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生物农药锐星对蔬菜害虫的毒效作用 被引量:1
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作者 徐健 王洪珍 +1 位作者 苏建坤 朱锦磊 《安徽农业科学》 CAS 2001年第2期223-224,共2页
比较 8种常用杀虫剂防治蔬菜害虫的效果 ,生物农药锐星对小菜蛾 (PlutellaxylostellaL .)、甜菜夜蛾 (LaphygmaexiguaH .)等防效显著 ,是无公害蔬菜生产的理想药剂。防治小菜蛾为主的害虫 ,以 1mg/g药液为宜 ,防治甜菜夜蛾则应用 1.6
关键词 生物农药 锐星 小菜蛾 甜菜夜蛾 Bt可湿性粉剂 蔬菜害虫 毒效作用
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河北省杀(抑)虫植物对淡色库蚊幼虫的毒效作用初步研究 被引量:21
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作者 黄钢 潘文亮 高占林 《中国媒介生物学及控制杂志》 CAS CSCD 2000年第1期27-29,共3页
目的 :了解河北地区杀虫植物资源概况 ,寻找和开发本省植物性杀 (抑 )虫剂。方法 :丙酮和植物干粉按 6∶1的比例浸泡提取 ,提取液以水稀释 30倍和 10 0倍浸渍处理淡色库蚊Ⅲ~Ⅳ龄幼虫。结果 :以 30倍稀释液处理 ,造成蚊幼虫死亡率达 5 ... 目的 :了解河北地区杀虫植物资源概况 ,寻找和开发本省植物性杀 (抑 )虫剂。方法 :丙酮和植物干粉按 6∶1的比例浸泡提取 ,提取液以水稀释 30倍和 10 0倍浸渍处理淡色库蚊Ⅲ~Ⅳ龄幼虫。结果 :以 30倍稀释液处理 ,造成蚊幼虫死亡率达 5 0 %以上的植物有 44种 ;以 10 0倍液浸渍 ,造成蚊幼虫死亡率 95 %以上的植物共 7种 ,其中茵陈蒿、薄荷提取液的死亡率达 10 0 % ;试验中发现一些植物提取液对蚊幼虫具有生长发育的抑制作用。结论 :杀虫植物所含成分对不同昆虫生物活性的敏感性不同 ,蒺藜、茵陈蒿、薄荷、佩兰、曼佗罗、艹律 草等植物 ,在防制蚊虫方面具有进一步开发利用的价值。 展开更多
关键词 淡色库蚊 杀虫植物 毒效作用 开发利用
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中药的心脏效-毒双向作用机制探析与用药警戒思考 被引量:9
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作者 殷玉玲 张晓朦 +2 位作者 张冰 林志健 韩宇 《中国药物警戒》 2022年第5期486-492,共7页
目的针对具有心脏治疗作用又可能引发心脏损伤的“效-毒双向作用”中药进行机制探析并提出用药警戒思考。方法检索中国知网、万方数据、维普网等数据库,检索时间为建库起至2021年11月30日。系统挖掘具有心脏效-毒双向作用的药物,结合文... 目的针对具有心脏治疗作用又可能引发心脏损伤的“效-毒双向作用”中药进行机制探析并提出用药警戒思考。方法检索中国知网、万方数据、维普网等数据库,检索时间为建库起至2021年11月30日。系统挖掘具有心脏效-毒双向作用的药物,结合文献学、生物信息技术手段,分析其效-毒双向作用成分、机制及“效-毒”转化因素。结果山豆根、吴茱萸、麦冬、两面针、香加皮等10味中药具有心脏效-毒双向作用,其作用成分类型包括生物碱类、强心苷类、皂苷类等,作用机制主要与AKT/AMPK/mTOR通路及心肌Ca^(2+)-Na^(+)-K^(+)通道有关。效-毒转化与机体原患心脏疾病、体质差异,用药剂量、用法、配伍,以及药物效-毒成分等多方面因素有关。结论心脏效-毒双向作用中药的用药需要多重措施警戒,防止该类中药由效转毒,特别要加强原患心脏疾病患者的用药监护。 展开更多
关键词 吴茱萸 麦冬 两面针 香加皮 心脏 -双向作用 机制探析 药物警戒
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基于网络药理学初探雷公藤干预狼疮性肾炎的效-毒作用 被引量:2
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作者 申安平 李桓 +2 位作者 王炳森 李晓坤 李松伟 《中国药理学通报》 CAS CSCD 北大核心 2022年第2期275-281,共7页
目的运用网络药理学方法探讨雷公藤对狼疮性肾炎(lupus nephritis,LN)的效-毒作用。方法通过TCMSP平台检索雷公藤活性成分和作用靶点;在CoolGeN、OMIM和Gene Cards数据库中收集LN的疾病基因;借助Cytoscape软件绘制药物-成分-靶点-疾病... 目的运用网络药理学方法探讨雷公藤对狼疮性肾炎(lupus nephritis,LN)的效-毒作用。方法通过TCMSP平台检索雷公藤活性成分和作用靶点;在CoolGeN、OMIM和Gene Cards数据库中收集LN的疾病基因;借助Cytoscape软件绘制药物-成分-靶点-疾病作用网络,利用STRING数据库进行蛋白相互作用网络分析;运用DAVID数据库对作用靶点进行GO和KEGG富集分析,结合文献探讨预测雷公藤对LN的效-毒作用及其机制。结果筛选得到雷公藤52个活性成分和与LN相关的38个靶点,大部分成分可通过NOD样受体、p53、TOLL样受体等信号通路调控免疫炎症、细胞增殖和细胞凋亡等过程而对LN起治疗作用,但雷公藤甲素(triptolide)、雷公藤红素(tripterine)、山萘酚(kaempferol)和β-谷甾醇(beta-sitosterol)等可能不利于LN病情好转。结论雷公藤的大部分成分对LN具有治疗作用,但部分有效成分可能同时存在促进足细胞凋亡、加速肾脏纤维化的副作用。 展开更多
