河北省农药可追溯管理的调查思考

本文对河北省农药可追溯管理现状进行了介绍和分析,介绍了河北省农药可追溯管理的形式,分析了目前存在的问题,并对下一步如何深入做好农药的可追溯管理提出了建议。     

二氯喹啉酸降解菌嗜麦芽寡养单胞菌菌株J03生长特性及其对烟草和水稻的安全性

二氯喹啉酸被广泛用于稻田除草,其残留易对后茬作物烟草的生长造成危害。本课题组前期从福建烟区植烟土壤中分离获得的嗜麦芽寡养单胞菌Stenotrophomonas maltophilia菌株J03对烟草二氯喹啉酸药害具有较好修复作用。为明确该菌株生长特性及其对烟草和水稻的安全性,本研究测定了J03菌株对烟草和水稻种子萌发及幼苗生长的影响,同时测定了环境因子温度和酸碱度对J03菌株生长的影响。结果表明:经J03菌株处理的烟草和水稻种子,发芽率分别大于80%和95%,与空白对照无显著差异。J03菌株处理的烟苗株高、叶片数和地上部鲜重分别为2.82 cm、6.4片和6.08 g,均显著高于空白对照,其他生长参数与对照无显著差异;J03菌株处理的水稻幼苗的株高和叶面积与空白对照相比均无显著差异。J03菌株在4~40℃内均可生长,但最适生长温度为30~37℃;在pH值为5.0~9.0的LB培养基中均可生长,但最适生长pH值为6.0~8.0。综合研究表明,嗜麦芽寡养单胞菌菌株J03对烟草和水稻生长安全,且其在田间的适合度较高。     

燕麦β-葡聚糖降血糖性能研究进展

本文从三个方面综述了燕麦β-葡聚糖降血糖性能研究进展。首先从食品血糖生成指数(glycemic index,GI)、餐后血糖、空腹血糖和α-淀粉酶活性等方面阐述了燕麦β-葡聚糖降血糖的功效,进而介绍了燕麦β-葡聚糖的结构因素——分子量和含量,以及食品加工过程对其降血糖功效的影响,最后综述了燕麦β-葡聚糖几种可能的降血糖机制,以期对后续研究提供参考。     

Effects of calpain-2 and autophagy-related protein 5 on hepatocyte apoptosis induced by endoplasmic reticulum stress

AIMTo investigate the effects of calpain-2 and autophagy-related protein 5 (Atg5) on apoptosis of BRL-3A rat normal liver cells during endoplasmic reticulum stress (ERS) induced by dithiothreitol (DTT). METH?ODS: BRL-3A cells were treated with DTT at 2.0 mmol/L for 0, 6, 12 and 24 h to induce ERS. Real-time cell analysis (RTCA) was used to measure the effect of DTT on BRL-3A cell proliferation. Apoptosis and cell cycle distribution were analyzed by flow cytometry. The mRNA expression of calpain-2 and Atg5 was detected by real-time PCR. The protein levels of calpain-2, Atg5, Atg7, Atg12 and microtubule-associated protein 1 light chain 3 (LC3) were determined by Western blot. The interaction between calpain-2 and Atg5 was investigated by co-immunoprecipitation (Co-IP). RESULTSThe proliferation of BRL-3A cells treated with DTT was significantly inhibited. The apoptosis of BRL-3A cells was significantly increased after DTT treatment for 6, 12 and 24 h as compared with 0 h group (P<0.05). The cell cycle was arrested in G₁ phase after DTT treatment (P<0.05). After DTT treatment for 6, 12 and 24 h, the mRNA expression of calpain-2 and Atg5 in the BRL-3A cells was significantly increased as compared with 0 h group (P<0.05). The protein levels of calpain-2, Atg12 and Atg7 in the cells treated with DTT for 6, 12 and 24 h were significantly higher than those in 0 h group, and the ratio of LC3-II/LC3-I was also significantly higher than that in 0 h group, while Atg5 expression was significantly lower than that in 0 h group (P<0.05). The results of Co-IP found that the anti-calpain-2 antibody precipitated Atg5 protein from the cell lysates, and the anti-Atg5 antibody also precipitated calpain-2 from the cell lysates, which confirmed the interaction between calpain-2 and Atg5. CONCLUSION Calpain-2 may participate in ERS-induced hepatocyte apoptosis by interacting with Atg5.     

