心痛方对心肌缺血模型大鼠MPO 活性 及PS 表达的干预作用

目的探讨心痛方对心肌缺血大鼠模型心肌梗死面积及髓过氧化物酶（MPO）、P 选择素（PS）的干预作 用。方法80 只清洁级SD 大鼠,随机分成假手术组、模型组、心痛方组、欣康组,采用结扎法造成心肌缺血模型,NBT 染色法测心肌梗死面积,比色法检测MPO 活性,免疫组化法检测PS 的表达。结果1.模型组、心痛方组、欣康组心肌梗 死面积、MPO 活性及PS 表达均显著高于假手术组,差异有统计学意义（P<0.01）;2.心肌梗死面积比较,心痛方组、欣康 组分别小于模型组（P<0.05）,差异均有统计学意义;3.MPO 活性比较,心痛方组、欣康组分别低于模型组（P<0.05）,而 心痛方组低于欣康组（P<0.05）,差异均有统计学意义;4.PS 表达比较,心痛方组、欣康组分别低于模型组（P<0.05）,差 异均有统计学意义。结论心痛方能缩小心肌梗死面积,抑制缺血心肌MPO 活性及PS 表达。在抑制MPO 活性方面心 痛方优于欣康。     

鬼臼多糖对免疫功能低下小鼠自由基产生酶活性的影响

采用环磷酰胺腹腔注射(50mg/kg)小鼠建立免疫抑制模型,观察鬼臼多糖(PEP)不同剂量(50,100,200mg/kg和400mg/kg)配合环磷酰胺应用后,对小鼠脾脏中黄嘌呤氧化酶(XOD)、髓过氧化物酶(MPO)及一氧化氮合成酶(NOS)水平的影响。结果表明,PEP能显著降低免疫抑制小鼠脾脏XOD、MPO的活性;对脾脏总NOS活性无显著影响,但400mg/kg多糖可降低小鼠脾脏诱导型NOS活性,提示PEP可通过降低免疫抑制小鼠体内自由基产生酶水平而起到抗氧化作用。     

Establishment and Evaluation of Mouse Model of Ulcerative Colitis

The experiment was aimed to establish mouse model of ulcerative colitis(uc) by screening the optimum concentration of dextran sulfate sodium salt(DSS).Thirty BALB/c mice were randomly assigned to control group, 3.5% DSS group and 5% DSS group, ten mice each group.Mice drank water freely for 5 days, the body weights of everyday were recorded, stool was observed and stool occult blood was tested.After the experiment, the changes of TNF-α, MPO, MDA and GSH were tested, and the colon weight/length ratio was calculated.Compared with control group, the activity of MPO and content of MDA in the experiment groups were significantly increased(P<0.05), and content of GSH was significantly decreased(P<0.05).3.5% and 5% DSS both could successfully establish mouse model of ulcerative colitis.Mice in 5% DSS group had poor mental state, such as lethargy, malaise;Mice in 3.5% DSS group were appropriate, the mice mental was good, MPO, MDA and GSH were significantly different compared with control group(P<0.05), but there were no difference compared with 5% DSS group(P>0.05).So 3.5% DSS was more appropriate than 5% DSS to establish mouse model of ulcerative colitis.     

白头翁汤对大肠杆菌造模腹泻小鼠血清和小肠组织中MPO含量的影响

使用致病性大肠杆菌O101经腹腔注射感染小鼠建立腹泻模型,4h后给予不同剂量白头翁汤灌胃治疗,治疗3d后,小鼠禁食不禁水12h后采样测定血清和小肠组织中MPO含量。模型组小鼠血清中髓过氧化物酶(MPO)含量升高,与空白组比较差异极显著(P<0.01),小肠组织匀浆液中MPO含量升高,与空白组比较差异显著(P<0.05);白头翁汤治疗组血清MPO含量均降低,与模型组比较差异极显著(P<0.01),白头翁汤治疗组小肠组织MPO含量降低,与模型组比较差异显著(P<0.05)。白头翁汤能降低致病性大肠杆菌诱发的腹泻小鼠血清和小肠组织中MPO含量,提示其能够抑制细菌性腹泻早期炎性细胞在小肠组织的浸润。     

病毒感染后杂色鲍部分血清免疫因子的变化

对杂色鲍(HaliotisdiversicolorReeve)进行病毒悬液和PBS(对照)注射感染,研究其血清免疫因子SOD、ACP、AKP、MPO活性的变化,并对实验结果进行统计学分析。结果表明,(1)注射病毒悬液组SOD活性变化为逐渐上升,至8h后达到最高点,然后逐渐下降;对照组SOD活力呈下降趋势,8h后上升,12h后恢复至初始水平,二者结果差异均为显著或极显著(P<0 05或P<0 01)。(2)注射病毒悬液组ACP与AKP活性的变化为:36h前变化不大,48h后明显上升;对照组ACP和AKP活性变化不大,二者结果除了第48小时外,差异均不显著(P>0 05)。(3)注射病毒悬液组MPO活性在第1小时内上升,然后逐渐下降,第8小时下降到最低点,随后逐渐上升;对照组在第1小时内下降,然后逐渐上升,第12小时升至最高点,然后逐渐下降,48h后与正常鲍活性基本一致。t检验显示,这两组结果在第1、4、8、24、36、48h差异显著或极显著(P<0 05或P<0 01),在第2、12小时差异不显著。结果显示,在人工感染病毒48h内,杂色鲍体内的免疫因子发生了明显的变化,血清中SOD活性降低,ACP及AKP活性显著升高,MPO活性显著升高。     

