皮下小血管 的英文怎麼說

中文拼音 [xiàxiǎoxiěguǎn]
皮下小血管 英文
small subcutaneous vessels
  • : Ⅰ名詞1 (人或物體表面的一層組織) skin 2 (皮革) leather; hide 3 (毛皮) fur 4 (包在外面的一層...
  • : 下動詞1. (用在動詞后,表示由高處到低處) 2. (用在動詞后, 表示有空間, 能容納) 3. (用在動詞后, 表示動作的完成或結果)
  • : Ⅰ形容詞1 (體積、面積、數量、強度等不大) small; little; petty; minor 2 (年紀小的; 年幼的) youn...
  • : 血名詞(血液 多用於口語) blood:吐血 spit (up) blood; 血的教訓 a lesson paid for [written] in b...
  • : Ⅰ名詞1 (管子) pipe; tube 2 (吹奏的樂器) wind musical instrument 3 (形狀似管的電器件) valve;...
  • 皮下 : subcutaneous皮下組織 [生理學] hypodermis; subcutis; hypoderm; subcutaneous tissue
  • 血管 : blood vessel; vascellum; vessel; rete
  1. Section two the evaluation of biocompatibility of the acellular dermal matrix by the method of cell culture. the new born rat ' s epdermic cells were cultured with the acellular dermal matrix together as experiment group, while the epdermic cell were cultured simply as control. 24 hours later, under the invert microscope, the epidermic cells anchored well and transparent flat cells were observed in both groups. 7 days later, both cultured cells were taked out and fixed in 95 % ethanol, stained with hematoxylin and were observed under light microscope. many cleaved cells were observed in both groups. during cell culture, no pathogenic microganism was observed. so we considered the acellular dermal matrix was aseptic and had good biocompatibility. section three subdermal implantation of the acellular dermal matrix. 24 rats were used in the experiments. a piece of acellular dermal matrix ( 1. 5 x 1. 5cm2 ) was implanted beneath the dorsum skin flaps of each rat, 1 week, 2 weeks, 3 weeks and 4 weeks after implantation, 6 pieces of acellular dermal matrix were harvested and the size of implanted acellular dermal matrix were measured, the sections were used for he staining and observed under light microscope. the result were as folio wing : 1 - 2 weeks after implantation, the acellular dermal matrix began to adhere to the tissue around and turned red gradually ; 3 - 4weeks after implantation, the acellular dermal matrix adhered closely to the tissue around and could be recognized easily, 1 - 3 weeks after implantation, the size of implanted acellular dermal matrix had no statistical difference ( p > 0. 05 ). 4 weeks after implantation implanted acellular dermal matrix contracted ( p < 0. 05 ). under light microscope, l - 2weeks after implantation, the fibroblast cells infiltrated the acellular dermal matrix and a small amount endothelial cells of vessel and lympho - histiocytic cells infiltrated the acellular dermal matrix. 3 - 4 weeks after implantation, infiltrating blood vessels were evident. so we think that the acellular dermal matrix had low immunological reactions and could induce the infiltration of fibroblast macrophage cell and the endothelial cells of vessel

    結果如包埋卜周者,無細胞真基質漸與周圍組織粘附,顏色由蒼白轉紅;包埋3周者,無細胞真基質與周圍組織緊密枯附,盾晰葉辯;術后卜周,包埋的基質面積變化較包埋前無統計學差異o川0引,術后4周包埋的無細胞真基質面積較包埋前縮j刃刀5 ) 。光鏡術后卜周,宿主的淋巳組織細胞、成纖維細胞浸入生長,釉附在膠原纖維上,少量細胞浸入基質;術后34周,無細胞真基質內較多的形成,故可認為無細胞真基質免疫原性低,能誘導宿主的成纖維細胞、巨噬細胞浸入生長,為一種新型的真替代物。第四部分無細胞真基質與自體斷層片復合移棺的研究, sd大鼠10隻,在其背部卜方造成全厚膚缺損的創面
  2. ( 2 ) common integument tissue venous vessel network can be divided into five layers from superficial layer to deep layer : cutaneous papillary layer, hypopapillary layer, hypodermis layer, subdermal layer and deep fascia layer. the artery branch and arteriole that shallowed up from hypopapillar layer get to papillar layer to form vessel network, circuitous and twisted, reflux and anastomose to become postcapillary micro veins and endothelial venule, then anastomose each other and accompanied with artery to enter hypo

    靜脈伴行動脈進入組織層、深筋膜層,並與組織層和深筋膜層動脈分支的伴行靜脈匯合,分別形成組織層、深筋膜層靜脈網,進而匯入軸心動脈的伴行靜脈。而真網中與動脈不伴行的微靜脈匯合成為靜脈,並逐漸聚集增粗,匯合加入淺非伴行靜脈屬支或即為屬支的起點。
  3. 2. mouse lung vessel endothelial cell was used for examining ha, hb and hpd ' s ic50 concentration under saturated light dose and ic50 light dose in saturated concentration irradiated by copper vapor laser of 510. 6nm and 578. 2nm separately

    應用體外培養的鼠肺細胞系( 1h11 )測定在飽和光劑量的條件,實驗光敏劑對細胞的殺傷作用,得出其半數殺傷濃度。
  4. From the view of cellular rheology, we examined the influence of fluid shear stress on the metabolism, morphology, structure and function of endothelia cells in our previous research. it is first time for us to develop the research between shear stress and apoptosis. in this study, we stimulate the human umbilical venous endothelial cells ( huvec ) by lps and apply different levels of fluid shear stress to them by a parallel plate flow chamber, then observe the change of apoptosis of endothelial cells by terminal deoxynucleotidyl transferase mediated dutp nick end labeling ( tunel )

    我們從細胞力學的角度,曾對細胞在剪切力作用的代謝、形態、結構及功能等進行過系統研究,但剪切力與內細胞凋亡的相關研究尚屬首次,我們希望通過探討細胞凋亡與剪切力大及作用時間的關系,為探索剪切力對細胞信號轉導的影響及作用機理提供有價值的參考數據和實驗資料。
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