The conserved DNA damage repair complex,MMS21-SMC5/6(Methyl methane sulfonate 21-Structural maintenance of chromosomes 5/6),has been extensively studied in yeast,animals,and plants.However,its role in phytopathogenic ...The conserved DNA damage repair complex,MMS21-SMC5/6(Methyl methane sulfonate 21-Structural maintenance of chromosomes 5/6),has been extensively studied in yeast,animals,and plants.However,its role in phytopathogenic fungi,particularly in the highly destructive rice blast fungus Magnaporthe oryzae,remains unknown.In this study,we functionally characterized the homologues of this complex,MoMMS21 and MoSMC5,in M.oryzae.We first demonstrated the importance of DNA damage repair in M.oryzae by showing that the DNA damage inducer phleomycin inhibited vegetative growth,infection-related development and pathogenicity in this fungus.Additionally,we discovered that MoMMS21 and MoSMC5 interacted in the nuclei,suggesting that they also function as a complex in M.oryzae.Gene deletion experiments revealed that both MoMMS21 and MoSMC5 are required for infection-related development and pathogenicity in M.oryzae,while only MoMMS21 deletion affected growth and sensitivity to phleomycin,indicating its specific involvement in DNA damage repair.Overall,our results provide insights into the roles of MoMMS21 and MoSMC5 in M.oryzae,highlighting their functions beyond DNA damage repair.展开更多
BACKGROUND Colon cancer(CC)occurrence and progression are considerably influenced by the tumor microenvironment.However,the exact underlying regulatory mechanisms remain unclear.AIM To investigate immune infiltration-...BACKGROUND Colon cancer(CC)occurrence and progression are considerably influenced by the tumor microenvironment.However,the exact underlying regulatory mechanisms remain unclear.AIM To investigate immune infiltration-related differentially expressed genes(DEGs)in CC and specifically explored the role and potential molecular mechanisms of complement factor I(CFI).METHODS Immune infiltration-associated DEGs were screened for CC using bioinformatics.Quantitative reverse transcription polymerase chain reaction was used to examine hub DEGs expression in the CC cell lines.Stable CFI-knockdown HT29 and HCT116 cell lines were constructed,and the diverse roles of CFI in vitro were assessed using CCK-8,5-ethynyl-2’-deoxyuridine,wound healing,and transwell assays.Hematoxylin and eosin staining and immunohistochemistry staining were employed to evaluate the influence of CFI on the tumorigenesis of CC xenograft models constructed using BALB/c male nude mice.Key proteins associated with glycolysis and the Wnt pathway were measured using western blotting.RESULTS Six key immune infiltration-related DEGs were screened,among which the expression of CFI,complement factor B,lymphoid enhancer binding factor 1,and SRY-related high-mobility-group box 4 was upregulated,whereas that of fatty acid-binding protein 1,and bone morphogenic protein-2 was downregulated.Furthermore,CFI could be used as a diagnostic biomarker for CC.Functionally,CFI silencing inhibited CC cell proliferation,migration,invasion,and tumor growth.Mechanistically,CFI knockdown downregulated the expression of key glycolysis-related proteins(glucose transporter type 1,hexokinase 2,lactate dehydrogenase A,and pyruvate kinase M2)and the Wnt pathway-related proteins(β-catenin and c-Myc).Further investigation indicated that CFI knockdown inhibited glycolysis in CC by blocking the Wnt/β-catenin/c-Myc pathway.CONCLUSION The findings of the present study demonstrate that CFI plays a crucial role in CC development by influencing glycolysis and the Wnt/β-catenin/c-Myc pathway,indicating that it could serve as a promising target for therapeutic intervention in CC.展开更多
目的观察柚皮苷对去卵巢骨质疏松大鼠骨组织HIF-1α/VEGF信号通路和H型血管形成的影响,探讨柚皮苷防治骨质疏松症的作用机制。方法建立去卵巢骨质疏松大鼠模型(随机将36只大鼠分为去卵巢组、假手术组和柚皮苷治疗组)。柚皮苷治疗3个月后...目的观察柚皮苷对去卵巢骨质疏松大鼠骨组织HIF-1α/VEGF信号通路和H型血管形成的影响,探讨柚皮苷防治骨质疏松症的作用机制。方法建立去卵巢骨质疏松大鼠模型(随机将36只大鼠分为去卵巢组、假手术组和柚皮苷治疗组)。柚皮苷治疗3个月后,检测血清和骨髓上清骨代谢指标和HIF-1α/VEGF信号通路变化,检测骨密度(bone mineral density,BMD)、骨微结构及H型血管变化。结果柚皮苷治疗组大鼠血清中成骨代谢指标[骨特异性碱性磷酸酶(BALP)、骨钙素(BGP)、I型原胶原分子N端前肽(PINP)]升高;而骨吸收标志物血清C端交联肽(CTX)降低;HIF-1α在血清和骨髓上清中表达均升高;VEGF在骨髓上清中表达升高,而血清中无明显改变;BMD和Micro-CT结果显示柚皮苷治疗组大鼠骨密度和骨量增加;同时股骨近端H型血管表达升高。结论柚皮苷可以调节骨代谢,改善骨质疏松大鼠骨密度,发挥抗骨质疏松作用,其作用机制可能是通过调节HIF-1α/VEGF信号通路、促进H型血管形成来实现的。展开更多
