导,Ｃ端突变体Ｅｃｓ抑制血小板凝聚的活性约为野生型４倍。得到了Ｅｃｓ的Ｃ端突变后使Ｅｃｓ抑制血小板凝聚的活性提高的结果。     

生态农业与乡村经济持续发展

生态农业与乡村经济持续发展张壬午,计文瑛,孙鸿良（天津农业部环境保护研究所,３００１９１）（中国农科院,北京１０００８１）ＥｃｏｌｏｇｉｃａｌＡｇｒｉｃｕｌｔｕｒｅａｎｄＳｕｓｔａｉｎａｂｌｅＤｅｖｅｌｏｐｍｅｎｔｏｆＲｕｒａｌＥｃｏｎｏｍｙ￥．ＺｈａｎｇＲｅｎｗｕ;ＪｉＷｅｎｙｉｎｇ（Ａｇｒｏ－ｅｎｖｉｒｏｎｍｅｎｔＰｒｏｔｅｃｌｉｏｎＩｎｓｔｉｔｕｔｅ,Ｔｉａｎｊｉｎ３００１９１）,ＳｕｎＨｏｎｇｌｉａｎｇ（ＣｈｉｎｅｓｅＡｃａｄｅｍｙｏｆＡｇｒｉｃｕｌｔｕｒａｌＳｃｉｅｎｃｃｓ,Ｂｅｉｊｉｎｇ１０００８１）．ＣｈｉｎｅｓｅＪｏｕｒｎａｌｏｆＥｃｏｌｏｇｙ,１９９３,１２（２）：１９—２０．ＴｈｉｓｐａｐｅｒｂｒｉｅｆｌｙｐｒｅｓｅｎｔｓｔｈｅｃｕｒｒｅｎｔｄｅｖｅｌｏｐｍｅｎｔｏｆｅｃｏｌｏｇｉｃａｌａｇｒｉｃｕｌｔｕｒｅｉｎＣｈｉｎａａｎｄｃｏｍｐａｒｅｓｗｉｔｈｔｈｅ＇＇ｓｕｓｔａｉｎａｂｌｅａｇｒｉｃｕｌｔｕｒｅａｎｄｒｕｒａｌｄｅｖｅｌｏｐｍｅｎｔ＇＇（ＳＡＲＤ）ｐｕｔｆｏｒｗａｒｄｂｙＦＡＯ,Ｃｈｉｎａ’ｓｓｕｓｔａｉｎａｂｌｅａ－ｇｒｉｃｕｌｔｕｒｅｉｓｎｏｔｏｎｌｙａｎｉｎｇｅｎｉｏｕｓ     

豆薯种子中两种蛋白质的分离纯化及其性质研究

豆薯（Ｐａｃｈｙｒｒｈｉｚｕｓｅｒｏｓｕｓ）种子经磷酸盐缓冲液抽提,Ｓ－ＳｅｐｈａｒｏｓｅＦａｓｔＦｌｏｗ柱,ＤＥ－５２纤维素柱和ＳｅｐｈａｄｅｘＧ－７５柱层析,提取出两种高纯度的蛋白成分,命名为ＰａｃｈｙｒｉｎＩ和ＩＩ,ＳＤＳ－ＰＡＧＥ测得其分子量分别为３３ｋＤ和１４．５ｋＤ,但ＨＰＬＣ分子筛的结果显示ＰａｃｈｙｒｉｎⅡ的分子量为２８ｋＤ,无论在还原条件下,还是在非还原条件下,ＰａｃｈｙｒｉｎＩ     

Anticancer activity and mechanism of Scutellaria barbata extract on human lung cancer cell line A549

Scutellaria barbata (S. barbata), a traditional Chinese herbal medicine native to southern China, is widely used as an anti-inflammatory and a diuretic in China. Several studies have indicated that extracts of S. barbata have growth inhibitory effects on a number of human cancers. Treatment of lung cancer, digestive system cancers, hepatoma, breast cancer, and chorioepithelioma by S. barbata extracts was reported. However, the mechanism underlying the antitumor activity was unclear. In this study, we studied the growth inhibitory effect of S. barbata and determined its mechanism of antitumor activity using human lung cancer cell line A549. Our results showed that ethanol extracts of S. barbata greatly inhibited A549 cell growth, with IC50 of 0.21 mg/ml. The major mechanisms of inhibition included cell apoptosis and cytotoxic effects. cDNA microarray analysis showed that 16 genes, involved in DNA damage, cell cycle control, nucleic acid binding and protein phosphorylation, underwent more than 5-fold change. These data indicated that these processes are involved in S. barbata-mediated killing of cancer cells. A surprising finding is that CD209, related to dendritic cell (DC) function, was dramatically downregulated by 102-fold. Further functional studies are needed to assess the role of the array-identified genes in S. barbata mediated anticancer activity.     

