Qiang GENG, Fu WANG, Qiang HAN, 等. Antioxidant Mechanism of Xiaojin Pill (小金丸) for Treatment of Peyronie's Disease in Rats Based on Matrix Metalloproteinases[J]. Chinese Journal of Integrative Medicine, 2019,25(9):671-676.
Qiang GENG, Fu WANG, Qiang HAN, et al. Antioxidant Mechanism of Xiaojin Pill (小金丸) for Treatment of Peyronie's Disease in Rats Based on Matrix Metalloproteinases[J]. Chinese Journal of Integrative Medicine, 2019,25(9):671-676.
Qiang GENG, Fu WANG, Qiang HAN, 等. Antioxidant Mechanism of Xiaojin Pill (小金丸) for Treatment of Peyronie's Disease in Rats Based on Matrix Metalloproteinases[J]. Chinese Journal of Integrative Medicine, 2019,25(9):671-676. DOI: 10.1007/s11655-019-3203-7.
Qiang GENG, Fu WANG, Qiang HAN, et al. Antioxidant Mechanism of Xiaojin Pill (小金丸) for Treatment of Peyronie's Disease in Rats Based on Matrix Metalloproteinases[J]. Chinese Journal of Integrative Medicine, 2019,25(9):671-676. DOI: 10.1007/s11655-019-3203-7.
Antioxidant Mechanism of Xiaojin Pill (小金丸) for Treatment of Peyronie's Disease in Rats Based on Matrix Metalloproteinases
摘要
Abstract
Objective:
2
To evaluate the effects of Xiaojin Pill (小金丸) in the treatment of Peyronie's disease (PD) in a rat model.
Methods:
2
Twenty-four male Sprague-Dawley rats were randomly divided into four groups with 6 in each: sham operation
PD model
vehicle control and Xiaojin Pill groups. The rats in the sham operation group received penile tunica albsginea (TA) injection with 50 μL vehicle
while the rats in the other 3 groups received 50 μL penile TA injection of 50 μg transforming growth factor (TGF)-β1. Forty-two days after the injection
rats in the vehicle control and Xiaojin Pill groups received 0.5 mL water and Xiaojin Pill solution (107 mg/kg of body weight)
respectively by gavage for 28 days
while those in the sham operation and PD model groups did not receive any intervention. After intervention
the expressions of matrix metalloproteinase 2/9 (MMP2/9)
nitric oxidesynthase (NOS)
superoxide dismutase (SOD) and malondialdehyde (MDA) were measured.
Results:
2
Rats in the PD model and vehicle control groups presented obvious fibrosis in corpus cavernosum (CC) and demonstrated a significantly increased expressions of MMP2 and MMP9 in the CC compared with the sham operation group (all
P
<
0.01). In contrast
the expressions of MMP2 and MMP9 in the Xiaojin Pill group were significantly down-regulated (both
P
<
0.01). In addition
the levels of NOS and MDA in CC were significantly increased while the activity of SOD was decreased in the PD model and vehicle control groups compared with the sham operation group (all
P
<
0.01). After Xiaojin Pill treatment
the levels of MDA
NOS and SOD appeared to be corrected (all
P
<
0.01).
Conclusions:
2
Xiaojin Pill could reduce fibrosis in the CC by decreasing the expressions of MMPs
NOS and MDA
and by increasing the activity of SOD. Therefore
Xiaojin Pill might be a therapeutic option for PD.
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相关作者
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相关机构
Key Laboratory of Shaanxi Administration of Traditional Chinese Medicine for TCM Compatibility, Shaanxi University of Chinese Medicine
State Key Laboratory of Cellular Stress Biology, School of Life Sciences, Faculty of Medicine and Life Science, Xiamen University
Fujian Pien Tze Huang Enterprise Key Laboratory of Natural Medicine Research and Development
Department of General Surgery, First People's Hospital of Hangzhou Lin'an District
Research Center of Neuroscience, School of Basic Medical Sciences, Chongqing Medical University