关键词 雷公藤 狼疮性肾炎 网络药理学 作用 作用机制 信号通路
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不同胆汁炮制方法对天南星解毒存效作用的实验研究 被引量:11
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作者 杨伟鹏 王怡薇 +3 位作者 王彦礼 毛淑杰 顾雪竹 李先端 《中国实验方剂学杂志》 CAS 北大核心 2009年第12期33-35,共3页
目的:考察以猪胆汁、牛胆汁作为辅料炮制天南星是否具有减毒增(存)效作用。方法:以小鼠的急性毒性试验考察不同胆汁炮制方法对天南星的减毒作用,以小鼠自主活动、睡眠时间及戊四氮引起的惊厥试验考察不同胆汁炮制方法对天南星的增(存)... 目的:考察以猪胆汁、牛胆汁作为辅料炮制天南星是否具有减毒增(存)效作用。方法:以小鼠的急性毒性试验考察不同胆汁炮制方法对天南星的减毒作用,以小鼠自主活动、睡眠时间及戊四氮引起的惊厥试验考察不同胆汁炮制方法对天南星的增(存)效作用。结果:小鼠急性毒性试验中,与对照组比较天南星组小鼠的体重、食量有显著性降低,猪胆星(猪胆汁炮制)组和牛胆星(牛胆汁炮制)组小鼠的体重、食量没有显著性影响(除牛胆星组雌性小鼠I^8 d体重较对照组增长略缓外),牛胆星组和猪胆星组动物的体重与天南星组相比有显著性著异;天南星、猪胆星、牛胆星均能够明显减少小鼠自主活动次数、延长小鼠睡眠时间、降低戊四氮引起的惊厥率,炮制前后无显著性差异。结论:以猪胆汁、牛胆汁作为辅料炮制天南星能够起到减毒存效的作用。 展开更多
关键词 天南星 炮制方法 作用
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大黄素对结肠Cajal间质细胞毒-效作用的研究 被引量:2
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作者 王嫣虹 彭成 +2 位作者 朱力阳 谢晓芳 郑桃 《中国中西医结合消化杂志》 CAS 2010年第3期141-144,共4页
[目的]建立小鼠结肠Cajal间质细胞(ICC)的体外培养方法,探讨大黄素对体外培养结肠ICC的毒-效作用。[方法]酶解消化法体外培养KM乳鼠结肠ICC,运用免疫荧光法鉴定结肠ICC,并用光学显微镜观察其生长期的形态变化。应用均匀设计法和MTT比... [目的]建立小鼠结肠Cajal间质细胞(ICC)的体外培养方法,探讨大黄素对体外培养结肠ICC的毒-效作用。[方法]酶解消化法体外培养KM乳鼠结肠ICC,运用免疫荧光法鉴定结肠ICC,并用光学显微镜观察其生长期的形态变化。应用均匀设计法和MTT比色法探索大黄素不同浓度和作用时间对结肠ICC的影响。[结果]大黄素对结肠ICC最大毒性浓度为1%,最小毒性浓度为0.001%;最大药效浓度为0.000 1%,最小药效浓度为0.000 008%。[结论]成功建立了体外培养KM乳鼠的结肠ICC的方法。大黄素对结肠ICC既有毒性又有药效作用,毒性浓度范围为0.001%~1%;药效浓度范围为0.000 008%~0.000 1%。 展开更多
关键词 大黄素 结肠CAJAL间质细胞 -作用
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基于物质基础探析十八反中“藻戟遂芫俱战草”配伍禁忌
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作者 安卓佳 张可怡 +2 位作者 周密迦 黄礼杰 修琳琳 《中国药物警戒》 2023年第12期1435-1440,共6页
目的基于物质基础探析十八反中“藻戟遂芫俱战草”配伍禁忌,为完善中药配伍禁忌理论和指导临床应用提供依据。方法通过检索近年来国内外文献,从物质基础角度分析“藻戟遂芫俱战草”甘草组反药组合配伍前后物质基础变化和其对毒效作用的... 目的基于物质基础探析十八反中“藻戟遂芫俱战草”配伍禁忌,为完善中药配伍禁忌理论和指导临床应用提供依据。方法通过检索近年来国内外文献,从物质基础角度分析“藻戟遂芫俱战草”甘草组反药组合配伍前后物质基础变化和其对毒效作用的影响。结果海藻、大戟、甘遂、芫花与甘草配伍对反药组合的毒、效成分溶出有影响,配伍后,可能通过促进毒性成分溶出、抑制毒性成分代谢、抑制有效成分溶出、产生新的物质、破坏物质结构等途径产生增毒减效的“毒”或增效减毒的“效”作用。结论甘草组反药组合并非绝对的配伍禁忌,还需继续基于物质基础,结合药物毒理基因组学和代谢组学等方法及高效技术进行研究。 展开更多
关键词 十八反 海藻 大戟 甘遂 芫花 甘草 物质基础 配伍禁忌 毒效作用
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小柴胡汤治疗肝炎时出现肝损伤的“效-毒”作用网络分析与机制预测 被引量:19
