935 resultados para Proteína ciclina D1


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选择条斑紫菜(Porphyra yezoensis)两个不同发育阶段(孢子体和配子体)作为研究对象,分别从孢子体与配子体的类囊体膜上分离到具有高放氧活性的PSII复合物。配子体PSII复合物的放氧活性为2269.77±152.94 μmolO2/chl(mg).h,孢子体PSII复合物的放氧活性为2256.33±141.81 μmolO2/chl(mg).h。对分离到的PSII复合物的稳定性和放氧活性进行了研究,结果表明:孢子体和配子体的PSII复合物,在4℃条件下保存比-80℃下放氧活性高,稳定性高。配子体跟孢子体比较,在-80℃保存条件下第六天就已经没有放氧活性,而此时-80℃下孢子体PSII复合物仍然具有放氧活性。同时对4℃下保存的PSII复合物进行分子筛柱层析,室温吸收光谱测定以及放氧活性测定,发现随着放氧活性逐渐降低的同时,蛋白大分子有聚合现象。室温吸收光谱表明经过长期的保存,吸收峰向短波长方向偏移,同时叶绿素易降解成为脱镁叶绿素。分别测定了配子体与孢子体PSII复合物的SDS-PAGE电泳蛋白条带的氨基酸序列,配子体PSII复合物经过SDS-PAGE电泳后的蛋白条带,经过质谱测定,鉴定出CP-47、D2、D1蛋白。孢子体PSII复合物,经过SDS-PAGE电泳后的蛋白条带,经过质谱分析鉴定出CP-47、CP-43、D2、D1蛋白。CP-47, CP-43蛋为PSII反应中心叶绿素P680的脱辅基蛋白,D1 与D2蛋白为PSII的反应中心蛋白。对纯化的PSII复合物,并首次采用单颗粒技术分析比较其形态结构,电镜观察证实纯化的PSII复合物为二聚体,颗粒大小约为13nm×7.8nm,经过计算总分子量约为500kDa,但是孢子体与配子体的PSII复合物在形态上有轻微差别,配子PSII复合物要略宽于孢子体复合物,孢子体PSII复合物周边棱角形较配子体明显。

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近年来,分子生物学技术与方法被越来越多地应用于有害赤潮研究。其中,单细胞PCR方法是对难以室内培养的有害赤潮藻种进行遗传特征研究的一项重要技术。本实验尝试建立微藻的单细胞PCR方法,并将其应用于鳍藻研究。 应用室内培养的亚历山大藻,研究了微藻的单细胞PCR方法,并对藻细胞的固定和保存方法进行了比较。结果表明,浮游植物研究中常用的甲醛固定方法只能用于短期保存样品(少于5天),而乙醇固定、鲁格氏液固定、或者在-20℃下冷冻保存的样品,在较长的时间后(60天)仍可以得到比较理想的PCR扩增结果。 应用单细胞PCR方法,对青岛近海采集的鳍藻进行了研究,扩增并测定了包括核糖体大亚基(LSU)rDNA的5’端D1-D2区序列,以及5.8S rDNA和ITS区的部分序列信息。通过分析软件对所得到的鳍藻序列信息与基因库中已知的鳍藻序列信息进行了分析与对比。根据ITS和LSU序列信息构建的系统进化树都显示,本文采集的鳍藻藻种与国外报道的圆形鳍藻聚为一支,初步确定采集的鳍藻应为圆形鳍藻,对该藻种形态学特征的观察也支持这一结果。该藻种部分LSU rDNA序列与欧洲同种鳍藻相似度达到99%,与其它等鳍藻遗传距离在18%-20%之间。测定的ITS区序列与同种圆形鳍藻有62个碱基的差异,与LSU rDNA序列相比,ITS序列变异更大。应用LC-MS方法对该鳍藻的进行了DSP毒素分析,结果未检测到OA或DTX1毒素。 这是我国首次应用单细胞PCR方法对鳍藻开展的研究工作,首次报道了我国鳍藻的核糖体部分序列信息。圆形鳍藻在青岛近海海域是初次报道,显示了单细胞PCR方法在鳍藻研究中的重要意义。

