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Des(rhamnosyl)verbascoside抗HBV作用的定量蛋白质组学研究
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作者 邓洁 赵童诗尧 +2 位作者 牟俊飞 梁成钦 周先丽 《广西科学》 CAS 2024年第1期197-204,共8页
为探究des(rhamnosyl)verbascoside体外抗乙型肝炎病毒(HBV)的活性作用和机制,本研究以des(rhamnosyl)verbascoside为实验药物对HepG2.2.15细胞进行干预,实验分为药物干预组和对照组,采用串联质谱标签(Tandem Mass Tag,TMT)蛋白质组学... 为探究des(rhamnosyl)verbascoside体外抗乙型肝炎病毒(HBV)的活性作用和机制,本研究以des(rhamnosyl)verbascoside为实验药物对HepG2.2.15细胞进行干预,实验分为药物干预组和对照组,采用串联质谱标签(Tandem Mass Tag,TMT)蛋白质组学方法对提取的总蛋白进行分析。结果表明,共筛选得到300个差异表达蛋白,其中有109个上调蛋白,191个下调蛋白。基因本体论(Gene Ontology,GO)分析结果显示,差异蛋白主要参与DNA复制(DNA replication)、鞘糖脂代谢(Glycosphingolipid metabolic process)、细胞增殖(Cell proliferation)、寡糖分解代谢(Oligosaccharide catabolic process)等生物学过程,以及DNA聚合酶活性(DNA polymerase activity)、丝氨酸型羧肽酶活性(Serine type carboxypeptidase activity)、DNA引物酶活性(DNA primase activity)等分子功能。京都基因与基因组百科全书(Kyoto Encyclopedia of Genes and Genomes,KEGG)分析结果显示,差异蛋白主要参与细胞代谢(Metabolism)、遗传信息传导(Genetic information processing)、生物系统通路(Organismal systems)等相关信号通路。亚细胞定位分析表明,差异蛋白大多定位在细胞质和细胞核。本研究共筛选出13个与抗HBV密切相关的蛋白。通过定量蛋白组学初步揭示des(rhamnosyl)verbascoside可能通过增加HGF、SORT1、MAN2B1,减少PRIM1、PRIM2、POLA1、POLD3、POLD2、POLD1、POLE、ERCC2、LAMC1、SDC1等蛋白表达来起到体外抗HBV的作用。 展开更多
关键词 des(rhamnosyl)verbascoside 蛋白组学 乙型肝炎病毒 生物信息学 旱田草
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Verbascoside exerts an anti-atherosclerotic effect by regulating liver glycerophospholipid metabolism
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作者 Peng Lei Jialin Lü +4 位作者 Tie Yao Peng Zhang Xin Chai Yuefei Wang Miaomiao Jiang 《Food Science and Human Wellness》 SCIE CSCD 2023年第6期2314-2323,共10页
Verbascoside,abundant in olive mill wastewater,is a phenylethanolic glycoside with a wide range of pharmacological activities.Atherosclerosis(AS)is a common metabolic disease and abnormal lipid metabolism in liver is ... Verbascoside,abundant in olive mill wastewater,is a phenylethanolic glycoside with a wide range of pharmacological activities.Atherosclerosis(AS)is a common metabolic disease and abnormal lipid metabolism in liver is inseparable from its formation and development.In this study,the anti-atherosclerotic effect of verbascoside was evaluated by establishing an atherosclerosis model based on western diet feeding of apolipoprotein E-defi cient mice for 16 weeks.After 12 weeks of administration during the feeding period,the levels of total cholesterol(TC),triglyceride(TG),low density lipoprotein cholesterol(LDL-C)in the plasma of mice were signifi cantly decreased,the formation of arterial plaques was delayed,and the levels of alanine aminotransferase(ALT),aspartate aminotransferase(AST)and lactate dehydrogenase(LDH)in plasma were alleviated,showing the hepatoprotective effect.In addition,based on untargeted lipidomic analysis,verbascoside stabilized glycerophospholipid metabolism,modulated lipid metabolism disorders and reduced lipid deposition in the liver to achieve the therapeutic effi cacy against atherosclerosis by regulating cardiolipin(CL),ether-linked phosphatidylcholine(ether-PC),lysophophatidylcholine(LPC),phosphatidylcholine(PC),oxidized phosphatidylcholine(OxPC),oxidized phosphatidylethanolamine(OxPE),triacylglycerol(TG),sphingomyelin(SM)back to normal levels. 展开更多
关键词 ATHEROSCLEROSIS verbascoside Lipid deposition LIPIDOMICS Glycerophospholipid metabolism
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Mechanism of action of verbascoside in mice with Parkinson's disease based on molecular docking,molecular dynamics and in vivo experiments