目的探讨单侧上尿路梗阻解除前后肾皮质厚度(RCT)与肾小球滤过率(GFR)的关系。方法选取2015年7月-2016年6月该院泌尿外科收治的63例上泌尿道梗阻患者为研究对象。其中,男34例,女29例,年龄22~73(52.21±11.56)岁;手术方式:输尿管镜碎...目的探讨单侧上尿路梗阻解除前后肾皮质厚度(RCT)与肾小球滤过率(GFR)的关系。方法选取2015年7月-2016年6月该院泌尿外科收治的63例上泌尿道梗阻患者为研究对象。其中,男34例,女29例,年龄22~73(52.21±11.56)岁;手术方式:输尿管镜碎石+取石术24例,一期经皮肾造瘘+二期经皮肾镜取石术(PCNL)21例,一期PCNL 18例。采用腹部增强CT、单光子发射计算机断层(SPECT)扫描分别测量RCT和GFR,根据术前患肾GFR情况分为3组:A组(中度肾损害,15.0 ml/min≤GFR<30.0 ml/min)、B组(重度肾损害,7.5 ml/min≤GFR<15.0 ml/min)、C组(极重度肾损害,GFR<7.5 ml/min),比较3组的手术前后的GFR变化。采用简单线性相关分析A和B组患者术前RCT与各指标的相关性。结果 9例患者因肾积水严重未测量RCT,患者的术前RCT>10 mm 20例,5~10 mm 23例,<5 mm 11例,平均值为(10.75±4.91)mm。A组术前RCT明显高于B组,差异有统计学意义(P<0.05)。3组患者术后1和9个月的GFR均明显高于同组术前,差异均有统计学意义(P<0.05)。A组术后1和9个月的GFR均明显高于另外两组,B组术后9个月的GFR明显高于C组,差异均有统计学意义(P<0.05),但术后1个月B组和C组的GFR差异无统计学意义(P>0.05)。B组术后1个月的GFR恢复值明显低于另外两组,差异有统计学意义(P<0.05),3组术后9个月的GFR恢复值比较差异无统计学意义(P>0.05)。术前RCT与术前GFR(r=0.613)、术后1个月GFR(r=0.697)及恢复值(r=0.552)、术后9个月GFR(r=0.589)及恢复值(r=0.488)均呈显著正相关,差异有统计学意义(P<0.05)。结论解除上泌尿道梗阻后患者的肾功能得到不同程度的恢复,即使是极重度肾功能损伤者,多数均能挽回患肾。术前RCT能有助于判断围手术期的肾功能,尤其是术后肾功能恢复情况。展开更多
For the experiment, 8 newborn male Holstein calves were selected that had the same feeding environment, and were of similar ages. They were randomly <span style="font-family:Verdana;">divided into 2 gr...For the experiment, 8 newborn male Holstein calves were selected that had the same feeding environment, and were of similar ages. They were randomly <span style="font-family:Verdana;">divided into 2 groups, with 4 in each group. The treatments consisted of </span><span style="font-family:Verdana;">feeding active probiotics (Group P) and a normal fed control group (Group C). The growth performance and blood indices were measured;rumen fluid samples were collected after weaning, and 16SrDNA sequencing and LC-MS metabolome detection were performed. Compared with the control group, </span><span style="font-family:Verdana;">relative abundances of Deltaproteobacteria, Desulfovibrionales, Bacteroi</span><span style="font-family:Verdana;">dales_ </span><span style="font-family:Verdana;">BS11_gut_group, Desulfovibrionaceae, Bacteroidales_S24-7_group, Acet</span><span style="font-family:Verdana;">obacteraceae, Ruminococcaceae_NK4A214_group, Asaia, [</span><i><span style="font-family:Verdana;">Ruminococcus</span></i><span style="font-family:Verdana;">] </span><i><span style="font-family:Verdana;">gauvreauii</span></i><span style="font-family:Verdana;">_group, </span><i><span style="font-family:Verdana;">Desulfovibrio</span></i><span style="font-family:Verdana;">, </span><i><span style="font-family:Verdana;">Kingella</span></i><span style="font-family:Verdana;">, </span><i><span style="font-family:Verdana;">Selenomonas</span></i><span style="font-family:Verdana;">, Lachnoclostri</span><span style="font-family:Verdana;">dium in group P were significantly different (P < 0.05). In group P, the metabolite </span><span style="font-family:Verdana;">of </span><span style="font-family:Verdana;">2-methylbenzoic acid and myo-inositol were significantly increased (P <</span><span style="font-family:Verdana;"> 0.05). These results showed that compared with normally fed calves, the growth performance and blood indices of probiotic-fed calves were changed, but the differences were not significant. Probiotic-fed calves showed significant differences in rumen fluid and a small number of metabolites, which were mainly involved in the pathway of carbohydrate metabolism. It proves </span><span style="font-family:Verdana;">that the supplemental active probiotics had an effect on the rumen microflora.</span>展开更多
法尼酯X受体(farnesoid X receptor,FXR),是由配体激活、维持机体稳态的一种转录因子。作为一种多功能核受体,入核后与视黄醛衍生物受体(retinoid X receptor,RXR)形成异质二聚体,与反向重复序列-1(inverted repeat-1,IR1)结合调节靶基...法尼酯X受体(farnesoid X receptor,FXR),是由配体激活、维持机体稳态的一种转录因子。作为一种多功能核受体,入核后与视黄醛衍生物受体(retinoid X receptor,RXR)形成异质二聚体,与反向重复序列-1(inverted repeat-1,IR1)结合调节靶基因表达。其靶基因涉及脂肪酸、胆汁酸、葡萄糖代谢,进而决定了FXR与胆汁淤积、糖尿病、高血压、脂质紊乱等代谢性疾病的密切联系。研究表明,多个FXR基因多态性位点与代谢性疾病的发生密切相关,如rs56163822与糖代谢紊乱相关,rs35724和rs10860603会影响身体质量指数(body mass index,BMI)。本文拟就近年来FXR参与代谢途径及其基因多态性与代谢性疾病的相关性作一综述,为代谢性疾病的发生几率评估及提前干预提供新思路。展开更多
