中华实验外科杂志
中華實驗外科雜誌
중화실험외과잡지
CHINESE JOURNAL OF EXPERIMENTAL SURGERY
2008年
9期
1100-1102
,共3页
张浩%宋智钢%姚颖龙%段炼%邹毅清%李白翎%黄盛东%徐志云
張浩%宋智鋼%姚穎龍%段煉%鄒毅清%李白翎%黃盛東%徐誌雲
장호%송지강%요영룡%단련%추의청%리백령%황성동%서지운
生物起搏%电子起搏%窦房结/细胞学%自体移植%心脏
生物起搏%電子起搏%竇房結/細胞學%自體移植%心髒
생물기박%전자기박%두방결/세포학%자체이식%심장
Biological pacemaker%Electronic pacemaker%Sino-atrial node/eytology%Autograft%Heart
目的 观察自体窦房结细胞移植与电子起搏器"串联"起搏心脏的作用.方法 健康成年犬12条,随机分为实验组和对照组(n=6).所有犬安置电子心脏起搏器以保证存活,然后切取窦房结.将实验组犬窦房结组织消化成细胞悬液后,注射到自体右室前壁心肌内,对照组相同部位注射等量培养液.2周后射频消融希氏束,建立完全性房室传导阻滞犬模型,观察并记录犬心律.对实验组犬经股静脉应用异丙肾上腺素,研究心律变化.免疫荧光染色观察移植的细胞存活状况及其与心室肌细胞形成的缝隙连接结构.结果 建立完全性房室传导阻滞犬模型1 h后,实验组心率高于对照组(P<0.01).注射异丙肾上腺素后,实验组心率变化明显(P<0.01).实验组心律在14 d内保持稳定.免疫荧光染色法证实,移植的细胞在移植部位存活,且细胞间有缝隙连接结构形成.结论 自体窦房结细胞移植是一种对儿茶酚胺类物质的调节作用反应敏感的生物起搏技术,并且在与电子起搏技术串联后,其起搏作用在14 d内保持稳定.移植的窦房结细胞可与周围细胞形成电-机械耦联的结构基础.
目的 觀察自體竇房結細胞移植與電子起搏器"串聯"起搏心髒的作用.方法 健康成年犬12條,隨機分為實驗組和對照組(n=6).所有犬安置電子心髒起搏器以保證存活,然後切取竇房結.將實驗組犬竇房結組織消化成細胞懸液後,註射到自體右室前壁心肌內,對照組相同部位註射等量培養液.2週後射頻消融希氏束,建立完全性房室傳導阻滯犬模型,觀察併記錄犬心律.對實驗組犬經股靜脈應用異丙腎上腺素,研究心律變化.免疫熒光染色觀察移植的細胞存活狀況及其與心室肌細胞形成的縫隙連接結構.結果 建立完全性房室傳導阻滯犬模型1 h後,實驗組心率高于對照組(P<0.01).註射異丙腎上腺素後,實驗組心率變化明顯(P<0.01).實驗組心律在14 d內保持穩定.免疫熒光染色法證實,移植的細胞在移植部位存活,且細胞間有縫隙連接結構形成.結論 自體竇房結細胞移植是一種對兒茶酚胺類物質的調節作用反應敏感的生物起搏技術,併且在與電子起搏技術串聯後,其起搏作用在14 d內保持穩定.移植的竇房結細胞可與週圍細胞形成電-機械耦聯的結構基礎.
목적 관찰자체두방결세포이식여전자기박기"천련"기박심장적작용.방법 건강성년견12조,수궤분위실험조화대조조(n=6).소유견안치전자심장기박기이보증존활,연후절취두방결.장실험조견두방결조직소화성세포현액후,주사도자체우실전벽심기내,대조조상동부위주사등량배양액.2주후사빈소융희씨속,건립완전성방실전도조체견모형,관찰병기록견심률.대실험조견경고정맥응용이병신상선소,연구심률변화.면역형광염색관찰이식적세포존활상황급기여심실기세포형성적봉극련접결구.결과 건립완전성방실전도조체견모형1 h후,실험조심솔고우대조조(P<0.01).주사이병신상선소후,실험조심솔변화명현(P<0.01).실험조심률재14 d내보지은정.면역형광염색법증실,이식적세포재이식부위존활,차세포간유봉극련접결구형성.결론 자체두방결세포이식시일충대인다분알류물질적조절작용반응민감적생물기박기술,병차재여전자기박기술천련후,기기박작용재14 d내보지은정.이식적두방결세포가여주위세포형성전-궤계우련적결구기출.
Objective To explore the effect of autograft of sino-atrial nodal cells for pacing heart working with electronic pacemaker.Methods Twelve healthy adult dogs were randomly assigned to experimental group or control group.The sino-atrial node(SAN)Was harvested after the electronic pacemaker was implanted into the dogs.The SAN from dogs in experimental group was digested into cell suspension,then injected into autogenic right ventricular anterior wall.Commensurable culture medium Was injected into the same position in control group.Two week later,all dogs underwent electrophysiologic study and transeatheter ablation of His bundle to create three-degree AV block models.Isopmterenol(ISO)was administrated to the dogs in experimental group to investigate the change of the rhythm.Immunofluorescent staining Was done to investigate the survival of grafted cells and gap junction formed between cells.Results One h after the establishment of three-degree AV block models,heart rates in the dogs from experimental group were quicker than those in control group(P<0.01).This escape rhythm Was altered remarkably when ISO was administrated(P<0.01).And this rhythm maintained for 14 days.Immunofluoreacent staining suggested that the grafted SAN cells survived in ventficular myocardium and gap junctions expressed betwoen cells.Conclusion Autograft of SAN cells from adult dogs is a kind of biopacing techniques sensirive to ISO.This effect is stable during 14 days.Grafted SAN cells carl form gap junctions with adjacent myocytes.