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作者 刘静 李晓宇 +2 位作者 吴恺怿 黄娜娜 孙蓉 《中草药》 CAS CSCD 北大核心 2019年第21期5135-5144,共10页
目的运用网络药理学研究模式,基于小柴胡汤治疗肝炎过程中造成药物性肝损的临床不良反应伤(ADR)信息挖掘,探讨小柴胡汤治疗肝炎时产生肝损伤的"效-毒"作用靶点、通路和机制。方法以小柴胡汤为研究对象,借助整合药理学平台构建... 目的运用网络药理学研究模式,基于小柴胡汤治疗肝炎过程中造成药物性肝损的临床不良反应伤(ADR)信息挖掘,探讨小柴胡汤治疗肝炎时产生肝损伤的"效-毒"作用靶点、通路和机制。方法以小柴胡汤为研究对象,借助整合药理学平台构建"效-毒"作用网络,预测分析其关键靶点和通路,应用Cytoscape软件对关键靶标所参与的通路整理分析,得到"效-毒"共同参与的通路及作用机制。结果小柴胡汤治疗肝炎时产生肝损伤的"效-毒"作用分析得出,在度值排名前100的候选靶标中共同靶标有HADHA、HADH、NSDHL、ADH1A、ALDH3A2、GCK等40个,小柴胡汤中共同参与"效-毒"作用的化学成分包括柴胡27个、人参74个、半夏13个、生姜8个、甘草32个、大枣39个、黄芩33个,共226个成分,共同作用于内分泌系统、神经系统、雌激素信号通路、趋化因子信号通路、内分泌和代谢疾病、非酒精性脂肪肝病(NAFLD)、神经退行性疾病7条通路参与"效-毒"过程。结论小柴胡汤治疗肝炎时产生肝损伤的"效-毒"作用可能与Ras/Raf/MEK/ERK、NF-κB、PI3K/AKT信号传导途径密切相关,通过调控细胞增殖、细胞凋亡、调控炎症因子的表达发挥作用。 展开更多
关键词 小柴胡汤 肝炎 药物性肝损伤 网络药理学 -作用
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Study on Tolerance and Biosorption of Various Microalgae Species to Arsenic
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作者 李妍丽 柯林 《Agricultural Science & Technology》 CAS 2012年第6期1303-1308,1327,共7页
[Objective] This study aimed to select microalgae species which are capable to effectively remove arsenic contamination from water under natural conditions. [Method] Four microalgae species [Chlorella sp. (zfsaia), ... [Objective] This study aimed to select microalgae species which are capable to effectively remove arsenic contamination from water under natural conditions. [Method] Four microalgae species [Chlorella sp. (zfsaia), Chlorella minata, Chlorella vulgaris and Selenastrum capricormulum] were used as experimental materials and cultured with six different concentrations of As (Ⅲ) (0.5, 1.0, 2.0, 5.0, 10.0, 20.0 mg/L). Biomass, chlorophyll a content and other physiological indicators were determined to investigate the arsenic tolerance and biosorption of four microalgae species. [Result] Chlorella sp. is sensitive to arsenic toxicity, its growth was inhibited when arsenic concentration exceeded 10 mg/L, with an EC 50 of 17.32 mg/L; when the arsenic concentration was 0-20 mg/L, growth of S.c, ww1 and C.v was not affected, which showed relatively high tolerance to arsenic, with arsenic removal rates of 77.02% , 72.18% and 81.36% respectively after 24 h. [Conclusion] This study indicates that microalgae have good application prospects for processing arsenic wastewater and being indicator plants of arsenic wastewater. 展开更多