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近年来,世界沿海国家有害赤潮发生的频率、规模及危害都有上升趋势,有害赤潮已经成为重要的近海环境问题之一。要有效防范有害赤潮带来的危害效应,建立和发展可靠、有效的赤潮监测手段非常重要。目前,对于赤潮藻种的监测主要依靠显微观察的方法,在实际应用中经常遇到困难。首先,亲缘关系相近的物种在形态上差异很小,如甲藻门亚历山大藻属的一些种类,仅细胞壁上个别甲片的结构有细微差别,并且这些形态学指标还容易受环境条件及生长阶段的影响。另外,这种以形态学为基础的分析方法,分析速度慢、耗时长,对操作人员的要求较高,难以满足浮游植物种群动力学监测“量大、连续”的要求。因此,本研究将分子生物学的技术和方法应用于赤潮监测,力求提高赤潮藻种鉴定的准确性和检测工作的效率。 亚历山大藻是一类重要的有害赤潮藻,该藻属中一些产毒特性差别很大的藻种,单从表形特征难以明确区分,从而限制了基于形态观察的监测技术的应用。本研究中,我们尝试应用分子生物学技术与方法,开展了该藻属藻种分子鉴定和荧光原位杂交检测方法的研究。在亚历山大藻的分子鉴定方面,我们采用了核糖体RNA基因(rDNA)序列分析的方法,首次测定了9株分离自中国沿海的(以及实验室保有的其它两株)亚历山大藻的rDNA序列全长,其中包括核糖体小亚基(SSU)rDNA、大亚基(LSU)rDNA、5.8S rDNA及内转录间隔区(ITS)区序列。序列分析结果显示,这些藻株包含了5种核糖体类型,分别是塔玛复合种亚洲温带(Temperate Asian)核糖体类型(TSC-TA),塔玛复合种西欧(West European)核糖体类型(TSC-WE),相关亚历山大藻(A. affine)核糖体类型(AF),微小亚历山大藻(A. minutum)葡萄牙(Portugal)核糖体类型(M-PO)和微小亚历山大藻新西兰(New Zealand)核糖体类型(M-NZ)。将测获的rDNA序列划分为若干保守性不同的区段,分别进行系统发育分析(结合GenBank数据库中保存的其它亚历山大藻相关序列)。结果显示,LSU rDNA D1-D2区是对该藻属藻种进行分子鉴定和系统发育研究的较好区段。同时,为解决建立亚历山大藻克隆培养的困难,我们应用单细胞rDNA序列分析方法,对亚历山大藻单个细胞直接进行了种类鉴定。结果表明,该方法适用于不同生活史阶段的亚历山大藻。 在亚历山大藻的检测技术方面,我们进一步扩展和完善了针对完整细胞的荧光原位杂交检测方法。首先,通过对不同核糖体类型藻株rDNA序列信息的对比分析,针对各自特异的序列位点,设计了特异性rRNA标记探针。经荧光原位杂交实验检验,实现了对5种核糖体类型亚历山大藻的特异性标记。其中,针对WE、M-PO及M-NZ核糖体型的特异性探针为首次获得,另外两个探针是针对TA和AF核糖体类型rRNA新的位点所设计。同时,对影响探针标记效果的诸多因素进行了分析和探讨。此外,在2007年春季长江口海域赤潮调查中,首次应用特异性核酸探针和荧光原位杂交检测方法,调查了该海域亚历山大藻的丰度。结果表明,在4月4日-4月10日的样品中,亚历山大藻达到了较高的密度,最高密度达到103cells/L。同时发现,实验中样品的保存方法有待改进。随后的研究表明,盐醇固定方法及多聚甲醛/甲醇固定方法,可以较好的保持rRNA不被降解并适宜杂交(至少3个月时间)。 总之,本研究首次测定并分析了11株亚历山大藻(9株分离自中国沿海)的rDNA全序列信息。在此基础上,获得了5种核糖体类型亚历山大藻的特异性rRNA标记探针,其中3种为首次获得。另外,实验证明,单细胞rDNA分析技术和荧光原位杂交检测方法,在自然水体中亚历山大藻的直接鉴定及丰度调查中,均具有良好的应用前景。这一工作为我国近海亚历山大藻的鉴定和检测提供了理论依据和方法学基础,希望对该藻赤潮的监测工作有推动作用。 关键词:亚历山大藻 遗传探针 rRNA rDNA 荧光原位杂交 系统发育

