甲硫氨酸诱导高Hcy血症的抗氧化作用研究

为探讨甲硫氨酸在诱导高Hcy血症过程中的抗氧化作用,将Wistar大鼠随机分为正常组和1%甲硫氨酸组,喂养6周后,采用高效液相色谱法测定血清中同型半胱氨酸(Hcy)和谷胱甘肽含量(GSH),全自动氨基酸分析仪测定蛋氨酸和牛磺酸含量,转氨酶活性采用试剂盒测定。肝组织丙二醛(MDA)含量采用硫代巴比妥酸法,黄嘌呤氧化酶法和比色法测定肝组织超氧化物歧化酶(SOD)活性、总抗氧化能力(FRAP值)和还原性谷胱甘肽含量。结果表明,1%甲硫氨酸组血清Hcy和牛磺酸含量分别为3.56±0.68μmol·L-1和568.68±57.02μmol·L-1,较正常组显著升高(p<0.05)。1%甲硫氨酸组肝组织GSH含量和SOD活性分别为132.19±25.49mg·g-1和6.86±1.46U·mg-1,较正常组103.97±16.30mg·g-1和5.01±1.24U·mg-1显著升高(p<0.05)。1%甲硫氨酸组较正常组肝组织FRAP值亦升高而MDA含量降低。结果表明,甲硫氨酸在诱导高Hcy血症过程中同时具有抗氧化作用。     

蓝莓的成分与保健功能的研究进展

越橘属蓝莓含有花青苷（花青素或酚配基,与糖的结合体）。紫檀芪、鞣花酸、超氧化物歧化酶、熊果酸、酚酸及不同维生素等生物活性成分。很早就报道蓝莓所含花青苷可加速视紫素的再生而有益于视力及眼部健康。近年的研究显示蓝莓具有抗氧化作用,预防癌症、降血脂、降胆固醇、增强记忆、抗衰老、增强人体免疫、保护视力、抗糖尿病等保健功能。因此蓝莓被认为是最有营养的食物之一。     

不同特性粘数壳聚糖降血浆胆固醇、甘油三酯及抗氧化活性研究

通过醋酸-H2O2氧化降解法制备三种不同特性粘数（50℃时,η=4．76mL／g,29．39mL／g和54．93mL／g）的壳聚糖。以小鼠为实验对象,采取灌胃给药方式,考察其降低血浆TCH、TG的能力,并以血浆SOD酶活及MDA含量为指标,进行抗氧化药效学评价。结果显示,给药21d后,三种壳聚糖均能显著降低小鼠血浆TCH和TG含量,降幅分别大于28．2％和22．5％;且三种壳聚糖也能显著降低小鼠血浆MDA含量,降幅大于30．0％,但对小鼠血浆SOD酶活则无显著影响。     

Alcalase碱性蛋白酶对中华稻蝗蛋白水解条件的研究

本试验采用Alcalase碱性蛋白酶对中华稻蝗蛋白进行水解,研究其蛋白酶解条件和酶解物的抗氧化性(用抑制邻苯三酚自氧化率来表示).结果表明,实验室最佳酶解条件为:底物浓度1%,pH值8.0,温度55℃,水解时间4 h,加酶量(V/V,%)为10%.在此条件下其酶解物具有明显的抗氧化活性,对邻苯三酚自氧化的抑制率可达40%,水解度为51%.     

Antioxidation and Tyrosinase Inhibition of Polyphenolic Curcumin Analogs

A series of polyphenolic curcumin analogs were synthesized and their inhibitory effects on mushroom tyrosinase and the inhibition of 1,1-diphenyl-2-picryl-hydrazyl (DPPH) free radical formation were evaluated. The results indictated that the analogs possessing m-diphenols and o-diphenols exhibited more potent inhibitory activity on tyrosinase than reference compound rojic acid, and that the analogs with o-diphenols exhibited more potent inhibitory activity of DPPH free-radical formation than reference compound vitamin C. The inhibition kinetics, analyzed by Lineweaver–Burk plots, revealed that compounds B₂ and C₂ bearing o-diphenols were non-competitive inhibitors, while compounds B₁₁ and C₁₁ bearing m-diphenols were competitive inhibitors. In particular, representative compounds C₂ and B₁₁ showed no side effects at a dose of 2,000 mg/kg in a preliminary evaluation of acute toxicity in mice. These results suggest that such polyphenolic curcumin analogs might serve as lead compounds for further design of new potential tyrosinase inhibitors.     

