【摘 要】
:
Sargassum fusiforme(S.fusiforme)has been used as an ingredient in Chinese herbal medicine for thousands of years.However,there are a limited number of studies concerning its therapeutic mechanism.High performance gel permeation chromato-graphy(HPGPC)analy
【机 构】
:
College of Biological and Environmental Sciences,Zhejiang Wanli University,Ningbo 315100,China;Schoo
论文部分内容阅读
Sargassum fusiforme(S.fusiforme)has been used as an ingredient in Chinese herbal medicine for thousands of years.However,there are a limited number of studies concerning its therapeutic mechanism.High performance gel permeation chromato-graphy(HPGPC)analysis showed that the average molecular weight of the S.fusiforme polysaccharide,SFPS 191212,is 43 kDa.SFPS 191212 is composed of mannose,rhamnose,galactose,xylose,glucose,and fucose(at a molar ratio:2.1 ∶ 2.9 ∶ 1.8 ∶ 15.5 ∶ 4.6 ∶62.5)with α-and β-configurations.The present research evaluated the anti-tumor potential of the S.fusiforme polysaccharide in hu-man erythroleukemia(HEL)cells in vitro.To explore the SFPS 191212\'s apoptosis mechanism in HEL cells,transcriptome analysis was performed on HEL cells that were incubated with SFPS 191212.The inhibitory effect of SFPS 191212 on HEL cell growth was also analyzed.It was found that SFPS 191212 inhibited HEL cell proliferation,reduced cell viability in a concentration-dependent manner,and induced an insignificant toxic effect on normal human embryonic lung(MRC-5)cells.Compared with the control group,transcriptome analysis identified a total of 598 differentially expressed genes(DEGs),including 243 up-regulated genes and 355 down-regulated genes.Gene Ontology(GO)and Kyoto Encyclopedia of Genes and Genomes(KEGG)enrichment analyses were performed on all DEGs,and 900 GO terms and 52 pathways were found to be significantly enriched.Finally,23 DEGs were randomly selected and confirmed by quantitative real-time polymerase chain reaction(qRT-PCR).Moreover,SFPS 191212 down-regulated the PI3K/Akt signal transduction pathway.Our results provide a framework for understanding the effect of SFPS 191212 on cancer cells and can serve as a resource for delineating the anti-tumor mechanisms of S.fusiforme.
其他文献
报道1例T2DM患者,应用达格列净后出现直立性低血压.达格列净是钠-葡萄糖协同转运蛋白2抑制剂(SGLT2i),因存在降糖外心血管获益,在T2DM合并动脉粥样硬化性心血管疾病的治疗中日益普及.目前,SGLT2i导致直立性低血压不良反应无明确报道.临床应用此类药物时应特别注意基线BP、联合用药情况及糖尿病自主神经病变.
甘精胰岛素U300更接近人体生理状态下基础胰岛素的分泌模式,降糖作用平稳,有效控制血糖的同时低血糖发生风险更低.此外,甘精胰岛素U300在一些特殊患者降糖治疗、用药依从性和灵活性等方面也存在优势,为糖尿病患者的血糖管理提供了更佳选择.
目的 探讨α-硫辛酸(LA)通过激活腺苷酸活化蛋白激酶(AMPK)/哺乳动物雷帕霉素靶蛋白(mTOR)通路改善T2DM大鼠肾脏病变.方法 40只大鼠分为正常对照组(Con)、T2DM组、LA组、复合物C组(Comp C)和LA+Comp C组,每组各8只.检测各组大鼠FPG、24 h尿蛋白水平,计算肾脏肥大指数,光镜和电镜观察大鼠肾脏病理变化,Weatern blot检测大鼠肾脏相关蛋白表达水平.结果 与NC组比较,T2DM组FPG、肾脏肥大指数、24 h尿蛋白升高(P<0.01),光镜和电镜下均可见肾脏
DKD是DM常见微血管并发症,由于长期高血糖及高胰岛素血症,机体处于血栓前状态,易伴发肾小球微血栓(GMT)形成.炎症信号通路和炎症因子参与GMT形成,引起微循环障碍,加速肾小球硬化,加重肾脏损伤.本文对DKD引起的GMT与炎症相关性研究进展进行综述.
动态血糖监测(CGM)技术迅速发展,已成为DM管理的重要方法.规范合理应用CGM系统可明显降低DM患者HbA1c水平,减少血糖波动及低血糖风险,提高血糖控制效果和生活质量,对改善DM患者预后意义重大.本文对CGM技术与临床研究进展进行综述.
中南大学湘雅二医院国家代谢性疾病临床医学研究中心、中国民族卫生协会、《糖尿病天地》杂志社共同主办的“第十六届湘雅国际糖尿病免疫学论坛”(以下简称“论坛”)于2021年4月23~25日在湖南长沙举行.
一、Ins治疗现状及挑战rn中国DM患者负担沉重,约占全球DM患者的1/4[1].尽管DM防控工作取得一定进步,但我国仍有50. 6%的T2DM患者未能实现良好的血糖控制[2].DM作为一种进展性疾病[3],起始Ins治疗是疾病管理的必经阶段[4].基础胰岛素方案是国内外指南[5-6]共同推荐的Ins起始方案,且一旦起始基础胰岛素治疗,为实现良好的血糖控制,对Ins剂量的合理调整十分必要.
Physalin B(PB),one of the major active steroidal constituents of Solanaceae Physalis plants,has a wide variety of bio-logical activities.We found that PB significantly down-regulated β-amyloid(Aβ)secretion in N2a/APPsw cells.However,the underly-ing mechan
During the pathogensis of rheumatoid arthritis(RA),activated RA fibroblast-like synoviocytes(RA-FLSs)combines similar proliferative features as tumor and inflammatory features as osteoarthritis,which eventually leads to joint erosion.Therefore,it is imper
Ocotillol(OT)-type ginsenosides,one subtype of ginsenosides,consist of a dammarane skeleton and a tetrahydrofuiran ring.Most naturally-occurring OT-type ginsenosides exist in Panax species,particularly in Panax quinquefolius,which may be attrib-uted to th