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浮游动物在海洋生态系统物质循环和能量流动中起着至关重要的作用。浮游动物物种组成、生物量和次级生产力的变化会改变生态系统的结构和功能。在黄海生态系统中如何描述这个过程,并使它易于模拟是本论文的研究目的。生物量和生产力是海洋生态系统食物网的基础。谁是浮游动物生物量和次级生产力的基础?哪些种类在生态系统中起关键作用?这些问题在黄海这样的温带陆架边缘海区很难回答,原因是物种组成、生物量和生产力的季节变化显著。因此,在对黄海食物产出的关键过程进行模拟时,需要应用既准确又简便的方法来对浮游动物群落的生态过程进行模拟。在对黄海浮游动物群落结构和物理海洋学特征进行充分的分析之后,浮游动物功能群的方法被确定用来进行黄海生态系统结构和功能的模拟。 根据浮游动物的粒径、摄食习性和营养功能,黄海浮游动物被分为6个功能群:大型浮游甲壳动物功能群(Giant crustacean,GC)、大型桡足类功能群(Large copepods, LC)、小型桡足类功能群(Small copepods,SC)、毛颚类功能群(Chaetognaths)、水母类功能群(Medusae)和海樽类功能群(Salps)。GC、LC和SC是按照粒径大小而划分的功能群,他们是高营养层次的主要食物资源。毛颚类和水母类是两类胶质性的肉食性浮游动物功能群,他们与高营养层次竞争摄食饵料浮游动物;海樽类与其他浮游动物种类竞争摄食浮游植物,而本身的物质和能量却不能有效的传递到高营养层次。本文研究报道了浮游动物各功能群的时空分布、基于浮游动物动能群的黄海生态区划分、饵料浮游动物功能群的生产力、毛颚类对浮游动物的摄食压力以及中华哲水蚤(Calanus sinicus)的摄食生态学。 春季,浮游动物生物量为2.1 g m–2,GC、LC和SC对生物量的贡献率分别为19, 44 和 26%。高生物量的LC和SC功能群主要分布于山东半岛南岸的近岸海域,而GC主要分布在远岸站位。夏季,浮游动物的生物量为3.1 g m–2,GC贡献了73%。GC、LC和SC主要分布在黄海的中部海域。秋季,浮游动物生物量为1.8 g m–2,GC、LC和SC的贡献率相似,分别为36, 33和23%,高生物量的GC和LC分布在黄海中部,而SC主要分布在远岸站位。GC和LC是冬季浮游动物生物量(2.9 g m–2)的优势功能群,分别贡献率了57%和27%,高生物量的GC、LC和SC都分布在黄海的中部海域。与GC、LC和SC相比,毛颚类生物量较低,主要分布于黄海的中北部海域。水母类(本文中指小型水母类)和海樽类斑块分布明显,主要分布于黄海沿岸和北部海域。属于不同功能群的约10个种类为浮游动物的优势种,控制着浮游动物群落的动态。 春季,黄海可以被分成4个浮游动物生态区,浮游动物生物量的分布中心位于山东半岛南岸近岸海域,与第一个生态区相对应,LC和SC在分布中心起主要的控制作用;夏、秋和冬季,黄海分别被分成3、4和3个生态区,浮游动物生物量的分布中心均位于黄海的中部海域,均与各季节的第一个生态区相对应,GC和LC是分布中心生态区的优势功能群,对分布中心起主要的控制作用。黄海冷水团(YSCBW)在GC、LC和SC的空间分布模式中起着重要的作用。黄海不同季节浮游动物生态区的空间分布模式及生态区中起控制作用的优势功能群类别有着重要的生态学意义。 我们将饵料浮游动物功能群细化为0.16–0.25 mm、0.25–0.5 mm、0.5–1 mm、1–2 mm和 >2 mm5个粒径组。应用生物能量学的方法研究了不同粒径浮游动物的生产力。