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1.
China Journal of Chinese Materia Medica ; (24): 1982-1986, 2013.
Artigo em Chinês | WPRIM | ID: wpr-346459

RESUMO

<p><b>OBJECTIVE</b>To study the effect and mechanism of Coicis Semen oil (Kanglaite injection, KLT) on renal interstitial fibrosis induced by unilateral ureteral obstruction (UUO).</p><p><b>METHOD</b>Fifty-four male SD rats were randomly divided into 3 groups, 6 in each group, the sham operated group, the model group, and the KLT group. Renal interstitial fibrosis model was established in rats by UUO. After administration of KLT (15 mL x kg(-1) x d(-1)) for 3, 7 and 14 days, the dynamic histological changes of renal interstitial tissues were observed and renal damage including tubular impairment and interstitial fibrosis were quantified on HE and Masson stained tissue sections. The expression of alpha-smooth muscle actin (alpha-SMA) and transforming growth factor-beta1 (TGF-beta1) were measured by immunohistochemistry staining sections. The protein expression of p-Smad2 and Smad7 were detected by Western blot respectively.</p><p><b>RESULT</b>The degree of tubular damage in KLT group was much lower than that in UUO group (P < 0.05). The expression of alpha-SMA and TGF-beta1 was decreased in both UUO group and KLT group, while it was significantly lower in KLT group at every time point. The protein expression of p-Smad2 was obviously decreased while the protein expressions of Smad7 was obviously increased in KLT group, compared with the UUO group (P < 0.05).</p><p><b>CONCLUSION</b>Coicis Semen oil could attenuate the tubulo-interstitial fibrosis, probable by intervening the TGF-beta/Smads signal transduction pathway of UUO rats.</p>


Assuntos
Animais , Masculino , Ratos , Coix , Fibrose , Injeções , Rim , Patologia , Óleos de Plantas , Usos Terapêuticos , Ratos Sprague-Dawley , Transdução de Sinais , Proteína Smad2 , Metabolismo , Fator de Crescimento Transformador beta1 , Fisiologia , Obstrução Uretral , Tratamento Farmacológico , Patologia
2.
Journal of Zhejiang University. Medical sciences ; (6): 511-516, 2010.
Artigo em Chinês | WPRIM | ID: wpr-319867

RESUMO

<p><b>OBJECTIVE</b>To investigate the effects of low-dose simvastatin on the expression of connective tissue growth factor (CTGF) and α-smooth muscle actin (α-SMA) in the renal tubulointerstitium of rats with diabetic nephropathy.</p><p><b>METHODS</b>Sixty male SD rats were randomly divided into three groups: Group C (control group), Group D, in which diabetes was induced by stroptozotocin (STZ) and Group DS, in which STZ-induced diabetic rats were treated with low-dose (no cholesterol-lowering effect) simvastatin. The following parameters were measured after 6 weeks and 12 weeks in each groups, respectively: body weight and kidney weight, 24-h urinary albumin excretion (UAE), biochemical indexes including blood glucose (GLU), low density lipoprotein (LDL), high density lipoprotein (HDL), triglycerides (TG) and serum creatinine (SCr). The expression of CTGF and α-SMA in renal tubulointerstitium was assessed by immunohistochemical method.</p><p><b>RESULT</b>After 6 and 12 weeks, there were no significant differences in SCr, LDL, HDL and TG levels among all three groups. The expression levels of CTGF and α-SMA in the tubulointerstitium of Group DS were significantly decreased compared with those of Group D at week 6 (P<0.05); there were no significant differences compared with Group C (P>0.05). After 12 weeks, CTGF and α-SMA expressions in Group DS were also lower than those in Group D (P<0.05); while higher than those in Group C (P<0.05).</p><p><b>CONCLUSION</b>Simvastatin with a under cholesterol-lowering dose, can decrease the expression levels of CTGF and α-SMA in renal tubulointerstitium of rats with diabetic nephropathy, by which the progression of the tubulointerstitial fibrosis would be delayed.</p>


Assuntos
Animais , Masculino , Ratos , Actinas , Metabolismo , Fator de Crescimento do Tecido Conjuntivo , Metabolismo , Diabetes Mellitus Experimental , Tratamento Farmacológico , Metabolismo , Rim , Metabolismo , Distribuição Aleatória , Ratos Sprague-Dawley , Sinvastatina , Farmacologia , Usos Terapêuticos
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