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作者 ADILAI Aibibuli KELIBINUER Saidierding +1 位作者 LU Ran-ran YANG Xin-ling 《Journal of Hainan Medical University》 CAS 2023年第24期9-17,共9页
Objective:To explore the improving effect of verbascoside on Parkinson's disease(PD)model mice and to clarify the possible mechanism.Methods:60 C57BL/6 male mice were randomly divided into normal group,model group... Objective:To explore the improving effect of verbascoside on Parkinson's disease(PD)model mice and to clarify the possible mechanism.Methods:60 C57BL/6 male mice were randomly divided into normal group,model group,low,middle and high dose groups(30,60 and 120 mg/kg,respectively).After a week of adaptive culture,except for the blank group,the subacute model of PD was established by intraperitoneal injection of 1-methyl-4-phenyl-1(MPTP)in each group for 5 consecutive days.After a week of adaptive culture,except for the blank group,the subacute model of PD was established by intraperitoneal injection of 1-methyl-4-phenyl-1(MPTP)in each group for 5 consecutive days.The establishment of the model,the drug group was intragastrically administered continuously for 7 d,and the mice in the normal group were injected with the same amount of saline.The behavioral changes of mice were observed by open field test,pole climbing test and grip test;the morphology,apoptosis and Nissl bodies of substantia nigra neurons were observed by HE staining and Nissl staining;the ultrastructural changes of neurons were observed by transmission electron microscope;the positive expressions of tyrosine hydroxylase(TH),α-synuclein(α-Syn)and toll-like receptor 4(TLR4)were detected by immunohistochemistry.The protein levels of TH,α-Syn,TLR4,NF-κB and P-NF-κB in substantia nigra of mice were detected by Western blot,and the levels of inflammatory factors IL-1β,IL-6 and tumor necrosis factor-α(TNF-α)in serum were detected by Elisa.Molecular docking was used to verify the binding ability of verbascoside to TLR4/NF-κB signal pathway and related factors,and molecular dynamics was used to verify the binding mode and stability of verbascoside with compounds.Results:compared with the normal group,the total walking distance,average speed,free activity time,pole climbing time and forelimb grip in the model group were significantly longer than those in the normal group(P<0.05).The ultrastructural changes of neurons,nuclear lysis,deformation and mitochondrial damage were observed under transmission electron microscope,and the number and morphological changes of HE staining substantia nigra neurons were decreased(P<0.05).Nissl staining showed that the number of Nissl positive cells decreased(P<0.05),the positive expression of TH decreased and the positive expression of α-syn and TLR4 increased(P<0.05).Western blotting showed that the expression of TH protein decreased,the expression of α-syn,TLR4,NF-κB p65 protein increased(P<0.05),and the expression of IL-1β,IL-6 and TNF-α in serum increased significantly(P<0.05).Compared with the model group,the activity ability of mice in the treatment group was significantly improved(P<0.05),the morphology of neurons gradually recovered and the number of neurons increased(P<0.05).The number of Nissl positive cells increased(P<0.05).The expression of TH protein increased,while the expression of α-syn,TLR4,NF-κBp65 protein decreased(P<0.05),and the expression of IL-1β,IL-6,TNF-α in serum decreased significantly(P<0.05).The results of molecular docking and molecular dynamics simulation show that the combination of mulberry glycoside with the compound is good and the property is stable.Conclusion:verbascoside has protective effect on PD mice,and its mechanism may be related to TLR4/NF-κB pathway,and then regulate neuroimmunity. 展开更多
