FOLLOWUS
1. State Discipline and State Key Laboratory of Kidney Disease (Chinese PLA General Hospital, 2011DAV),Beijing,China,00088
2. Medical School of Nankai University,Tianjin,China
纸质出版日期:2014,
网络出版日期:2014-1-24,
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Yang, Y., Wei, Rb., Zheng, Xy. et al. Effects of Compound Shenhua Tablet (复方肾华片) on renal tubular Na+-K+-ATPase in rats with acute ischemic reperfusion injury., Chin. J. Integr. Med. 20, 200–208 (2014). https://doi.org/10.1007/s11655-014-1740-7
Yue Yang, Ri-bao Wei, Xiao-yong Zheng, et al. Effects of Compound Shenhua Tablet (复方肾华片) on renal tubular Na+-K+-ATPase in rats with acute ischemic reperfusion injury[J]. Chinese Journal of Integrative Medicine, 2014,20(3):200-208.
Yang, Y., Wei, Rb., Zheng, Xy. et al. Effects of Compound Shenhua Tablet (复方肾华片) on renal tubular Na+-K+-ATPase in rats with acute ischemic reperfusion injury., Chin. J. Integr. Med. 20, 200–208 (2014). https://doi.org/10.1007/s11655-014-1740-7 DOI:
Yue Yang, Ri-bao Wei, Xiao-yong Zheng, et al. Effects of Compound Shenhua Tablet (复方肾华片) on renal tubular Na+-K+-ATPase in rats with acute ischemic reperfusion injury[J]. Chinese Journal of Integrative Medicine, 2014,20(3):200-208. DOI: 10.1007/s11655-014-1740-7.
To observe the effect of Compound Shenhua Tablet (复方肾华片
SHT) on the sodiumpotassium- exchanging adenosinetriphosphatase (Na+-K+-ATPase) in the renal tubular epithelial cells of rats with acute ischemic reperfusion and to investigate the mechanisms underlying the effects of SHT on renal ischemic reperfusion injury (RIRI). Fifty male Wistar rats were randomly divided into the sham surgery group
model group
astragaloside group [150 mg/(kg·d)]
SHT low-dose group [1.5 g/(kg·d)] and SHT high-dose group [3.0 g/(kg·d)]
with 10 rats in each group. After 1 week of continuous intragastric drug administration
surgery was performed to establish the model. At either 24 or 72 h after the surgery
5 rats in each group were sacrificed
blood biochemistry
renal pathology
immunoblot and immunohistochemical examinations were performed
and double immunofluorescence staining was observed under a laser confocal microscope. Compared with the sham surgery group
the serum creatinine (SCr) and blood urea nitrogen (BUN) levels were significantly increased
Na+-K+-ATPase protein level was decreased
and kidney injury molecule-1 (KIM-1) protein level was increased in the model group after the surgery (P<0.01 or P<0.05). Compared with the model group
the SCr
BUN
pathological scores
Na+-K+-ATPase
and the KIM-1 protein level of the three treatment groups were significantly improved at 72 h after the surgery (P<0.05 or P<0.01). And the SCr
BUN of the SHT low- and high-dose groups
and the pathological scores of the SHT high-dose group were significantly lower than those of the astragaloside group (P<0.05). The localizations of Na+-K+-ATPase and megalin of the model group were disrupted
with the distribution areas overlapping with each other and alternately arranged. The severity of the disruption was slightly milder in three treatment groups compared with that of the model group. The results of immunofluorescence staining showed that the SHT high-dose group had a superior effect as compared with the astragaloside group and the SHT low-dose group. The SHT effectively alleviated RIRI caused by ischemic reperfusion
promoted the recovery of the polarity of renal tubular epithelial cells
and protected the renal tubules. The therapeutic effects of SHT were superior to those of astragaloside as a single agent.
To observe the effect of Compound Shenhua Tablet (复方肾华片
SHT) on the sodiumpotassium- exchanging adenosinetriphosphatase (Na+-K+-ATPase) in the renal tubular epithelial cells of rats with acute ischemic reperfusion and to investigate the mechanisms underlying the effects of SHT on renal ischemic reperfusion injury (RIRI). Fifty male Wistar rats were randomly divided into the sham surgery group
model group
astragaloside group [150 mg/(kg·d)]
SHT low-dose group [1.5 g/(kg·d)] and SHT high-dose group [3.0 g/(kg·d)]
with 10 rats in each group. After 1 week of continuous intragastric drug administration
surgery was performed to establish the model. At either 24 or 72 h after the surgery
5 rats in each group were sacrificed
blood biochemistry
renal pathology
immunoblot and immunohistochemical examinations were performed
and double immunofluorescence staining was observed under a laser confocal microscope. Compared with the sham surgery group
the serum creatinine (SCr) and blood urea nitrogen (BUN) levels were significantly increased
Na+-K+-ATPase protein level was decreased
and kidney injury molecule-1 (KIM-1) protein level was increased in the model group after the surgery (P<0.01 or P<0.05). Compared with the model group
the SCr
BUN
pathological scores
Na+-K+-ATPase
and the KIM-1 protein level of the three treatment groups were significantly improved at 72 h after the surgery (P<0.05 or P<0.01). And the SCr
BUN of the SHT low- and high-dose groups
and the pathological scores of the SHT high-dose group were significantly lower than those of the astragaloside group (P<0.05). The localizations of Na+-K+-ATPase and megalin of the model group were disrupted
with the distribution areas overlapping with each other and alternately arranged. The severity of the disruption was slightly milder in three treatment groups compared with that of the model group. The results of immunofluorescence staining showed that the SHT high-dose group had a superior effect as compared with the astragaloside group and the SHT low-dose group. The SHT effectively alleviated RIRI caused by ischemic reperfusion
promoted the recovery of the polarity of renal tubular epithelial cells
and protected the renal tubules. The therapeutic effects of SHT were superior to those of astragaloside as a single agent.
Compound Shenhua TabletAstragalosiderenal ischemic reperfusion injuryNa+-K+- adenosinetriphosphatase
Compound Shenhua TabletAstragalosiderenal ischemic reperfusion injuryNa+-K+- adenosinetriphosphatase
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