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College of Traditional Chinese Medicine, Guangdong Pharmaceutical University,Guangzhou,China
Published:2017,
Published Online:24 January 2017,
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Han, B., Zhu, Cx., Shi, W. et al. Effect of Rhizoma Polygoni Cuspidati and Ramulus Cinnamomi compatibility on uric acid metabolism and urinary neutrophil gelatinase-associated lipocalin and kidney injury molecule-1 in rats with hyperuricemia., Chin. J. Integr. Med. 23, 535–542 (2017). https://doi.org/10.1007/s11655-016-2649-0
Bin Han, Chun-xia Zhu, Wan Shi, et al. Effect of Rhizoma Polygoni Cuspidati and Ramulus Cinnamomi compatibility on uric acid metabolism and urinary neutrophil gelatinase-associated lipocalin and kidney injury molecule-1 in rats with hyperuricemia. [J]. Chinese Journal of Integrative Medicine 23(7):535-542(2017)
Han, B., Zhu, Cx., Shi, W. et al. Effect of Rhizoma Polygoni Cuspidati and Ramulus Cinnamomi compatibility on uric acid metabolism and urinary neutrophil gelatinase-associated lipocalin and kidney injury molecule-1 in rats with hyperuricemia., Chin. J. Integr. Med. 23, 535–542 (2017). https://doi.org/10.1007/s11655-016-2649-0 DOI:
Bin Han, Chun-xia Zhu, Wan Shi, et al. Effect of Rhizoma Polygoni Cuspidati and Ramulus Cinnamomi compatibility on uric acid metabolism and urinary neutrophil gelatinase-associated lipocalin and kidney injury molecule-1 in rats with hyperuricemia. [J]. Chinese Journal of Integrative Medicine 23(7):535-542(2017) DOI: 10.1007/s11655-016-2649-0.
To explore the effects of Rhizoma Polygoni Cuspidati and Ramulus Cinnamomi compatibility (PR) on uric acid metabolism and the expression of urinary neutrophil gelatinase-associated lipocalin (NGAL) and kidney injury molecule-1 (KIM-1) in rats with hyperuricemia. Seventy male Sprague Dawley (SD) rats were randomly divided into 7 groups with 10 rats per group
including the normal group
model group
allopurinol group
benzbromarone group and PR groups at 3 doses (3.5
7
14 g/kg). Except the normal group
rats of the other groups were intragastrically administered 100 mg/kg hypoxanthine and 250 mg/kg ethambutol
and subcutaneously injected with 200 mg/kg potassium oxonate. All rats were continuously modeled for 17 days
and gavaged with corresponding drugs. The rats of the normal and model groups were gavaged with saline
once a day
for 2 weeks. The levels of serum uric acid (SUA)
blood urea nitrogen (BUN) and creatinine (Cr) were determined. In addition
the contents of NGAL and KIM-1 in urine and the mRNA and protein expressions of xanthine oxidase (XOD) in liver of hyperuricemia rats were measured by reverse transcription polymerase chain reaction (RT-PCR) and Western blot
respectively. Moreover
the pathological changes of kidney were analyzed by hematoxylin and eosin (HE) stain method. Compared with the normal group
the levels of SUA
BUN
NGAL and KIM-1 and the expressions of hepatic XOD mRNA and protein in the hyperuricemia rats were increased signifificantly (P<0.01). PR signifificantly decreased the levels of SUA
BUN
NGAL and KIM-1 and down-regulated the mRNA and protein expressions of hepatic XOD (P<0.05 or P<0.01). In addition
the pathological changes of kidney were signifificantly suppressed by oral administration of PR. PR ameliorated uric acid metabolism and protected renal function
the underlying mechanism was mediated by decreasing the levels of SUA
BUN
NGAL and KIM-1
inhibiting the expression of hepatic XOD and ameliorating the pathological change of kidney.
To explore the effects of Rhizoma Polygoni Cuspidati and Ramulus Cinnamomi compatibility (PR) on uric acid metabolism and the expression of urinary neutrophil gelatinase-associated lipocalin (NGAL) and kidney injury molecule-1 (KIM-1) in rats with hyperuricemia. Seventy male Sprague Dawley (SD) rats were randomly divided into 7 groups with 10 rats per group
including the normal group
model group
allopurinol group
benzbromarone group and PR groups at 3 doses (3.5
7
14 g/kg). Except the normal group
rats of the other groups were intragastrically administered 100 mg/kg hypoxanthine and 250 mg/kg ethambutol
and subcutaneously injected with 200 mg/kg potassium oxonate. All rats were continuously modeled for 17 days
and gavaged with corresponding drugs. The rats of the normal and model groups were gavaged with saline
once a day
for 2 weeks. The levels of serum uric acid (SUA)
blood urea nitrogen (BUN) and creatinine (Cr) were determined. In addition
the contents of NGAL and KIM-1 in urine and the mRNA and protein expressions of xanthine oxidase (XOD) in liver of hyperuricemia rats were measured by reverse transcription polymerase chain reaction (RT-PCR) and Western blot
respectively. Moreover
the pathological changes of kidney were analyzed by hematoxylin and eosin (HE) stain method. Compared with the normal group
the levels of SUA
BUN
NGAL and KIM-1 and the expressions of hepatic XOD mRNA and protein in the hyperuricemia rats were increased signifificantly (P<0.01). PR signifificantly decreased the levels of SUA
BUN
NGAL and KIM-1 and down-regulated the mRNA and protein expressions of hepatic XOD (P<0.05 or P<0.01). In addition
the pathological changes of kidney were signifificantly suppressed by oral administration of PR. PR ameliorated uric acid metabolism and protected renal function
the underlying mechanism was mediated by decreasing the levels of SUA
BUN
NGAL and KIM-1
inhibiting the expression of hepatic XOD and ameliorating the pathological change of kidney.
hyperuricemiaRhizoma Polygoni Cuspidati and Ramulus Cinnamomi compatibilityXanthine Oxidaseneutrophil gelatinase-associated lipocalinkidney injury molecule-1Chinese Medicine
hyperuricemiaRhizoma Polygoni Cuspidati and Ramulus Cinnamomi compatibilityXanthine Oxidaseneutrophil gelatinase-associated lipocalinkidney injury molecule-1Chinese Medicine
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