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灵芝孢子粉是灵芝的生殖细胞,包含灵芝所有的化学成分,主要含有灵芝三萜类、多糖类、甾体类、脂肪酸类和蛋白质类等多种化合物。灵芝孢子粉具有抗肿瘤、免疫调节、抗氧化、保护心血管、保肝护肝等药理作用。《中国药典》2020年版对灵芝孢子粉的质量控制标准尚未明确规定,就灵芝孢子粉化学成分和药理作用研究进展进行综述,并基于质量标志物(quality marker,Q-Marker)理论,从植物亲缘性与特有性、有效性、可测性、临床应用、可入血成分等方面进行Q-Marker预测分析,初步推测多糖类、灵芝酸、甾醇类(麦角甾醇)、不饱和脂肪酸(油酸)等成分为其Q-Marker,为规范灵芝孢子粉质量研究和建立、完善灵芝孢子粉质量标准提供参考。 相似文献
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猴头菌醇提浸膏和水提浸膏甾醇类化合物的比较研究 总被引:3,自引:0,他引:3
目的 :研究猴头菌甾醇类化合物 ,探讨醇提和水提浸膏疗效差异的药化基础。方法 :利用GC-MS方法对猴头菌甾醇类物质组成进行分析 ,并采用气相色谱、反相HPLC及其他生化分析手段比较了猴头菌及其 2种方法提取物的成分。结果 :醇提浸膏较水提浸膏在粗多糖、水溶性蛋白、脂肪酸方面没有明显优势 ,但醇提与水提浸膏在甾醇类物质含量上存在显著差异。在猴头菌丝体中存在含量较高的不同双键形式的麦角甾醇类化合物、β谷甾醇和 4个双键的C28甾醇化合物。结论 :猴头菌甾醇类化合物主要存在于醇提浸膏中 ,其中麦角甾醇含量最高。同时首次发现猴头菌含有麦角甾 8(14) 烯 3β-醇、β-谷甾醇和 4个双键的C28甾醇化合物。 相似文献
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姜旭 《国际中医中药杂志》2005,27(2):111-112
从灵芝中分离得到的具有高氧合性和生物活性的羊毛甾烷型三萜显示细胞毒作用。从其水溶性部分分得的多糖和糖蛋白具有抗肿瘤和免疫调节活性。本次比较了灵芝的未成熟和成熟的鹿角型子实体水溶性部分在体内外对LLC细胞的抗肿瘤作用,确定了二者三萜和多糖类的成分和组成。 相似文献
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百合科(Liliaceae)藜芦属(Veratrum)植物的化学成分包括甾体生物碱类、二苯乙烯类、黄酮类、二肽类及其它类化合物,其中甾体生物碱是其主要活性成分。近年来,其抗肿瘤活性得到了广泛的关注和研究。本文综述了近10年来分离得到的新异甾体生物碱,及在化合物单体层面的抗肿瘤活性研究,包括在细胞水平上的抗肿瘤活性筛选、化合物结构修饰、构效关系及作用机制等,并结合蒙药藜芦“泻痞”应用的文献研究,提出了其中甾体生物碱可能是其抗肿瘤药效物质基础。该文献研究为藜芦甾体生物碱的抗肿瘤作用提供研究思路,并为蒙药藜芦抗肿瘤制剂的开发提供参考。 相似文献
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冬虫夏草是中国的一种传统名贵中药,富含了虫草多糖、虫草素、虫草酸、虫草多肽、麦角甾醇等多种单体活性成分。现代医学发现其具有抗肿瘤、免疫调节、降血糖、抗氧化、对肾脏的保护作用等广泛的药理学功能。目前的研究已证实冬虫夏草及其单体活性成分可以有效的治疗多种疾病。本文在检索近几年来有关冬虫夏草及单体活性成分药理作用的相关研究资料的基础上,主要从冬虫夏草的单体活性成分的研究现状及冬虫夏草的药理学作用的研究进展两个方面对目前冬虫夏草及单体活性成分药理作用进行归纳和总结,为今后进一步开发和利用冬虫夏草提供帮助。 相似文献
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马勃Lasiosphaera Calvatia是一种常用的真菌类药材,具有较高的药用价值,广泛用于多种传统处方中,应用前景广阔。马勃中的化学成分主要有甾体类、酚类、挥发性、氨基酸类等,其活性成分主要有甾体类、多糖、多肽类等,其中麦角甾醇是真菌类的特征甾醇,本文的化学成分总结为《中国药典》后续马勃指标成分的规定提供理论依据。现代药理活性研究表明,马勃具有抗肿瘤、止血、抑菌、止咳、抗氧化、抗炎等作用。本文对2020年版《中国药典》规定的3种基原植物以及脱皮马勃属、秃马勃属的马勃类药材的化学成分和药理活性进行了全面系统的总结,以期为马勃的深入研究和开发利用提供科学参考。 相似文献
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白花蛇舌草的化学成分及功效研究综述 总被引:2,自引:0,他引:2
白花蛇舌草是一种传统中药,目前从中分离得到的化学成分共有50余种,主要为黄酮类、蒽醌类、萜类、甾醇类、酚酸类和糖类等。白花蛇舌草各类溶剂的提取物及部分单体成分具有抗肿瘤、调节免疫、抗炎、抗氧化等作用。单体成分的功效及作用机制研究是其今后研究的主要方向。 相似文献
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Ganoderma lucidum (G. lucidum), a basidiomycete white rot fungus, has long been prescribed to prevent and treat various human diseases, particularly in China, Japan, and Korea. Several classes of bioactive substances have been isolated and identified from G. lucidum, such as triterpenoids, polysaccharides, nucleosides, sterols, and alkaloids, among others. This paper examines the potential role of G. lucidum polysaccharide (GLPS) in tumor therapy and the possible mechanisms involved. Both in vitro and in vivo studies suggested that the anti-tumor activities of GLPS are mediated by its immunomodulatory, anti-angiogenic, and cytotoxic effects. GLPS affects immune cells and immune-related cells including B lymphocytes, T lymphocytes, dendritic cells, macrophages, and natural killer cells. In addition, recent data also suggest that GLPS suppresses tumorigenesis or inhibits tumor growth through direct cytotoxic effect and anti-angiogenic actions. However, many questions still need to be answered before both G. lucidum and GLPS can be widely accepted and used as anti-tumor agents. 相似文献