关键词 As(Ⅲ) MICROALGAE Toxicity effect BIOSORPTION
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The Effect of Biological and Cytotoxic Therapy for Rheumatoid Arthritis on Human Chromosomes
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作者 Sekib Sokolovic Sida Kasumagic +1 位作者 Mirela Mackic-Curovic Izeta Aganovic-Musinovic 《Journal of Life Sciences》 2010年第7期30-32,共3页
Objectives: An open-label prospective, combined basic and clinical controlled study was done to investigate the effects of biological therapy using rituximab, and cytotoxic drug treatment with methotrexate on morphol... Objectives: An open-label prospective, combined basic and clinical controlled study was done to investigate the effects of biological therapy using rituximab, and cytotoxic drug treatment with methotrexate on morphology and quantifitiation of chromosomes in rheumatoid arthritis patients. Methods: This study is follow-up of a prior publication, with new observations in comparison with control subjects. A total of 16 subjects were divided into two groups. Group I comprised 8 seropositive rheumatoid arthritis patients who were analysed for the primary end point of possible cytotoxic effects of rituximab and methotrexate. Group II included 8 healthy individuals who served as controls. Assessment was done before treatment with rituximab, and 4 weeks after initiation of therapy. Patients were randomly assigned to receive infusion of rituximab in a full dose of 2.0 g divided into two doses of 1.0 g on days I and 15. The lymphocytes from periphereal blood was cultured by the Moorhead method. Results: Normal male and female Karyograms were observed after full courses of therapy with rituximab. In one female patient who had been receiving longstanding cytotoxic therapy with methotrexate, 2% of chromosomal mitosis showed structural abnormalities. Following the discontinuation of methotrexate and the administration of rituximab, her karyogram became normal. Conclusion: The results from this study indicated that rituximab therapy was safe for the number and structure of human chromosomes, while methotrexate showed chromosomal aberration in one female RA patient. After discontinuation of this longstanding treatment, the karyogram of the same patient returned to normal. 展开更多
关键词 RITUXIMAB CHROMOSOME rheumatoid arthritis structure and number.