目的·分析比较新型冠状病毒肺炎(coronavirus disease 2019,COVID-19)普通型和重型患者的糖脂代谢特点。方法·2020年2—3月,将武汉雷神山医院普通病房住院的36例COVID-19普通型患者和重症监护室(intensive care unit,ICU)的50...目的·分析比较新型冠状病毒肺炎(coronavirus disease 2019,COVID-19)普通型和重型患者的糖脂代谢特点。方法·2020年2—3月,将武汉雷神山医院普通病房住院的36例COVID-19普通型患者和重症监护室(intensive care unit,ICU)的50例COVID-19重型患者设为普通型患者组和重型患者组,对他们的电子病历进行提取和分析。收集2组的人口学资料、临床资料、实验室检查结果、合并疾病和临床结局,并采用独立样本t检验、非参数检验、χ^(2)检验等比较2组之间的差异。从糖脂代谢角度初步分析COVID-19普通型和重型患者的特点及患者入住ICU的相关因素。结果·2组患者的性别、合并糖尿病或冠心病的人数间无统计学差异;重型患者平均年龄较普通型患者明显偏大(P<0.05);重型患者组患高血压的比例(52.0%)显著高于普通型患者(22.2%)(P<0.05);重型患者组淋巴细胞计数明显低于普通型患者组(P<0.05);2组患者间谷丙转氨酶、谷草转氨酶、血清肌酐、血尿酸值无统计学差异;重型患者组血清白蛋白、校正钙离子浓度、总胆固醇、三酰甘油、高密度脂蛋白和低密度脂蛋白均显著低于普通型患者组(均P<0.05);重型患者组的空腹血糖水平显著高于普通型患者组(P=0.001)。多因素Logistic回归发现空腹血糖、总胆固醇、高密度脂蛋白、低密度脂蛋白、血清白蛋白水平与COVID-19患者入住ICU存在一定的相关性。结论·COVID-19患者,尤其是重型患者,存在更加严重的糖脂代谢紊乱。空腹血糖、总胆固醇、高密度脂蛋白、低密度脂蛋白和血清白蛋白水平可能与患者入住ICU相关。展开更多
In order to realize the application of corn stalk in cow feed, we designed experiments to explore the effect of a certain proportion of corn stalk on the performance of lactating dairy cows. 9 multiparous mid-lactatin...In order to realize the application of corn stalk in cow feed, we designed experiments to explore the effect of a certain proportion of corn stalk on the performance of lactating dairy cows. 9 multiparous mid-lactating cows were allocated at random to three groups, each containing 3 intact cows. The trial <span style="font-family:Verdana;">consisted of three periods and three dietary treatments with a 3 × 3 Latin</span> <span style="font-family:Verdana;">square design. The diets were normal concentrats plus dried corn stalk</span><span style="font-family:Verdana;"> chopped to 5 - 8 cm long (N), high concentrates plus dried corn stalks chopped to a length of approximately 5 - 8 cm by a mower (H) while the milled corn stalks were passed through a pulviser with a 2 cm pore size (MH). Each cow was measured for dry matter intake (DMI), ruminal pH, rumen fermentation, se</span><span style="font-family:Verdana;">lective feeding behavior and production performance. The results showed</span><span style="font-family:Verdana;"> that MH led to a significantly higher intake of DM, neutral detergent fiber (NDF), forage NDF (FNDF), acid detergent fiber (ADF), crude protein (CP) and organic matter (OM) than N and H (</span><i><span style="font-family:Verdana;">P</span></i><span style="font-family:Verdana;"> < 0.05). Cows fed H and MH showed similar selective feeding behavior, while those fed H showed various selectiv</span><span style="font-family:Verdana;">ity for the dietary component. MH resulted in a significantly higher milk</span><span style="font-family:Verdana;"> production (</span><i><span style="font-family:Verdana;">P</span></i><span style="font-family:Verdana;"> < 0.05), and tended to have a higher milk fat production than N (</span><i><span style="font-family:Verdana;">P</span></i><span style="font-family:Verdana;"> = 0.055). There were no significant differences in the milk components (</span><i><span style="font-family:Verdana;">P</span></i><span style="font-family:Verdana;"> = 0.424) and lactose (</span><i><span style="font-family:Verdana;">P</span></i><span style="font-family:Verdana;"> = 0.113) between cows fed N and MH. The high-con</span><span style="font-family:Verdana;">centrates plus milled corn stalk diet can increase the milk yield under the</span><span style="font-family:Verdana;"> premise of normal rumen pH in dairy cows, thereby generating higher economic benefits. And milled corn stalk can effectively inhibit the cow’s selective eating of low-quality roughage.</span>展开更多
The aim of this study was to investigate the effects of </span><i><span style="font-family:Verdana;">Saccharomyces cerevisiae</span></i><span style="font-family:Verdana;...The aim of this study was to investigate the effects of </span><i><span style="font-family:Verdana;">Saccharomyces cerevisiae</span></i><span style="font-family:Verdana;"> and its fermentation products on performance, blood hormone levels and rumen floral composition in peripartum dairy cows. Sixty perinatal cows were selected and allocated to two groups according to parity and expected date of delivery. Each group was supplemented with </span><i><span style="font-family:Verdana;">Saccharomyces cerevisiae</span></i><span style="font-family:Verdana;"> and its fermentation product 0 or 100 g. The results showed that </span><i><span style="font-family:Verdana;">Saccharomyces cerevisiae</span></i><span style="font-family:Verdana;"> and its fermentation products could significantly increase the feed intake of peripartum dairy cows (P < 0.01), increase the lactose content after 21 days postpartum (P < 0.01), and tend to increase milk production (P = 0.052). There was no significant effect on other milk components, the apparent digestibility of nutrients. There was a tendency to increase milk production and reduce the number of somatic cells in milk;increase blood levels of glucagon (P < 0.01) and </span><i><span style="font-family:Verdana;">β</span></i><span style="font-family:Verdana;">-hydroxybutyrate (P = 0.01), reducing the insulin content (P = 0.02).