Comparison of effects of dietary‐specific fatty acids on growth and lipid metabolism in Nile tilapia

The dominant fatty acids (FAs) in oils are often used to explain different nutritional effects of dietary oils in fish. However, the amounts of dominant FAs among oils are different, and the nutritional roles of these important FAs in fish have not been precisely compared at similar levels in feeding trials. In the present study, different amounts of palmitic acid were added to safflower oil (SO), olive oil (OO) and fish oil (FO) to obtain comparable amounts (about 550 g/kg of total FAs) of 18:2n‐6, 18:1n‐9 and 20:5n‐3 + 22:6n‐3 and subsequently fed to Nile tilapia (11.1 ± 0.01 g) for 8 weeks. The results showed similar growth among groups but FO group obtained lower fat deposition, serum ALT and AST activities, compared to OO. Lipogenesis‐related gene expressions were higher in OO group than FO group in liver, muscle and adipose tissue, but there were only few differences in these genes between SO and FO groups. Lipid catabolism genes in FO group were higher than OO and SO groups in adipose tissue, but not in muscle, and the significantly higher expressions of CPT1b and PPARα were only observed in liver. Overall, dietary 18:2n‐6, 20:5n‐3 and 22:6n‐3 were beneficial to normal growth and lipid metabolism, whereas high amount of 18:1n‐9 induced lipid deposition and liver damage in Nile tilapia.     

花生硬脂酰-ACP酸脱饱和基因FAB2表达的分子机制

FAB2位于油酸合成通路的上游,编码硬脂酰-ACP脱饱和酶,调控硬脂酸(C18:0)向油酸(C18:1)转化。本研究发现高油酸品种开农176种子发育前期FAB2的表达量升高,而成熟期油酸过量积累会抑制FAB2的表达。利用开农176与开农70构建F2杂交群体,发现当植株油酸含量超过60%时会从整体水平上抑制FAB2的表达。种子发育前期,油酸不断积累会导致过氧化物酶活性升高,并且活性氧含量随之增加;但是在种子发育后期均降低,该结果与FAB2的表达量变化趋势相同。亚细胞定位结果表明, FAB2与FAD2分别定位于叶绿体与内质网。FAB2编码区序列多态性分析显示,该蛋白序列氮端的氨基酸结构缺失可能会导致硬脂酸含量升高。FAB2启动子序列存在大量AT碱基的富集区域,并且含有光响应、激素调控、转录因子结合的保守顺式元件。本研究发现过量积累的油酸会激活过氧化物酶介导的活性氧信号途径,进而通过细胞核内的未知转录因子调节上游基因FAB2的表达量,该结果不仅拓展了对FAB2的功能认知,也为培育高油酸花生品种提供了相关的理论指导。     

Effects of apelin-13 on oxidative stress induced by high uric acid in adipocytes

AIM: To study the effects of apelin-13 on oxidative stress induced by high uric acid in 3T3-L1 adipocytes and its underlying mechanisms. METHODS: 3T3-L1 adipocytes were stimulated with uric acid at 10 mg/dL for 48 h. Some of the adipocytes were administered with 1 μmol/L apelin-13 in the presence of uric acid at 10 mg/dL. The adipocytes stimulated with 100 μmol/L H₂O₂ were served as positive controls. The intracellular reactive oxygen species (ROS) concentrations were detected by flow cytometry. The biochemical kits were used to measure the activities of superotide dismutase (SOD), glutathione peroxidase (GSH-Px), catalase (CAT) and NADPH oxidase (NOX) activity, and the content of malondialdehyde (MDA) in the cell lysate and the supernatant. The mRNA levels of renin-angiotensin system (RAS) components, including angiotensinogen (AGT), angiotensin-converting enzyrne1 (ACE1), angiotensin II type 1 receptor (AT1R) and AT2R, as well as angiotensin II receptor -like 1 (APJ) were measured by real-time PCR. The concentrations of angiotensin II (AngⅡ) in the cell lysate and the supernatant were measured by ELISA. RESULTS: Adipocytes stimulated with uric acid at 10 mg/dL had lower activities of antioxidant enzymes (SOD, GSH-PX and CAT) and higher levels of NOX activity and MDA content (P < 0.05). Accordingly, the intracellular ROS levels were found to be dramatically increased. However, apelin-13 administration attenuated uric acid-induced oxidative stress in the 3T3-L1 adipocytes. Uric acid at 10 mg/dL upregulated the mRNA expression of local RAS, enhanced AngⅡ concentrations both in the cell lysate and the supernatant, and down-regulated the mRNA level of APJ in the adipocytes (P < 0.05). Conversely, apelin-13 partially reversed these parameters. CONCLUSION: Apelin-13 attenuates oxidative stress induced by uric acid, may be via down-regulation of local RAS expression in the 3T3-L1 adipocytes.     

