中国糖尿病杂志
中國糖尿病雜誌
중국당뇨병잡지
CHINESE JOURNAL OF DIABETES
2008年
10期
622-624
,共3页
谷宝军%YANG Zhong-guang%司捷旻%刘峰%徐月敏
穀寶軍%YANG Zhong-guang%司捷旻%劉峰%徐月敏
곡보군%YANG Zhong-guang%사첩민%류봉%서월민
糖尿病%大鼠%尿道外括约肌
糖尿病%大鼠%尿道外括約肌
당뇨병%대서%뇨도외괄약기
External urethral sphincter
目的 利用大鼠模型研究糖尿病(DM)对尿道外括约肌功能的影响.方法以雌性SD大鼠制成DM模型,6~8周后测定DM大鼠和正常对照(NC)大鼠膀胱等容收缩状态下的膀胱内压、尿道充盈压和括约肌肌电图(EUS-EMG).结果 与NC大鼠对比,DM大鼠体重明显降低,血糖明显升高,膀胱容量明显增大;膀胱排尿收缩时尿道压力病理性增高;EUS-EMG表现为排尿过程中应有的尿道外括约肌高频舒张收缩减弱或消失,引发的尿道压力曲线上的高频振动波振幅降低或消失.结论 DM在损伤大鼠膀胱功能的同时,还损伤排尿时尿道外括约肌正常的高频收缩舒张功能.
目的 利用大鼠模型研究糖尿病(DM)對尿道外括約肌功能的影響.方法以雌性SD大鼠製成DM模型,6~8週後測定DM大鼠和正常對照(NC)大鼠膀胱等容收縮狀態下的膀胱內壓、尿道充盈壓和括約肌肌電圖(EUS-EMG).結果 與NC大鼠對比,DM大鼠體重明顯降低,血糖明顯升高,膀胱容量明顯增大;膀胱排尿收縮時尿道壓力病理性增高;EUS-EMG錶現為排尿過程中應有的尿道外括約肌高頻舒張收縮減弱或消失,引髮的尿道壓力麯線上的高頻振動波振幅降低或消失.結論 DM在損傷大鼠膀胱功能的同時,還損傷排尿時尿道外括約肌正常的高頻收縮舒張功能.
목적 이용대서모형연구당뇨병(DM)대뇨도외괄약기공능적영향.방법이자성SD대서제성DM모형,6~8주후측정DM대서화정상대조(NC)대서방광등용수축상태하적방광내압、뇨도충영압화괄약기기전도(EUS-EMG).결과 여NC대서대비,DM대서체중명현강저,혈당명현승고,방광용량명현증대;방광배뇨수축시뇨도압력병이성증고;EUS-EMG표현위배뇨과정중응유적뇨도외괄약기고빈서장수축감약혹소실,인발적뇨도압력곡선상적고빈진동파진폭강저혹소실.결론 DM재손상대서방광공능적동시,환손상배뇨시뇨도외괄약기정상적고빈수축서장공능.
Objective Urethral function is essential for efficient voiding.This study focused on the function of the external urethral sphincter (EUS) in DM rats. Methods Female SD rats with the weight of 250-275g weight initially were used.DM (n=6) was induced by an i.p.injection of streptozotocin (65 mg/kg) and allowed to progress for 6 to 8 weeks,and age-matched normal rats (n=5) were taken as control.A double lumen catheter was used to simultaneously record isovolumetric bladder pressure and urethral perfusion pressure (UPP) under urethane anesthesia.EUS-EMG(electromyogram) activities were also recorded using fine wired electrodes. Results Blood glucose of all DM rats was>300 mg/dl.High frequency oscillations (HFOs) of UPP were significantly reduced in some diabetic rats, but never in controls.The increased tonic EUS activity in diabetic rats resulted in increased urethral resistance (UPP was 23.5±1.6mmHg in DM rats compared with 7.9±1.8mmHg in controls,P<0.05). Conclusions These results demonstrate that DM induces EUS dysfunctions, decreases urethral relaxation and increases urethral outlet resistance during reflex voiding