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排序方式: 共有860条查询结果,搜索用时 15 毫秒
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Do Thi Thanh HUONG Vidya JAYASANKAR Safiah JASMANI Hisako SAIDO-SAKANAKA Andrew J. WIGGINTON Marcy N. WILDER 《Fisheries Science》2004,70(3):518-520
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Nadezhda E. Ustyuzhanina Maria I. Bilan Andrey S. Dmitrenok Eugenia A. Tsvetkova Sofya P. Nikogosova Cao Thi Thuy Hang Pham Duc Thinh Dinh Thanh Trung Tran Thi Thanh Van Alexander S. Shashkov Anatolii I. Usov Nikolay E. Nifantiev 《Marine drugs》2022,20(6)
Fucosylated chondroitin sulfates (FCSs) FCS-BA and FCS-HS, as well as fucan sulfates (FSs) FS-BA-AT and FS-HS-AT were isolated from the sea cucumbers Bohadschia argus and Holothuria (Theelothuria) spinifera, respectively. Purification of the polysaccharides was carried out by anion-exchange chromatography on DEAE-Sephacel column. Structural characterization of polysaccharides was performed in terms of monosaccharide and sulfate content, as well as using a series of non-destructive NMR spectroscopic methods. Both FCSs were shown to contain a chondroitin core [→3)-β-d-GalNAc-(1→4)-β-d-GlcA-(1→]n bearing sulfated fucosyl branches at O-3 of every GlcA residue in the chain. These fucosyl residues were different in pattern of sulfation: FCS-BA contained Fuc2S4S, Fuc3S4S and Fuc4S at a ratio of 1:8:2, while FCS-HS contained these residues at a ratio of 2:2:1. Polysaccharides differed also in content of GalNAc4S6S and GalNAc4S units, the ratios being 14:1 for FCS-BA and 4:1 for FCS-HS. Both FCSs demonstrated significant anticoagulant activity in clotting time assay and potentiated inhibition of thrombin, but not of factor Xa. FS-BA-AT was shown to be a regular linear polymer of 4-linked α-L-fucopyranose 3-sulfate, the structure being confirmed by NMR spectra of desulfated polysaccharide. In spite of considerable sulfate content, FS-BA-AT was practically devoid of anticoagulant activity. FS-HS-AT cannot be purified completely from contamination of some FCS. Its structure was tentatively represented as a mixture of chains identical with FS-BA-AT and other chains built up of randomly sulfated alternating 4- and 3-linked α-L-fucopyranose residues. 相似文献
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通过鸡接种不同剂量的SL8132、SL8786、SL8132/pcDNA3s与SL8786/pcDNA3s,测定其致病力与免疫效果,检测了诱导乙肝表面抗体(抗-HBs)的动态变化.结果表明减毒鼠伤寒沙门菌原菌SL8132、SL8786接种后连续观察雏鸡10d,不同剂量组的感染均未引起死亡.接种后7周,肝脏、脾脏中已没有菌落,粪便中仅有极少量的菌落.口服减毒鼠伤寒沙门菌在完成抗原呈递后即被鸡体免疫系统所清除,未发现雏鸡出现明显毒副作用.SL8132/pcDNA3s与SL8786/pcDNA3s疫苗诱导的抗-HBs动态检测发现,抗-HBs在免疫后水平逐渐升高,到第8周最高,此后逐渐下降.原菌SL8132与SL8786与重组菌株SL8132/pcDNA3s与SL8786/pcDNA3s均具有良好的安全性与免疫原性. 相似文献
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高脂日粮对小鼠消化系统自由基水平与物质消化、吸收的影响 总被引:1,自引:0,他引:1
选取6周龄雄性昆明种小鼠40只,按体质量随机分成4组:即对照组(正常日粮),高脂日粮组(粗脂肪含量18%),LA组(高脂日粮+0.05%LA和高脂日粮+0.1%LA).小鼠预饲1周后正式饲喂,饲喂5周后进行代谢试验.6周后测定小鼠消化系统自由基水平和肠道黏膜脂肪酶、蛋白酶和淀粉酶活性.结果表明,长期饲喂高脂日粮可显著提高小鼠消化系统自由基水平(P<0.05),降低肠道淀粉酶和蛋白酶活性(P<0.05),但肠道脂肪酶活性显著提高(P<0.05);小鼠对粗脂肪和粗蛋白消化率降低(P<0.05),蛋白沉积率降低(P<0.05).添加0.05%LA后,能显著降低高脂饲喂小鼠消化系统自由基水平(P<0.05),提高小鼠对粗脂肪、粗蛋白消化率(P<0.05),和蛋白沉积率(P<0.05);添加0.1%LA可使小鼠全血及系统自由基水平恢复到接近正常水平.由此得出:高脂摄入,增加小鼠消化系统自由基生成,降低消化酶活性、降低机体对营养物质的消化吸收.适宜的LA添加可有效清除小鼠消化系统自由基,提高消化酶活性,提高营养物质的利用率,缓解营养性氧化应激. 相似文献
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氮添加对天山高寒草原土壤酶活性和酶化学计量特征的影响 总被引:1,自引:0,他引:1
为探究氮添加对高寒草原生态系统土壤酶活性的影响,于2018年在中国科学院巴音布鲁克草原生态系统研究站,选择4个氮添加水平(对照,N0,0 kg·hm^-2·a^-1;低氮,N1,10 kg·hm^-2·a^-1;中氮,N3,30 kg·hm^-2·a^-1;高氮,N9,90 kg·hm^-2·a^-1),开展土壤酶活性对氮添加响应的研究,分析土壤酶活性对氮添加的响应特点,土壤酶化学计量比以及土壤酶活性与土壤环境因子的关系。结果表明:与对照相比,氮添加在N3水平显著增加β-1,4葡萄糖苷酶(βG)、β-D-纤维二糖水解酶(CBH)和β-1,4木糖苷酶(βX)酶活性(P<0.05),N1和N3水平显著增加碱性磷酸酶(AKP)活性(P<0.05),N3水平显著降低多酚氧化酶(PPO)活性(P<0.05),氮添加对亮氨酸氨基肽酶(LAP)活性影响不显著,N3水平下显著增加N-乙酰-β-D氨基葡萄糖苷酶(NAG)活性(P<0.05)。相关分析表明,8种土壤酶活性均与土壤有机碳(SOC、NAG除外)和总磷(TP)显著相关,与土壤总氮(TN)不相关。研究区土壤酶活性C∶N∶P化学计量比为1∶1∶1.2,与全球生态系统的土壤酶活性C∶N∶P的比值1∶1∶1相偏离,表明该研究区土壤微生物生长受磷素限制。冗余分析(RDA)进一步揭示出土壤有机碳和土壤全磷含量是影响土壤酶活性的主要因子。 相似文献
