浙江中西医结合杂志
浙江中西醫結閤雜誌
절강중서의결합잡지
ZHEJIANG JOURNAL OF INTEGRATED TRADITIONAL CHINESE AND WESTERN MEDICINE
2015年
5期
439-442
,共4页
宋晨%诸靖宇%吴金星%徐智慧%张大宏
宋晨%諸靖宇%吳金星%徐智慧%張大宏
송신%제정우%오금성%서지혜%장대굉
大鼠%脊髓损伤%骶3神经电调节%逼尿肌细胞凋亡%膀胱纤维化
大鼠%脊髓損傷%骶3神經電調節%逼尿肌細胞凋亡%膀胱纖維化
대서%척수손상%저3신경전조절%핍뇨기세포조망%방광섬유화
rats%spinal cord injury%S3 neuromodulation%detrusor cell apoptosis%bladder fibrosis
目的:观察骶3神经电调节对脊髓损伤早期大鼠逼尿肌细胞凋亡及膀胱纤维化影响。方法取雌性成年SD大鼠90只,随机分成实验组60只,空白对照组30只,采用脊髓横断法建立大鼠神经源性膀胱的模型。实验组大鼠随机分为电针组及阴性对照组,各30只。电针组进行电极植入,并行电调节治疗2周。3组大鼠2周后同时处死取材,均分别采用胶原染色、苦杏酸天狼星红染色、免疫组化方法来观察逼尿肌纤维化程度。采用透射电镜观察逼尿肌细胞超微结构改变。结果①胶原染色及苦杏酸天狼星红染色观察,电针组同阴性对照组相比,平滑肌细胞之间胶原纤维的数量明显减少,细胞排列规则。②电针组膀胱组织Collagen Ⅰ和Collagen Ⅲ表达分别为(1.042±0.213)、(1.532±0.141),均明显低于阴性对照组的(2.049±0.246)、(3.901±0.208),电针组Ⅰ/Ⅲ型胶原比例较阴性对照组明显减少,差异有统计学意义(P<0.05)。阴性对照组CollagenⅠ和CollagenⅢ表达显著高于空白对照组的(1.154±0.124)、(0.780±0.127),阴性对照组Ⅰ/Ⅲ型胶原比例较空白对照组明显增高,差异有统计学意义(P<0.05)。③电镜观察,电针组与阴性对照组相比,逼尿肌细胞表面平滑,排列均匀,胞浆内线粒体结构完整,无肿胀破裂现象,细胞结构接近于空白对照组。结论骶3神经电调节能抑制脊髓损伤早期大鼠膀胱逼尿肌间质中胶原纤维的表达,减少脊髓损伤后大鼠逼尿肌细胞的凋亡,促进膀胱功能恢复。
目的:觀察骶3神經電調節對脊髓損傷早期大鼠逼尿肌細胞凋亡及膀胱纖維化影響。方法取雌性成年SD大鼠90隻,隨機分成實驗組60隻,空白對照組30隻,採用脊髓橫斷法建立大鼠神經源性膀胱的模型。實驗組大鼠隨機分為電針組及陰性對照組,各30隻。電針組進行電極植入,併行電調節治療2週。3組大鼠2週後同時處死取材,均分彆採用膠原染色、苦杏痠天狼星紅染色、免疫組化方法來觀察逼尿肌纖維化程度。採用透射電鏡觀察逼尿肌細胞超微結構改變。結果①膠原染色及苦杏痠天狼星紅染色觀察,電針組同陰性對照組相比,平滑肌細胞之間膠原纖維的數量明顯減少,細胞排列規則。②電針組膀胱組織Collagen Ⅰ和Collagen Ⅲ錶達分彆為(1.042±0.213)、(1.532±0.141),均明顯低于陰性對照組的(2.049±0.246)、(3.901±0.208),電針組Ⅰ/Ⅲ型膠原比例較陰性對照組明顯減少,差異有統計學意義(P<0.05)。陰性對照組CollagenⅠ和CollagenⅢ錶達顯著高于空白對照組的(1.154±0.124)、(0.780±0.127),陰性對照組Ⅰ/Ⅲ型膠原比例較空白對照組明顯增高,差異有統計學意義(P<0.05)。③電鏡觀察,電針組與陰性對照組相比,逼尿肌細胞錶麵平滑,排列均勻,胞漿內線粒體結構完整,無腫脹破裂現象,細胞結構接近于空白對照組。結論骶3神經電調節能抑製脊髓損傷早期大鼠膀胱逼尿肌間質中膠原纖維的錶達,減少脊髓損傷後大鼠逼尿肌細胞的凋亡,促進膀胱功能恢複。
목적:관찰저3신경전조절대척수손상조기대서핍뇨기세포조망급방광섬유화영향。방법취자성성년SD대서90지,수궤분성실험조60지,공백대조조30지,채용척수횡단법건립대서신경원성방광적모형。실험조대서수궤분위전침조급음성대조조,각30지。전침조진행전겁식입,병행전조절치료2주。3조대서2주후동시처사취재,균분별채용효원염색、고행산천랑성홍염색、면역조화방법래관찰핍뇨기섬유화정도。채용투사전경관찰핍뇨기세포초미결구개변。결과①효원염색급고행산천랑성홍염색관찰,전침조동음성대조조상비,평활기세포지간효원섬유적수량명현감소,세포배렬규칙。②전침조방광조직Collagen Ⅰ화Collagen Ⅲ표체분별위(1.042±0.213)、(1.532±0.141),균명현저우음성대조조적(2.049±0.246)、(3.901±0.208),전침조Ⅰ/Ⅲ형효원비례교음성대조조명현감소,차이유통계학의의(P<0.05)。음성대조조CollagenⅠ화CollagenⅢ표체현저고우공백대조조적(1.154±0.124)、(0.780±0.127),음성대조조Ⅰ/Ⅲ형효원비례교공백대조조명현증고,차이유통계학의의(P<0.05)。③전경관찰,전침조여음성대조조상비,핍뇨기세포표면평활,배렬균균,포장내선립체결구완정,무종창파렬현상,세포결구접근우공백대조조。결론저3신경전조절능억제척수손상조기대서방광핍뇨기간질중효원섬유적표체,감소척수손상후대서핍뇨기세포적조망,촉진방광공능회복。