结果表明:浮游动物次级生产力5月份最高,为91.9 mg C m–2 d–1,其次是6月和9月,分别为75.6 mg C m–2 d–1和65.5 mg C m–2 d–1,8月、3月和12月较低,仅为42.3 mg C m–2 d–1、35.9 mg C m–2 d–1和27.9 mg C m–2 d–1。根据这些结果,黄海浮游动物年次级生产力为18.9 g C m–2 year–1。0.16–0.25 mm和 0.25–0.5 mm 两个粒径组对浮游动物次级生产力的贡献率为58–79%,即相对应的SC功能群的周转率(P/B, 0.091–0.193 d–1)要高于GC和LC。 黄海毛颚类功能群的优势种类为强壮箭虫(Sagitta crassa)、纳嘎箭虫(S. nagae)、肥胖箭虫(S. enflata)和百陶箭虫(S. bedoti)。我们对这四种箭虫的生产力和对浮游动物生物量和生产力的摄食压力进行了研究。结果表明:黄海毛颚类总的生物量为98–217 mg m–2,总的生产力为1.22–2.36 mg C m–2 d–1。黄海毛颚类的生物量占浮游动物总生物量的6.35–14.47%,而生产力仅占浮游动物总生产力的2.54–6.04%。强壮箭虫和纳嘎箭虫是黄海毛颚类功能群的绝对优势种,控制着黄海毛颚类群落的动态。黄海毛颚类总的摄食率为4.24–8.18 mg C m–2d–1,对浮游动物现存量和生产力总的摄食压力分别为为0.94%和12.56%。黄海冬季,浮游动物的现存量和生产力为0.4 g C m–2和0.026 g C m–2d–1,而毛颚类的摄食压力却达到了全年的最大值,为1.4%和20.94%。因此,毛颚类的摄食可能对冬季浮游动物群落结构造成重要的影响。通过不同体长组箭虫的摄食率可以推断,黄海毛颚类全年主要摄食小型桡足类,对SC功能群的摄食压力最大。但是在夏季黄海冷水团形成的月份,毛颚类对前体长为2 mm的LC功能群中的种类摄食压力也较大,但此时,由于优势种中华哲水蚤进入滞育阶段,因此毛颚类的摄食会对其种群数量造成严重的影响。 中华哲水蚤在春、秋季的摄食率分别为2.08–11.46和0.26–3.70 µg C female–1 day–1,与微型浮游生物的现存量呈显著的正相关。春季,在黄海的北部,中华哲水蚤通过摄食微型浮游生物吸收的碳量能够满足其代谢和繁殖需求,而在黄海的南部和秋季黄海冷水团锋区附近,中华哲水蚤必须通过摄食其他类型的食物资源来维持其代谢和生殖需求。较低的摄食率、无产卵以及种群中CV期桡足幼体占优势表明,秋季中华哲水蚤在黄海冷水团区域内处于滞育状态。中华哲水蚤优先摄食微型原生动物,并且春季中华哲水蚤总的生长效率(GGE, 3–39%)与食物中微型原生动物的比例呈显著的正相关,表明微型原生动物具有较高的营养价值。但是,因较低的产卵率(0.16–12.6 eggs female–1 day–1)而导致的中华哲水蚤较低的总生长效率(13.4%),可能就是由于其食物中的必需营养成分含量不足(或缺乏)造成的。 本文从生物量的角度,对黄海浮游动物各功能群的时空分布、生态区划分进行了研究报道,对GC、LC和SC功能群的生产力、毛颚类对浮游动物的摄食压力和中华哲水蚤的摄食生态学进行了较为深入的研究,这些结果为黄海食物产出的关键过程的模拟提供了基础资料。今后的研究重点应搞清楚黄海水母类对浮游动物次级生产力的摄食压力和海樽类在食物产出模型中产生的负效应的程度,浮游动物各功能群的组成、季节变化和空间分布模式的长期变化,尤其是在气候变化和人类活动的影响下,将是今后研究的重点。