Sulodexide protects against hyperglycemia-induced retinal vascular injury via suppressing NOX4/NLRP3 pathway

AIM To investigate the effect of sulodexide (SDX) on high glucose-induced damage in retinal microvascular endothelial cells. METHODS (1) High-fat diet combined with intraperitoneal injection of streptozocin were used to induce type 2 diabetes mellitus (DM) followed by injection of saline or SDX in C57BL/6J male mice. Retinal microvascular leakage and density, and the protein levels of NLRP3 inflammasome-related proteins, zonula occludens-1 (ZO-1) and NADPH oxidase 4 (NOX4) were measured. (2) Human retinal microvascular endothelial cells (HRMECs) were treated with normal glucose or high glucose with or without SDX, and were further transfected with siRNA to knock down NOX4, or infected by adenovirus to over-express NOX4. The protein levels of ZO-1, VE-cadherin (VE-Cad), NOX4 and NLRP3 inflammasome-related proteins as well as the level of reactive oxygen species (ROS) were detected. RESULTS Treatment with SDX increased the protein level of ZO-1, attenuated retinal leakage and NLRP3 inflammasome activation, and enhanced the density of microvasculature and the number of ganglion cells in diabetic retinas. The protein levels of ZO-1 and VE-Cad were decreased, while the levels of NOX4, NLRP3 inflammasome-related proteins and ROS generation were increased in high glucose-treated HRMECs. Silencing of NOX4 inhibited high glucose-induced increases in NLRP3 inflammasome and ROS generation, and decreases in the protein levels of ZO-1 and VE-Cad. Over-expression of NOX4 significantly increased the levels of NLRP3 inflammasome-related proteins and ROS generation in HRMECs, and reduced the protein levels of ZO-1 and VE-Cad. Treatment with SDX partly reversed NOX4 over-expression-induced changes. CONCLUSION SDX alleviates hyperglycemia-induced retinal microvascular endothelial injury via inhibiting NOX4/ROS/NLRP3 pathways.     

Mechanism of elemene enhancing radiosensitivity of human glioma U251 cells

AIM To investigate the effect of elemene on the radiosensitivity of human glioma U251 cells and its mechanism. METHODS The U251 cells were used as a glioma model in vitro, and were exposed to different concentrations of elemene and different doses of radiation. The cell viability was measured by MTT assay, the apoptosis and cell cycle distribution were analyzed by flow cytometry, and the related protein levels were determined by Western blot. RESULTS Elemene inhibited the viability of U251 cells in vitro and enhanced the radiosensitivity of the cells. The cells in radiotherapy combined with elemene group had higher rates of early apoptosis, secondary necrosis and total cell death than those in radiation group. Elemene induced G₂/M phase arrest in the U251 cells. Elemene reduced the protein expression of cell division cycle protein 2 （Cdc2）, which resulted in the decrease in cyclin B1 expression induced by radiotherapy, thereby inhibiting the formation of cyclin B-Cdc2 complex. Elemene reduced Cdc2 activity by inhibiting the phosphorylation of Cdc2 protein at threonine 161, thereby inducing G₂/M phase arrest in the cells. It also mediated apoptosis by down-regulating survivin expression. CONCLUSION Elemene may increase the sensitivity of U251 cells to radiotherapy by down-regulating Cdc2 protein, decreasing cyclin B1 expression, inhibiting the formation of cylcin B-Cdc2 complex and down-regulating the expression of survivin.     

CD36/Src/ERK pathway is involved in process of monocyte differentiation into macrophages

AIM To investigate the role of fatty acid translocase (FAT/CD36) on differentiation of monocytes to macrophages. METHODS Human monocyte THP-1 cells were treated with phorbol 12-myristate 13-acetate (PMA) at 0, 100 and 200 μg /L. Small interfering RNA (siRNA) targeting CD36 (siCD36) was employed to knock down the expression of CD36 in THP-1 cells. The CD36 over-expression (CD36OE) cell line was constructed by transfection with a recombinant lentivirus containing CD36 cDNA. Optical microscopy and crystal violet staining were used to detect the monocyte morphological changes and adhesion ability. The protein expression of CD36 was measured by flow cytometry and Western blot. The mRNA levels of CD36, CD11b and CD80 were detected by real-time PCR. The protein levels of extracellular signal-regulated kinase (ERK） and Src tyrosine kinase were determined by Western blot. RESULTS The cellular adhesiveness of THP-1 cells was elevated in the process of monocytes differentiation, and the expression of CD36 was increased in this process as well (P<0.01). siCD36 was transfected into the THP-1 cells (CD36i group) and the silencing efficiency was approximately 80%. The cell surface area and cellular adhesiveness were significantly decreased in CD36i group compared with scrambled siRNA (NCi) group (P<0.01). The mRNA levels of CD11b and CD80 were decreased in CD36i group compared with NCi group (P<0.01). The cell surface area and cellular adhesiveness were increased in CD36OE group compared with empty vector (vector) group (P<0.05). The mRNA levels of CD11b and CD80 were increased in CD36OE group compared with vector group (P<0.01). The phosphorylation levels of ERK and Src were decreased in CD36i group compared with NCi group (P<0.05). CONCLUSION CD36 promotes the differentiation of human monocyte THP-1 cells to macrophages by increasing the phosphorylation of Src and further activating ERK.     