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Anti-angiogenic and inhibitory activity on inducible nitric oxide production of the mushroom Ganoderma lucidum 总被引:5,自引:0,他引:5
Fresh fruit bodies of Ganoderma lucidum were extracted with 70% ethanol at room temperature. The extract (GL) showed significant anti-angiogenic activity, which was detected using a chick embryo chorioallantoic membrane assay. GL significantly inhibited LPS-induced NO production in RAW 264.7 macrophages. These results support the anti-tumor effect of Ganoderma lucidum. 相似文献
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Hsu SC Ou CC Li JW Chuang TC Kuo HP Liu JY Chen CS Lin SC Su CH Kao MC 《Journal of ethnopharmacology》2008,120(3):394-401
Ethnopharmacological relevance
Ganoderma, known as Lingzhi or Reishi, has been traditionally administered throughout Asia for centuries as a cancer treatment and for other medicinal purposes.Aim of the study
To investigate the inhibitory activity and explore the molecular mechanisms of anti-tumor effect on colorectal cancer cells in vitro and in vivo as well as to test the side effects of Ganoderma tsugae.Materials and methods
Methanol fraction was obtained from dried fruiting bodies of Ganoderma. TLC and HPLC were performed to differentiate and confirm the identification of different species as well as to quantify the bioactive molecules in methanol extracts of Ganoderma species. MTT and Trypan blue exclusion assay as well as tumorigenesis study were used to assess the anti-tumor effect in vitro and in vivo. Using flow cytometry and Western Blots, we examined further the molecular mechanisms of anti-tumor effect. Finally, biochemical and hematological profiles and pathological examinations were used to evaluate the safety.Results
The Ganoderma tsugae extracts inhibit colorectal cancer cell proliferation caused by accumulating cells in G2/M phase, and it may be through downregulation of cyclin A and B1 and upregulation of p21 and p27. Tumorigenesis study in nude mice revealed the extracts caused tumor shrinkage. Additionally, safety assay showed Ganoderma tsugae extracts caused no significant side effects in an animal model.Conclusions
This study provides molecular evidence that Ganoderma tsugae extracts exert anti-tumor effects both in vitro and in vivo on colorectal adenocarcinoma cells by inducing G2/M cell cycle arrest. More importantly, no significant physiological changes resulting from treatment with Ganoderma tsugae extracts were observed in the animal model. Therefore, these data provide new insights into the possible therapeutic use of Ganoderma tsugae for treating colorectal cancer. 相似文献14.
