Physiological and biochemical changes of females of Piracanjuba,subjected to induced reproduction

The aim of this experiment was to compare the level of fish female stress during induced reproduction with pituitary extract by two different methods, natural and semiextruded. The reproductive efficiency was 62.5% in the seminatural treatment and 100% in the extruded. Obtained egg volume was 5200 ml and 4000 ml, for seminatural and extruded treatments respectively. The mean number of eggs was 46.7 for the seminatural and 52.0 and for the extruded treatment. The percentage of viable eggs was, respectively, 87.2% and 8.17% for the natural treatment and extruded semimethods. Blood samples were collected to quantify cortisol and glucose levels, as well as red cell series and lymphocyte count. Fishes submitted to induction procedures showed elevated cortisol and glucose levels, compared to the control animals. The results for haematocrit, haemoglobin concentration and red blood cell count showed no significant differences among groups. Significant differences found in the number of lymphocytes and monocytes suggest the general adaptation syndrome. Our results suggest the reproductive induction process with extrusion of gametes as a more stressful method than seminatural reproduction process.     

葡萄糖和尿素对新鲜水稻秸秆氨化品质的影响

为研究葡萄糖和尿素对新鲜水稻秸秆氨化品质的影响,采用不同质量分数的葡萄糖(0、4 g/kg)和尿素(0、2、4和6 g/kg)对水稻卓两优141的新鲜秸秆进行氨化处理,常温氨化50 d后开包取样分析各项指标。结果表明:氨化饲料中黄曲霉毒素、伏马毒素、玉米赤酶烯酮含量检测结果符合饲料卫生标准;尿素和葡萄糖的交互作用对氨态氮、可溶性碳水化合物和半纤维素含量有显著作用。随着尿素浓度的增加,各处理的pH值显著升高,氨态氮和粗蛋白(CP)含量显著增加,6 g/kg尿素处理组的中性洗涤纤维(NDF)、酸性洗涤纤维(ADF)、酸性洗涤木质素(ADL)降解效果最好;4 g/kg葡萄糖处理显著降低了秸秆NDF、ADF、ADL和氨态氮含量,显著增加了秸秆可溶性碳水化合物(WSC)和粗蛋白(CP)的含量。综合分析,添加葡萄糖可以提高水稻秸秆的营养价值,4 g/kg葡萄糖+6 g/kg尿素处理组的氨化效果最佳。     

不同金属盐强化乙醇/水预处理对蔗渣酶解效率的影响

预处理过程可以破坏木质纤维素生物质的致密结构、降低生物抗性,是木质纤维素生物质经酶解制备糖基平台化学的重要步骤。该研究以蔗渣为原料,在预处理温度为160 ℃、预处理时间为10 min时,选取0.025 mol/L 的不同金属盐FeCl₃、CrCl₃、AlCl₃、CuCl₂、FeCl₂、ZnCl₂、MnCl₂、MgCl₂、CaCl₂、NaCl、LiCl、Na₂CO₃对蔗渣进行乙醇/水预处理,并对预处理后样品进行酶解,探究不同金属盐强化乙醇/水预处理对蔗渣酶解效率的影响和规律,并进一步通过扫描电镜（scanning electron microscopy, SEM）、X射线衍射（X-ray diffraction, XRD）、傅里叶变换红外光谱（fourier transform infrared spectroscopy, FT-IR）和热重（thermogravimetric, TG）对蔗渣原料和预处理后的固体进行表征,探究金属盐强化乙醇/水预处理后蔗渣表面形貌与结构变化对酶解效率的影响,分析作用机理。结果表明:与原料甘蔗渣相比,不同金属盐强化乙醇/水预处理后样品中葡聚糖的质量分数从45.5%增加到77.2%,预处理后样品酶解48h后的葡萄糖得率也由51.14%增加到最高93.08%。其中,三价金属盐（FeCl₃、CrCl₃和AlCl₃）对蔗渣酶解效率的提升最为显著,这可归因于三价金属盐强化乙醇/水预处理可以更加有效的去除蔗渣中的半纤维素和木质素,增加酶对纤维素的可及性。后续表征分析也表明经过三价金属盐（FeCl₃、CrCl₃和AlCl₃）强化乙醇/水预处理后的样品比经过二价金属盐（CuCl₂、FeCl₂、ZnCl₂、MnCl₂、MgCl₂和CaCl₂）和一价金属盐（NaCl、LiCl和Na₂CO₃）强化乙醇/水预处理表面结构破坏更为彻底,结晶度相对增加最大,木素和半纤维素去除率最多,热稳定性也相对最高。该研究结果将为后续木质纤维素生物质的高效转化与利用提供参考。     

