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Therapeutic potential and pharmacological mechanism of visnagin
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作者 Poonam Yadav Sumeet Kumar Singh +7 位作者 Sayantap Datta Saloni Verma Aarti Verma Arnab Rakshit Anjana Bali Jasvinder Singh Bhatti Amit Khurana Umashanker Navik 《Journal of Integrative Medicine》 SCIE CAS CSCD 2024年第4期399-412,共14页
Visnagin is a furanochromone and one of the most important compound in the Ammi visnaga(L.)Lam(a synonym of Visnaga daucoides Gaertn.)plant,which is used to cure various ailments.Many investigations into the bioactive... Visnagin is a furanochromone and one of the most important compound in the Ammi visnaga(L.)Lam(a synonym of Visnaga daucoides Gaertn.)plant,which is used to cure various ailments.Many investigations into the bioactive properties of visnagin have been studied to date.The literature on visnagin demonstrates its biological properties,including anti-inflammatory,anti-diabetic,and beneficial effects in cardiovascular and renal diseases.Moreover,visnagin improves sperm quality parameters,stimulates steroidogenesis,and increases serum gonadotropins and testosterone levels,while decreasing proinflammatory cytokines,oxidative damage,genomic instability,and it modulates apoptosis.Thus,visnagin has emerged as an exciting lead for further research,owing to its potential in various unmet clinical needs.The current review summarized its basic structure,pharmacokinetics,and pharmacological effects,focusing on its mechanisms of action.The review will help to understand the potential of visnagin as an alternative treatment strategy for several diseases and provide insight into research topics that need further exploration for visnagin’s safe clinical use. 展开更多
关键词 visnagin PHYTOCHEMICAL ANTI-INFLAMMATORY Ammi visnaga L. Visnaga daucoides Gaertn CANCER
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齿阿米素对大鼠心肌缺血再灌注损伤的保护作用及其机制研究 被引量:2
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作者 付海荣 谭家华 +3 位作者 邓雪松 李晶 张永慧 庞毅 《中药新药与临床药理》 CAS CSCD 北大核心 2021年第9期1238-1244,共7页
目的探讨齿阿米素对大鼠心肌缺血再灌注损伤(MI/RI)的保护作用及其机制。方法将60只大鼠随机分为假手术组、模型组、复方丹参片组(阳性药组,200 mg·kg^(-1))及齿阿米素高、中、低剂量组(4、2、1 mg·kg^(-1)),每组10只。大鼠... 目的探讨齿阿米素对大鼠心肌缺血再灌注损伤(MI/RI)的保护作用及其机制。方法将60只大鼠随机分为假手术组、模型组、复方丹参片组(阳性药组,200 mg·kg^(-1))及齿阿米素高、中、低剂量组(4、2、1 mg·kg^(-1)),每组10只。大鼠灌胃给药,每日1次,连续7 d。末次给药后24 h,采用左冠状动脉前降支结扎法建立MI/RI大鼠模型。造模2 h后,记录各组大鼠的左室舒张末期内压(LVEDP)、左室收缩内压(LVSP)、左室内压最大上升/下降速率(LV±dp/dtmax)及平均动脉压(MABP);测定大鼠血清乳酸脱氢酶(LDH)、C反应蛋白(CRP)、肌酸激酶(CK)、肌酸激酶同工酶(CK-MB)含量及大鼠心肌组织超氧化物歧化酶(SOD)、谷胱甘肽过氧化物酶(GSH-Px)、丙二醛(MDA)及总抗氧化能力(T-AOC)水平;采用HE染色法观察大鼠心肌组织病理学形态变化;RT-PCR法检测大鼠心肌组织核转录因子-κB(NF-κB)、NF-κB抑制蛋白α(IκBα)及IκB激酶β(IKKβ)mRNA的表达水平;Western Blot法检测大鼠心肌组织p65、p-p65、IκBα、p-IκBα、IKKβ及p-IKKβ蛋白的表达水平。结果与假手术组比较,模型组大鼠心脏的LVEDP明显升高(P<0.01),LV±dp/dtmax、LVSP及MABP明显下降(P<0.01);血清中的LDH、CRP、CK及CK-MB活性明显增加(P<0.01);心肌组织纤维排列紊乱,有核固缩、溶解现象,有炎性细胞浸润;心肌组织的SOD、GSH-Px及T-AOC水平显著降低(P<0.01),MDA含量显著增加(P<0.01);心肌组织的NF-κB、IKKβmRNA表达水平显著上调(P<0.01),IκBαmRNA表达水平显著下调(P<0.01);心肌组织的p-p65、p-IKKβ蛋白表达水平显著上调(P<0.01),p-IκBα蛋白表达水平显著下调(P<0.01)。与模型组比较,齿阿米素高、中剂量组大鼠心脏的LVEDP明显降低(P<0.01),LV±dp/dtmax、LVSP及MABP明显升高(P<0.05,P<0.01);LDH、CRP、CK及CK-MB活性明显下降(P<0.01);心肌组织病理损伤明显改善;心肌组织SOD、GSH-Px及T-AOC水平明显升高(P<0.05,P<0.01),MDA含量明显降低(P<0.05,P<0.01);心肌组织NF-κB、IKKβmRNA表达水平明显下调(P<0.01),IκBαmRNA表达水平明显上调(P<0.01);心肌组织p-p65、p-IKKβ蛋白表达水平明显下调(P<0.01),p-IκBα蛋白表达水平明显上调(P<0.01)。结论齿阿米素对大鼠心肌缺血再灌注损伤具有保护作用,其作用机制与抗氧化应激和抑制NF-κB信号通路有关。 展开更多
关键词 齿阿米素 心肌缺血再灌注损伤 氧化应激 NF-ΚB信号通路 大鼠
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Mosquitocidal Activity of Extracts from Ammi visnaga (Apiaceae) Seeds
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作者 Kumudini M. Meepagala Alden S. Estep James J. Becnel 《Journal of Agricultural Chemistry and Environment》 2016年第4期170-178,共9页