Preparative separation of four individual flavonoids in Scutellaria barbata D. Don based on high selectivity polymeric adsorbents with different polarities

The individual flavonoid component, scutellarin, scutellarein, luteolin and apigenin, in Scutellaria barbata plant was isolated based on the macro porous adsorbent with high adsorption selectivity. These adsorbents were synthesized based on the copolymerization of methyl acrylate and divinylbenzene (MA-co-DVB). So the polarity and the adsorption affinity of these adsorbents can be adjusted through changing MA content in the adsorbents. And then the ability of the adsorbent with different MA contents for isolation of these four individual flavonoid was also investigated. Adsorbents M2 and M4, with MA content of 25% and 45%, respectively, demonstrated the best separation ability. Complete separation of the four flavone compounds was achieved in a continuous process based on combination of adsorbents with different polarities (M2 and M4). Gradient elution using adsorbent M4 separated the four flavonoids into three fractions, which were determined to contain scutellarin, scutellarein and a mixture of luteolin and apigenin. The latter was separated completely by adsorbent M2 subsequently. All four compounds were obtained at high resolution and high recovery yield (96.7%, 94.1%, 95.8% and 93.8%, respectively), suggesting the efficiency of sequentially combined columns with different segregation patterns.     

半枝莲化学成分及药理活性研究进展(综述)

半枝莲Scutellaria barbata为我国传统中药,具清热解毒、化瘀止痛、排石利尿等多重功效。化学成分研究表明,半枝莲含有大量黄酮类、二萜类、挥发油类及多糖等化学成分;药理研究表明,半枝莲具有抗肿瘤、抗氧化、抗菌及免疫调节等药理活性。本文综述半枝莲的化学成分及其药理活性研究概况,为其进一步开发利用提供参考。     

Two new species and combinations of Stipa L. (Graminae) from northwest Africa

Two new species of Stipa L. S. meridionalis and S. magrebensis, are described from northern Africa, and two new combinations have been made: V. barbata subsp. breripila and S. gigantea subsp. maroccana.     

DPPH·–luminol chemiluminescence system and its application in the determination of scutellarin in pharmaceutical injections and rat plasma with flow injection analysis

In this article, a DPPH·–luminol chemiluminescence (CL) system was reported and the CL mechanism was discussed according to the CL kinetic properties after sequence injecting DPPH· into the DPPH·–luminol reaction mixture. It was observed that scutellarin could inhibit the CL response of the DPPH·–luminol system. Based on this observation, a simple and rapid flow injection CL method was developed for the determination of scutellarin using the inhibition effect in alkaline medium. The optimized chemical conditions for the CL reaction were 5 × 10^?6 mol/L DPPH · and 1.0 × 10^?4 mol/L luminol in 0.01 mol/L NaOH. Under optimized conditions, the CL intensity was inversely proportional to the concentration of scutellarin over the ranges 5–2000 and 40–3200 ng/ml in pharmaceutical injection and rat plasma, respectively. The limits of detection (S/N  = 3) were 5 and 40 ng/ml in preparations and rat plasma, respectively. Furthermore, the precision, recovery and stability of the validated method were acceptable for the determination of scutellarin in both pharmaceutical injections and rat plasma. The presented method was successfully applied in the determination of scutellarin in pharmaceutical injections and real rat plasma samples.     

Determination of scutellarin in rat plasma by high-performance liquid chromatography with ultraviolet detection

A validated high-performance liquid chromatography method is described for the determination of scutellarin in rat plasma using a liquid-liquid extraction and ultraviolet (UV) absorbance detection. The separation used a Diamonsil ODS column (250 mm x 4.6mm i.d., 5 microm particle size) with an isocratic mobile phase consisting of methanol-acetonitrile-50mM dihydrogen ammonium phosphate buffer (22:15:63 (v/v/v), adjusted to pH 2.5 with 1M phosphoric acid). The ultraviolet detector operated at 335 nm. Plasma samples were extracted with ethyl acetate after acidification. The extraction recovery of scutellarin ranged from 68.1 to 80.5%. High selectivity and a low quantitation limit (0.050 microg/ml) were achieved. The linear range was 0.050-12.5 microg/ml, correlation coefficient r=0.9981. The method has a good reproducibility, R.S.D. values were below 7.9% for within-day and between-day precision. The method is simple, rapid, and applicable to preliminary pharmacokinetic studies of scutellarin in rats.     