葡萄糖水热过程中焦炭结构演变特性

为了解生物质水热炭化过程中焦炭的形成机制及其理化结构的演变机理,该文以葡萄糖为原料,利用高温高压反应釜,对葡萄糖在水热环境中炭化的反应过程和焦炭的表面物理结构及微观化学组成进行了系统的分析。研究发现,葡萄糖经过水热处理,可以获得富含炭微球的无定形水热焦炭,这些炭微球粒径分布在0.6～7 μm之间,而通过控制水热过程的温度、葡萄糖添加量和停留时间,则可对其收率、形貌、化学组成等理化性质产生重要影响。在220℃,4 h,6 g/100 mL的水热条件下,炭微球粒径最小且均匀,平均粒径约为1.54 μm;在220℃,4 h,12 g/100 mL的水热条件下,焦炭收率最高为38.92%。水热焦炭中含有大量的芳香环结构和含氧官能团,具有很强的亲水性,其表面碳化程度高于内核。水热焦炭的形成主要是一系列脱水、聚合、凝结、芳香化、胶体作用的结果。研究结果为生物质水热法制备炭微球的过程控制提供参考。     

Effects of cage netting colour and density on the skin pigmentation and stress response of Australian snapper Pagrus auratus (Bloch & Schneider, 1801)

The unnaturally dark pigmentation of cultured Australian snapper Pagrus auratus can be improved through dietary astaxanthin supplementation and by holding fish in tanks with a white background. The practical application of these laboratory‐based findings was examined with two experiments to establish if the advantages of transferring fish to light coloured tanks before harvest could be achieved on‐farm using white cages and to determine the effects of fish density on skin colour. For the first experiment, snapper (mean TL=29.7 cm) were transferred from a commercial snapper sea cage to black or white netted cages and fed diets supplemented with unesterified astaxanthin (supplied as Lucantin^® Pink, BASF) at 0 or 39 mg kg^?1 for 42 days. Skin colour was measured using the CIE (black–white), (green–red), (blue–yellow) colour scale. Snapper held in white netting cages became significantly lighter (higher ) than snapper held in black cages; however, values were not as high as previous laboratory‐based studies in which snapper were held in white plastic‐lined cages. Snapper fed astaxanthin displayed significantly greater and values, and total carotenoid concentrations after 42 days. In addition, total carotenoids were higher in fish from black than white cages. The second experiment was designed to investigate whether density reduced the improvements in skin colour achieved by holding fish in white coloured cages and whether cage colour affected stress. Snapper (mean weight=435 g) were acclimated to black cages and fed 39 mg kg^?1 astaxanthin for 44 days before transferring to black or white plastic‐lined cages at 14 (low), 29 (mid) or 45 (high) kg m^?3 for 7 days after which time skin colour, plasma cortisol and plasma glucose concentrations were measured. Skin lightness () was greater in snapper transferred to white plastic‐lined cages with the lightest coloured fish obtained from the lowest density after 7 days. Density had no effect on plasma cortisol or glucose levels after 7 days, although plasma cortisol was elevated in snapper from black cages. For improved skin colouration we recommend feeding unesterified astaxanthin at 39 mg kg^?1 for approximately 6 weeks and transferring snapper to white plastic‐lined cages or similar at low densities for short periods before harvest rather than producing fish in white netting sea cages subject to biofouling.     

Mechanism of quercetin improving rat coronary artery myogenic response under high glucose