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Use of liposomal doxorubicin for adjuvant chemotherapy of breast cancer in clinical practice 被引量:1
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作者 Ming ZHAO Xian-feng DING +3 位作者 Jian-yu SHEN Xi-ping ZHANG Xiao-wen DING Bin XU 《Journal of Zhejiang University-Science B(Biomedicine & Biotechnology)》 SCIE CAS CSCD 2017年第1期15-26,共12页
Breast cancer is one of the malignant tumors with the highest morbidity and mortality. It is helpful to reduce the rate of tumor recurrence and metastasis by treating breast cancer with adjuvant chemotherapy, so as to... Breast cancer is one of the malignant tumors with the highest morbidity and mortality. It is helpful to reduce the rate of tumor recurrence and metastasis by treating breast cancer with adjuvant chemotherapy, so as to increase the cure rate or survival of patients. In recent years, liposomes have been regarded as a kind of new carrier for targeted drugs. Being effective for enhancing drug efficacy and reducing side effects, they have been widely used for devel- oping anticancer drugs. As a kind of anthracycline with high anticancer activity, doxorubicin can treat or alleviate a variety of malignant tumors effectively when it is used on its own or in combination with other anticancer drugs~ Alt- hough liposomal doxorubicin has been extensively used in the adjuvant chemotherapy of breast cancer, its exact therapeutic efficacy and side effects have not been definitely proven. Various clinical studies have adopted different combined regimes, dosages, and staging, so their findings differ to certain extent. This paper reviews the clinical application of liposomal doxorubicin in the adjuvant chemotherapy of breast cancer and illustrates therapeutic effects and side effects of pegylated liposomal doxorubicin (PLD) and non-PLD (NPLD) in clinical research, in order to discuss the strategies for applying these drugs in such adjuvant chemotherapy, looking forward to providing references for related research and clinical treatment in terms of dosage, staging, combined regimes, and analysis methods and so on. 展开更多
关键词 Liposomal doxorubicin Breast cancer Adjuvant chemotherapy Therapeutic effect Toxic and side effects
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Advances in environmental behaviors and effects of dissolved organic matter in aquatic ecosystems 被引量:6
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作者 HE Wei BAI ZeLin +5 位作者 LI YiLong KONG XiangZhen LIU WenXiu YANG Chen YANG Bin XU FuLiu 《Science China Earth Sciences》 SCIE EI CAS CSCD 2016年第4期746-759,共14页
Dissolved organic matter(DOM) is a group of compounds that have complex chemical structures and multiple interactions with their surrounding materials. More than one trillion tons of DOM are stocked in the world's... Dissolved organic matter(DOM) is a group of compounds that have complex chemical structures and multiple interactions with their surrounding materials. More than one trillion tons of DOM are stocked in the world's aquatic ecosystems. DOM is a very important part of aquatic ecosystem productivity and plays a crucial role in global carbon cycling. DOM has rich environmental behaviors and effects such as influencing the bioavailability of contaminants, serving as an important inducer of reactive oxygen species(ROS), and protecting aquatic organisms from the harm of dangerous ultraviolet radiation. There have been many systematic studies on the composition, structure, and sources of DOM because such studies are much easier to conduct than studies on the environmental behaviors and effects of DOM. Due to many factors, the research systems of DOM's environmental behaviors and effects are still being developed and have become a hotspot of environmental science. This review paper focuses on some critical progress, problems, and trends of DOM's environmental behaviors and effects in aquatic ecosystems, including mutual exchange mechanisms between DOM and particulate organic matter(POM) with influencing factors, photochemical behaviors of DOM especially inducing ROS, binding interactions between DOM and anthropogenic organic contaminants(AOC), interactions between DOM and microorganisms, effects of DOM on pollutants' bioavailability, ecotoxicity, and ecological risks. Hopefully, this paper will contribute to a more systematic understanding of the DOM environmental behaviors and effects and to promoting further relevant studies. 展开更多
关键词 Dissolved organic matter Mutual exchange mechanisms Photochemical behavior Binding interaction BIOAVAILABILITY
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A novel bone marrow targeted gadofullerene agent protect against oxidative injury in chemotherapy 被引量:1
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作者 张莹 舒春英 +7 位作者 甄明明 李杰 于童 贾旺 李雪 邓睿君 周悦 王春儒 《Science China Materials》 SCIE EI CSCD 2017年第9期866-880,共15页
Chemotherapy as an effective cancer treatment technique has been widely used in tumor therapy. However, it is still a challenge to overcome the serious side effects of chemotherapy, especially for its myelotoxicity. H... Chemotherapy as an effective cancer treatment technique has been widely used in tumor therapy. However, it is still a challenge to overcome the serious side effects of chemotherapy, especially for its myelotoxicity. Here we report a novel strategy using the water soluble gadofullerene nanocrystals(GFNCs) to protect against chemotherapy injury in hepatocarcinoma bearing mice, which was induced by the commonly chemotherapeutic agent cyclophosphamide(CTX).The GFNCs were revealed to specifically accumulate in the bone marrow after intravenously injecting to mice and they exhibited excellent radical scavenging function, resulting in a prominent increase of mice blood cells and pathological improvements of the primary organs in the GFNCs(15 mg kg-(-1))treated mice after the CTX(60 mg kg-(-1)) therapy. Moreover,the GFNCs maintained and even strengthened the antineoplastic activity of the CTX agent. Therefore, the GFNCs would be the promising chemoprotective agents in chemotherapy based on their high efficiency, low toxicity and metabolizable property. 展开更多
关键词 gadofullerene nanocrystals chemopreventive agent MYELOSUPPRESSION radical scavenging chemotherapy drug
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