Analysis of Phytosterol,Fatty Acid,and Carotenoid Composition of 19 Microalgae and 6 Bivalve Species

ABSTRACT

In this study, the functional components of 19 microalgae and 6 bivalve species were investigated in the context of the application in bivalve feeding and human health food. Principal component analysis was performed to detect any association between the functional components and individual microalgal species or taxonomic group. The proportions of the functional components differed depending on the taxonomic group or species of microalga. The genera Cheatoceros, Thalassiosira, and Isochrysis contained high concentrations of fucosterol and fucoxanthin, which are present in large amounts in brown algae. Diatoms, haptophytes, and eustigmatophytes, which are used as feed for bivalves, were rich in fucosterol and eicosapentenoic acid (EPA); further, haptophytes were rich in docosahexaenoic acid (DHA). In addition, the microalgae associated with red tide, i.e., the raphidophytes, were found to be rich in fucoxanthin, β-sitosterol, and EPA, whereas dinoflagellates were rich in DHA. Seven bivalve species also contained high concentrations of fucosterol, EPA, and DHA, as did microalgae, which were used to feed by bivalves. These results are useful in selecting microalgae effectively as feed of the bivalves.     

Evaluation of cytokines and sialic acids contents in horses naturally infected with Theileria equi

This study was undertaken to assess the effects of T. equi infection on serum concentrations of some important cytokines including interferon-γ (IFN-γ), tumor necrosis factor-α (TNF-α), and interleukin-1 beta (IL-1β), IL-1α, IL-4, IL-6, IL-8, IL-10, IL-12α, IL-12β, IL-18, as well as total, protein and lipid binding sialic acids (TSA, PBSA and LBSA). Furthermore, any probable relation among the parasitemia, cytokines and sialic acids (SAs) were calculated using Pearson correlation and simple linear regression. Almost 300 draft horses (Kurdish-breed) with age of 3–4 years old from north-west of Iran were examined and an infected group comprised of 28 mares, naturally infected with T. equi, was identified and divided into 3 subgroups according to their parasitemia rates (low <1 %, moderate 1–3 % and high 3–5 %). Twenty healthy horses were considered as a control. Characterization and differentiation of piroplasmosis were conducted using routine hematological procedures and specific PCR assay. The results revealed a significant increase (P < 0.05) in all of the cytokines and SAs in a parasitic burden-dependent fashion. Additionally, a strong and positive relation was detected among the parasitemia, cytokines and SAs. Conclusively, T. equi infection is associated with induction of severe inflammatory processes in horses and SA plays a pivotal role in pathophysiology of the disease as it is tightly correlated with the parasitemia rate.     

Role of chlorogenic acid in endothelial dysfunction in db/db mice

AIM: To explore the effects of chlorogenic acid (CGA) on endothelial dysfunction in db/db mice and the possible mechanism. METHODS: Male db/db mice (n=12) were divided into control group and CGA group, with 6 mice in each group. The mice in CGA group were treated with diet containing 0.02% CGA, while the mice in control group were given normal diet only. The observation period was 12 weeks. Fasting blood glucose level, tail blood pressure and the body weight were analyzed each week. At the end of the 12th week, the mice were anesthetized and blood was taken from carotid artery. The plasma levels of heme oxygenase-1 (HO-1), catalase (CAT), NAD(P)H dehydrogenase quinone 1 (NQO1) and glutathione peroxidase-1 (GPx-1) were measured by ELISA. The mouse aortas were isolated, and the superoxide anion and nitric oxide (NO) levels were measured by DHE and DAF-2 DA staining, respectively. Wire Myograph System was used to detect the vasorelaxation of db/db mouse aorta. The protein levels of peroxisome proliferator-activated receptor α (PPARα), nuclear factor E2-related factor 2 (Nrf2), phosphorylated AMP-activated protein kinase (p-AMPK), phosphorylated endothelial NO synthase (p-eNOS), P22^phox and P47^phox were determined by Western blot. RESULTS: Dietary CGA decreased fasting blood glucose and body weight in db/db mice as compared with control group (P<0.01 or P<0.05). The plasma levels of HO-1, CAT, NQO1 and GPx-1 in CGA group were higher than those in control group (P<0.01 or P<0.05). Administration of CGA for 12 weeks attenuated superoxide anion level, increased NO level in the mouse endothelium and improved endothelium-dependent relaxation of the db/db mouse aorta. CGA also increased the protein levels of PPARα, Nrf2, p-AMPK and p-eNOS, and decreased P22^phox and P47^phox levels (P<0.01). CONCLUSION: Dietary CGA improves db/db mouse endothelium-dependent relaxation. This effect may be related to the increases in the levels of antioxidant molecules PPARα, Nrf2 and p-AMPK, and the up-regulation of antioxidant capacity, thus decreasing the oxidative stress, promoting eNOS phosphorylation, and increasing NO level.     