关键词 Parkinson's disease verbascoside Toll-like receptor 4 Molecular docking
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Verbascoside—A Review of Its Antitumor Activities
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作者 Hasan Alaa Aldeen Khalaf Ruaa Azziz Jasim Ismail Taha Ibrahim 《Pharmacology & Pharmacy》 2021年第6期109-126,共18页
Cancer is a set of diseases including abnormal growth of cells that can spread to another tissue. Verbascoside (or acteoside) is a naturally occurring, water-soluble secondary metabolite with significant biological pr... Cancer is a set of diseases including abnormal growth of cells that can spread to another tissue. Verbascoside (or acteoside) is a naturally occurring, water-soluble secondary metabolite with significant biological properties, which is distributed widely in plant kingdom. Verbascoside is pharmacologically active compounds with many recent evidences that support its biological activities and safety. This review focus</span><span lang="EN-US" style="font-family:"">es</span><span lang="EN-US" style="font-family:""> on the recent studies that concerned with the antitumor activities of verbascoside alone and as a synergistic agent as well as nanoproduct. It also shows the latest advances in its antitumor effects, cytotoxic selectivity and its efficiencies in treating cancer, <i>in vitro</i> and/or <i>vivo</i>. 展开更多
关键词 verbascoside Phenylethanoids PHENYLPROPANOIDS GLYCOSIDES CYTOTOXIC ANTITUMOR
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Verbascoside promotes the regeneration of tyrosine hydroxylase-immunoreactive neurons in the substantia nigra 被引量:11
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作者 Jian-qing Liang Li Wang +1 位作者 Jian-cheng He Xian-dong Hua 《Neural Regeneration Research》 SCIE CAS CSCD 2016年第1期101-106,共6页
Tyrosine hydroxylase is a key enzyme in dopamine biosynthesis. Change in tyrosine hydroxylase expression in the nigrostriatal system is closely related to the occurrence and development of Parkinson's disease. Ver... Tyrosine hydroxylase is a key enzyme in dopamine biosynthesis. Change in tyrosine hydroxylase expression in the nigrostriatal system is closely related to the occurrence and development of Parkinson's disease. Verbascoside, an extract from Radix Rehmanniae Praeparata has been shown to be clinically effective in treating Parkinson's disease. However, the underlying mechanisms remain unclear. It is hypothesized that the effects of verbascoside on Parkinson's disease are related to tyrosine hydroxylase expression change in the nigrostriatal system. Rat models of Parkinson's disease were established and verbascoside(60 mg/kg) was administered intraperitoneally once a day. After 6 weeks of verbascoside treatment, rat rotational behavior was alleviated; tyrosine hydroxylase m RNA and protein expression and the number of tyrosine hydroxylase-immunoreactive neurons in the rat right substantia nigra were significantly higher than the Parkinson's model group. These findings suggest that the mechanism by which verbascoside treats Parkinson's disease is related to the regeneration of tyrosine hydroxylase-immunoreactive neurons in the substantia nigra. 展开更多
关键词 酪氨酸羟化酶 阳性神经元 毛蕊花 糖苷 黑质 再生 帕金森氏症 帕金森病
