中国烧伤创疡杂志
中國燒傷創瘍雜誌
중국소상창양잡지
2014年
4期
287-294
,共8页
何仁亮%余志和%李红毅%王洪生%李凤春%梁家芬%吴树毅
何仁亮%餘誌和%李紅毅%王洪生%李鳳春%樑傢芬%吳樹毅
하인량%여지화%리홍의%왕홍생%리봉춘%량가분%오수의
湿润烧伤膏%毛囊单位%成纤维细胞%原位再生技术
濕潤燒傷膏%毛囊單位%成纖維細胞%原位再生技術
습윤소상고%모낭단위%성섬유세포%원위재생기술
MEBO%Follicular Unit%Fibroblast%In situ regeneration technology
目的:探讨毛囊单位移植联合原位再生技术对创面修复的作用。方法将24只SD大鼠(雌雄各半)随机分为实验组A(毛囊单位移植组)、实验组B(毛囊单位移植联合原位再生技术组)、对照组C(自体微粒皮移植组)、对照组D (自体微粒皮移植联合原位再生技术组),每组6只,制成SD大鼠体表创面模型,并在制备好的创面上分别覆盖相应的湿润烧伤膏药纱(B、 D组)及凡士林纱布(A、 C组),每天换药1次。5 d后,创面肉芽组织生长,此时剪取A、 B组大鼠的单侧鼠须垫皮肤,并分割鼠须垫毛囊,切取带有毛囊乳头、毛囊周围组织及部分表皮的毛囊单位复合组织,植入已制备好的创面中;从C、 D组大鼠的全层皮肤中切取表皮和部分真皮组织,植入已制备好的创面中; A、 C组创面覆盖凡士林纱布,B、 D组创面覆盖湿润烧伤膏药纱。分别于术后第1、2、3、4、5周取各组创面标本,镜下观察其组织学改变。结果 B组大鼠的创面愈合情况明显优于A、C、 D组,组织病理学观察可见,B组创面术后成纤维细胞及新生毛细血管的数量均多于A、 C、 D组,且其后期减少较明显; B组创面上皮组织生长速度及创面缩小速度均较A、 C、 D组快。结论湿润烧伤膏能加速实验性大鼠皮肤溃疡创面的愈合,使炎症细胞不断减少,毛细血管和细胞排列有序,调节细胞的数量和形态,促进成纤维细胞逐渐产生胶原纤维,转变成纤维细胞,从而修复创面。
目的:探討毛囊單位移植聯閤原位再生技術對創麵脩複的作用。方法將24隻SD大鼠(雌雄各半)隨機分為實驗組A(毛囊單位移植組)、實驗組B(毛囊單位移植聯閤原位再生技術組)、對照組C(自體微粒皮移植組)、對照組D (自體微粒皮移植聯閤原位再生技術組),每組6隻,製成SD大鼠體錶創麵模型,併在製備好的創麵上分彆覆蓋相應的濕潤燒傷膏藥紗(B、 D組)及凡士林紗佈(A、 C組),每天換藥1次。5 d後,創麵肉芽組織生長,此時剪取A、 B組大鼠的單側鼠鬚墊皮膚,併分割鼠鬚墊毛囊,切取帶有毛囊乳頭、毛囊週圍組織及部分錶皮的毛囊單位複閤組織,植入已製備好的創麵中;從C、 D組大鼠的全層皮膚中切取錶皮和部分真皮組織,植入已製備好的創麵中; A、 C組創麵覆蓋凡士林紗佈,B、 D組創麵覆蓋濕潤燒傷膏藥紗。分彆于術後第1、2、3、4、5週取各組創麵標本,鏡下觀察其組織學改變。結果 B組大鼠的創麵愈閤情況明顯優于A、C、 D組,組織病理學觀察可見,B組創麵術後成纖維細胞及新生毛細血管的數量均多于A、 C、 D組,且其後期減少較明顯; B組創麵上皮組織生長速度及創麵縮小速度均較A、 C、 D組快。結論濕潤燒傷膏能加速實驗性大鼠皮膚潰瘍創麵的愈閤,使炎癥細胞不斷減少,毛細血管和細胞排列有序,調節細胞的數量和形態,促進成纖維細胞逐漸產生膠原纖維,轉變成纖維細胞,從而脩複創麵。
목적:탐토모낭단위이식연합원위재생기술대창면수복적작용。방법장24지SD대서(자웅각반)수궤분위실험조A(모낭단위이식조)、실험조B(모낭단위이식연합원위재생기술조)、대조조C(자체미립피이식조)、대조조D (자체미립피이식연합원위재생기술조),매조6지,제성SD대서체표창면모형,병재제비호적창면상분별복개상응적습윤소상고약사(B、 D조)급범사림사포(A、 C조),매천환약1차。5 d후,창면육아조직생장,차시전취A、 B조대서적단측서수점피부,병분할서수점모낭,절취대유모낭유두、모낭주위조직급부분표피적모낭단위복합조직,식입이제비호적창면중;종C、 D조대서적전층피부중절취표피화부분진피조직,식입이제비호적창면중; A、 C조창면복개범사림사포,B、 D조창면복개습윤소상고약사。분별우술후제1、2、3、4、5주취각조창면표본,경하관찰기조직학개변。결과 B조대서적창면유합정황명현우우A、C、 D조,조직병이학관찰가견,B조창면술후성섬유세포급신생모세혈관적수량균다우A、 C、 D조,차기후기감소교명현; B조창면상피조직생장속도급창면축소속도균교A、 C、 D조쾌。결론습윤소상고능가속실험성대서피부궤양창면적유합,사염증세포불단감소,모세혈관화세포배렬유서,조절세포적수량화형태,촉진성섬유세포축점산생효원섬유,전변성섬유세포,종이수복창면。
Objective Explore the effect of the combination of follicular unit transplantation andin-situ skin regen-eration technology on wound repair. Method All the 24 SD rats, ( half female and half male) , wererandomly divided into four groups ( 6 rats each group ) : experiment group A ( follicular unit transplantation group ) , experimental group B ( follicular unit transplantation combined with in-situ regeneration technology) , control groupC ( autologous micro skin par-ticle transplant group) and control group D ( autologous micro skin particle transplant combined with in-situ regeneration technology). Wound model was established in every rat and covered by MEBO gauze (group B and D) or vaseline gauze (group A and C) which was changed once aday. Five days later, granulation tissue grew on the wound. At this time, sheared the skin ofone side beardsof rats in group A and B, and separated follicleswhich were then cut into follicular units consisting of follicle papilla, surrounding tissues and some epidermal skin, and the follicular units were transplanted into the prepared wound models of their own. In group C and D, epidermis with part of dermal skin was cut from the full-thickness skin of each rat and transplanted into its own wound model. Vaseline gauzeswere used to cover the wounds in group A and C, MEBO gauzes were used to cover the wounds in group B and D. Tissue samples on wounds in all groups were taken in week 1, 2, 3, 4, 5 after operation, and histological changes were observedunder a microscope. Results The status of wound healing in group B was obviously better than group A, C and D. In view of histopathological observation, newly gen-eratedfibroblasts and capillaries in group B were morethan that in group A, C and D, and their late term decrease were more apparent. The epithelium growth and wound area decrease in group B was faster that that in group A, C and D. Conclusion MEBO can accelerate the wound healing of experimental skin ulcers in rats, by decreasing inflammatory cells, arranging the capillaries and cells in order, regulating the quantity and morphology of cells, and promoting fibroblasts producing col-lagen fibers and turning intofibrocytes thereby repairing the wounds.