浅析新媒体时代广告传播新特点

在新媒体时代下,广告传播作为信息传播的一种重要形式,呈现出一些新的特点。本文先对新媒体的概念进行界定,并展示当前新媒体的发展状况,然后分析新媒体时代广告传播所呈现出的新特点

远红外陶瓷微珠干预对急性损伤大鼠LZM、MPO、IL-8和IL-10指标影响的研究

利用远红外陶瓷微珠作为干预手段,对大鼠肌肉急性损伤后进行恢复治疗,探讨其对骨骼肌血清炎症指标LZM、MPO和免疫学IL-10、IL-8指标的影响.将88只SD雄性大鼠分为A组安静对照组; B组模型组; C组模型+热水组; D组模型+陶瓷微珠组,大鼠急性损伤造模成功后自然休息48 h后,各组实验大鼠按照设计分别取干预后第3 d、4 d、6 d、7 d时相点数据进行组内、组间分析.结果:(1)干预后第3 d,D组血LZM、IL-10恢复后各时相水平均显著高于自然恢复B组与模型C组(P <0. 05);(2)干预后7 d,D组血MPO、IL-8恢复水平均显著低于自然恢复B组与模型C组(P <0. 01).结论:(1)远红外陶瓷微珠干预下,发现降低了MPO水平而提升了LZM水平,说明干预后急性损伤炎性细胞对损伤肌肉的破坏进一步减小;(2)远红外陶瓷微珠干预可提升IL-10浓度水平和降低IL-8的浓度水平,验证其影响炎症反应过程,促进急性损伤的快速恢复.福建省自然科学基金资助项目(2016J01404);;莆田学院育苗基金资助项目(2017014);莆田学院国家基金预研资助项目(2016076);;国家体育总局科技服务资助项目(2017HT008

Experimental study on effect of Changrun Formula in regulating expression of AQP3 and AQP9 in colon mucosa of functional constipation rats

目的:观察肠润方对功能性便秘模型大鼠结肠黏膜AQP3、AQP9表达的影响,探究其调控AQP3、AQP9表达的分子机制。方法:60只SD大鼠随机分为空白组、模型组、阳性对照组(麻仁丸组)、肠润方组、肠润方联合P38MAPK抑制剂SB203580组。用复方地芬诺酯制造大鼠便秘模型,采用免疫组织化学及实时荧光定量PCR(q RT-PCR)检测大鼠便秘模型近端及远端结肠黏膜AQP3、AQP9的表达;Western Blot检测信号传导通路相关分子P38MAPK及P-P38MAPK的表达。结果:造模成功后,模型组近端结肠黏膜AQP3表达较空白组明显上升,而远端结肠黏膜AQP9表达较空白组明显下降(t值分别为3.148和7.069,P值均0.05)。肠润方联合P38MAPK抑制剂SB203580治疗后,近端结肠黏膜AQP3 m RNA水平显著上升(t=5.922,P0.05). The level of AQP3 m RNA in proximal colonic mucosa was significantly increased(t=5.922, P<0.01), and AQP9 m RNA was significantly decreased in distal colonic mucosa(t=4.038, P<0.01); The relative expression of P-P38/P38 protein was significantly decreased(t=19.419, P<0.01). Conclusion: The therapeutic action ofChangrun Formula on functional constipation rat models might through inhibiting the expression of AQP3 in proximal colon, and accelerating on expression of AQP9 in distal colon, and the regulating mechanism might relate with the inhibition on P38 MAPK and AKT phosphorylation.福建省自然科学基金项目(No.2012D043)~

湛江湾和平水母属2新种（软水母亚纲，锥螅水母目，和平水母科）

采自广东湛江湾海域软水母亚纲(Leptomedusae Claus,1877)、锥螅水母目(Conica Broch,1916)、和平水母科(Eirenidae Haeckel, 1879)、和平水母属(Eirene Eschscholtz,1829) 2新种,即大腺和平水母新种(E. macrogonia Huang, Sun et Liu,sp. nov.)和湛江和平水母新种(E. zhanjiangensis Huang, Zhang et Zao, sp.nov.)。其鉴别特征如下:(1)大腺和平水母,新种;伞扁于半球形,胶质中等厚;胃柄基部塔状,胃柄较长,伸出伞腔口外;垂管长度短于口唇,4个发达口唇边缘呈齿状皱褶;生殖腺发达波状弯曲,着生于辐管下伞部,从胃柄基部延伸到伞缘外;19～24条缘触手,5～8个缘疣,触手基部呈球状,无排泄乳突;每2条触手间或触手和缘疣间有1个平衡囊,每个平衡囊有1～2个平衡石;4条辐管,1条环管。(2)湛江和平水母,新种;伞半球形,胶质厚;胃柄基部呈塔形,末端变窄;垂管较长,约等于口唇长度,口唇边缘有齿状皱褶;生殖腺带状,从胃柄基部延伸至近伞缘;缘触手多,70～125条,触手基球有排泄乳突;平衡囊数目约为触手数的1/2;4条辐管,1条环管。国家海洋局海洋公益性科研专项（No.201505027

Preparation and application of monoclonal antibodies against Herpes simplex virus-1

目的:制备并筛选HSV-1单抗,建立定量检测HSV-1病毒颗粒抗原的双抗体夹心ElISA方法,用于HSV-1病毒颗粒的质控。方法:以HSV-1免疫bAlb/C小鼠制备单克隆抗体,以筛选的中和单克隆抗体1f6为捕捉抗体,HrP标记的2b1为检测抗体,构建定量检测HSV-1病毒颗粒抗原的双抗体夹心ElISA方法,并对本方法的特异性、灵敏度、精密度、准确性和线性等性能进行验证。用本方法定量检测的病毒量与病毒滴度作回归分析。结果:构建的双抗体夹心定量检测HSV-1病毒颗粒抗原的ElISA方法,线性范围为0.125~2μg/Ml,相关系数为r2=0.995 5,定量限度为0.125μg/Ml,试剂的变异系数CV<10%,抗原回收率介于85.6%~107.1%之间。与HSV-1以外的其他样本无交叉反应。本方法检测与病毒感染滴度具有很好的相关性。结论:成功构建了定量检测HSV-1含量的ElISA方法,为HSV-1病毒颗粒抗原定量检测提供快速手段。Objective: To prepare and screen monoclonal antibodies against Herpes simplex virus-1( HSV-1),and develop a double antibody sandwich quantitative enzyme-linked immunosorbent assay( Q-ELISA) for detection of HSV-1 particle.This method was used to control the quality of viral particle in the developing and manufacturing process of HSV-1.Methods: BALB / c mice was immunized with HSV-1 to prepare monoclonal antibodies.A double antibody sandwich Q-ELISA was developed to determine concentration of HSV-1 particle,which was based on the neutralizing monoclonal antibody 1F6 as capture antibody,and 2B1 as HRP-conjugated antibody.The performance of the reagent was evaluated,including specificity,sensitivity,precision,accuracy and linear.And the relation between the amount of virus detected by this method and the virus titer was analyzed by regression analysis method.Results: The QELISA for HSV-1 particle was developed.The quantitation scope was 0.125- 2 μg / ml,the coefficient correlation was 0.995 5,the limit of detection was 0.125 μg / ml,the recovery was between 85.6% and 107.1%,the variation coefficient was lower than 10%,and the reagent does not react with other samples except HSV-1 antigen.This method has a good correlation with virus titer.Conclusion: The QELISA for HSV-1 particle was successfully developed,which provide a new approach for rapid and quantitative detection of HSV-1 antigen