腎球囊 的英文怎麼說
中文拼音 [shènqiúnáng]
腎球囊
英文
glomerular capsule-
Abstract : the anti - inflammatory effect of n - butanol extract of xanthocerassorbifolia bunge ( bex ) was studied in this paper. the ear edema resulted from dimethyl benzene, paw edema induced by carrageenin, the increase of vascular permeability caused by acetic acid, the chemotaxis of wbc induced by cmc and the weight of cotton granuloma in mice and hind paw edema induced by fresh egg white in rats were inhibited significantly by ig bex daily for 7 days, respectively. the carrageenin - induced paw edema was also inhibited markedly in adrenal - ectomiced mice. no changes in weight of adrenal and the concentration of vitamin c were observed, indicating that the anti - inflammatory effect of bex was not related to pituitary - adrenal system
文摘:文冠木正丁醇提取物對二甲苯致小鼠耳腫脹、蛋清致大鼠足腫脹、角叉菜膠致小鼠足腫脹、醋酸致小鼠腹腔毛細血管通透性增加、小鼠羧甲基纖維素囊中白細胞遊走、小鼠棉球肉芽腫生長均有顯著的抑制作用，同樣劑量下，文冠木正丁醇提取物對角叉菜膠致去雙側腎上腺小鼠足腫脹仍有顯著的抑制作用，且對小鼠腎上腺重量及腎上腺中維生素c的含量沒有明顯影響。Necropsy at the end of the experiment indicated that histopathological abnormalities were found in kidneys, such as increase of gelatinous material and some white cell infiltration
組織病理學檢查中，腎組織的膠脂球明顯增多，部分腎小囊外周有炎性細胞浸潤。In this report, we mainly covered the following aspects of " tissue organ regeneration and replication in situ " : 1 ) procedures of tissue organd regeneration and replication and replication in clnical practice ; 2 ) the discover and existence of potentiald regenerative cell ( prc ) ; 3 ) the proliferation, differentiation and regeneration law of potential law of potential regenerative cells ; 4 ) study procedure on tissue organ regeneration and replication from prcs in vitro based on the model of full skin organ regeneration in situ after extensive in vitro, set up the method and technology of searching life regenerative substance required in tissue organ regeneration and replication in situ. in this study, first, the whole human body is divided into 206 function units, which are the " tissue organ " in regeneration study. then the histology foundation of tissue organ regeneration and replication in situ is set up. in ordre to prove the existence of the potential regenerative cells and their potential baility and function, we established clinical tracking rechnique of skin organ regeneration in situ ; meanwhile, several tissue organ regeneration and replication in vitro models which represent different kinds of runctions were sucessfully set up, with all these techniques and models, we confirmed : 1 ) the existence, function and ability of pptemtoa regenerative cells ; 2 ) the importance of life regenerative substance ; 3 ) the feasibility of tissue organ regeneration and replication in situ ; 4 ) the big value of tissue organ regeneration and replication in situ in life science and medicine progerss. we also showed the possible foreground of capture cancer with this method and technologh. in this report, nearly 200 photographs of several tissue organ regeneration and replication in situ or in vitro demonstrated the whole process of tissue organ and big organ entities regeneration and replication from cells. the results of tissue organ regeneration and replication in situ mainly include : 1 ) whole skin organ regeneration and replication in situ ; 2 ) gastrointestinal mucosa tissue organ regeneration in vitro ; 3 ) hair follicle tissue organ regeneration in situ or in vitro ; 4 ) never tissue organ regeneration in situ ; 5 ) pancreas tissue organ regeneration and replication in vitro ; 5 ) marrow tissue regeneration in vitro ; 6 ) renal glomerulus and tubule tissue organ tugeneraation in vitro ; 7 ) heart muscle regeneration in vitro, etcl. in order to let more and more people know and understand this technology of tissue organd regeneration and replication in situ, herein, for the first time, we publicize the key points of actualizing this technology. also, we publicized the technology procedures and the frame constitute of life substances. we bilieve this is a big contribution to human science