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Photoinhibition is a central problem for the understanding of plasticity in photosynthesis vs. irradiance response. It effectively reduces the photosynthetic rate. In this contribution, we present a mechanistic model of algal photoinhibition induced by photodamage to photosystem-II. Photosystem-IIs (PSIIs) are assumed to exist in three states: open, closed and inhibited. Photosynthesis is closely associated with the transitions between the three states. The present model is defined by four parameters: effective cross section of PSII, number of PSIIs, turnover time of electron transfer chains and the ratio of rate constant of damage to that of repair of D1 proteins in PSIIs. It gives a photosynthetic response curve of phytoplankton to irradiance (PI-curve). Without photoinhibition, the PI-curve is in hyperbola with the first three parameters. The PI-curve with photoinhibition can be simplified to the same form as the hyperbola by replacing either the number of PSIIs with the number of functional PSIIs or the turnover time of electron transfer chains with the average turnover time.

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为了有效地利用从国内其他地区引进的低蛋白弱筋种质材料,采用SDS-PAGE技术对63份材料进行了高分子量谷蛋白亚基组成的分析.结果表明,参试材料中共有14种HMW-GS类型,Glu-A1位点上有Null、1和2~*三种类型,以Null为主(52.4%);Glu-B1位点上有13+16、17+18、7、7+8、7+8+9和7+9六种类型,以7+8为主(55.6%);Glu-D1位点上有10、12、2+12、5+10、5+12五种类型,以2+12为主(61.9%),而5+10为27%.亚基组合类型共有22种,以"1,7+8,2+12"为主(22.2%).品质评分频率最高的是8分,为38.1%,其次为6分,为14.3%,5分的为9.5%,但品质评分为10分的也有5个材料,频率为7.9%.优质亚基含量等同或高于其他同类研究,品质评分也相对较高,这说明我国弱筋小麦的选择,需要加强对HMW-GS组成的分析.

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对CIMMYT的99份硬粒小麦-节节麦人工合成种(简称合成种)的HMW-GS组成分析发现,Glu-B1和Glu-D1位点的变异类型比普通小麦丰富,分别有9种和12种亚基类型;筛选出含有比5+10亚基更优质的1.5+10和5+12亚基的合成种分别有8份和1份;含有优质亚基1.5+10的合成种与普通小麦杂交结实正常;对2个合成种与2个普通小麦品种的8个止反交组合F1种子电泳发现,优质亚基1.5+10在F1代能正常表达,双亲所有亚基任F1代都得到表达,表现共显性遗传。本研究为优质亚基1.5+10和5+12转育到普通小麦中奠定了基础。

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为了给青海高原春小麦改良提供资料,分析了于海育成和国内外引进的125个春小麦品种(系)的HMW-GS等位基因变异,并测定了其中58个品种(系)在青海高原环境下的面团流变学特性。结果表明:(1)参试春小麦品种(系)的HMW-GS存在广泛的变异,Glu-A1位点出现3个等位基因,Glu-B1位点出现5个等位基因,Glu-D1位点出现4个等位基因;共出现了22种HMW-GS组合形式,其中1,7+8,2+12和N,7+8,2+12组合类型出现频率最高,并发现了个别罕见的变异类型,如2+10,10。(2)亚基组合类型对沉淀值、形成时间、稳定时间、评价值等品质性状影响较大,对籽粒蛋白质含量、出粉率和面粉吸水率的影响不显著。试验还表明,HMW-GS组成与面粉的筋力有密切关系。

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The chlorophyll fluorescence in soybean leaves was observed by a portable fluorometer CF-1000 under field conditions. On clear days, F-0 increased while F, and F-v/F-m decreased gradually in the morning. At midday F-O reached its maximum while F-v and F-v/F-m reached their minimum. The reverse changes occurred in the afternoon. At dusk these parameters could return to levels near those at dawn. Following exposure to a strong sunlight for more than 3 h, the dark-recovery process displayed three phases: (1) slow increases in F-0, F-v and F-v/F-m within the first hour; (2) a faster decrease in F-0 and faster increases in F-v and F-v/F-m within subsequent two hours; (3) a slow decrease in F-0 and slow increases in F-v and F-v/F-m within the fourth hour. In comparison with darkness, weak irradiance had no stimulating effect on the recovery from photoinhibition. Hence the photoinhibition in soybean leaves is mainly the reflection of reversible inactivation of some photosystem 2 reaction centres, but not the result of D1 protein loss.