AIM: To investigate the mechanism of quercetin improving rat coronary artery myogenic response under high glucose (HG) by measuring muscle tension of coronary arterial ring and recording voltage-gated K⁺ channel (Kv) current of coronary artery smooth muscle cells by whole cell patch clamp. METHODS: The coronary rings from the normal SD rats were acutely isolated, and then divided into 6 groups: (1) control group; (2) HG group; (3) HG+low dose (3 μmol/L) of quercetin group; (4) HG+moderate dose (10 μmol/L) of quercetin group; (5) HG+high dose (30 μmol/L) of quercetin group; (6) HG+C6303 (PKC inhibitor)+high dose of quercetin group. Determinations of coronary artery response to vasoconstrictor (60 mmol/L KCl or 0.1 mmol/L U46619) or vasodilator (ACh at 10^-9~10^-5 mol/L) were performed, and the percentage of coronary ring tension was calculated using the contraction as 100% caused by 60 mmol/L KCl. The rat coronary artery smooth muscle cells were acutely isolated for recording the Kv current using whole cell patch clamp. RESULTS: Compared with control group, the contraction amplitudes to 60 mmol/L KCl or 0.1 mmol/L U46619 were significantly increased under HG incubation. Quercetin intervention concentration-dependently reduced the coronary artery contraction amplitude. Incubation of PKC specific inhibitor C6303 attenuated the effect of quercetin. Compared with control group, the diastolic amplitude to ACh decreased significantly in HG group, and quercetin intervention concentration-dependently increased the coronary artery diastolic amplitude. Incubation of PKC specific inhibitor C6303 attenuated the effect of quercetin. Compared with control group, HG incubation inhibited Kv current of coronary artery vascular smooth muscle cells significantly, and quercetin intervention attenuated the inhibitory effect of HG on Kv current intensity. Incubation of PKC specific inhibitor C6303 attenuated the effect of quercetin. CONCLUSION: Quercetin has a protective effect on myogenic response of coronary artery under HG and the effects is related to the increase in Kv current and the activation of PKC in vascular smooth muscle cells.     

黄绿木霉菌诱变菌株的初步研究

通过对木霉的孢悬液进行紫外线和亚硝酸钠复合诱变，经刚果红培养基鉴定筛得5株突变菌株。利用液体培养发酵，对各菌株的CMC酶活测定发现，其中Ⅱ号：Ⅲ号突变菌株的CMC酶活分别比原菌株提高了150％和65％，并均具有很好的抗葡萄糖阻遏效应。     

ROCK promotes high glucose-induced cardiomyocyte apoptosis by inhi-biting PI3K/Akt signaling pathway

AIMTo investigate whether Rho-associated coiled-coil kinase (ROCK) is involved in high glucose-induced apoptosis of primary cardiomyocytes by regulating PI3K/Akt signaling pathway. METHODSPrimary Wistar rat cardiomyocytes were cultured and identified by α-sarcomeric actin (α-SCA) immunohistochemistry. Cardiomyocytes were treated with 5.5, 33 and 40 mmol/L glucose for 48 h. The cell viability was measured by MTT assay, and the mRNA expression of ROCK1 and ROCK2 in the cardiomyocytes was detected by RT-qPCR. Flow cytometry was used to analyze the apoptosis of the cardiomyocytes. The protein levels of ROCK1, ROCK2, cleaved caspase-3, Bcl-2, PI3K, Akt and p-Akt were determined by Western blot. In order to confirm the regulatory effect of ROCKs on PI3K/Akt signaling pathway, the cells were divided into control group (5.5 mmol/L glucose), high glucose group (33 mmol/L glucose) and high glucose+Y27632 (ROCK inhibitor) group. Western blot was used to detect the protein levels of ROCK1, ROCK2, PI3K, Akt and p-Akt. RESULTSAfter 48 h of high glucose exposure, the values of relative cell viability in 33 and 40 mmol/L glucose groups were (79.71±2.43)% and (68.41±7.49)%, respectively, both of which were significantly decreased compared with normal control group (P<0.05). After 48 h of high glucose exposure, the relative mRNA levels of ROCK1 and ROCK2 in 33 and 40 mmol/L glucose groups were significantly increased compared with normal control group (P<0.05). Compared with normal control group, the apoptotic rate in 33 and 40 mmol/L glucose groups was increased significantly (P<0.05). Compared with normal control group, the protein expression of ROCK1, ROCK2 and cleaved caspase-3 in 33 and 40 mmol/L glucose groups was increased (P<0.05), while the protein expression of Bcl-2 was decreased (P<0.05). No significant difference in the protein levels of PI3K and Akt among the 3 groups was observed, while the protein level of p-Akt in 33 and 40 mmol/L glucose groups was decreased compared with normal control group (P<0.05). Compared with high glucose group, the expression of ROCK1 and ROCK2 was decreased in high glucose+Y27632 group. No significant difference in the protein levels of PI3K and Akt among the 3 groups was observed. Compared with normal control group, the protein level of p-Akt in high glucose group was decreased, and the protein level of p-Akt in high glucose+Y27632 group was increased significantly compared with high glucose group. CONCLUSION Under high glucose environment, ROCK may reduce the level of p-Akt by inhibiting the PI3K/Akt signaling pathway, thus promoting the apoptosis of cardiomyocytes.