富硒鸡不同部位硒含量及脂肪酸组成研究

本文探讨通过富硒饲料饲养的富硒鸡不同部位中硒含量及脂肪酸组成。分别取富硒饲养鸡不同部位,包括皮、褐色脂肪、白色脂肪、胸肌、腿肌、肌胃、心脏、肾脏、肝脏、蛋;各样本采用微波消解法(MD)消解,然后用电感耦合等离子体质谱法(ICP-MS)检测硒含量。以正己烷抽提样本中脂肪,经三氯化硼-甲醇甲酯化后,采用GC-MS进行脂肪酸组成进行分析。各检测部位中,硒含量依次为:肌胃>白色脂肪>皮>蛋>肾脏>肝脏>腿肌>心脏>褐色脂肪>胸肌。肌胃中硒含量最高为2639.19 ng/g,胸肌中硒含量最低为129.76 ng/g。脂肪酸组成分析结果显示,白色脂肪中饱和脂肪酸含量最高为88.07%,胸肌不饱和脂肪酸含量最高为68.44%。本次检测结果显示富硒饲料在母鸡不同部位硒含量不同,不同部位脂肪酸组成也不相同,本实验结果对富硒鸡中营养成分的利用提供参考。     

断奶对仔猪肠道屏障的影响及营养调控

在集约化养殖中,3~4周龄早期断奶是仔猪生命周期中一个非常紧张的时期,此时仔猪胃肠道还未发育成熟。肠道屏障由上皮、免疫和肠神经系统组成,这些系统控制上皮屏障的完整性以及肠道功能,包括肠腔营养物质、水和电解质的运输。早期断奶导致肠道通透性增加,出现胃肠功能紊乱的情况,可能对猪只一生产生长期的影响。因此,仔猪断奶饲粮需要正确水平的营养素、营养源和高质量的添加剂,鼓励仔猪快速进食,减轻或消除断奶应激综合症,降低死亡率和发病率。养猪就是养"肠道",合理使用功能性氨基酸、植物化学物质和有机酸等添加剂,能够修复由于断奶应激综合症导致的肠道屏障功能障碍。     

油菜高亚麻酸育种探析

为促进通过提高油菜种子亚麻酸含量途径增加中国人群亚麻酸的摄入量,提高健康水平的工作进程。结合文献资料,在剖析开展油菜高亚麻酸育种的意义、可行性、难点及可利用的有利条件的基础上,提出油菜高亚麻酸育种策略与技术途径。在工作实践中,陕西省杂交油菜研究中心研究团队创建并完善"油菜高亚麻酸种质的筛选方法",利用该方法开展油菜高亚麻酸种质资源筛选和高亚麻酸育种取得良好成效:油菜种质资源的整体亚麻酸含量、具有较高亚麻酸含量种质的百分比率、亚麻酸含量最高值、亚麻酸含量15%的种质数量均明显增加;获得一批亚麻酸含量大于15%(最高含量达21%)的甘蓝型油菜非转基因种质,育成高亚麻酸的不育系和恢复系;甘蓝型油菜高亚麻酸杂交种‘秦杂油7号’通过国家品种登记;2个亚麻酸含量15%左右的杂交种正在申请品种登记。发现在A02、C02及A06染色体上存在多个与亚麻酸显著关联SNP位点。提出开展基础机理研究和分子设计育种创新体系建设,开展高亚麻酸种质资源创新、综合评价和利用研究,构建高亚麻酸育种体系,规化高效保优栽培技术路线,开展油菜籽加工技术、抗氧化研究,构建标准体系等6方面建议。