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Mental dependence, characterized by craving and impulsive seeking behavior, is the matter of intensive study in the field of drug addiction. The mesolimbic dopamine system has been suggested to play an important role in rewarding of drugs and relapse. Although chronic drug use can induce neuroadaptations of the mesolimbic system and changes of drug reinforcement, these mechanisms cannot fully account for the craving and the compulsive drug-using behavior of addicts. Acknowledging the reinforcement effects of drugs, most previous studies have studied the impact of environmental cues and conditioned learning on addiction behavior, often using established classical or operant conditioning model. These studies, however, paid little attention to the role of cognitive control and emotion in addiction. These mental factors that are believed to have an important influence on conditioned learning. The medial prefrontal cortex (mPFC) has close anatomic and functional connections with the mesolimbic dopamine system. A number of the cognitive neurological studies demonstrate that mPFC is involved in motivation, emotional regulation, monitoring of responses and other executive functions. Thus we speculated that the function of abnormality in mPFC following chronic drug use would cause related to the abnormal behavior in addicts including impulse and emotional changes. In the present study of a series of experiments, we used functional magnetic resonance imaging to examine the hemodynamic response of the mPFC and related circuits to various cognitive and emotional stimuli in heroin addicts and to explore the underlying dopamine neuromechnism by microinjection of tool drugs into the mPFC in laboratory animals. In the first experiment, we found that heroin patients, relative to the normal controls, took a much shorter time and committed more errors in completing the more demanding of cognitive regulation in the reverse condition of the task, while the neural activity in anterior cingulate cortex (ACC) was attenuated. In the second experiment, the scores of the heroin patients in self-rating depression scale (SDS) and Self-rating anxiety scale (SAS) were significantly higher than the normal controls and they rated the negative pictures more aversive than the normal controls. Being congruent with the behavioral results, hemodynamic response to negative pictures showed significant difference between the two groups in bilateral ventral mPFC (VMPFC), amygdala, and right thalamus. The VMPFC of patients showed increased activation than normal controls, whereas activation in the amygdala of patients was weaker than that in normal subjects. Our third experiment showed that microinjection of D1 receptor agonist SKF38393 into the mPFC of rats decreased hyperactivity, which was induced by morphine injection, in contrast, D1 receptor antagonist SCH23390 increased the hyperactivity, These findings suggest: (1) The behavior and neural activity in ACC of addicts changed in chronic drug users. Their impulsive behavior might result from the abnormal neural activity in the mPFC especially the ACC. (2) Heroine patients were more depress and anxiety than normal controls. The dysfunction of the mPFC---amygdala circuit of heroine addicts might be related to the abnormal emotion response. (3) Dopamine in the mPFC has an inhibitory effect on morphine induced behavior. The hyperactivity induced by chronic morphine was reduced by dopamine increase with D1 receptor agonist, confirm the first experiment that the neuroadaption of mPFC system induced by chronic morphine administration appears to be the substrate the impulse behavior of drug users.