</span></span><span style="font-family:""> </span><i><span style="font-family:Verdana;">Saccharomyces cerevisiae</span></i><span style="font-family:""><span style="font-family:Verdana;"> reduced the abundance of rumen microbes in peripartum dairy cows but had no effect on rumen microbial diversity. Compared with the control group, the supplemented group showed reductions in the abundance of genera </span><i><span style="font-family:Verdana;">Bacillus</span></i><span style="font-family:Verdana;"> (P = 0.03), </span><i><span style="font-family:Verdana;">Butyrivibrio</span></i><span style="font-family:Verdana;"> (P = 0.01), </span><i><span style="font-family:Verdana;">Denitrobacterium</span></i><span style="font-family:Verdana;"> (P = 0.01), and </span><i><span style="font-family:Verdana;">Mogibacterium</span></i><span style="font-family:Verdana;"> (P < 0.01), </span><i><span style="font-family:Verdana;">Porphyromonas</span></i><span style="font-family:Verdana;"> (P = 0.05), </span><i><span style="font-family:Verdana;">Saccharofermentans</span></i><span style="font-family:Verdana;"> (P < 0.01), </span><i><span style="font-family:Verdana;">Sphaerochaeta</span></i><span style="font-family:Verdana;"> (P = 0.02), </span><i><span style="font-family:Verdana;">Streptococcus</span></i><span style="font-family:Verdana;"> (P = 0.04) and other genera. There were significant increase in the content of </span><i><span style="font-family:Verdana;">Acidaminococcus</span></i><span style="font-family:Verdana;"> (P = 0.03), </span><i><span style="font-family:Verdana;">Allisonella</span></i><span style="font-family:Verdana;"> (P < 0.01), </span><i><span style="font-family:Verdana;">Bulleidia</span></i><span style="font-family:Verdana;"> (P < 0.01), </span><i><span style="font-family:Verdana;">Corynebacterium</span></i><span style="font-family:Verdana;"> (P = 0.01), </span><i><span style="font-family:Verdana;">Dialister</span></i><span style="font-family:Verdana;"> (P < 0.01), </span><i><span style="font-family:Verdana;">Faecalibacterium</span></i><span style="font-family:Verdana;"> (P = 0.02), </span><i><span style="font-family:Verdana;">Faekalitalea</span></i><span style="font-family:Verdana;"> (P = 0.03), </span><i><span style="font-family:Verdana;">Fibrobacter</span></i><span style="font-family:Verdana;"> (P = 0.04), </span><i><span style="font-family:Verdana;">Flavobacterium</span></i><span style="font-family:Verdana;"> (P = 0.03), </span><i><span style="font-family:Verdana;">Kandleria</span></i><span style="font-family:Verdana;"> (P < 0.01), </span><i><span style="font-family:Verdana;">Paraprevotella</span></i><span style="font-family:Verdana;"> (P < 0.01), </span><i><span style="font-family:Verdana;">Pyramidobacter</span></i><span style="font-family:Verdana;"> (P = 0.05), </span><i><span style="font-family:Verdana;">Roseburia</span></i><span style="font-family:Verdana;"> (P < 0.01), </span><i><span style="font-family:Verdana;">Succinivibrio</span></i><span style="font-family:Verdana;"> (P < 0.01) and other genera.</span></span><span style="font-family:""> </span><span style="font-family:""><span style="font-family:Verdana;">The main metabolic pathways such as tryptophan metabolism and steroid hormone biosynthesis in perinatal dairy cows were determined for </span><i><span style="font-family:Verdana;">Saccharomyces cerevisiae</span></i><span style="font-family:Verdana;"> and its fermentation products.展开更多
基金Research and Development Program of China(2023YFD1400200)the Natural Science Foundation of Fujian Province,China(2022J01125)+2 种基金the Fujian Key Laboratory for Monitoring and Integrated Management of Crop Pests,China(MIMCP-202301)the Fujian Provincial Science and Technology Key Project,China(2022NZ030014)the National Natural Science Foundation of China(NSFC31871914).