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Chang‐Hoon Shin Hien Thi Dieu Bui Samad Rahimnejad Ji‐Hoon Cha Byung‐Woo Yoo Bo‐Kyeun Lee Hyung‐Jin Ahn Soo‐Il Choi Yun‐Jeong Choi Yong‐Ho Park Jeong‐Dae Kim Kyeong‐Jun Lee 《Journal of the World Aquaculture Society》2014,45(3):258-268
This study was conducted to evaluate the effects of dietary supplementation of Barodon, an anionic alkali mineral complex, on growth, feed utilization, humoral innate immunity and disease resistance of olive flounder. A basal experimental diet was used as a control and supplemented with 0.1, 0.2, 0.3, 0.4, or 0.5% Barodon. Triplicate groups of fish (26.4 ± 0.2 g) were fed one of the diets to apparent satiation twice daily for 10 wk. The growth performance was enhanced (P < 0.05) linearly and quadratically in fish fed diets containing Barodon compared with that in fish fed the control. Feed utilization was significantly improved by Barodon supplementation. Serum lysozyme and antiprotease activities were increased quadratically in Barodon fed groups. Also, significantly higher superoxide dismutase activity was found in Barodon‐fed fish. Dietary supplementation of 0.1–0.3% Barodon resulted in significant enhancement of fish disease resistance against Streptococcus iniae. The findings in this study indicate that dietary supplementation of Barodon can enhance growth, feed utilization, innate immunity, and disease resistance of olive flounder and that the optimum level seems to be 0.1% in diets. 相似文献
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Kosuke SODA Maya YAMANE Chiharu HIDAKA Kozue MIURA Trang T. H. UNG Hang L. K. NGUYEN Hiroshi ITO Mai Q. LE Toshihiro ITO 《The Journal of veterinary medical science / the Japanese Society of Veterinary Science》2021,83(12):1899
Low and highly pathogenic avian influenza viruses (LPAIVs and HPAIVs, respectively) have been co-circulating in poultry populations in Asian, Middle Eastern, and African countries. In our avian-flu surveillance in Vietnamese domestic ducks, viral genes of LPAIV and HPAIV have been frequently detected in the same individual. To assess the influence of LPAIV on the pathogenicity of H5 HPAIV in domestic ducks, an experimental co-infection study was performed. One-week-old domestic ducks were inoculated intranasally and orally with phosphate-buffered saline (PBS) (control) or 106 EID50 of LPAIVs (A/duck/Vietnam/LBM678/2014 (H6N6) or A/Muscovy duck/Vietnam/LBM694/2014 (H9N2)). Seven days later, these ducks were inoculated with HPAIV (A/Muscovy duck/Vietnam/LBM808/2015 (H5N6)) in the same manner. The respective survival rates were 100% and 50% in ducks pre-infected with LBM694 or LBM678 strains and both higher than the survival of the control group (25%). The virus titers in oral/cloacal swabs of each LPAIV pre-inoculation group were significantly lower at 3–5 days post-HPAIV inoculation. Notably, almost no virus was detected in swabs from surviving individuals of the LBM678 pre-inoculation group. Antigenic cross-reactivity among the viruses was not observed in the neutralization test. These results suggest that pre-infection with LPAIV attenuates the pathogenicity of HPAIV in domestic ducks, which might be explained by innate and/or cell-mediated immunity induced by the initial infection with LPAIV. 相似文献
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