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Complete biosynthesis of the phenylethanoid glycoside verbascoside 被引量:1
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作者 Yihan Yang Daoyi Xi +1 位作者 Yanan Wu Tao Liu 《Plant Communications》 SCIE CSCD 2023年第4期286-300,共15页
Verbascoside,which was first discovered in 1963,is a well-known phenylethanoid glycoside(PhG)that exhibits antioxidant,anti-inflammatory,antimicrobial,and neuroprotective activities and contributes to the therapeutic ... Verbascoside,which was first discovered in 1963,is a well-known phenylethanoid glycoside(PhG)that exhibits antioxidant,anti-inflammatory,antimicrobial,and neuroprotective activities and contributes to the therapeutic effects of many medicinal plants.However,the biosynthetic pathway of verbascoside remains to be fully elucidated.Here,we report the identification of two missing enzymes in the verbascoside biosynthesis pathway by transcriptome mining and in vitro enzymatic assays.Specifically,a BAHD acyltransferase(hydroxycinnamoyl-CoA:salidroside hydroxycinnamoyltransferase[SHCT])was shown to catalyze the regioselective acylation of salidroside to form osmanthuside A,and a CYP98 hydroxylase(osmanthuside B 3,30-hydroxylase[OBH])was shown to catalyze meta-hydroxylations of the p-coumaroyl and tyrosol moieties of osmanthuside B to complete the biosynthesis of verbascoside.Because SHCTs and OBHs are found in many Lamiales species that produce verbascoside,this pathway may be general.The findings from the study provide novel insights into the formation of caffeoyl and hydroxytyrosol moieties in natural product biosynthetic pathways.In addition,with the newly acquired enzymes,we achieved heterologous production of osmanthuside B,verbascoside,and ligupurpuroside B in Escherichia coli;this work lays a foundation for sustainable production of verbascoside and other PhGs in micro-organisms. 展开更多
关键词 ACYLTRANSFERASE cytochrome P450 microbial synthesis verbascoside ACTEOSIDE PHENYLPROPANOID
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Efficacy of verbascoside,echinacoside,crenatoside on altitudeinduced fatigue in rats and possible mechanism
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作者 GUO Ziliang QIAN Qingyuan +3 位作者 LI Xiaolin ZHU Yuting REN Jun LI Maoxing 《Journal of Traditional Chinese Medicine》 SCIE CSCD 2023年第5期934-943,共10页
OBJECTIVE:To study the efficacy and mechanism of three phenylethanoid glycosides(PhG s)(verbascoside,echinacoside,and crenatoside)on altitude-induced fatigue in rats.METHODS:Altitude-induced fatigue model rats were es... OBJECTIVE:To study the efficacy and mechanism of three phenylethanoid glycosides(PhG s)(verbascoside,echinacoside,and crenatoside)on altitude-induced fatigue in rats.METHODS:Altitude-induced fatigue model rats were established in a large hypobaric chamber.Swimming time,energy storage substances,metabolic enzymes,and metabolites were used to evaluate the anti-fatigue activities and mechanism of three PhG s(verbascoside,echinacoside,and crenatoside)(150 mg/kg,intragastric administration)in the hypoxic environment.RESULTS:The three PhGs,especially verbascoside,could prolong the swimming time of rats,ameliorate the edema and inflammatory infiltration of liver and skeletal muscle,increase the level of energy storage substances,reduce the decomposition of proteins,and exhibit positive effects on the metabolism-related enzyme activity and metabolites.CONCLUSIONS:The PhG s,especially verbascoside,are very potential with anti-fatigue activity in hypoxia.The mechanism may be explained with regulation of energy metabolism and reduction of oxidative stress. 展开更多