脱水导致的胞内溶质变化与植物耐干性的获得

植物耐干性是指许多植物个体和部分植物种子能在含水量极低的条件下存活,在回水的过程中迅速启动修复机制,细胞经重新水合修复所受损伤的能力。在脱水过程中,植物会合成和积累某些小分子物质、碳水化合物和特殊的蛋白质;在极度脱水状态下,多组分参与的玻璃化的形成和两性物质的重新分配、耐干性植物中特有的抗氧化机制都是植物获得耐干性的重要条件。复苏植物(resurrection plant)和部分被子植物种子是当前研究植物耐干性的模式材料。     

栎金钱菌活性提取物抗衰老研究

用栎金钱菌活性提取物灌胃衰老模型小鼠,观察其对小鼠血清SOD活性、肝组织MDA和脂褐素的含量、脾指数、胸腺指数和肾指数的影响。结果表明,栎金钱菌活性提取物能使雄性小鼠血清SOD活性提高40.16%,肝MDA含量减少47.12%,肝脂褐素含量减少89.48%,脾指数增加35.13%,胸腺指数增加48.92%,肾指数增加11.26%,表明栎金钱菌活性提取物具有良好的抗衰老作用。栎金钱菌活性提取物800mg/kg·d的剂量具有最好的抗衰老效果,且具有性别的差异,对雄性小鼠的抗衰老作用略优于对雌性小鼠的。     

New therapy with XLQ® to suppress chronic prostatitis through its anti-inflammatory and antioxidative activities

Chronic prostatitis is a common urological disease. The etiology of this disease and effective therapy for its treatment are yet to be elucidated. We investigated the functions of XLQ^® in chronic nonbacterial prostatitis using a complete Freund's adjuvant-induced rat model. Prostates and blood samples were collected for further evaluation after oral gavage with XLQ ^® or a vehicle for 4 weeks. The results showed that XLQ ^® significantly decreased the prostate index, ameliorated the histopathologic changes, and reduced CD3+ and CD45+ cell infiltration in the prostate stroma. Further study showed that XLQ ^® suppressed the expression of proinflammatory cytokines, such as interleukin (IL)-1β, IL-2, IL-6, IL-17A, monocyte chemoattractant protein-1, and tumor necrosis factor-α. XLQ ^® showed a strong antioxidant capacity by enhancing the activities of antioxidative enzymes (e.g., total superoxide dismutase, catalase, and glutathione peroxidase) and decreasing the level of lipid peroxidation products (malondialdehyde). Moreover, XLQ ^® can suppress the activation of nuclear factor-κB and P38-mitogen-activated protein kinase signaling pathways. In summary, XLQ ^® has affirmative effects on chronic prostatitis, which could be attributed to its anti-inflammatory and antioxidative capacities. On the basis of these results, XLQ ^® can be developed as an effective and safe therapy for chronic prostatitis.     

Scutellarin exerts protective effects against atherosclerosis in rats by regulating the Hippo–FOXO3A and PI3K/AKT signaling pathways

Atherosclerosis (AS), a progressive disorder, is one of the tough challenges in the clinic. Scutellarin, an extract from Herba Erigerontis, is found to have oxygen-free radicals scavenging effects and antioxidant effects. In this study, we aimed to investigate the anti-AS effects of scutellarin is related to controlling the Hippo–FOXO3A and PI3K/AKT signal pathway. To establish an AS model, the rats in the scutellarin and model groups were intraperitoneally injected with vitamin D ₃ and then fed a high-fat diet for 12 weeks. In addition, in vitro angiotensin II-induced apoptosis of human aortic endothelial cells (HAECs) were used to establish models. Scutellarin significantly reduced blood lipid levels and increased antioxidase levels in both models. Additionally, scutellarin inhibited reactive oxygen species generation and apoptosis in HAECs. The impaired vascular barrier function was restored by using scutellarin in AS rats and in HAECs cells characterized by inhibiting mammalian sterile-20-like kinases 1 (Mst1) phosphorylation, Yes-associated protein (YAP) phosphorylation, forkhead box O3A (FOXO3A) phosphorylation at serine 207, nuclear translocation of FOXO3A, and upregulating protein expression of AKT and FOXO3A phosphorylation at serine 253. Scutellarin significantly reduced Bcl-2 interacting mediator of cell death (Bim), caspase-3, APO-1, CD95 (Fas), and Bax: Bcl-2-associated X (Bax) levels and activated Bcl-2: B-cell lymphoma-2 (Bcl-2). Scutellarin also significantly inhibited the expression of Mst1, YAP, FOXO3A at the messenger RNA level. When Mst1 was overexpressed or phosphoinositide 3-kinases suppressed, the effects of scutellarin were significantly blocked. In conclusion, the results of the present study suggest that scutellarin exerts protective effects against AS by inhibiting endothelial cell injury and apoptosis by regulating the Hippo–FOXO3A and PI3K/AKT signal pathways.