Aedes aegypti mosquitoes are responsible for transmission of many viral diseases, such as Zika fever, dengue fever, yellow fever, and chikungunya. Emergence of resistance to currently used pesticides among mosquitoes ... Aedes aegypti mosquitoes are responsible for transmission of many viral diseases, such as Zika fever, dengue fever, yellow fever, and chikungunya. Emergence of resistance to currently used pesticides among mosquitoes has increased the importance for the search for novel mosquito control agents. Natural products, particularly plant and microbe derived secondary metabolites, are good sources in the search for such compounds. Ammi visnaga (Lam.) Lamarck is a plant in the Apiaceae family native to North Africa, Europe, and Asia. In the search for environmentally benign and effective insecticides as part of an ongoing joint effort between the USDA (US Department of Agriculture) and the DWFP (Deployed War Fighter Protection) program sponsored by the Department of Defense, we have investigated ethyl acetate extract of A. visnaga seeds. Two furanochromones, khellin and visnagin that exhibited larvicide activity against Aedes aegypti mosquito larvae were isolated from the ethyl acetate extract of the seeds by bioassay-guided fractionation. This is the first report of mosquito larvicidal activity of khellin and visnagin. 展开更多
关键词 Aedes aegypt Ammi visnaga Mosquito Larvicide Apiaceae Khellin visnagin
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阿密茴素拮抗多柔比星组织毒性及其机制研究
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作者 周文娟 王玓玥 +1 位作者 赵淼淼 刘岩 《四川大学学报(自然科学版)》 CAS CSCD 北大核心 2022年第2期177-181,共5页
多柔比星(Doxorubicin, DOX)是临床上使用最广泛的蒽环家族化疗药物.为了研究阿密茴素(Visnagin, VIS)能否缓解DOX诱发的肝、肾毒性及其相关机制,此研究首先构建DOX急性、慢性肝肾损伤小鼠模型,通过观察小鼠肝肾细胞死亡率、肝肾功能变... 多柔比星(Doxorubicin, DOX)是临床上使用最广泛的蒽环家族化疗药物.为了研究阿密茴素(Visnagin, VIS)能否缓解DOX诱发的肝、肾毒性及其相关机制,此研究首先构建DOX急性、慢性肝肾损伤小鼠模型,通过观察小鼠肝肾细胞死亡率、肝肾功能变化评价VIS对肝肾损伤的保护作用.在急性和慢性损伤模型中,原位末端凋亡实验(TUNEL)结果表明VIS可以显著降低肝肾细胞凋亡率;而慢性模型中,VIS还能缓解肝肾功能损伤.此外,实验结果表明VIS可以显著抑制DOX诱发的TOP2-DNA共价复合物形成,提示VIS可能通过抑制DOX下游的TOP2通路起保护作用.研究结果将为后续深入探究降低DOX毒副作用的课题提供参考. 展开更多
关键词 癌症治疗 多柔比星 阿密茴素 毒副作用
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Aflatoxin B1: Toxicity, bioactivation and detoxification in the polyphagous caterpillar Trichoplusia ni 被引量:1
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作者 Ren Sen Zeng Zhimou Wen +1 位作者 Guodong Niu R. Berenbaum 《Insect Science》 SCIE CAS CSCD 2013年第3期318-328,共11页
Trichoplusia ni caterpillars are polyphagous foliage-feeders and rarely likely to encounter aflatoxin B1 (AFB1), a mycotoxin produced by Aspergillus flavus and A. parasiticus, in their host plants. To determine how ... Trichoplusia ni caterpillars are polyphagous foliage-feeders and rarely likely to encounter aflatoxin B1 (AFB1), a mycotoxin produced by Aspergillus flavus and A. parasiticus, in their host plants. To determine how T. ni copes with AFB 1, we evaluated the toxicity ofAFB 1 to T. ni caterpillars at different developmental stages and found that AFB 1 tolerance significantly increases with larval development. Diet incorporation of AFB 1 at 1μg/g completely inhibited larval growth and pupation of newly hatched larvae, but 3μg/g AFB 1 did not have apparent toxic effects on larval growth and pupation of caterpillars that first consume this compound 10 days after hatching. Piperonyl butoxide, a general inhibitor of cytochrome P450 monooxygenases (P450s), reduced the toxicity of AFB 1, suggesting that AFB1 is bioactivated in T. ni and this bioactivation is mediated by P450s. Some plant allelochemicals, including flavonoids such as fiavones, furanocoumarins such as xanthotoxin and imperatorin, and furanochromones such as visnagin, that induce P450s in other lepidopteran larvae ameliorated AFBI toxicity, suggesting that P450s are also involved in AFB 1 detoxification in T. ni. 展开更多
关键词 aflatoxin ALLELOCHEMICAL BIOACTIVATION cytochrome P450 monooxygenase flavone Helicoverpa zea IMPERATORIN mycotoxin piperonyl butoxide Trichoplusia ni visnagin XANTHOTOXIN
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