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hyperosmotic in Chinese

Pronunciation:
How to pronounce "hyperosmotic""hyperosmotic" in a sentence"hyperosmotic" meaning

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  • 高滲的

Examples

  • This structure increased obviously following hyperosmotic stimulation
    高滲刺激后， edas的數(shù)量明顯增多。
  • While it is not clear that whether son astrocytes respond to hyperosmotic stimuli and what ' s the relationship between them and neurons
    但是，關(guān)于膠質(zhì)細(xì)胞在高滲刺激狀況下，是否參與滲透壓的調(diào)節(jié)及其與神經(jīng)元的關(guān)系的研究尚未見報(bào)道。
  • Treat primary cultured neurons and astrocytes with hyperosmotic stimulation . immunofluorescence was used to study the expression of cx43 and cx32 in son neurons and astrocytes
    應(yīng)用westernblot技術(shù)檢測(cè)高滲刺激后視上核縫隙連接蛋白（ connexin ， cx ） 32和43含量。
  • After hyperosmotic treatment , cx43 - li granules increased quickly on the plasm of the cultured astrocytes and cx32 - li increased apparently in the cultured neurons
    而對(duì)培養(yǎng)的神經(jīng)元和星形膠質(zhì)細(xì)胞施予高滲刺激，星形膠質(zhì)細(xì)胞膜上cx43樣陽性顆粒迅速增多，神經(jīng)元cx32表達(dá)明顯增強(qiáng)。
  • Objective : in this study we try to simultaneously investigate the response of neurons and astrocytes of rats following hyperosmotic stimulation and focus attention on the role of neuronal - astrocytic complex in the osmotic reglution
    目的：本研究試圖從整體水平共同觀察神經(jīng)元和ast對(duì)高滲透壓刺激的反應(yīng)，探討神經(jīng)膠質(zhì)細(xì)胞?神經(jīng)元復(fù)合體在滲透壓調(diào)控過程中的作用。
  • 5 , after being treated with hyperosmotic stimulation , the cultured astrocytes and microglias showed a fast increase of intracellular calcium concentration followed by a decrease . the [ ca2 + ] j of astrocytes decreased slower than that of microglias . according to the r
    根據(jù)實(shí)驗(yàn)結(jié)果，得出以下結(jié)論： l 、高滲刺激可以引起大鼠son內(nèi)的星形膠質(zhì)細(xì)胞和小膠質(zhì)細(xì)胞快速的反應(yīng)，星形膠質(zhì)細(xì)胞的反應(yīng)要早于神經(jīng)元。
  • Based on the previous researches , the present study investigated the response of son neurons and glias ( astrocytes and microglias ) to hyperosmotic stimulation and their relationship to find out the roles of glias in regulating hyperosmotic stimulation
    因此在以往研究的基礎(chǔ)上，本課題通過觀察視上核神經(jīng)元和膠質(zhì)細(xì)胞(星形膠質(zhì)細(xì)胞和小膠質(zhì)細(xì)胞)對(duì)高滲刺激的反應(yīng)及其相互關(guān)系，探討視上核膠質(zhì)細(xì)胞在高滲刺激后調(diào)節(jié)過程中的作用。
  • Conclusions : the present results indicated that the brain areas involving in the heperosmotic regulation mainly located in mvz son and pvn . the neurons and astrocytes might be very active following hyperosmotic pressure and n - asc as a functional unit might serve to modulate osmotic pressure . there was reciprocal osmoregulation pathways between the mvz and son or pvn in the brain
    結(jié)論：參與大鼠高滲性滲透壓調(diào)節(jié)的中樞主要位于mvz 、 son和pvn等核團(tuán)，神經(jīng)元和ast以n asc的形式共同參與滲透壓調(diào)節(jié)反應(yīng)，體內(nèi)存在mvz和son或pvn之間往返的滲透壓調(diào)節(jié)通路。
  • Methods : hyperosmotic pressure animal model was established by administering 3 % sodium chloride as drinking water to rats or increasing osmotic pressure of the culture medium . osmoregulation positions in the brain , reciprocal projection pathways between the medullary visceral zone ( mvz ) and supraoptic nucleus ( son ) or hypothalamic paraventricular nucleus ( pvn ) , oscillation of intracellular calcium in cultured neurons and astrocytes were studied by means of anti - fos , glial fibrillary acidic protein ( gfap ) , tyrosine hydroxylase ( th ) or vasopressin ( vp ) multiple imrnunohistochemical staining , immuno - electronic microscope , wga - hrp retrogradely tracing and cell culture methods . results : ( 1 ) fos positive neurons within the mvz , parabrachial nuclei , locus ceruleus , pvn , son , subfomical organ increased markedly
    方法：通過給予大鼠飲用3氯化鈉或提高培養(yǎng)基滲透壓濃度的方法復(fù)制高滲刺激模型，主要采用抗fos 、膠質(zhì)原纖維酸性蛋白( gfap )和酪氨酸羥化酶( th ) (或加壓素? vp )免疫組織化學(xué)多重染色、免疫電鏡、 wga - hrp束路追蹤結(jié)合免疫組織化學(xué)多重染色、細(xì)胞培養(yǎng)等實(shí)驗(yàn)方法，系統(tǒng)觀察了中樞參與滲透壓反射的調(diào)控部位、下丘腦視上核( son )神經(jīng)元? ast超微結(jié)構(gòu)的變化、延髓內(nèi)臟帶( mvz )和son及下丘腦室旁核( pvn )之間往返投射通路和神經(jīng)元的性質(zhì)及其與ast的關(guān)系、培養(yǎng)神經(jīng)元和ast內(nèi)鈣波的變化。
  • An acellular dermal matrix was prepared from allogenic skin by removing epidermis with a hyperosmotic salt solution and cross - linking with glutaralaldehyde , then clear away acellular components in dermis with naoh - maceration . the light and sme observation of the acellular dermal matrix revealed that the epidermis and cellular component in dermis were eliminated
    本研究共分四部分：第一部分無細(xì)胞真皮基質(zhì)的制備用高滲鹽除去異體皮膚的表皮細(xì)胞，經(jīng)戊二醛交聯(lián)后以低濃度naoh消蝕以除去真皮中的所有細(xì)胞成分，得到無細(xì)胞真皮基質(zhì)。
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