中南大学学报(医学版)
中南大學學報(醫學版)
중남대학학보(의학판)
JOURNAL OF CENTRAL SOUTH UNIVERSITY (MEDICAL SCIENCES)
2010年
8期
800-806
,共7页
贺志飚%彭再梅%金丽艳%徐军美%柴湘平
賀誌飚%彭再梅%金麗豔%徐軍美%柴湘平
하지표%팽재매%금려염%서군미%시상평
吗啡%药物预处理%缺血再灌注损伤%线粒体%通透性转换孔
嗎啡%藥物預處理%缺血再灌註損傷%線粒體%通透性轉換孔
마배%약물예처리%결혈재관주손상%선립체%통투성전환공
morphine%medicine preconditioning%ischemia-reperfusion injury%mitochondria%permeability transition pore
目的:探讨吗啡预处理对大鼠缺血再灌注损伤心肌保护作用及对线粒体通透性转换孔(mitochondrial permeability transition pore,MPTP)的影响.方法:40只SD成年雄性大鼠,体质量220~280 g,随机分为S组(假手术组,仅穿线,不结扎冠状动脉前降支),IR组(缺血再灌注组),Mp+IR组(吗啡预处理缺血再灌注组),CsA+IR组 (环孢霉素A预处理缺血再灌注组), 每组10只.除S组外,其余大鼠心脏都经历30 min缺血和180 min再灌注,再灌注180 min时抽血测血清中磷酸肌酸同工酶(creatine kinase-Mb,CK-Mb)和心肌肌钙蛋白I(cardiac troponin I,cTnI),分离心肌线粒体,测定缺血再灌注心肌线粒体2-3[H]DOG,Cyt C,[Ca2+]m 和Ca2+摄取速率及MPTP t1/2(MPTP达到50%开放所需时间)并比较4组之间的差异.结果:Mp+IR组和CsA+IR组CK-Mb与cTnI明显较IR组降低(P<0.01).IR组心肌细胞线粒体2-3[H]DOG和[Ca2+]m 明显增加,高于S组,Cyt C含量明显低于S组,Mp+IR组较IR组2-3[H]DOG和[Ca2+]m下降,Cyt C 含量增加(P<0.01).2-3[H]DOG与[Ca2+]m呈正相关(r=0.797,P<0.01), Cyt C与2-3[H]DOG呈负相关(r=-0.805,P<0.01),Cyt C与[Ca2+]m呈负相关(r=-0.648,P<0.01).缺血再灌注后MPTP t1/2明显缩短,用吗啡和CsA干预使MPTP t1/2明显延长.结论:用吗啡预处理可以起到保护心肌的作用,其机制可能与降低钙超载,延长MPTPt1/2有关.
目的:探討嗎啡預處理對大鼠缺血再灌註損傷心肌保護作用及對線粒體通透性轉換孔(mitochondrial permeability transition pore,MPTP)的影響.方法:40隻SD成年雄性大鼠,體質量220~280 g,隨機分為S組(假手術組,僅穿線,不結扎冠狀動脈前降支),IR組(缺血再灌註組),Mp+IR組(嗎啡預處理缺血再灌註組),CsA+IR組 (環孢黴素A預處理缺血再灌註組), 每組10隻.除S組外,其餘大鼠心髒都經歷30 min缺血和180 min再灌註,再灌註180 min時抽血測血清中燐痠肌痠同工酶(creatine kinase-Mb,CK-Mb)和心肌肌鈣蛋白I(cardiac troponin I,cTnI),分離心肌線粒體,測定缺血再灌註心肌線粒體2-3[H]DOG,Cyt C,[Ca2+]m 和Ca2+攝取速率及MPTP t1/2(MPTP達到50%開放所需時間)併比較4組之間的差異.結果:Mp+IR組和CsA+IR組CK-Mb與cTnI明顯較IR組降低(P<0.01).IR組心肌細胞線粒體2-3[H]DOG和[Ca2+]m 明顯增加,高于S組,Cyt C含量明顯低于S組,Mp+IR組較IR組2-3[H]DOG和[Ca2+]m下降,Cyt C 含量增加(P<0.01).2-3[H]DOG與[Ca2+]m呈正相關(r=0.797,P<0.01), Cyt C與2-3[H]DOG呈負相關(r=-0.805,P<0.01),Cyt C與[Ca2+]m呈負相關(r=-0.648,P<0.01).缺血再灌註後MPTP t1/2明顯縮短,用嗎啡和CsA榦預使MPTP t1/2明顯延長.結論:用嗎啡預處理可以起到保護心肌的作用,其機製可能與降低鈣超載,延長MPTPt1/2有關.
