中国临床药理学杂志
中國臨床藥理學雜誌
중국림상약이학잡지
The Chinese Journal of Clinical Pharmacology
2015年
15期
1530-1532
,共3页
姜黄素%糖尿病肾病%转化生长因子
薑黃素%糖尿病腎病%轉化生長因子
강황소%당뇨병신병%전화생장인자
curcumin%diabetic nephropathy%transforming growth factor-β1
目的:探讨姜黄素对糖尿病肾病大鼠的肾内转化生长因子表达的影响。方法采用一次性腹腔注射链脲佐菌素58 mg· kg-1(5.8 mL· kg-1)建立糖尿病肾病大鼠模型。实验组灌胃姜黄素混悬液200 mg· kg-1,正常组与模型组则灌服等体积的1%羟甲基纤维素钠。用免疫组化法观察肾小球、肾小管区域转化生长因子的表达。结果与模型组比较,实验组大鼠24 h尿微量白蛋白、空腹血糖、血浆转化生长因子的含量均明显降低(P<0.01),肾小球、肾小管区域转化生长因子的表达也有显著降低( P<0.01)。结论姜黄素能下调转化生长因子在血清及肾的表达,对糖尿病肾病大鼠的肾有一定的保护作用。
目的:探討薑黃素對糖尿病腎病大鼠的腎內轉化生長因子錶達的影響。方法採用一次性腹腔註射鏈脲佐菌素58 mg· kg-1(5.8 mL· kg-1)建立糖尿病腎病大鼠模型。實驗組灌胃薑黃素混懸液200 mg· kg-1,正常組與模型組則灌服等體積的1%羥甲基纖維素鈉。用免疫組化法觀察腎小毬、腎小管區域轉化生長因子的錶達。結果與模型組比較,實驗組大鼠24 h尿微量白蛋白、空腹血糖、血漿轉化生長因子的含量均明顯降低(P<0.01),腎小毬、腎小管區域轉化生長因子的錶達也有顯著降低( P<0.01)。結論薑黃素能下調轉化生長因子在血清及腎的錶達,對糖尿病腎病大鼠的腎有一定的保護作用。
목적:탐토강황소대당뇨병신병대서적신내전화생장인자표체적영향。방법채용일차성복강주사련뇨좌균소58 mg· kg-1(5.8 mL· kg-1)건립당뇨병신병대서모형。실험조관위강황소혼현액200 mg· kg-1,정상조여모형조칙관복등체적적1%간갑기섬유소납。용면역조화법관찰신소구、신소관구역전화생장인자적표체。결과여모형조비교,실험조대서24 h뇨미량백단백、공복혈당、혈장전화생장인자적함량균명현강저(P<0.01),신소구、신소관구역전화생장인자적표체야유현저강저( P<0.01)。결론강황소능하조전화생장인자재혈청급신적표체,대당뇨병신병대서적신유일정적보호작용。
Objective To study effect of curcumin on expression of transforming growth factor in rats with diabetic kidney nephropathy.Methods The use of a single intraperitoneal injection of streptozotocin 58 mg · kg -1 to establish diabetic nephropathy in rats.Experimental group were given curcumin suspension 200 mg· kg-1 gavage, the normal group and model group were given equal 1%sodium carboxymethylcellu-lose volume.Observed by immunohistochemical staining of glomerular tubular regional expression of transforming growth factor.Results Com-pared with the model group, the rats of the experimental group 24 h urinary albumin, fasting blood glucose, serum transforming growth factor levels were significantly decreased (P<0.01).The glomerular, tubular region of transforming growth factor expression also decreased significantly ( P<0.01).Conclusion Curcumin can decrease the level of transfor-ming growth factor in serum and renal expression, and it has certain protective effect on diabetic nephropathy rats kidney.