Scutellarin inhibits the glioma cell proliferation by downregulating BIRC5 to promote cell apoptosis

The expression changes of baculovirus inhibitor of apoptosis repeat-containing protein5 in brain glioma after administration of Scutellarin was detected. To explore the effort of scutellarin on anti-glioma by downregulating BIRC5.The effect of scutellarin on tumour growth and animal survival was detected by administering scutellarin to nude mice subcutaneous tumour formation and SD rats in situ tumour formation models. A significantly different gene BIRC5 was found by using the combination of TCGA databases and network pharmacology. And then qPCR was performed to detect the expression of BIRC5 in glioma tissues, cells and normal brain tissues and glial cells. CCK-8 was used to detect the IC50 of scutellarin on glioma cells. The wound healing assay, flow cytometry and MTT test were used to detect the effect of scutellarin on the apoptosis and proliferation of glioma cells. The expression of BIRC5 in glioma tissues was significantly higher than that in normal brain tissues. Scutellarin can significantly reduce tumour growth and improve animal's survival. After scutellarin was administered, the expression of BIRC5 in U251 cells was significantly reduced. And after same time, apoptosis increased and cell proliferation was inhibited. This original research showed that scutellarin can promote the apoptosis of glioma cells and inhibit the proliferation by downregulating the expression of BIRC5.     

土壤类型对短葶飞蓬灯盏乙素和咖啡酸酯积累的影响

在相同栽培管理条件下,分别以黑色石灰土、红色石灰土、红壤、黄红壤、紫色土和腐殖土为生长介质对短葶飞蓬（Erigeron breviscapus）进行了人工栽培试验。结果显示,生长在不同土壤类型的短葶飞蓬植株体内总咖啡酸酯和灯盏乙素含量有显著的差异。红色石灰土、紫色土及黄红壤生长的植株总咖啡酸酯和灯盏乙素含量最高,黑色石灰土和腐殖土的最低。相同土类的不同亚类土壤生长植株间2种次生代谢产物含量的差异程度,会超过不同土类间的。植株总咖啡酸酯和灯盏乙素含量与土壤P和K含量没有显著相关关系,但与土壤速效N含量及植株含N量则都有极显著负相关关系。不同土壤生长植株叶片的最大光能转换效率（Fv／Fm）值与灯盏乙素和总咖啡酸酯含量都表现出极显著负相关关系。土壤类型对短葶飞蓬次生代谢影响规律与碳素／营养平衡假说（CNB）及资源获得假说（HA）的预测一致。     

Probing the binding of scutellarin to human serum albumin by circular dichroism, fluorescence spectroscopy, FTIR, and molecular modeling method

The binding of scutellarin with human serum albumin (HSA) was investigated at four temperatures, 296, 303, 310, and 318 K, by fluorescence, circular dichroism (CD), Fourier transform infrared spectroscopy (FT-IR), and molecular modeling study at pH 7.40. The binding parameters were determined by Scatchard's procedure, which are approximately consistent with the results of Stern-Volmer equation. The thermodynamic parameters were calculated according to the dependence of enthalpy change on the temperature as follows: DeltaH degrees is a small negative value (-8.55 kJ/mol), whereas DeltaS degrees is a positive value (65.15 J/mol K). Quenching of the fluorescence HSA in the presence of scutellarin was observed. Data obtained by fluorescence spectroscopy and CD experiment, FT-IR experiment, and molecular modeling method suggested that scutellarin can strongly bind to the HSA and the primary binding site of scutellarin is located in site I of HSA. It is considered that scutellarin binds to site I (subdomain II) mainly by a hydrophobic interaction and there are hydrogen bond interactions between the scutellarin and the residues Arg222 and Arg257.     

Antagonistic effect of scutellarin on the toxicity of selenium in rat livers

Selenium has both nutritional function and toxicity according to its concentration and species. To counteract the toxicity of selenium, scutellarin was investigated. Wistar rats were supplemented with 40 μg Se/kg/d as sodium selenite, 40 μg Se/kg/d with 20 mg/kg/d scutellarin, and 20 mg/kg/d scutellarin, respectively, for 15 d. The mRNA levels and activities of glutathione peroxidase (GSH-Px) and thioredoxin reductase (TR), and the malondialdehyde (MDA) contents were measured. Reactive oxygen species (ROS) were detected by chemiluminescence assay, and tissue conformation was investigated by histological study. The results showed significant decreases of mRNA levels and activities of GSH-Px and TR and a significant increase of MDA content in livers of the Se-treated rats (p<0.05, compared with the control). Supplementation of scutellarin to the Se-treated group significantly inhibited the decreases of mRNA levels and activities, and the increase of MDA content (p<0.05, compared with the Setreated group). Meanwhile, scutellarin-scavenged ROS generated in the mixture of sodium selenite, reduced glutathione, and oxygen. Liver injury was displayed in slices exposed to selenium at the present dose. The groups treated with both selenium and scutellarin or only scutellarin did not show significant tissue damage. Thus, scutellarin had an antagonistic effect against the toxicity of selenium.