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991.
Liza Wittenberg-Voges Sabine BR. Kästner Marja Raekallio Outi M. Vainio Karl Rohn Klaus Hopster 《Veterinary anaesthesia and analgesia》2018,45(2):165-174
Objective
To compare the effects of MK-467 during isoflurane anaesthesia combined with xylazine or dexmedetomidine on global and gastrointestinal perfusion parameters.Study design
Prospective, randomized experimental trial.Animals
A total of 15 warmblood horses.Methods
Horses were divided into two groups for administration of either dexmedetomidine (D) or xylazine (X) for premedication (D: 3.5 μg kg?1; X: 0.5 mg kg?1) and as constant rate infusion during isoflurane anaesthesia (D: 7 μg kg?1 hour?1; X: 1 mg kg?1 hour?1). During anaesthesia, heart rate, mean arterial blood pressure (MAP), systemic vascular resistance index (SVRI) and cardiac index (CI) were measured. Microperfusion of the colon, jejunum and stomach was measured using laser Doppler flowmetry. After 2 hours of stabilization, MK-467 (250 μg kg?1) was administered, and measurements were continued for another 90 minutes. For statistical analysis, the permutation test and Wilcoxon rank-sum test were used (p < 0.05).Results
There were no differences in baseline measurements between groups. The MK-467 bolus resulted in a significant decrease in MAP (D: –58%; X: –48%) and SVRI (D: –68%; X: –65%) lasting longer in group D (90 minutes) compared to group X (60 minutes). While CI increased (D: +31%; X: +35%), microperfusion was reduced in the colon (D: –44%; X: –34%), jejunum (D: –26%; X: –33%) and stomach (D: –37%; X: –35%).Conclusions and clinical relevance
Alpha-2-agonist induced vasoconstriction was reversed by the MK-467 dose used, resulting in hypotension and rise in CI. Gastrointestinal microperfusion decreased, probably as a result of insufficient perfusion pressure. An infusion rate for MK-467 as well as an ideal agonist/antagonist ratio should be determined. 相似文献992.
选用1日龄的雌性岭南黄肉鸡99只,随机分为3组,分别为对照组、试验Ⅰ组和试验Ⅱ组,每组33只。对照组常规饲养,试验Ⅰ组和Ⅱ组分别在饮水中添加0.012 mL/L和0.020 mL/L的茶树油,试验至45日龄结束。解剖取十二指肠、空肠、回肠进行HE染色和PAS染色,观察小肠黏膜形态、上皮内淋巴细胞及杯状细胞数目。结果显示,2个试验组与对照组相比,各段小肠的绒毛长度增加,肠壁变薄,隐窝深度变浅,肠绒毛高度/隐窝深度比值增加;2个试验组的上皮内杯状细胞和淋巴细胞的数目高于对照组。结果表明,茶树油能够改善肉鸡小肠黏膜结构,增加小肠上皮内免疫细胞数量,提示茶树油对肉鸡的肠道吸收和肠道免疫功能具有增强作用。 相似文献
993.
凋亡素基因真核表达载体的构建及在人肿瘤细胞中的表达 总被引：2，自引：1，他引：2
为探讨凋亡素对肿瘤的基因治疗效果,构建了凋亡素基因的真核表达载体。将凋亡素基因重组入 ｐｃ Ｄ Ｎ Ａ３ 载体,并通过脂质体介导凋亡素在人喉癌、人肺癌细胞系中表达;通过 Ｒ Ｔ Ｐ Ｃ Ｒ 在转染细胞中检测到了凋亡素的 ｍ Ｒ Ｎ Ａ,这为应用凋亡素进行肿瘤的基因治疗奠定了基础。 相似文献
994.
