Protective effect of salidroside on contrast-induced nephropathy in comparison with N-acetylcysteine and its underlying mechanism
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OriginalPaper|Updated:2021-08-27
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Protective effect of salidroside on contrast-induced nephropathy in comparison with N-acetylcysteine and its underlying mechanism
Protective effect of salidroside on contrast-induced nephropathy in comparison with N-acetylcysteine and its underlying mechanism
中国结合医学杂志(英文版)2015年21卷第4期 页码:266-273
Affiliations:
1. State Discipline and State Key Laboratory of Kidney Disease (Chinese PLA General Hospital, 2011DAV),Beijing,China,00088
2. Department of Rheumatism Immunity, Tianjin First Center Hospital,Tianjin,China
Author bio:
Funds:
Supported by the National Nature Science Foundation of China (No. 81273968 and No. 81471027), and Ministerial Project of the National Working Commission on Aging (No. QLB2014W002)
Xing, Y., Wei, Rb., Tang, L. et al. Protective effect of salidroside on contrast-induced nephropathy in comparison with N-acetylcysteine and its underlying mechanism., Chin. J. Integr. Med. 21, 266–273 (2015). https://doi.org/10.1007/s11655-015-2137-y
Yue Xing, Ri-bao Wei, Lu Tang, et al. Protective effect of salidroside on contrast-induced nephropathy in comparison with N-acetylcysteine and its underlying mechanism[J]. Chinese Journal of Integrative Medicine, 2015,21(4):266-273.
Xing, Y., Wei, Rb., Tang, L. et al. Protective effect of salidroside on contrast-induced nephropathy in comparison with N-acetylcysteine and its underlying mechanism., Chin. J. Integr. Med. 21, 266–273 (2015). https://doi.org/10.1007/s11655-015-2137-yDOI:
Yue Xing, Ri-bao Wei, Lu Tang, et al. Protective effect of salidroside on contrast-induced nephropathy in comparison with N-acetylcysteine and its underlying mechanism[J]. Chinese Journal of Integrative Medicine, 2015,21(4):266-273. DOI: 10.1007/s11655-015-2137-y.
Protective effect of salidroside on contrast-induced nephropathy in comparison with N-acetylcysteine and its underlying mechanism
摘要
To study the prevention effect of salidroside on contrast-induced-nephropathy (CIN) and its underlying mechanism. A total of 24 Wistar rats were randomly divided into 4 groups with 6 in each group. Rats were firstly administrated with normal saline (control and model groups)
N-acetylcysteine (NAC
NAC group) and salidroside (salidroside group) for 7 days before model establishment in each group
respectively. Histopathological analysis was performed by periodic acid-Schiff (PAS) staining. Oxidative stress related parameters including superoxide dismutase (SOD) and methane dicarboxylic aldehyde (MDA)
nitric oxide (NO)
angiotensin II (Ang II)
8-hydroxy-2′-deoxyguanosine (8-OHdG)
mRNA and protein levels of endothelial nitric oxide synthase (eNOS)
and nitric oxide synthase (NOS) activity were measured. Compared with the control group
the levels of MDA
Ang II and 8-OHdG were all significantly increased and levels of SOD
NO
and eNOS mRNA and protein were decreased significantly in the model group (P<0.05). Meanwhile
the NOS activity was also significantly decreased in the model group (P<0.05). In addition
the levels of these parameters were all improved in the NAC (P<0.05) and salidroside groups and no significant different was found between these two groups (P>0.05). Salidroside can be the potential substitute of NAC to prevent CIN. The underlying mechanism may be associated with oxidative stress damage caused by contrast agents.
Abstract
To study the prevention effect of salidroside on contrast-induced-nephropathy (CIN) and its underlying mechanism. A total of 24 Wistar rats were randomly divided into 4 groups with 6 in each group. Rats were firstly administrated with normal saline (control and model groups)
N-acetylcysteine (NAC
NAC group) and salidroside (salidroside group) for 7 days before model establishment in each group
respectively. Histopathological analysis was performed by periodic acid-Schiff (PAS) staining. Oxidative stress related parameters including superoxide dismutase (SOD) and methane dicarboxylic aldehyde (MDA)
nitric oxide (NO)
angiotensin II (Ang II)
8-hydroxy-2′-deoxyguanosine (8-OHdG)
mRNA and protein levels of endothelial nitric oxide synthase (eNOS)
and nitric oxide synthase (NOS) activity were measured. Compared with the control group
the levels of MDA
Ang II and 8-OHdG were all significantly increased and levels of SOD
NO
and eNOS mRNA and protein were decreased significantly in the model group (P<0.05). Meanwhile
the NOS activity was also significantly decreased in the model group (P<0.05). In addition
the levels of these parameters were all improved in the NAC (P<0.05) and salidroside groups and no significant different was found between these two groups (P>0.05). Salidroside can be the potential substitute of NAC to prevent CIN. The underlying mechanism may be associated with oxidative stress damage caused by contrast agents.
关键词
salidrosidecontrast-induced-nephropathyoxidative stressN-acetylcysteineChinese Medicine
Keywords
salidrosidecontrast-induced-nephropathyoxidative stressN-acetylcysteineChinese Medicine
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