关键词 phenylethanoid glycosides verbascoside HYPOXIA FATIGUE energy metabolism
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毛蕊花糖苷对腺嘌呤所致不育症大鼠的影响
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作者 王志 侯强 +1 位作者 冉峥 杨建华 《中成药》 CAS CSCD 2024年第3期771-779,共9页
目的 探讨毛蕊花糖苷对腺嘌呤诱导的不育症大鼠的作用及其机制。方法 大鼠随机分为空白组、模型组、阳性对照组(100 mg/kg复方玄驹胶囊)和毛蕊花糖苷低、高剂量组(50、100 mg/kg)。除空白组外,其余各组每天灌胃150 mg/kg腺嘌呤,连续14 d... 目的 探讨毛蕊花糖苷对腺嘌呤诱导的不育症大鼠的作用及其机制。方法 大鼠随机分为空白组、模型组、阳性对照组(100 mg/kg复方玄驹胶囊)和毛蕊花糖苷低、高剂量组(50、100 mg/kg)。除空白组外,其余各组每天灌胃150 mg/kg腺嘌呤,连续14 d,建立不育症大鼠模型。造模结束后,各组灌胃给予相应剂量药物,连续给药28 d。观察各组大鼠一般活动情况,计算脏器(肝脏、肾脏、睾丸、附睾)指数,于显微镜下观察精子情况,HE染色观察大鼠肝脏、肾脏及睾丸组织病理形态,并进行精子发生评估(Johnsen评分法),ELISA法检测血清T、LH、FSH、GnRH水平,RT-qPCR和Western blot法检测大鼠睾丸组织mTOR、LC3B、ULK1 mRNA和蛋白表达。结果 与空白组比较,模型组大鼠肾脏指数升高(P<0.05),精子计数、精子活动率及精子指数降低(P<0.05),血清T、GnRH水平降低(P<0.05),LH、FSH水平升高(P<0.05),肾脏和睾丸组织病理损伤明显,睾丸组织mTOR mRNA和蛋白表达升高(P<0.05),LC3B、ULK1 mRNA和蛋白表达降低(P<0.05),p-mTOR蛋白表达降低(P<0.05);与模型组比较,毛蕊花糖苷高剂量组肾脏指数降低(P<0.05),精子计数、精子活动率升高(P<0.05),血清T水平升高(P<0.05),LH、FSH水平降低(P<0.05),肾脏和睾丸组织病理损伤有不同程度改善,睾丸组织mTOR mRNA和蛋白表达降低(P<0.05),LC3B、ULK1 mRNA和蛋白表达升高(P<0.05),p-mTOR蛋白表达升高(P<0.05),且毛蕊花糖苷高剂量作用与阳性对照药复方玄驹胶囊相当。结论 毛蕊花糖苷能有效提高不育症大鼠的精子质量,改善性激素紊乱、生殖功能及肾脏、睾丸组织病理性损伤,其作用机制可能与增强正性调控自噬,调节下丘脑-垂体-睾丸轴紊乱有关。 展开更多
关键词 毛蕊花糖苷 不育症 腺嘌呤 自噬 MTOR LC3B ULK1
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Fast repair of dAMP hydroxyl radical adduct by verbascoside via electron transfer 被引量:1
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作者 石益民 王文锋 +5 位作者 姚思德 林维真 韩镇辉 师彦平 贾忠建 郑荣梁 《Science China(Life Sciences)》 SCIE CAS 1999年第6期621-627,共7页
DNA damaged by oxygen radicals has been implicated as a causative event in a number of degenerative diseases, including cancer and aging. So it is very impotant to look for ways in which either oxygen radicals are sca... DNA damaged by oxygen radicals has been implicated as a causative event in a number of degenerative diseases, including cancer and aging. So it is very impotant to look for ways in which either oxygen radicals are scavenged prior to DNA damage or damaged DNA is repaired to supplement the cells’ inadequate repair capacity. The repair activity and its mechanism of verbaseoside, isolated from Pedicularis species, towards dAMP-OH·was studied with pulse radiolytic technique. On pulse irradiation of nitrous oxide saturated 2 mmol/L dAMP aqueous solution containing verbascoside, the transient absorption spectrum of the hydroxyl adduct of dAMP decayed with the formation of that of the phenoxyl radical of verbascoside well under 100 microseconds after electron pulse irradiation. The result indicated that dAMP hydroxyl adducts can be repaired by verbascoside. The rate constants of the repair reaction was deduced to be 5.9×10<sup>8</sup> dm<sup>3</sup>·mol<sup>-1</sup>·s<sup>-1</sup>. A deeper understanding of this new repair mechanism will 展开更多
关键词 DNA damage DAMP HYDROXYL radical verbascoside electron transfer FAST repair.
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PROTECTIVE EFFECTS OF VERBASCOSIDE ON STATIN-INDUCED MYOTOXICITY IN ZEBRAFISH EMBRYOS
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作者 Elaine Wat Hin Fai Kwok +5 位作者 Chun Fai Ng Chi Man Koon Ysé Sallé de Chou Jessica Ferriere Brian Tomlinson Clara BS Lau 《World Journal of Traditional Chinese Medicine》 2015年第4期94-95,共2页