목적:탐토마배예처리대대서결혈재관주손상심기보호작용급대선립체통투성전환공(mitochondrial permeability transition pore,MPTP)적영향.방법:40지SD성년웅성대서,체질량220~280 g,수궤분위S조(가수술조,부천선,불결찰관상동맥전강지),IR조(결혈재관주조),Mp+IR조(마배예처리결혈재관주조),CsA+IR조 (배포매소A예처리결혈재관주조), 매조10지.제S조외,기여대서심장도경력30 min결혈화180 min재관주,재관주180 min시추혈측혈청중린산기산동공매(creatine kinase-Mb,CK-Mb)화심기기개단백I(cardiac troponin I,cTnI),분리심기선립체,측정결혈재관주심기선립체2-3[H]DOG,Cyt C,[Ca2+]m 화Ca2+섭취속솔급MPTP t1/2(MPTP체도50%개방소수시간)병비교4조지간적차이.결과:Mp+IR조화CsA+IR조CK-Mb여cTnI명현교IR조강저(P<0.01).IR조심기세포선립체2-3[H]DOG화[Ca2+]m 명현증가,고우S조,Cyt C함량명현저우S조,Mp+IR조교IR조2-3[H]DOG화[Ca2+]m하강,Cyt C 함량증가(P<0.01).2-3[H]DOG여[Ca2+]m정정상관(r=0.797,P<0.01), Cyt C여2-3[H]DOG정부상관(r=-0.805,P<0.01),Cyt C여[Ca2+]m정부상관(r=-0.648,P<0.01).결혈재관주후MPTP t1/2명현축단,용마배화CsA간예사MPTP t1/2명현연장.결론:용마배예처리가이기도보호심기적작용,기궤제가능여강저개초재,연장MPTPt1/2유관.
Objective To investigate the effect of morphine preconditioning on mitochondrial permeability transition pore (MPTP) and its protective mechanism after myocardial ischemia-reperfusion injury. Methods A rat model of ischemia-reperfusion injury was established. Forty rats were injected with 2-3[H] DOG and then divided into 4 groups randomly: a sham operation (S) group, an ischemia-reperfusion injury (IR) group, a morphine preconditioning (Mp+IR) group, and a cyclosporine A preconditioning (CsA+IR) group. We monitored the concentrations of serum creatine kinase-Mb (CK-Mb) and cardiac troponin I (cTnI), and measured myocardial mitochondrial 2-3[H] DOG, cytochrome c content, Ca2+ concentration ([Ca2+]m), the velocity of Ca2+ intake and reaction half time of mitochondrial permeability transition pore (MPTP t1/2) in the 4 groups. Results The concentrations of serum CK-Mb and cTnI decreased more in the Mp+IR group and the CsA+IR group than those of the IR group. The concentrations of 2-3[H]DOG and [Ca2+]m in the IR group were evidently higher but the level of cytochrome c was lower than those of the sham operation group. The concentrations of 2-3[H] DOG and [Ca2+]m in the Mp+IR group decreased whereas the concentration of cytochrome c increased compared with those in the IR group. Mitochondrial 2-3[H]DOG content was positively correlated with the concentration of calcium (r=0.797, P<0.01). The 2-3[H]DOG and [Ca2+]m content were negatively correlated with cytochrome c in the IR group (r=-0.805 and r=-0.648, respectively, P<0.01). MPTP t1/2 in the IR group was shortened evidently, and that in the Mp+IR and CsA+IR group was significantly lengthened. Conclusion Morphine preconditioning may have myocardial protective effect through unburdening the calcium overload and lengthening the MPTP t1/2.