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Niedermeyer TH Lindequist U Mentel R Gördes D Schmidt E Thurow K Lalk M 《Journal of natural products》2005,68(12):1728-1731
Four sterols and 10 triterpenes were isolated from the fruiting bodies of Ganoderma pfeifferi, including the three new triterpenes 3,7,11-trioxo-5alpha-lanosta-8,24-diene-26-al (lucialdehyde D, 1), 5alpha-lanosta-8,24-diene-26-hydroxy-3,7-dione (ganoderone A, 2), and 5alpha-lanosta-8-ene-24,25-epoxy-26-hydroxy-3,7-dione (ganoderone C, 3). The structures of 1-3 were determined on the basis of spectroscopic evidence. Antibacterial, antifungal, and antiviral activity were studied for some of the isolated compounds. Ganoderone A (2), lucialdehyde B (4), and ergosta-7,22-dien-3beta-ol (7) were found to exhibit potent inhibitory activity against herpes simplex virus. 相似文献
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目的 利用高分辨气相色谱-四级杆-静电轨道阱质谱法(GC-Q-Exactive-MS)定性分析灵芝孢子油的化学成分。方法 采用GC-Q-Exactive-MS,在电子轰击(EI)源下获取化合物的全扫描质谱数据,通过总结脂肪酸类、萜类、甾醇类及醛类化学成分的质谱裂解规律,并检索NIST、MassBank、HMDB、PubChem在线数据库及查阅相关文献,对灵芝孢子油的各类化学成分进行鉴定。结果 从灵芝孢子油中共鉴定了22个化学成分,包括3个脂肪酸类、4个萜类、4个甾醇类、4个醛类及7个其他类化合物。结论 研究结果为灵芝孢子油质量控制和中药弱极性化学成分定性分析提供了参考。 相似文献
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New lanostanoids from the mushroom Ganoderma lucidum. 总被引:3,自引:0,他引:3
Jiyuan Ma Qing Ye Yanjun Hua Decheng Zhang Raymond Cooper Michael N Chang Joseph Y Chang Hao H Sun 《Journal of natural products》2002,65(1):72-75
From a lipophilic extract of the fruiting body of Ganoderma lucidum, three new lanostanoids, 8beta,9alpha-dihydroganoderic acid J (1), methyl 8beta,9alpha-dihydroganoderate J (2), and 20-hydroxylganoderic acid G (3), along with 12 known lanostanoids and two ergostane sterols were isolated. The structures of 1-3 were determined by interpretation of their spectroscopic data. 相似文献
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??This article summarized the chemical constituents and pharmacological activities of Lysimachia L., thus providing scientific and theoretical basis for development of this genus. Literatures of experimental studies on Lysimachia genus at home and abroad were consulted and summarized. The chemical research showed that the main compounds in Lysimachia genus were triterpenoids and their glycosides, flavonoids and their glycosides, organic acids, and sterols. Pharmacological investigation showed that the plants of this genus had anti-tumor, anti-inflammatory, antioxidant, and ??-glucosidase inhibitory activities. Lysimachia genus should be further researched and utilized, which is abundant in our country. 相似文献