Myotoxicity is a well-known side effect of statins,the common lipid-lowering drug.Herba Cistanches(HC,Cistanche deserticola)is a Chinese herb traditionally used for muscle problems.Recent studies demonstrated that HC ... Myotoxicity is a well-known side effect of statins,the common lipid-lowering drug.Herba Cistanches(HC,Cistanche deserticola)is a Chinese herb traditionally used for muscle problems.Recent studies demonstrated that HC could reduce muscle damage in post-exercised rats.Verbascoside(Vb)was fournd as the major constituent in the active fraction of HC and is known to be muscle protective, 展开更多
关键词 VB PROTECTIVE EFFECTS OF verbascoside ON STATIN-INDUCED MYOTOXICITY IN ZEBRAFISH EMBRYOS
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基于LC-MS法研究百合地黄汤单煎及共煎液中化学成分变化
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作者 毛前程 马柯 +7 位作者 王嘉昀 房天赫 刘蔚然 张洪秀 张琦 田义昭 徐敏真 宗鑫 《辽宁中医药大学学报》 CAS 2024年第2期77-82,共6页
目的测定仲景古方百合地黄汤水煎液成分,并对鲜百合和鲜地黄的水煎液所含成分进行对比,为优化百合地黄汤提取工艺提供初步依据。方法以液相色谱-质谱联用(LC-MS)技术为基础,定性分析百合地黄汤水煎液所含化学成分并进行归属及聚类分析,... 目的测定仲景古方百合地黄汤水煎液成分,并对鲜百合和鲜地黄的水煎液所含成分进行对比,为优化百合地黄汤提取工艺提供初步依据。方法以液相色谱-质谱联用(LC-MS)技术为基础,定性分析百合地黄汤水煎液所含化学成分并进行归属及聚类分析,同时对百合水煎液、地黄汁所含化学成分进行比对。结果百合水煎液、鲜地黄汁中分别检测到35种、36种化学成分;古法煎煮后,在百合地黄汤水煎液中发现69种化学成分,其中有机酸类16种、糖类及苷类共6种、氨基酸及多肽类共8种、生物碱类3种;其中有8种物质为原百合水煎液与地黄汁共有,较两种原煎液新产生36种物质,且抗抑郁有效成分毛蕊花糖苷仅存在于共煎液中。结论古法百合地黄汤共煎液中抗抑郁有效成分比单煎液丰富,有助于抗抑郁有效成分的提取,LC-MS技术适用于复方提取液的含量测定,通过此研究,构建了基于质谱技术的中药复方化学物质组成表征的指纹图谱。 展开更多
关键词 百合地黄汤 液相色谱-质谱联用 百合水煎液 地黄汁 毛蕊花糖苷 阿魏酸
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毛蕊花糖苷对冠心病大鼠炎症及脂代谢的影响
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作者 任引刚 祝松涛 《山西医科大学学报》 CAS 2024年第2期131-139,共9页
目的 探讨毛蕊花糖苷(verbascoside, Verb)对冠心病(CHD)大鼠炎症及脂代谢的影响。方法 将SD大鼠随机分为对照组、模型组、毛蕊花糖苷低、中、高剂量组,每组12只。对照组大鼠正常饲料喂养,其他组大鼠高脂饮食联合腹腔注射垂体后叶素诱... 目的 探讨毛蕊花糖苷(verbascoside, Verb)对冠心病(CHD)大鼠炎症及脂代谢的影响。方法 将SD大鼠随机分为对照组、模型组、毛蕊花糖苷低、中、高剂量组,每组12只。对照组大鼠正常饲料喂养,其他组大鼠高脂饮食联合腹腔注射垂体后叶素诱导冠心病模型。建模后,对照组和模型组大鼠均每天灌胃2 mL生理盐水,低、中、高剂量组大鼠分别每日灌胃2 mL剂量为20,40,80 mg/kg的毛蕊花糖苷,共灌胃4周。末次给药后24 h,分别检测各组大鼠的心功能指标[射血分数(EF)和短轴缩短率(FS)]、血清心肌损伤标志物[肌酸激酶同工酶MB(CK-MB)和乳酸脱氢酶(LDH)]、血清脂代谢指标[总胆固醇(TC)、甘油三酯(TG)、低密度脂蛋白胆固醇(LDL-C)、高密度脂蛋白胆固醇(HDL-C)和游离脂肪酸(FFA)]和血清炎症指标[肿瘤坏死因子-α(TNF-α)、细胞间黏附分子-1(ICAM-1)和单核细胞趋化因子-1(MCP-1)]。通过苏木素伊红(HE)染色观察心肌形态。通过qRT-PCR检测心肌组织中AMP激活的蛋白激酶α(AMPKα)、过氧化物酶体增殖物激活受体α和γ(PPAR-α和PPAR-γ)和PPAR-γ激活分子1α(PGC-1α)的mRNA水平。通过Western blot检测心肌组织中核因子-κB(NF-κB) p65和AMPKα的磷酸化水平。结果 与对照组比较,模型组大鼠的EF和FS降低(P<0.05),血清中CK-MB、LDH、TC、TG、LDL-C、FFA、TNF-α、ICAM-1和MCP-1水平升高(P<0.05),血清HDL-C水平降低(P<0.05),心肌组织中NF-κB p65的磷酸化水平升高(P<0.05),心肌组织中AMPKα、PPAR-α、PPAR-γ和PGC-1α mRNA水平和AMPKα的磷酸化水平降低(P<0.05)。与模型组比较,低、中和高剂量组大鼠的EF和FS升高(P<0.05),血清中CK-MB、LDH、TC、TG、LDL-C、FFA、TNF-α、ICAM-1和MCP-1水平降低(P<0.05),血清HDL-C水平升高(P<0.05),心肌组织中NF-κB p65的磷酸化水平降低(P<0.05),心肌组织中AMPKα、PPAR-α、PPAR-γ和PGC-1α mRNA水平和AMPKα的磷酸化水平升高(P<0.05)。与低剂量组比较,中和高剂量组大鼠的EF和FS升高(P<0.05),血清中CK-MB、LDH、TC、TG、LDL-C、FFA、TNF-α、ICAM-1和MCP-1水平降低(P<0.05),血清HDL-C水平升高(P<0.05),心肌组织中NF-κB p65的磷酸化水平降低(P<0.05),心肌组织中AMPKα、PPAR-α、PPAR-γ和PGC-1α mRNA水平和AMPKα的磷酸化水平升高(P<0.05)。结论 毛蕊花糖苷有效改善了冠心病大鼠的心功能,减轻了心肌损伤,其机制可能与抑制NF-κB介导的炎症反应和激活AMPK介导的脂代谢基因转录和表达有关。 展开更多
关键词 毛蕊花糖苷 冠心病 炎症 脂代谢 大鼠
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地黄中毛蕊花糖苷对OxLDL诱导的人脐静脉内皮细胞凋亡与自噬的影响
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作者 王小兰 李孟 +3 位作者 孙墨 王笑阳 郑晓珂 冯卫生 《中药材》 CAS 北大核心 2023年第1期186-190,共5页
目的:研究从地黄中提取的毛蕊花糖苷对氧化低密度脂蛋白(OxLDL)诱导下人脐静脉内皮细胞(HUVEC)的保护作用,并进一步探究其对细胞炎症、凋亡与自噬的影响。方法:采用OxLDL(150μg/mL)处理HUVEC细胞建立内皮细胞损伤模型,实验设正常对照... 目的:研究从地黄中提取的毛蕊花糖苷对氧化低密度脂蛋白(OxLDL)诱导下人脐静脉内皮细胞(HUVEC)的保护作用,并进一步探究其对细胞炎症、凋亡与自噬的影响。方法:采用OxLDL(150μg/mL)处理HUVEC细胞建立内皮细胞损伤模型,实验设正常对照组、模型组及毛蕊花糖苷50、100μg/mL组。采用MTT法检测细胞相对存活率;亚硝酸盐显色法及ELISA法检测细胞上清液中NO、eNOS、IL-1β、IL-6、TNF-α含量;Annexin-V-PE/7AAD双染流式技术检测细胞凋亡;Flow Sight成像细胞仪检测自噬蛋白LC3A/B表达及自噬情况;Western Blot法检测细胞凋亡与自噬相关蛋白Bax、Bcl-2、LC3B的表达。结果:与模型组比较,毛蕊花糖苷可提高HUVEC细胞活力,降低炎症因子IL-1β、IL-6、TNF-α分泌及细胞凋亡率,促进细胞分泌NO与eNOS,升高LC3BⅡ/Ⅰ比值及自噬蛋白LC3A/B在细胞中标记的自噬百分率,降低凋亡相关蛋白Bax/Bcl-2比值(P<0.05或P<0.01)。结论:毛蕊花糖苷可抑制炎症因子,减少细胞凋亡,增加细胞保护性自噬,改善内皮功能障碍。 展开更多