文摘The conserved DNA damage repair complex,MMS21-SMC5/6(Methyl methane sulfonate 21-Structural maintenance of chromosomes 5/6),has been extensively studied in yeast,animals,and plants.However,its role in phytopathogenic fungi,particularly in the highly destructive rice blast fungus Magnaporthe oryzae,remains unknown.In this study,we functionally characterized the homologues of this complex,MoMMS21 and MoSMC5,in M.oryzae.We first demonstrated the importance of DNA damage repair in M.oryzae by showing that the DNA damage inducer phleomycin inhibited vegetative growth,infection-related development and pathogenicity in this fungus.Additionally,we discovered that MoMMS21 and MoSMC5 interacted in the nuclei,suggesting that they also function as a complex in M.oryzae.Gene deletion experiments revealed that both MoMMS21 and MoSMC5 are required for infection-related development and pathogenicity in M.oryzae,while only MoMMS21 deletion affected growth and sensitivity to phleomycin,indicating its specific involvement in DNA damage repair.Overall,our results provide insights into the roles of MoMMS21 and MoSMC5 in M.oryzae,highlighting their functions beyond DNA damage repair.
文摘BACKGROUND Colon cancer(CC)occurrence and progression are considerably influenced by the tumor microenvironment.However,the exact underlying regulatory mechanisms remain unclear.AIM To investigate immune infiltration-related differentially expressed genes(DEGs)in CC and specifically explored the role and potential molecular mechanisms of complement factor I(CFI).METHODS Immune infiltration-associated DEGs were screened for CC using bioinformatics.Quantitative reverse transcription polymerase chain reaction was used to examine hub DEGs expression in the CC cell lines.Stable CFI-knockdown HT29 and HCT116 cell lines were constructed,and the diverse roles of CFI in vitro were assessed using CCK-8,5-ethynyl-2’-deoxyuridine,wound healing,and transwell assays.Hematoxylin and eosin staining and immunohistochemistry staining were employed to evaluate the influence of CFI on the tumorigenesis of CC xenograft models constructed using BALB/c male nude mice.Key proteins associated with glycolysis and the Wnt pathway were measured using western blotting.RESULTS Six key immune infiltration-related DEGs were screened,among which the expression of CFI,complement factor B,lymphoid enhancer binding factor 1,and SRY-related high-mobility-group box 4 was upregulated,whereas that of fatty acid-binding protein 1,and bone morphogenic protein-2 was downregulated.Furthermore,CFI could be used as a diagnostic biomarker for CC.Functionally,CFI silencing inhibited CC cell proliferation,migration,invasion,and tumor growth.Mechanistically,CFI knockdown downregulated the expression of key glycolysis-related proteins(glucose transporter type 1,hexokinase 2,lactate dehydrogenase A,and pyruvate kinase M2)and the Wnt pathway-related proteins(β-catenin and c-Myc).Further investigation indicated that CFI knockdown inhibited glycolysis in CC by blocking the Wnt/β-catenin/c-Myc pathway.CONCLUSION The findings of the present study demonstrate that CFI plays a crucial role in CC development by influencing glycolysis and the Wnt/β-catenin/c-Myc pathway,indicating that it could serve as a promising target for therapeutic intervention in CC.