ZHENG Hao-long SONG Nan CAO Hui-min CHEN Si WANG Jie Lü Xiao-ming JIA Lian-qun 《园艺学报》2020,36(4):713-718
AIM To investigate the effects of different components of Gynostemma pentaphyllum ［gypenosides (Gps), gypenoside XLIX (GpXLIX) and ginsenoside Rb3 (GRb3)］ on mitochondrial energy metabolism-related proteins in endothelial cells induced by oxidized low-density lipoprotein (ox-LDL). METHODS EA.hy926 cells were divided into control group, model group, Gps group, GpXLIX group and GRb3 group. The cells in control group were cultured only in DMEM complete medium. The cells in model group were treated with 100 mg/L ox-LDL for 48 h. The cells in Gps group, GpXLIX group and GRb3 group were treated with 100 mg/L ox-LDL for 24 h, and then treated with Gps, GpXLIX and GRb3 at 100 mg/L for another 24 h, respectively. The ATP content in each group was detected by ELISA. The expression levels of mitochondrial energy metabolism-related proteins, cytochrome C oxidase subunit 5a （Cox5a）, NADH:ubiquinone oxidoreductase core subunit S1 （Ndufs1）, ATP synthase F1 subunit alpha (ATP5a) and cytochrome C (Cyt C）, were determined by Wes automatic Western blot quantitative analysis system and Western blot. RESULTS Compared with control group, the ATP content in model group was decreased (P <0.01). After drug intervention, the ATP content increased to different degrees in Gps group, GpXLIX group and GRb3 group (P <0.01). The results of Wes automatic Western blot quantitative analysis system were consistent with those of Western blot. These results showed that compared with control group, the protein expression of Cox5a, Ndufs1 and ATP5a in model group was decreased, and the protein expression of Cyt C was increased (P <0.01). After intervention, the protein expression of Cox5a, Ndufs1 and ATP5a was increased and the protein expression of Cyt C was decreased in Gps group, GpXLIX group and GRb3 group (P <0.05 or P <0.01). Among them, the effect of Gps on the protein expression of Cox5a, Ndufs1 and Cyt C was significantly stronger than those of the 2 monomer components, and the effect of GRb3 was found to be superior in the 2 monomer components. The effect of GpXLIX on ATP5a protein was superior to the other 2 components. CONCLUSION Gynostemma total saponins and related active ingredients protect ox-LDL-induced endothelial cells by affecting mitochondrial energy metabolism-related proteins, thereby preventing and treating atherosclerosis. 相似文献
995.
LI Xiang ZHANG Ling JIA Yue LI Zhen ZHAO Yu-jie MA Lan LI Rui-wen LI Li CAO Xiao-lu 《园艺学报》2020,36(4):673-680
996.
AIMTo investigate the role of soluble Klotho protein in THP-1-derived foam cell formation. METHODSTHP-1 monocytes were induced into macrophages by treatment with 160 nmol/L phorbol myristate acetate for 48 h, and then were divided into 6 groups: negative control group (THP-1-derived macrophages), positive control group [THP-1-derived foam cells induced by oxidized low-density lipoprotein (ox-LDL) for 48 h], and 25, 50, 100 and 200 μg/L soluble Klotho protein groups (THP-1-derived macrophages pretreated with soluble Klotho protein at the indicat?ed concentraions for 2 h and then induced by ox-LDL for 48 h). Lipid droplets in cytoplasm were observed by oil red O staining. The cholesterol outflow rate was detected by scintillation counting technique. The content of intracellular total cholesterol, free cholesterol and cholesterol ester was detected by enzyme fluorescence analysis. The expression of acyl-coenzyme A:cholesterol acyltransferase 1 （ACAT1） and ATP-binding cassette transport?er A1 (ABCA1) at mRNA and protein levels was determined by RT-qPCR and Western blot, respectively. RESULTSOil red O staining and lipid mass quantification showed that THP-1-derived foam cell formation was dose-dependently suppressed by soluble Klotho protein. The cholesterol efflux rate of THP-1-derived foam cells was increased by soluble Klotho protein in a dose-dependent manner (P <0.05). In addition, soluble Klotho protein decreased the expression of ACAT1 and increased the expression of ABCA1 in a dose-dependent manner (P <0.05). CONCLUSION The soluble Klotho protein inhibits THP-1-derived foam cell formation in a dose-dependent manner by down-regulating the expression of ACAT1 and up-regulating the expression of ABCA1. 相似文献
997.