关键词 毛蕊花糖苷 内皮功能障碍 凋亡 自噬 LC3A/B蛋白
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基于分子对接、分子动力学和体内实验研究毛蕊花苷对帕金森病小鼠的作用机制
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作者 阿迪莱·艾比布力 克力比奴儿·赛地尔丁 +1 位作者 逯冉冉 杨新玲 《海南医学院学报》 2023年第24期1855-1862,1869,共9页
目的:探讨毛蕊花苷(Verbascoside,VB)对帕金森(Parkinson′s disease,PD)模型小鼠的改善作用及明确可能的机制。方法:将60只C57BL/6雄性小鼠随机分为正常组、模型组、VB低、中、高剂量组(分别为30、60、120 mg/kg)。适应性培养一周以后... 目的:探讨毛蕊花苷(Verbascoside,VB)对帕金森(Parkinson′s disease,PD)模型小鼠的改善作用及明确可能的机制。方法:将60只C57BL/6雄性小鼠随机分为正常组、模型组、VB低、中、高剂量组(分别为30、60、120 mg/kg)。适应性培养一周以后,除空白组外,各组连续5 d腹腔注射1-甲基-4-苯基-1,2,3,6-四氢吡啶盐酸盐(MPTP)建立PD亚急性模型,造模后药物组连续灌胃给药7 d,正常组小鼠注射等量生理盐水。通过旷场实验、爬杆实验、抓力测试观察小鼠行为学改变;HE染色和Nissl染色观察黑质神经元组织病理结构;透射电镜观察神经元超微结构变化;免疫组织化学检测酪氨酸羟化酶(TH)、α-突触核蛋白(α-Syn)以及Toll样受体4(TLR4)蛋白阳性表达;Western blot检测小鼠黑质TH、α-Syn及TLR4、NF-κB、PNF-κB蛋白水平变化;Elisa法检测血清中炎症因子IL-1β、IL-6、肿瘤坏死因子-α(TNF-α)水平;利用分子对接和分子动力学验证VB与TLR4/NF-κB信号通路及相关因子的结合能力及稳定性。结果:与正常组相比,模型组小鼠行走总路程降低、爬杆时间显著延长,前肢抓力减弱(P<0.05);透射电镜观察神经元超微结构改变,细胞核溶解、变形,线粒体损伤;H&E染色和Nissl染色显示神经元数量减少,形态结构改变,神经元尼氏体阳性细胞数减少(P<0.05);免疫组织化学和Western blot结果显示α-syn、TLR4、NF-κB p65表达水平升高,TH水平明显降低(P<0.05),血清中IL-1β、IL-6、TNF-α表达显著升高(P<0.05);与模型组比较,VB治疗组明显改善小鼠活动能力(P<0.05),神经元细胞形态逐渐恢复,神经元尼氏体阳性细胞增多(P<0.05);α-syn、TLR4、NF-κB p65蛋白表达降低,TH蛋白表达升高(P<0.05),血清中IL-1β、IL-6、TNF-α水平明显降低(P<0.05)。分子对接及分子动力学模拟结果显示VB与蛋白结合优良,性质较稳定。结论:VB对PD小鼠具有保护作用,其作用机制可能与TLR4/NF-κB通路有关,进而调节神经免疫。 展开更多
关键词 帕金森病 毛蕊花苷 TOLL样受体4 分子对接
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复肝汤HPLC特征图谱及波长切换法同时测定6种成分的含量
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作者 袁文钦 黄伟鹏 +4 位作者 林雅丽 段崇申 刘怡馨 陈乃宏 刘应蛟 《中南药学》 2023年第8期2158-2162,共5页
目的建立复肝汤HPLC特征图谱,并测定复肝汤中毛蕊花糖苷、芦丁、槲皮素、木犀草素、芹菜素、丹参酮Ⅱ_(A)6种主要成分的含量。方法采用高效液相色谱法,色谱柱为Agilent 5TC-C_(18)色谱柱(4.6 mm×250 mm,5μm),流动相为甲醇-水,梯... 目的建立复肝汤HPLC特征图谱,并测定复肝汤中毛蕊花糖苷、芦丁、槲皮素、木犀草素、芹菜素、丹参酮Ⅱ_(A)6种主要成分的含量。方法采用高效液相色谱法,色谱柱为Agilent 5TC-C_(18)色谱柱(4.6 mm×250 mm,5μm),流动相为甲醇-水,梯度洗脱,流速为1.0 mL·min^(-1),检测波长分别为310 nm(毛蕊花糖苷)、370 nm(芦丁、槲皮素、木犀草素、芹菜素)、250 nm(丹参酮Ⅱ_(A)),柱温30℃,进样量20μL。结果确定复肝汤HPLC特征图谱13个共有峰,利用相似度软件对10批样品特征图谱进行分析,各批样品相似度均在0.95以上。毛蕊花糖苷、芦丁、槲皮素、木犀草素、芹菜素和丹参酮ⅡA的线性范围分别在4.394~87.880μg·mL^(-1)(r=0.9999)、1.501~30.020μg·mL^(-1)(r=0.9999)、0.475~9.505μg·mL^(-1)(r=0.9997)、0.547~10.945μg·mL^(-1)(r=0.9995)、1.028~20.550μg·mL^(-1)(r=0.9998)、0.854~17.070μg·mL^(-1)(r=1.000);平均加样回收率在92.1%~101.3%,RSD在0.78%~1.4%。结论该方法简便、准确、重复性高,并可同时测定复肝汤中6种成分的含量,为复肝汤质量控制提供了参考。 展开更多
关键词 高效液相色谱法 复肝汤 毛蕊花糖苷 芦丁 槲皮素 木犀草素 芹菜素 丹参酮Ⅱ_(A)
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毛蕊花糖苷防晒霜对紫外线辐射诱导大鼠皮肤损伤的保护作用研究
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作者 李晓琳 王芃 +1 位作者 李茂星 姜疆 《中南药学》 CAS 2023年第3期594-600,共7页
目的建立UVB辐射诱导大鼠皮肤损伤模型,探讨毛蕊花糖苷防晒霜抗紫外线辐射的作用及机制。方法选取背部皮肤恢复成光滑、无损伤的大鼠建立紫外损伤模型。照射条件为紫外线(320 nm)照射,照射强度为1.8 J·cm^(-2),每日照射3 min,连续... 目的建立UVB辐射诱导大鼠皮肤损伤模型,探讨毛蕊花糖苷防晒霜抗紫外线辐射的作用及机制。方法选取背部皮肤恢复成光滑、无损伤的大鼠建立紫外损伤模型。照射条件为紫外线(320 nm)照射,照射强度为1.8 J·cm^(-2),每日照射3 min,连续3 d。49只大鼠随机分为空白组(无紫外线照射)、模型组(紫外线照射)、基质组(紫外线照射+空白基质),高剂量组(紫外线照射+6%毛蕊花糖苷防晒霜)、中剂量组(紫外线照射+4%毛蕊花糖苷防晒霜)、低剂量组(紫外线照射+2%毛蕊花糖苷防晒霜)及阳性对照组(市售防晒霜)。大鼠照射期间,每日观察背部皮肤损伤情况。末次背部照射后,取照射区皮肤组织进行苏木精-伊红染色和天狼猩红染色观察皮肤组织形态及胶原纤维的变化,Tunel染色检测细胞凋亡情况,检测皮肤抗氧化能力[超氧化物歧化酶(SOD)、谷胱甘肽(GSH)、谷胱甘肽硫转移酶(GST)、过氧化氢(H_(2)O_(2))、羟脯氨酸(Hyp)],免疫组化检测cleaved caspase-3的变化。结果大鼠背部紫外照射后,皮肤呈现粗糙增厚、红肿溃烂等不同程度的损伤,胶原纤维变性紊乱。与模型组比较,毛蕊花糖苷不同剂量组皮肤损伤程度明显减轻,皮肤组织SOD活性、GSH含量和GST活力均升高,而H_(2)O_(2)、Hyp含量下降(P<0.05或P<0.01),其中毛蕊花糖苷高剂量组效果最好。同时,凋亡细胞及cleaved caspase-3的阳性细胞率减少,显示毛蕊花糖苷防晒霜处理后可减轻细胞凋亡。结论毛蕊花糖苷防晒霜可提高皮肤抗氧化应激活性,降低氧化产物含量,抑制细胞凋亡,达到抗紫外线辐射损伤作用。 展开更多