文摘目的观察柚皮苷对去卵巢骨质疏松大鼠骨组织HIF-1α/VEGF信号通路和H型血管形成的影响,探讨柚皮苷防治骨质疏松症的作用机制。方法建立去卵巢骨质疏松大鼠模型(随机将36只大鼠分为去卵巢组、假手术组和柚皮苷治疗组)。柚皮苷治疗3个月后,检测血清和骨髓上清骨代谢指标和HIF-1α/VEGF信号通路变化,检测骨密度(bone mineral density,BMD)、骨微结构及H型血管变化。结果柚皮苷治疗组大鼠血清中成骨代谢指标[骨特异性碱性磷酸酶(BALP)、骨钙素(BGP)、I型原胶原分子N端前肽(PINP)]升高;而骨吸收标志物血清C端交联肽(CTX)降低;HIF-1α在血清和骨髓上清中表达均升高;VEGF在骨髓上清中表达升高,而血清中无明显改变;BMD和Micro-CT结果显示柚皮苷治疗组大鼠骨密度和骨量增加;同时股骨近端H型血管表达升高。结论柚皮苷可以调节骨代谢,改善骨质疏松大鼠骨密度,发挥抗骨质疏松作用,其作用机制可能是通过调节HIF-1α/VEGF信号通路、促进H型血管形成来实现的。
文摘目的探讨单侧上尿路梗阻解除前后肾皮质厚度(RCT)与肾小球滤过率(GFR)的关系。方法选取2015年7月-2016年6月该院泌尿外科收治的63例上泌尿道梗阻患者为研究对象。其中,男34例,女29例,年龄22~73(52.21±11.56)岁;手术方式:输尿管镜碎石+取石术24例,一期经皮肾造瘘+二期经皮肾镜取石术(PCNL)21例,一期PCNL 18例。采用腹部增强CT、单光子发射计算机断层(SPECT)扫描分别测量RCT和GFR,根据术前患肾GFR情况分为3组:A组(中度肾损害,15.0 ml/min≤GFR<30.0 ml/min)、B组(重度肾损害,7.5 ml/min≤GFR<15.0 ml/min)、C组(极重度肾损害,GFR<7.5 ml/min),比较3组的手术前后的GFR变化。采用简单线性相关分析A和B组患者术前RCT与各指标的相关性。结果 9例患者因肾积水严重未测量RCT,患者的术前RCT>10 mm 20例,5~10 mm 23例,<5 mm 11例,平均值为(10.75±4.91)mm。A组术前RCT明显高于B组,差异有统计学意义(P<0.05)。3组患者术后1和9个月的GFR均明显高于同组术前,差异均有统计学意义(P<0.05)。A组术后1和9个月的GFR均明显高于另外两组,B组术后9个月的GFR明显高于C组,差异均有统计学意义(P<0.05),但术后1个月B组和C组的GFR差异无统计学意义(P>0.05)。B组术后1个月的GFR恢复值明显低于另外两组,差异有统计学意义(P<0.05),3组术后9个月的GFR恢复值比较差异无统计学意义(P>0.05)。术前RCT与术前GFR(r=0.613)、术后1个月GFR(r=0.697)及恢复值(r=0.552)、术后9个月GFR(r=0.589)及恢复值(r=0.488)均呈显著正相关,差异有统计学意义(P<0.05)。结论解除上泌尿道梗阻后患者的肾功能得到不同程度的恢复,即使是极重度肾功能损伤者,多数均能挽回患肾。术前RCT能有助于判断围手术期的肾功能,尤其是术后肾功能恢复情况。
文摘For the experiment, 8 newborn male Holstein calves were selected that had the same feeding environment, and were of similar ages. They were randomly <span style="font-family:Verdana;">divided into 2 groups, with 4 in each group. The treatments consisted of </span><span style="font-family:Verdana;">feeding active probiotics (Group P) and a normal fed control group (Group C). The growth performance and blood indices were measured;rumen fluid samples were collected after weaning, and 16SrDNA sequencing and LC-MS metabolome detection were performed. Compared with the control group, </span><span style="font-family:Verdana;">relative abundances of Deltaproteobacteria, Desulfovibrionales, Bacteroi</span><span style="font-family:Verdana;">dales_ </span><span style="font-family:Verdana;">BS11_gut_group, Desulfovibrionaceae, Bacteroidales_S24-7_group, Acet</span><span style="font-family:Verdana;">obacteraceae, Ruminococcaceae_NK4A214_group, Asaia, [</span><i><span style="font-family:Verdana;">Ruminococcus</span></i><span style="font-family:Verdana;">] </span><i><span style="font-family:Verdana;">gauvreauii</span></i><span style="font-family:Verdana;">_group, </span><i><span style="font-family:Verdana;">Desulfovibrio</span></i><span style="font-family:Verdana;">, </span><i><span style="font-family:Verdana;">Kingella</span></i><span style="font-family:Verdana;">, </span><i><span style="font-family:Verdana;">Selenomonas</span></i><span style="font-family:Verdana;">, Lachnoclostri</span><span style="font-family:Verdana;">dium in group P were significantly different (P < 0.05). In group P, the metabolite </span><span style="font-family:Verdana;">of </span><span style="font-family:Verdana;">2-methylbenzoic acid and myo-inositol were significantly increased (P <</span><span style="font-family:Verdana;"> 0.05). These results showed that compared with normally fed calves, the growth performance and blood indices of probiotic-fed calves were changed, but the differences were not significant. Probiotic-fed calves showed significant differences in rumen fluid and a small number of metabolites, which were mainly involved in the pathway of carbohydrate metabolism. It proves </span><span style="font-family:Verdana;">that the supplemental active probiotics had an effect on the rumen microflora.</span>
文摘法尼酯X受体(farnesoid X receptor,FXR),是由配体激活、维持机体稳态的一种转录因子。作为一种多功能核受体,入核后与视黄醛衍生物受体(retinoid X receptor,RXR)形成异质二聚体,与反向重复序列-1(inverted repeat-1,IR1)结合调节靶基因表达。其靶基因涉及脂肪酸、胆汁酸、葡萄糖代谢,进而决定了FXR与胆汁淤积、糖尿病、高血压、脂质紊乱等代谢性疾病的密切联系。研究表明,多个FXR基因多态性位点与代谢性疾病的发生密切相关,如rs56163822与糖代谢紊乱相关,rs35724和rs10860603会影响身体质量指数(body mass index,BMI)。本文拟就近年来FXR参与代谢途径及其基因多态性与代谢性疾病的相关性作一综述,为代谢性疾病的发生几率评估及提前干预提供新思路。
