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本文引用的文献

1
The cardiac sodium-calcium exchanger NCX1 is a key player in the initiation and maintenance of a stable heart rhythm.心脏钠离子-钙离子交换器 NCX1 是启动和维持稳定心律的关键因素。
Cardiovasc Res. 2013 Sep 1;99(4):780-8. doi: 10.1093/cvr/cvt154. Epub 2013 Jun 12.
2
Overactive bladder mediated by accelerated Ca2+ influx mode of Na+/Ca2+ exchanger in smooth muscle.平滑肌中通过钠/钙交换器的钙离子内流加速模式介导的膀胱过度活动。
Am J Physiol Cell Physiol. 2013 Aug 1;305(3):C299-308. doi: 10.1152/ajpcell.00065.2013. Epub 2013 May 22.
3
Reverse mode of the sodium/calcium exchanger subtype 3 in interstitial cells of Cajal from rat bladder.大鼠膀胱 Cajal 间质细胞中钠钙交换体亚型 3 的反向模式。
Urology. 2013 Jul;82(1):254.e7-12. doi: 10.1016/j.urology.2013.02.049. Epub 2013 May 17.
4
Anandamide reduces intracellular Ca2+ concentration through suppression of Na+/Ca2+ exchanger current in rat cardiac myocytes.花生四烯酸乙醇胺通过抑制大鼠心肌细胞中的钠/钙交换体电流来降低细胞内 Ca2+ 浓度。
PLoS One. 2013 May 7;8(5):e63386. doi: 10.1371/journal.pone.0063386. Print 2013.
5
Urinary nerve growth factor: a biomarker of detrusor overactivity? A systematic review.尿神经生长因子:逼尿肌过度活动的生物标志物?一项系统综述。
Int Urogynecol J. 2013 Oct;24(10):1603-9. doi: 10.1007/s00192-013-2104-0. Epub 2013 May 7.
6
Chronic cyclic bladder over distention up-regulates hypoxia dependent pathways.慢性周期性膀胱过度扩张上调缺氧依赖途径。
J Urol. 2013 Oct;190(4 Suppl):1603-9. doi: 10.1016/j.juro.2013.02.026. Epub 2013 Feb 19.
7
New insights into the contribution of arterial NCX to the regulation of myogenic tone and blood pressure.动脉 NCX 对肌源性张力和血压调节作用的新认识。
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8
Ca²⁺ channel and Na⁺/Ca²⁺ exchange localization in cardiac myocytes.钙离子通道和钠钙交换在心肌细胞中的定位。
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9
The Na+/Ca²+ exchanger in cardiac ischemia/reperfusion injury.心脏缺血/再灌注损伤中的 Na+/Ca²+ 交换体。
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10
Reverse-mode Na+/Ca2+ exchange is an important mediator of venous contraction.反向模式的 Na+/Ca2+ 交换是静脉收缩的一个重要介导者。
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钠/钙交换体1亚型的反向模式促成部分膀胱流出道梗阻大鼠的逼尿肌过度活动。

Reverse mode of sodium/calcium exchanger subtype 1 contributes to detrusor overactivity in rats with partial bladder outflow obstruction.

作者信息

Zhong Xiao, You Nan, Wang Qingqing, Li Longkun, Huang Chibing

机构信息

Department of Urology, Second Affiliated Hospital, Third Military Medical UniversityChongqing 400037, P. R. China.

Department of Hepatobiliary Surgery, Second Affiliated Hospital, Third Military Medical UniversityChongqing 400037, P. R. China.

出版信息

Am J Transl Res. 2018 Mar 15;10(3):806-815. eCollection 2018.

PMID:29636870
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5883121/
Abstract

To investigate whether the reverse mode of sodium/calcium exchanger subtype 1 (NCX1) plays an important role in the excitability of detrusor cells in rats with partial bladder outflow obstruction (PBOO), PBOO was maintained for 6 weeks in forty female Wistar rats. Thirty of the animals exhibited non-voiding bladder contraction and comprised the DO group. An additional thirty sham-operated female Wistar rats were used as the control group. The expression levels of NCX1 were compared between the two groups by quantitative reverse transcriptase-polymerase chain reaction (RT-PCR), western blotting (WB), and double-label immunofluorescence. The contractions of detrusor strips in NCX reverse mode were measured in both groups using isometric tension. The role of NCX in the regulation of the intracellular Ca concentration ([Ca]) of smooth muscle cells was observed in reverse mode using confocal microscopy, and the current was evaluated in the presence of the antagonist KB-R7943 (5 μM and 10 μM) using the whole-cell patch-clamp technique. The expression of NCX1 was significantly higher in the DO group than in the control group, as assessed by qRT-PCR, WB analysis and immunofluorescence. The volume and rate of Ca ion flux through the NCX, as well as the NCX currents, were higher in the DO group than in the control group in both modes. Increased NCX1 levels may contribute to the establishment of DO after PBOO by elevating [Ca] in reverse mode under depolarization, potentially inducing cell excitability.

摘要

为研究钠/钙交换体1亚型(NCX1)的反向模式是否在部分膀胱出口梗阻(PBOO)大鼠逼尿肌细胞的兴奋性中发挥重要作用,对40只雌性Wistar大鼠进行6周的PBOO造模。其中30只动物出现无排尿膀胱收缩,组成逼尿肌过度活动(DO)组。另外30只假手术雌性Wistar大鼠作为对照组。通过定量逆转录聚合酶链反应(RT-PCR)、蛋白质免疫印迹法(WB)和双标免疫荧光法比较两组NCX1的表达水平。使用等长张力测量两组中NCX反向模式下逼尿肌条的收缩情况。使用共聚焦显微镜观察NCX反向模式下其对平滑肌细胞内钙浓度([Ca])调节的作用,并使用全细胞膜片钳技术在拮抗剂KB-R7943(5 μM和10 μM)存在的情况下评估电流。通过qRT-PCR、WB分析和免疫荧光评估,DO组中NCX1的表达明显高于对照组。在两种模式下,DO组通过NCX的钙离子通量的体积和速率以及NCX电流均高于对照组。NCX1水平升高可能通过在去极化状态下以反向模式升高[Ca],潜在地诱导细胞兴奋性,从而有助于PBOO后DO的形成。