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Rewarding experience after drug use is one of the mechanisms of substance abuse. Previous evidence indicated that rewarding experience was closely related to learning processes. Neuroscience studies have already established multiple-mode learning model. Reference memory system and habit memory are associated with hippocampus and dorsa striatum respectively, which are also involved in the rewarding effect of morphine. However, the relationship between spatial/habit learning and morphine reward property is still unclear. After drug use, with sensitization to rewarding effect, spatial learning is also changed. To study the mechanism of increment of spatial learning would provide new perspective about reward learning. Based on the individual difference between spatial learning and reward learning, the experiments studied relationship between the two leaning abilities and tested the function of dorsal hippocampus and dorsal striatum in morphine-induced CPP. The results were summarized below: 1 In a single-rule learning water maze task, subjects better in spatial learning also excelled in rewarding learning. In a multi-rule learning task, morphine administration was more rewarding to subjects of use place strategy. 2 Treatment potentiating the rewarding effect of morphine also increased place-rule learning, with no significant improvement in habit learning. 3 Intracranial injections into CA1 of hippocampus or dorsal striatum of M1 antagonist, Pirenzepine, could block the establishment of morphine CPP after three days morphine treatment. In contrast, the antagonist of D1 receptor SCH23390 had no blocking effect. Both Pirenzepine and SCH23390 blocked the locomotor-stimulating effect of morphine. In summary, spatial learning stimulated the behavioral expression of morphine’s rewarding effect, in which CA1 of hippocampus was critically involved. On the other side, a pretreatment schedule of morphine, while increased the rewarding effect, improved place-rule learning, indicating that spatial learning might be one chain of sensitization to drug rewards effects

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The conceptualization of “depression” as a heterogenous disease has been widely accepted by most researchers. However, controlled experiments are rather sparse. To date, most studies demonstrated that animals with helplessness, a widely recognized behavioral index of “depression” also show varied comobidity expressions of other emotional behaviors, such as hightened or lightened anxiety level compared with controls. This means that distinct subtypes of “depression” may exist, in which different neural mechanisms may play roles. The present study aims to explore the possibility of behaviorally categorizing two depressive subtypes, referred as anxious helplessness and non-anxious helplessness, respectively. Then, by using RT-PCR, the dopamine D1, D2, D3 receptors mRNA expressions in medial prefrontal cortex (mPFC) and nucleus accubems (NAc) were quantified. The main findings are described as belows: 1. Uncontrollable shock could readily induce helpless behavior in shocked animals as a whole but with salient individual differences. Prior inescaoable shock induces subsuquent helplessness in approximately 40% shocked animals, while the other animals showed no sign of helpless expression, and were classified as non-helplessness. 2. Among helpless animals, the “subtype” of anxious helpless and non-anxious helpless could be identified according to the anxiety level evaluated by elevated plus maze. 3. D3 receptors mRNA expressions in the mPFC and NAc were increased in stressed animals after uncontrollable shock treatment. At the meanwhile, significant lower expressions of D2 receptors in the mPFC and NAc, and much lower expressions of D1 receptors in the mPFC were found in rats that did not become helpless after stress. In contrast, no significant difference between helpless and control animals was found in D1/D2 receptors mRNA expressions. 4. Based on above mentioned results, the up-regulation of D3 receptors in the mPFC and NAc may reflect a generalized effect of exposure to uncontrollalbe shock. While the down-regulation of D1\D2 receptors in the mPFC and decreased expression of D2 receptors in the NAc may be associated with adaptive or protective mechnisms which protecting animals from helplessness after uncontrollable shock treatment. 5. Futhermore, a significant negative relationship was found between anxiety level and D1 receptors expressions in the mPFC in helpless animals. Compared to the non-anxious helpless and control rats, the D1 receptors mRNA of anxious helpless rats were down-regulation in the mPFC. The present study indicated that the D1 dopamine receptor gene is associated with co-morbid depression and anxiety.

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A Proteômica surgiu como uma das vertentes da era pós-genômica e vem contribuindo significativamente para o entendimento global e integrado do sistema biológico. O estudo do proteoma envolve todo o conjunto de proteínas expresso pelo genoma de uma célula, como também pode ser direcionado somente àquelas que se expressam diferencialmente em condições específicas. Proteômica dedica-se também ao conjunto de isoformas de proteínas e modificações pós-traducionais, às interações entre elas, bem como à descrição estrutural de moléculas e seus complexos. Esta revisão apresenta as principais tecnologias empregadas em estudos proteômicos, e faz um levantamento de trabalhos recentes que utilizaram abordagens proteômicas para a identificação de genes e rotas envolvidos na resposta da planta a estresses bióticos e abióticos. Finalmente, são discutidos aspectos do potencial do emprego da proteômica na compreensão de questões biológicas complexas e no melhoramento genético de plantas na busca de genótipos superiores.