文摘目的·分析比较新型冠状病毒肺炎(coronavirus disease 2019,COVID-19)普通型和重型患者的糖脂代谢特点。方法·2020年2—3月,将武汉雷神山医院普通病房住院的36例COVID-19普通型患者和重症监护室(intensive care unit,ICU)的50例COVID-19重型患者设为普通型患者组和重型患者组,对他们的电子病历进行提取和分析。收集2组的人口学资料、临床资料、实验室检查结果、合并疾病和临床结局,并采用独立样本t检验、非参数检验、χ^(2)检验等比较2组之间的差异。从糖脂代谢角度初步分析COVID-19普通型和重型患者的特点及患者入住ICU的相关因素。结果·2组患者的性别、合并糖尿病或冠心病的人数间无统计学差异;重型患者平均年龄较普通型患者明显偏大(P<0.05);重型患者组患高血压的比例(52.0%)显著高于普通型患者(22.2%)(P<0.05);重型患者组淋巴细胞计数明显低于普通型患者组(P<0.05);2组患者间谷丙转氨酶、谷草转氨酶、血清肌酐、血尿酸值无统计学差异;重型患者组血清白蛋白、校正钙离子浓度、总胆固醇、三酰甘油、高密度脂蛋白和低密度脂蛋白均显著低于普通型患者组(均P<0.05);重型患者组的空腹血糖水平显著高于普通型患者组(P=0.001)。多因素Logistic回归发现空腹血糖、总胆固醇、高密度脂蛋白、低密度脂蛋白、血清白蛋白水平与COVID-19患者入住ICU存在一定的相关性。结论·COVID-19患者,尤其是重型患者,存在更加严重的糖脂代谢紊乱。空腹血糖、总胆固醇、高密度脂蛋白、低密度脂蛋白和血清白蛋白水平可能与患者入住ICU相关。
文摘In order to realize the application of corn stalk in cow feed, we designed experiments to explore the effect of a certain proportion of corn stalk on the performance of lactating dairy cows. 9 multiparous mid-lactating cows were allocated at random to three groups, each containing 3 intact cows. The trial <span style="font-family:Verdana;">consisted of three periods and three dietary treatments with a 3 × 3 Latin</span> <span style="font-family:Verdana;">square design. The diets were normal concentrats plus dried corn stalk</span><span style="font-family:Verdana;"> chopped to 5 - 8 cm long (N), high concentrates plus dried corn stalks chopped to a length of approximately 5 - 8 cm by a mower (H) while the milled corn stalks were passed through a pulviser with a 2 cm pore size (MH). Each cow was measured for dry matter intake (DMI), ruminal pH, rumen fermentation, se</span><span style="font-family:Verdana;">lective feeding behavior and production performance. The results showed</span><span style="font-family:Verdana;"> that MH led to a significantly higher intake of DM, neutral detergent fiber (NDF), forage NDF (FNDF), acid detergent fiber (ADF), crude protein (CP) and organic matter (OM) than N and H (</span><i><span style="font-family:Verdana;">P</span></i><span style="font-family:Verdana;"> < 0.05). Cows fed H and MH showed similar selective feeding behavior, while those fed H showed various selectiv</span><span style="font-family:Verdana;">ity for the dietary component. MH resulted in a significantly higher milk</span><span style="font-family:Verdana;"> production (</span><i><span style="font-family:Verdana;">P</span></i><span style="font-family:Verdana;"> < 0.05), and tended to have a higher milk fat production than N (</span><i><span style="font-family:Verdana;">P</span></i><span style="font-family:Verdana;"> = 0.055). There were no significant differences in the milk components (</span><i><span style="font-family:Verdana;">P</span></i><span style="font-family:Verdana;"> = 0.424) and lactose (</span><i><span style="font-family:Verdana;">P</span></i><span style="font-family:Verdana;"> = 0.113) between cows fed N and MH. The high-con</span><span style="font-family:Verdana;">centrates plus milled corn stalk diet can increase the milk yield under the</span><span style="font-family:Verdana;"> premise of normal rumen pH in dairy cows, thereby generating higher economic benefits. And milled corn stalk can effectively inhibit the cow’s selective eating of low-quality roughage.</span>
文摘The aim of this study was to investigate the effects of </span><i><span style="font-family:Verdana;">Saccharomyces cerevisiae</span></i><span style="font-family:Verdana;"> and its fermentation products on performance, blood hormone levels and rumen floral composition in peripartum dairy cows. Sixty perinatal cows were selected and allocated to two groups according to parity and expected date of delivery. Each group was supplemented with </span><i><span style="font-family:Verdana;">Saccharomyces cerevisiae</span></i><span style="font-family:Verdana;"> and its fermentation product 0 or 100 g. The results showed that </span><i><span style="font-family:Verdana;">Saccharomyces cerevisiae</span></i><span style="font-family:Verdana;"> and its fermentation products could significantly increase the feed intake of peripartum dairy cows (P < 0.01), increase the lactose content after 21 days postpartum (P < 0.01), and tend to increase milk production (P = 0.052). There was no significant effect on other milk components, the apparent digestibility of nutrients. There was a tendency to increase milk production and reduce the number of somatic cells in milk;increase blood levels of glucagon (P < 0.01) and </span><i><span style="font-family:Verdana;">β</span></i><span style="font-family:Verdana;">-hydroxybutyrate (P = 0.01), reducing the insulin content (P = 0.02).