Objective To investigate sacral nerve stimulation through S3 foramen for the treatment of detrusor cell apoptosis and neurogenic fibrosis of the bladder in rats with spinal cord injury(SCI). Methods Ninety SD fe-male rats were randomly divided into experimental group (n=30), control group (n=30), blank group (n=30). SCI model was established by crosscutting spine. Rats in experimental group were implanted with electrical acupuncture poles and had neruomodulation for 2 weeks. Rats in 3 groups were all sacrificed at the end of nerve stimulation and immunohistochemistry, collagen staining and Sirius Red F3B(SR) staining and transmission electron microscope (TEM) were used to observe the apoptosis and fibrosis of the detrusor muscle. Results Collagen and SR staining showed that less collagen fiber was seen between detrusor cells and the cells were more regular and smooth in ex-perimental group than those in control group. Collagen I and collagen III were decreased in experimental group than those in control group (collagen I:1.042±0.213 vs 2.049±0.246, collagen III:1.532±0.141 vs 3.901±0.208, P<0.05). The ratio of collagen I to collagen III in experimental group was lower than that in control group with sig-nificant difference (P<0.05). The collagen I and collagen III of control group was higher than that of blank group (collagen I:1.154±0.124, collagen III:0.780±0.127, P<0.05) and the ratio of collagen I to collagen III was also higher (P<0.05). TEM observed that the cells of experimental group were more regular and smoother than those of control group and no cell edema and destroied and the construction of the cells were similar to the normal cells (blank group). Conclusion The S3 nerve electrical stimulation may improve bladder function by inhibiting apopto-sis and fibrosis of detrusor cells in SCI rats.