硅藻土对5种储粮害虫和不同磷化氢抗性水平杂拟谷盗防治效果的研究

为初步了解硅藻土对储粮害虫的防治效果以及与害虫磷化氢抗性发生发展的关系, 本研究采用直接拌粮法(设置剂量梯度为0?0.2?0.4?0.6 g/kg和 0.8 g/kg)测定硅藻土对赤拟谷盗?杂拟谷盗?锈赤扁谷盗?谷蠹?玉米象的防治效果, 以及磷化氢抗性杂拟谷盗(抗性倍数为 2.3~144.7)对硅藻土的敏感性差异; 除此之外, 本研究还分析了0.4 g/kg硅藻土在 4 种粮食(小麦?玉米?大豆?稻谷)中对赤拟谷盗的杀虫效果?研究结果表明:一定剂量(0.2~0.8 g/kg)的硅藻土均能够在一定时间内有效杀死上述 5种储粮害虫, 不同储粮害虫对硅藻土的敏感性存在显著差异(P<0.05), 其中杂拟谷盗对硅藻土的耐受性最强, 玉米象对硅藻土最为敏感?除个别品系外, 不同磷化氢抗性品系的杂拟谷盗对硅藻土的敏感性不存在显著差异(P>0.05), 且与磷化氢抗性无关; 硅藻土在不同粮食中对害虫的作用效果存在显著性差异(P<0.05)(处理 7 d后, 死亡率为 13%~98%), 其中在大豆中对赤拟谷盗的杀虫效果最强, 在玉米中对其作用效果不明显?因此本研究得出结论:硅藻土对主要储粮害虫均具有一定的防治作用, 且对抗磷化氢的杂拟谷盗具有良好的致死效果?因此, 硅藻土具备成为储粮害虫防治及其磷化氢抗性治理药剂的潜力?     

基于主成分分析法的鸡汤与不同鸡肉酶解液中游离氨基酸的对比分析

为获得与鸡汤中组成成分差异性最小、风味类似的鸡肉蛋白酶解液,并为鸡肉香精制作提供理论依据和参考,选用6种蛋白酶(动物蛋白酶、复合蛋白酶、木瓜蛋白酶、碱性蛋白酶、风味蛋白酶和中性蛋白酶)对鸡肉进行酶解,检测鸡汤与不同鸡肉酶解液的组成成分与相对含量,分析17种游离氨基酸的呈味特性,并通过主成分分析法(principal component analysis, PCA)对比分析鸡汤与鸡肉酶解液中游离氨基酸组成的相似性与差异性。结果表明,动物蛋白酶对鸡肉酶解效果最好,水解度为19.21%;复合蛋白酶其次,水解度为18.52%。对比鸡汤及鸡肉酶解液组成成分发现,鸡汤中检测到33种物质,鸡肉酶解液中检测到36种物质,同时相对含量有差异。对比鸡汤与鸡肉酶解液中呈味氨基酸发现,复合蛋白酶酶解液中鲜味氨基酸与鸡汤中相对含量相近,为10.95%,且谷氨酸与天冬氨酸相对含量与鸡汤相比差异不显著。通过PCA对比发现,复合蛋白酶酶解的鸡肉酶解液中游离氨基酸种类和相对含量与鸡汤差异最小,同时呈味特性类似,具有相似的滋味。     

施肥对春青稞干物质积累、分配及产量的影响

为研究施肥对青稞干物质积累、分配及产量的调节作用,以‘藏青27’、‘QTB13’和‘QTB25’为试验材料,比较分析不同施肥处理下干物质积累、分配及产量的变化规律。结果表明：增加施肥量促进青稞分蘖期—成熟期的干物质积累及开花期和成熟期干物质向营养器官和籽粒的分配,提高了花前营养器官贮藏同化物转运量及对籽粒贡献率,降低了花后同化物输入籽粒量对籽粒贡献率。‘QTB13’和‘QTB25’在F₂条件下,更有利于干物质积累及向营养器官和穗部的分配,花后同化物输入籽粒量最大,产量也最大。‘藏青27’在F₃条件下,更有利于干物质积累及向营养器官和穗部的分配,花后同化物输入籽粒量和对籽粒贡献率最大,产量也最大。说明合理施肥有利于青稞干物质积累分配及产量提高。