2013Xiandai shengwu yixue jinzhanRequires access

Effect of Angiotensin II Receptor Antagonist on Expression of ICAM-1 in Renal Cortex of Experimental Diabetic Rats

Yang Xin-jun

Open publisher page 0 citations

Abstract

Objective: To investigate the mechanism of Valsartan in protecting the kidney of streptozotocin-induced diabetic rats.Methods: Sprague-dawley rats were randomly divided into diabetic model treated with Valsartan(10mg·kg-1/d)group(A),diabetic model group(B) and normal control group(C).Plasma glucose,kidney mass/body mass ratio,MAP,serum creatinine,urinary creatinine,24 urinary albumin excretion ratio were measured in the 4th,6th week respectively.ICAM-1 mRNA expression in renal cortinal were measured with RT-PCR in the 6th week.And the kidney sample were observed with light and electron microscope.Mean glomerular transverse sectional area and mean glomerular volume were calculated by analysis system of the image.Results: In both two stages,kidney mass/body mass ratio,Ccr,24 urinary albumin excretion ratio in both diabetic group(B) were higher than that of normal group(C)(P0.01),but they were decreased significantly in A group than that in B group.For the urinary albumin in two stages,there was no difference between A and C group(P0.05).In the 4th and 6th,the MGPA and MGV in group A were significantly smaller than that of B group(P0.01).ICAM-1 mRNA expression were higher in B group than that in A and C group.Conclusion: Valsartan could reduce the expression of ICAM-1 mRNA,it could reduce the level of urinary albumin and could prevent the glomerular sclerosis,so the pathological progress of kidney was delayed in diabetic rats.

About this research paper

What this paper is about

Objective: To investigate the mechanism of Valsartan in protecting the kidney of streptozotocin-induced diabetic rats.Methods: Sprague-dawley rats were randomly divided into diabetic model treated with Valsartan(10mg·kg-1/d)group(A),diabetic model group(B) and normal control group(C).Plasma glucose,kidney mass/body mass ratio,MAP,serum creatinine,urinary creatinine,24 urinary albumin excretion ratio were measured in the 4th,6th week respectively.ICAM-1 mRNA expression in renal cortinal were measured with RT-PCR in the 6th week.And the kidney sample were observed with light and electron microscope.Mean glomerular transverse sectional area and mean glomerular volume were calculated by analysis system of the image.Results: In both two stages,kidney mass/body mass ratio,Ccr,24 urinary albumin excretion ratio in both diabetic group(B) were higher than that of normal group(C)(P0.01),but they were decreased significantly in A group than that in B group.For the urinary albumin in two stages,there was no difference between A and C group(P0.05).In the 4th and 6th,the MGPA and MGV in group A were significantly smaller than that of B group(P0.01).ICAM-1 mRNA expression were higher in B group than that in A and C group.Conclusion: Valsartan could reduce the expression of ICAM-1 mRNA,it could reduce the level of urinary albumin and could prevent the glomerular sclerosis,so the pathological progress of kidney was delayed in diabetic rats.

Why it matters

A significance statement is not available in the OpenAlex record.

Key contribution

A contribution statement is not available in the OpenAlex record.

Method / approach

Method details are not available in the OpenAlex metadata.

Main findings

Findings are not separately available in the OpenAlex metadata.

Limitations

Limitations are not available in the OpenAlex metadata.

Applications

Application details are not available in the OpenAlex metadata.

Available abstract

Objective: To investigate the mechanism of Valsartan in protecting the kidney of streptozotocin-induced diabetic rats.Methods: Sprague-dawley rats were randomly divided into diabetic model treated with Valsartan(10mg·kg-1/d)group(A),diabetic model group(B) and normal control group(C).Plasma glucose,kidney mass/body mass ratio,MAP,serum creatinine,urinary creatinine,24 urinary albumin excretion ratio were measured in the 4th,6th week respectively.ICAM-1 mRNA expression in renal cortinal were measured with RT-PCR in the 6th week.And the kidney sample were observed with light and electron microscope.Mean glomerular transverse sectional area and mean glomerular volume were calculated by analysis system of the image.Results: In both two stages,kidney mass/body mass ratio,Ccr,24 urinary albumin excretion ratio in both diabetic group(B) were higher than that of normal group(C)(P0.01),but they were decreased significantly in A group than that in B group.For the urinary albumin in two stages,there was no difference between A and C group(P0.05).In the 4th and 6th,the MGPA and MGV in group A were significantly smaller than that of B group(P0.01).ICAM-1 mRNA expression were higher in B group than that in A and C group.Conclusion: Valsartan could reduce the expression of ICAM-1 mRNA,it could reduce the level of urinary albumin and could prevent the glomerular sclerosis,so the pathological progress of kidney was delayed in diabetic rats.

Key concepts: Endocrinology, Internal medicine, Valsartan, Creatinine, Diabetic nephropathy, Kidney, Renal cortex, Chemistry

Related papers

Back to paper searchBrowse research topicsOriginal source
Effect of Angiotensin II Receptor Antagonist on Expression of ICAM-1 in Renal Cortex of Experimental Diabetic Rats — Research Paper | ScholarLens