</span></span><span style="font-family:""> </span><i><span style="font-family:Verdana;">Saccharomyces cerevisiae</span></i><span style="font-family:""><span style="font-family:Verdana;"> reduced the abundance of rumen microbes in peripartum dairy cows but had no effect on rumen microbial diversity. Compared with the control group, the supplemented group showed reductions in the abundance of genera </span><i><span style="font-family:Verdana;">Bacillus</span></i><span style="font-family:Verdana;"> (P = 0.03), </span><i><span style="font-family:Verdana;">Butyrivibrio</span></i><span style="font-family:Verdana;"> (P = 0.01), </span><i><span style="font-family:Verdana;">Denitrobacterium</span></i><span style="font-family:Verdana;"> (P = 0.01), and </span><i><span style="font-family:Verdana;">Mogibacterium</span></i><span style="font-family:Verdana;"> (P < 0.01), </span><i><span style="font-family:Verdana;">Porphyromonas</span></i><span style="font-family:Verdana;"> (P = 0.05), </span><i><span style="font-family:Verdana;">Saccharofermentans</span></i><span style="font-family:Verdana;"> (P < 0.01), </span><i><span style="font-family:Verdana;">Sphaerochaeta</span></i><span style="font-family:Verdana;"> (P = 0.02), </span><i><span style="font-family:Verdana;">Streptococcus</span></i><span style="font-family:Verdana;"> (P = 0.04) and other genera. There were significant increase in the content of </span><i><span style="font-family:Verdana;">Acidaminococcus</span></i><span style="font-family:Verdana;"> (P = 0.03), </span><i><span style="font-family:Verdana;">Allisonella</span></i><span style="font-family:Verdana;"> (P < 0.01), </span><i><span style="font-family:Verdana;">Bulleidia</span></i><span style="font-family:Verdana;"> (P < 0.01), </span><i><span style="font-family:Verdana;">Corynebacterium</span></i><span style="font-family:Verdana;"> (P = 0.01), </span><i><span style="font-family:Verdana;">Dialister</span></i><span style="font-family:Verdana;"> (P < 0.01), </span><i><span style="font-family:Verdana;">Faecalibacterium</span></i><span style="font-family:Verdana;"> (P = 0.02), </span><i><span style="font-family:Verdana;">Faekalitalea</span></i><span style="font-family:Verdana;"> (P = 0.03), </span><i><span style="font-family:Verdana;">Fibrobacter</span></i><span style="font-family:Verdana;"> (P = 0.04), </span><i><span style="font-family:Verdana;">Flavobacterium</span></i><span style="font-family:Verdana;"> (P = 0.03), </span><i><span style="font-family:Verdana;">Kandleria</span></i><span style="font-family:Verdana;"> (P < 0.01), </span><i><span style="font-family:Verdana;">Paraprevotella</span></i><span style="font-family:Verdana;"> (P < 0.01), </span><i><span style="font-family:Verdana;">Pyramidobacter</span></i><span style="font-family:Verdana;"> (P = 0.05), </span><i><span style="font-family:Verdana;">Roseburia</span></i><span style="font-family:Verdana;"> (P < 0.01), </span><i><span style="font-family:Verdana;">Succinivibrio</span></i><span style="font-family:Verdana;"> (P < 0.01) and other genera.</span></span><span style="font-family:""> </span><span style="font-family:""><span style="font-family:Verdana;">The main metabolic pathways such as tryptophan metabolism and steroid hormone biosynthesis in perinatal dairy cows were determined for </span><i><span style="font-family:Verdana;">Saccharomyces cerevisiae</span></i><span style="font-family:Verdana;"> and its fermentation products.