试验旨在探索奶牛对气候变化较为敏感的血液常规指标,为荷斯坦奶牛低温应激研究提供相关数据支撑及科学依据,并对该地区冬季奶牛饲养管理及耐应激个体选育提供理论依据。以河北省承德市围场县某规模化奶牛场的健康荷斯坦泌乳奶牛为研究对象,连续监测了秋季（2018年10月24日至2018年10月30日）、初冬（2018年12月4日至2018年12月10日）和深冬（2018年12月25日至2018年12月31日）牛舍温湿指数（THI）,并分别采集了15头荷斯坦奶牛血液样本,测定了9种血液常规指标,同时收集了试验牛群的8项产奶性能数据,分析荷斯坦奶牛在秋冬季节产奶性能及血液常规指标的变化规律,筛选气候变化较为敏感的血液常规指标。结果显示：秋季,牛舍平均温度为8.0 ℃,平均THI为49.38,说明试验牛群在该时期处于非低温应激状态;初冬,牛舍平均温度为－6.4 ℃,平均THI达到23.56,在168 h监测期,有92 h －8≤THI < 25,76 h 25≤THI < 39,试验牛群在该时期大部分时间处于中度低温应激状态;深冬,牛舍平均温度为－7.59 ℃,平均THI达到21.86,有43 h 25≤THI < 39,117 h 8≤THI < 25,试验牛群在该时期绝大部分时间处于中度低温应激状态。随着温度下降,奶牛直肠温度、呼吸频率显著降低（P < 0.05）;冬季奶牛血中白细胞计数（WBC）、红细胞计数（RBC）、血红蛋白（HGB）、红细胞压积（HCT）、血小板总数（PLT）、血小板压积（PCT）、单核细胞数（MO）、淋巴细胞数（LY）极显著或显著升高（P < 0.01;P < 0.05）;除红细胞压积（HCT）、白细胞计数外,其他各指标在初冬与深冬间差异不显著（P > 0.05）;红细胞平均体积（MCV）在各季节间变化不显著（P > 0.05）;与秋季相比,初冬、深冬奶牛平均日产奶量（AMY）分别下降0.71和1.17 kg/d（P < 0.01）;初冬乳脂率（FP）、乳蛋白率（PP）、脂蛋比（F/P）显著或极显著下降（P < 0.05;P<0.01）,深冬时期恢复至秋季水平（P > 0.05）;乳中非脂肪固体物质率（SP）在初冬显著下降,在深冬显著上升（P < 0.05）;初冬、深冬乳中体细胞数（SCC）分别比秋季高1.84×105、1.63×105 个/mL（P < 0.05）;乳糖率（LP）及酸度在各时期均无显著差异（P > 0.05）。综合以上结果,冀北寒区荷斯坦奶牛在秋季处于非应激状态,在初冬和深冬处于中度低温应激状态,且牛群的生理指标和产奶性能受气候影响较为严重;奶牛血液红细胞、白细胞、淋巴细胞和单核细胞数为受气候影响变化较为灵敏的血液常规指标。 相似文献
999.
WEN Ren-hui KE Shi-ye SHI Guang-yao LIU Ding-hui YU Xian-guan LING Ye-sheng ZHU Jie-ming QIAN Xiao-xian 《园艺学报》2020,36(2):193-199
AIM: To investigate whether endoplasmic reticulum stress is involved in trimethylamine N -oxide (TMAO)-mediated oxidative stress in human umbilical vein endothelial cells (HUVECs). METHODS: The cell viability was examined by CCK-8 assay. The cells were stained by DCFH-DA, and the intracellular level of reactive oxygen species (ROS) was observed by phase-contrast microscopy and detected by flow cytometric analysis. The protein levels of phospho-IRE-1α, IRE-1α and GRP78/BiP were detected by Western blot. RESULTS: TMAO exerted no significant effect on the viability of HUVECs. For a long period (>24 h), even a low concentration (10 μmol/L) of TMAO increased the oxidative stress level in the HUVECs (P <0.05). TMAO increased the phosphorylation level of IRE-1α and significantly up-regulated the protein level of GRP78/BiP in HUVECs (P <0.01). Pretreatment with STF-083010, an inhibitor of IRE1α, for 1 h reduced TMAO-induced oxidative stress in HUVECs (P <0.05). CONCLUSION: Endoplasmic reticulum stress is involved in TMAO-induced oxidative stress in HUVECs. 相似文献
1000.
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. 相似文献