本研究報告，重點報道了組織器官的原位再生復制的臨床程序，報道了組織潛能再生細胞的發現和存在，以及該細胞的增殖分化和形成組織器官的變化規律.以燒傷后皮膚組織器官的原位再生復制為模型，研究出了體外組織潛能再生細胞復制組織器官的培養方法;以體外組織器官的復制為模型，建立了尋找原位組織器官再生復制所需生命物質的方法和技術.本研究，首先按人體的器官功能，分解為206個功能單位，確立了所復制的人體器官中的組織功能單位為組織器官，從而建立了原位組織器官再生復制的組織學基礎.為了驗證組織潛能再生細胞的再生潛能，建立了皮膚器官原位再生的實體臨床跟蹤技術，同時又建立了能代表有關器官功能類別的代表組織器官的原位和體外復制模型，以多組織器官的成功復制確定潛能再生細胞的作用，確定生命研究再生物質的重要性，確定組織器官原位再生復制的可行性，確定了組織器官原位再生復制的生命科學研究和醫學進步的重大應用價值，同時展示了用此方法和技術攻克癌癥的前景.本研究報告，以近二百幅多個組織器官原位和體外再生復制的實體圖片，展示了潛能再生細胞復制的組織器官和大器官司實體;展示了細胞再生復制器官的全過程.真實的報告了組織器官原位再生復制的成果.所公布的主要成果為:皮膚器官的原位再生復制;胃腸黏膜組織器官的原位和體外再生復制;毛囊組織器官的原位和體外再生復制;神經組織器官的原位復制;胰腺組織器官的體外復制;骨髓組織的體外復制;腎小球小管組織器官的體外復制;心肌的體外復制等.為了讓更多的人學會和掌握組織器官原位再生復制技術，本報告首次公布實施技術的重要環節和技術流程;首次公布了生命再生物質的框架和組成.作者自費研究成果對人類生命科學的一大貢獻Pathologically noted differences in renal size between the two entities, with gcd showing moderate renomegaly and ipcd marked renomegaly, have not been appreciated on us
這兩種疾病在病理改變上表現為腎大小存在顯著的區別，腎小球疾病顯示腎中度腫大，嬰兒多囊病腎顯著增大，在超聲上是無法鑒別的。Experimentally, gcd can be induced by administration of long - acting mineralocorticoids, reversible on withdrawal of the steroids < 9 >
經實驗研究，腎小球囊性腎病可以被長效的腎上腺皮質激素誘發，停用該類類固醇激素后其可以恢復< 9 > 。In previously reported cases, renal appearances in gcd were indistinguishable from ipcd or apcd with marked renomegaly, increased cortical and medullary echogenicity, loss of cortico - medullary differentiation and small cortical cysts
在以往的病例報道中，腎小球囊性腎病病例的腎臟外觀與嬰兒多囊病或成人多囊腎疾病是難以區別的，都表現為腎腫大、皮髓質回聲增強、皮髓質回聲的差別消失、皮質小囊腫。The term gcd has been loosely used in the literature and many conditions with only occasional cortical cysts e. g. trisomy 13 - 15 and zellweger ' s syndrome, have been included < 2 >
「腎小球囊性腎病」已經被廣泛的使用在文獻和偶爾出現在皮質囊腫的病例中，這些病例包括13 15三體和腦肝腎綜合征< 2 > 。The microscopic appearance of multicystic dysplastic kidney ( cystic renal dysplasia, or potter ' s type ii ) is characterized by large cysts lined by flattened cuboidal epithelium and an intervening parenchyma that is fibrotic with islands of bluish cartilage and rare glomeruli
多囊性發育不良腎（多囊腎發育不良）的顯微鏡下特點：囊腫較大，內層為扁平立方上皮，受累實質纖維化，內有島狀的藍色軟骨和少量的小球。Gcd may be the result of teratogenic insult rather than a genetic defect < 5, 7 >, and may be at least partially reversible in some patients < 5 >
腎小球囊性腎病可能是由致畸的創傷所致，而遺傳性缺陷的可能要相對小一些< 5 ， 7 > ，這種改變至少在某些病人是局部可逆的< 5 > 。Post mortem reports of liver findings in gcd include subcapsular cysts < 3 > and adenomas < 4, 5 >
屍檢報告發現，在腎小球囊性腎病，可見肝臟包膜下囊腫< 3 >和腺瘤< 4 ， 5 > 。The diagnosis of gcd must be considered in neonates and young children where us demonstrates bilateral marked renomegaly, increased cortical echogenicity with or without small visible cysts, normal medullary pyramids, and liver lesions not in keeping with periportal fibrosis
腎小球囊性腎病的診斷必須考慮到患者是年齡較小的兒童或新生兒，超聲可見雙腎顯著腫大，腎皮質回聲增強，其內可見或沒有大小不等的小囊腫，腎錐體回聲正常，沒有門脈周圍纖維化的肝損害。Gcd is a rare condition, characterised by diffuse dilatation of bowman ' s spaces with occasional involvement of collecting tubules
腎小球囊性腎病是一種罕見的以鮑曼（氏）腔彌漫型擴張為特徵的，偶爾會累積到集合小管的疾病。Effect of n - terminal fragment fusion protein of polycystin - 1 on collagen synthesis and degradation in rat glomerular mesangial cells
多囊蛋白1氨基段融合蛋白對腎小球系膜細胞細胞外基質及其降解基因表達的影響Glomerulocystic renal disease ( gcd ) is characterized histologically by uniform cystic dilatation of bowman ' s spaces
腎小球囊性腎病（ gcd ）在組織學上的特徵性表現為均勻一致的鮑曼（氏）腔的囊狀擴張。Results tsl could decrease the levels of fbg, hbalc, 24 h malb p005 or p001, ameliorate the thickness of glomerular basement membrane, decrease the components of ecm, downregulate tgf 1 and timp2 expression, and upregulate mmp2 expression p005 or p001
結果通腎絡膠囊可降低dn大鼠fbg hba1c 24h malb的水平wtbxp005或p001 ，減輕腎小球基底膜增厚程度，減少ecm成分，降低tgf 1 timp2的表達，升高mmp2的表達p005或p001 。Appearances were typical of glomerutocystic kidneys ( fig. 2 )
典型的腎小球囊性腎病表現（圖2 ） 。分享友人