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A anaplasmose bovina é causada pela riquétsia intra-eritrocítica Anaplasma marginale, responsável por importantes prejuízos econômicos, por causa da alta morbidade e mortalidade em rebanhos bovinos suscetíveis. A vacinação tem sido uma forma econômica e eficiente de controlar a enfermidade. No entanto, os métodos de imunização tradicionais apresentam efeitos adversos em algumas categorias de animais. Nas últimas décadas, os estudos sobre imunização contra Anaplasma concentraram-se nas proteínas de superfície MSP1a, 1b, 2, 3, 4 e 5. No entanto, até o momento, os resultados foram pouco promissores, apontando a necessidade de ampliar o conhecimento sobre o rol das proteínas de membrana da riquétsia e das relações estruturais entre elas. Nesse contexto, os estudos do genoma e do proteoma da riquétsia têm contribuído com essa finalidade. Pela análise genômica, 14 genes para novas proteínas de membrana externa foram identificados (omp 1-14), dentre os quais, omp2, 3 e 6 não são transcritos. Esses genes ostraram-se altamente conservados entre isolados da riquétsia. As proteínas OMP4, 7, 10 e 14 foram reconhecidas por soros de bovinos imunizados com membrana de A. marginale, mostrando potencial para desenvolvimento de imunógenos. Além disso, mediante análise proteômica, foi possível detectar novas proteínas de membrana, negligenciadas pela anotação genômica. Dentre elas estão AM097 - conjugal transfer protein, AM956 - PepA citosol amino peptidase, AM254 - fator de elongação Tu e quatro proteínas de função desconhecida: AM127, 197, 387 e 854, as quais também foram reconhecidas por soros de bovinos imunizados com membrana de A. marginale.

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Os objetivos buscados pelos autores neste estudo foram produzir e solubilizar a proteína MSP5 recombinante truncada de Anaplasma marginale e avaliar seu desempenho em um ensaio de imunoadsorção enzimática indireto para detecção de anticorpos contra a riquétsia. O gene msp5, exceto a região N-terminal hidrofóbica, foi amplificado por reação em cadeia da polimerase, clonado em plasmídeo pTrcHis-TOPO e expresso em Escherichia coli. A solubilização da proteína recombinante foi avaliada em diferentes pHs e concentrações de uréia. A sensibilidade e a especificidade do ensaio foram avaliados testando-se 66 soros de animais infectados experimentalmente com A. marginale e 96 soros negativos, com o estado de infecção desses animais confirmado por reação em cadeia da polimerase. Um total de 1.666 amostras de soros bovinos, provenientes do Brasil - Rio Grande do Sul (73), Mato Grosso do Sul (91), Pernambuco (86), Bahia (314) e Minas Gerais (267), assim como do Uruguai (32) e Costa Rica (803) foram testadas nos ELISAs com MSP5 truncada e com MSP1a recombinantes, e a concordância entre os dois testes foi avaliada. O ELISA indireto com MSP5 truncada foi capaz de detectar animais infectados com 96,97% de sensibilidade e 100% de especificidade. Nos animais infectados experimentalmente, o ELISA detectou anticorpos do 12o dia após a inoculação (DPI) até o último dia de observação (37o DPI). Os ELISAs para MSP5 e MSP1a apresentaram concordância de 95,67%, com índice kappa de 0,81. Os resultados discordantes apresentaram uma diferença significativa (P < 0,001). Anticorpos contra A. marginale foram detectados em animais de todas asregiões estudadas. O ELISA com MSP5 recombinante truncada apresentou bom desempenho na detecção de anticorpos contra A. marginale, com alta sensibilidade e especificidade, representando uma importante ferramenta para o diagnóstico da anaplasmose bovina em estudos epidemiológicos.