小鼠溃疡性结肠炎模型的建立与评价

本试验旨在通过筛选葡聚糖硫酸钠盐(DSS)最佳浓度建立小鼠溃疡性结肠炎模型。将30只BALB/c小鼠随机分为对照组、3.5% DSS组、5% DSS组,每组10只。小鼠自由饮水5 d,每天记录小鼠体重,观察粪便性状,测便潜血。试验结束后测血清TNF-α、结肠组织髓过氧化物酶(MPO)、丙二醛(MDA)、还原性谷胱甘肽(GSH)活性变化等指标,计算结肠重量/长度比值。与对照组相比,两试验组结肠组织中MPO活性显著升高(P<0.05),MDA含量显著升高(P<0.05),GSH含量显著降低(P<0.05)。结果表明,两种浓度葡聚糖硫酸钠盐均可造模成功,5% DSS组小鼠精神状态很差,表现嗜睡、萎靡状态,而3.5% DSS组小鼠精神状态良好,且组织中MPO、MDA、GSH与对照组相比均差异显著(P<0.05),与5% DSS组相比差异不显著(P>0.05),因此,选用浓度为3.5% DSS造模更合适。     

内脂素对脂多糖刺激的大鼠肝脏组织结构和髓过氧化物酶的影响

本试验旨在观察内脂素(visfatin)对脂多糖(LPS)刺激的大鼠肝脏组织结构和髓过氧化物酶(myeloperoxidase,MPO)的影响.试验选用24只8周龄Wistar大鼠,随机分成4组:生理盐水组、visfatin组、LPS组、visfatin+LPS组.其中生理盐水组和LPS组每天注射生理盐水,visfatin组和visfatin+LPS组每天注射visfatin,1周后,LPS组和visfatin+LPS组的Wistar大鼠注射一定量的LPS,6 h后剖杀全部Wistar大鼠.采用HE和免疫组化染色观察各组Wistar大鼠肝脏的组织结构和MPO,结果发现,与生理盐水组相比,visfatin组的巨噬细胞增多,MPO表达水平显著降低(P< 0.05);与LPS组相比,visfatin+LPS组的Wistar大鼠肝细胞形态变得模糊不清,炎性细胞的浸润更加明显,MPO的水平表达也显著降低(P< 0.05).结果表明,visfatin可增加肝脏中巨噬细胞的数量且对肝脏中的MPO表达水平也有显著的影响.     

小鼠髓过氧化物酶(MPO)基因克隆分析及真核表达载体的构建

髓过氧化物酶(myeloperoxidase,MPO)是一种血红素辅基蛋白酶,是血红素过氧化物酶超家族成员之一,参与多种疾病的发生和发展过程.本研究旨在克隆小鼠MPO基因CDS全长序列,检测该基因在小鼠神经细胞的表达谱.首先利用RT-PCR法与克隆载体克隆小鼠MPO基因CDS全长序列,对其进行生物信息学分析;然后构建真...     

Fenvalerate induced stress mitigation by dietary supplementation of multispecies probiotic mixture in a tropical freshwater fish, Labeo rohita (Hamilton)

Five experimental diets with various combinations of probiotics, namely T1 & T6 (basal feed (BF) without probiotics), T2 & T7 (BF + Bacillus subtilis + Lactococcus lactis), T3 & T8 (BF + L. lactis + Saccharomyces cerevisiae), T4 & T9 (BF + B. subtilis + S. cerevisiae) and T5 & T10 (BF + B. subtilis + L. lactis + S. cerevisiae) were fed to Labeo rohita fingerlings for 30 days. Treatment groups T1, T2, T3, T4 and T5 were exposed to Fenvalerate, at a concentration of 1.79 μg L⁻¹. The SOD and CAT activity was significantly affected (P < 0.01) in fenvalerate treated groups. However, the supplementation of the three-probiotic mixture at equal concentration showed markedly reduced activity. Similarly, RBC, Hb, NBT, total protein and albumin values were reduced significantly (P < 0.01) in the fenvalerate exposed fish as compared to the probiotic supplemented fish. Fenvalerate exposure also showed increased serum ALP, ACP and Bilirubin values (P < 0.01) in comparison to the non-exposed fish. Histological observations of the gills, kidney and liver showed tissue degeneration after fenvalerate exposure, which however showed marked recovery on the three-probiotic mixture supplementation. Therefore, these results indicate that a mixture of multi-species probiotic supplementation in equal concentration acts beneficially in mitigating the stressful effects of fenvalerate.     

Chlorogenic acid protects paraoxonase 1 activity in high density lipoprotein from inactivation caused by physiological concentrations of hypochlorite

We hypothesized that chlorogenic acids, the main phenolics in coffee, many fruits and Ilex paraguariensis extracts, protect paraoxonase 1 activity in HDL from inactivation by chlorination at concentrations of HOCl (50 μM) and chlorogenic acid (2–10 μM) compatible with those found in humans.