关键词 毛蕊花糖苷 抗紫外线辐射 抗氧化 细胞凋亡
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藓生马先蒿质量标准研究
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作者 焦兴苹 达洛嘉 杨凤梅 《中成药》 CAS CSCD 北大核心 2023年第10期3342-3346,共5页
目的建立藓生马先蒿质量标准。方法采用显微鉴别、TLC进行定性鉴别,2020年版《中国药典》方法检测其水分、总灰分、酸不溶性灰分、浸出物含量,HPLC法测定京尼平苷酸、毛蕊花糖苷含量。结果显微鉴别特征明显,可见花粉粒、草酸钙晶体、网... 目的建立藓生马先蒿质量标准。方法采用显微鉴别、TLC进行定性鉴别,2020年版《中国药典》方法检测其水分、总灰分、酸不溶性灰分、浸出物含量,HPLC法测定京尼平苷酸、毛蕊花糖苷含量。结果显微鉴别特征明显,可见花粉粒、草酸钙晶体、网纹状细胞、螺纹导管。TLC特征斑点分离清晰。10批样品水分、总灰分、酸不溶性灰分、浸出物平均含量分别为8.3%、15.8%、2.0%、36.7%。京尼平苷酸、毛蕊花糖苷分别在12.83~128.31、11.77~117.75μg/mL范围内线性关系良好(r≥0.9997),平均加样回收率分别为101%、101%,RSD分别为1.16%、1.08%,平均含量分别为0.31%、1.78%。结论藓生马先蒿质量标准为水分、总灰分、酸不溶性灰分分别不得超过15%、20%、4.0%,浸出物不得少于33.0%,京尼平苷酸、毛蕊花糖苷含量分别不得少于0.25%、1.70%。 展开更多
关键词 藓生马先蒿 京尼平苷酸 毛蕊花糖苷 TLC HPLC 2020年版《中国药典》
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毛蕊花糖苷调节HMGB1/RAGE/NF-κB信号通路对动脉粥样硬化大鼠内皮功能障碍的影响
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作者 刘艳文 刘水清 +1 位作者 林少伟 刘协红 《天津医药》 CAS 北大核心 2023年第12期1339-1343,共5页
目的 探讨毛蕊花糖苷(VB)调节高迁移率族蛋白B1(HMGB1)/晚期糖基化终产物受体(RAGE)/核因子κB(NF-κB)信号通路对动脉粥样硬化(AS)大鼠内皮功能障碍的影响机制。方法 采用高脂饲料喂养联合维生素D3溶液腹腔注射的方法建立AS大鼠模型。... 目的 探讨毛蕊花糖苷(VB)调节高迁移率族蛋白B1(HMGB1)/晚期糖基化终产物受体(RAGE)/核因子κB(NF-κB)信号通路对动脉粥样硬化(AS)大鼠内皮功能障碍的影响机制。方法 采用高脂饲料喂养联合维生素D3溶液腹腔注射的方法建立AS大鼠模型。将大鼠分为对照组(10只),模型组(12只),毛蕊花糖苷低、中、高剂量组(VB-L、M、H,2、5、10 mg/kg,每组10只)和阳性对照组(辛伐他汀,5 mg/kg,10只)。全自动生化分析仪检测血清中血脂水平;HE染色观察大鼠主动脉组织病理变化;酶联免疫吸附试验(ELISA)法检测血清中炎性因子及内皮细胞因子水平;微量法试剂盒检测大鼠氧化应激水平;Western blot检测主动脉HMGB1/RAGE信号通路蛋白表达。结果 与对照组相比,模型组大鼠主动脉内膜增厚、血管出现斑块,并伴有脂质沉积和炎性细胞浸润,血清中总胆固醇(TC)、三酰甘油(TG)、低密度脂蛋白胆固醇(LDL-C)、肿瘤坏死因子α(TNF-α)、白细胞介素1β(IL-1β)、C反应蛋白(CRP)、基质金属蛋白酶9(MMP-9)、内皮素1(ET-1)、内脂素、细胞间黏附分子1(ICAM-1)、丙二醛(MDA)及主动脉中HMGB1、RAGE、NF-κB磷酸化水平升高,高密度脂蛋白胆固醇(HDL-C)、一氧化氮(NO)、超氧化物歧化酶(SOD)、谷胱甘肽过氧化物酶(GSH-Px)水平降低(P<0.05);与模型组相比,VB各组及辛伐他汀组大鼠病理学变化明显改善,血清中TC、TG、LDL-C、TNF-α、IL-1β、CRP、MMP-9、ET-1、内脂素、ICAM-1、MDA及主动脉中HMGB1、RAGE、NF-κB磷酸化水平降低,血清HDL-C、NO、SOD、GSH-Px水平升高(P<0.05)。结论 VB可下调HMGB1/RAGE/NF-κB信号通路蛋白表达,抑制AS大鼠炎症和氧化应激,改善脂质代谢和血管内皮功能。 展开更多
关键词 麦角甾苷 动脉粥样硬化 HMGB1蛋白质 高级糖化终产物受体 内皮功能障碍 毛蕊花糖苷
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UPLC-MS/MS法测定右归丸中毛蕊花糖苷的含量
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作者 邓杰华 周云峰 +3 位作者 黄招光 吴喆 黄炳泉 李存金 《江西中医药大学学报》 2023年第4期74-76,共3页
目的:建立右归丸中毛蕊花糖苷的含量测定方法。方法:采用Waters ACQUITY UPLC BEH C_(18)色谱柱(2.1 mm×100 mm,1.7μm),以乙腈-0.1%甲酸溶液为流动相,梯度洗脱,流速0.3 mL/min,柱温30℃;质谱条件以623→161和623→133为特征离子对... 目的:建立右归丸中毛蕊花糖苷的含量测定方法。方法:采用Waters ACQUITY UPLC BEH C_(18)色谱柱(2.1 mm×100 mm,1.7μm),以乙腈-0.1%甲酸溶液为流动相,梯度洗脱,流速0.3 mL/min,柱温30℃;质谱条件以623→161和623→133为特征离子对,采用电喷雾离子源(ESI)和负离子扫描方式,进行多反应离子监测(MRM)定量分析。结果:毛蕊花糖苷在质量浓度175.739 2~1 757.392 0 ng/mL范围内呈良好线性关系,方法学考察良好。9批样品中毛蕊花糖苷的含量范围为33.40~53.20μg/g。结论:所建方法能测定右归丸中熟地黄的主要化学成分的含量,可用于右归丸的质量控制。 展开更多
关键词 右归丸 熟地黄 毛蕊花糖苷 液质联用 含量
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痹痛散的质量标准研究
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作者 苏捷 杨贤海 +3 位作者 付大清 阳国彬 郑光明 马小青 《中医药导报》 2023年第6期51-54,共4页
目的:建立痹痛散的质量标准。方法:采用薄层色谱法(TLC)分别对痹痛散中地黄、当归和三七进行定性鉴别;通过高效液相色谱法(HPLC)对痹痛散中毛蕊花糖苷、阿魏酸及丹酚酸B进行含量测定。结果:地黄、当归和三七薄层色谱斑点清晰,专属性强,... 目的:建立痹痛散的质量标准。方法:采用薄层色谱法(TLC)分别对痹痛散中地黄、当归和三七进行定性鉴别;通过高效液相色谱法(HPLC)对痹痛散中毛蕊花糖苷、阿魏酸及丹酚酸B进行含量测定。结果:地黄、当归和三七薄层色谱斑点清晰,专属性强,阴性对照无干扰。含量测定结果显示,毛蕊花糖苷、阿魏酸和丹酚酸B分别在6.06~96.88μg/mL(r=0.9998)、7.70~123.12μg/mL(r=0.9990)、31.16~498.56μg/mL(r=0.9995)范围内呈良好的线性关系;平均加样回收率分别为97.80%、96.21%、99.78%,RSD分别为1.62%、1.21%、1.06%。结论:建立的方法准确、可靠,可用于痹痛散的质量评价。 展开更多
关键词 痹痛散 质量标准 毛蕊花糖苷 阿魏酸 丹酚酸B
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