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Reduced cortical renal GLUT1 expression induced by angiotensin-converting enzyme inhibition in diabetic spontaneously hypertensive rats
Souza, M. S; Machado, U. F; Okamoto, M; Bertoluci, M. C; Ponpermeyer, C; Leguisamo, N; Azambuja, F; Irigoyen, M. C; Schaan, B. D.
  • Souza, M. S; Fundação Universit¨¢ria de Cardiologia. Instituto de Cardiologia do Rio Grande do Sul. Porto Alegre. BR
  • Machado, U. F; Universidade de São Paulo. Instituto de Ci¨ºncias Biom¨¦dicas. Departamento de Fisiologia e Biof¨ªsica. São Paulo. BR
  • Okamoto, M; Universidade de São Paulo. Instituto de Ci¨ºncias Biom¨¦dicas. Departamento de Fisiologia e Biof¨ªsica. São Paulo. BR
  • Bertoluci, M. C; Universidade Federal do Rio Grande do Sul. Hospital de Cl¨ªnicas de Porto Alegre. Serviços de Endocrinologia e Medicina Interna. Porto Alegre. BR
  • Ponpermeyer, C; Fundação Universit¨¢ria de Cardiologia. Instituto de Cardiologia do Rio Grande do Sul. Porto Alegre. BR
  • Leguisamo, N; Fundação Universit¨¢ria de Cardiologia. Instituto de Cardiologia do Rio Grande do Sul. Porto Alegre. BR
  • Azambuja, F; Fundação Universit¨¢ria de Cardiologia. Instituto de Cardiologia do Rio Grande do Sul. Porto Alegre. BR
  • Irigoyen, M. C; Fundação Universit¨¢ria de Cardiologia. Instituto de Cardiologia do Rio Grande do Sul. Porto Alegre. BR
  • Schaan, B. D; Fundação Universit¨¢ria de Cardiologia. Instituto de Cardiologia do Rio Grande do Sul. Porto Alegre. BR
Braz. j. med. biol. res ; 41(11): 960-968, Nov. 2008. graf, tab
Article in English | LILACS | ID: lil-500363
ABSTRACT
Diabetes in spontaneously hypertensive rats is associated with cortical renal GLUT1 and GLUT2 overexpression. Our objective was to evaluate the effect of the angiotensin-converting enzyme blockade on cortical renal GLUT1 and GLUT2 expression, urinary albumin and urinary TGF-¦Â1. Streptozotocin, 50 mg/kg, or citrate buffer (N = 16) was administered as a single injection into the tail vein in adult spontaneously hypertensive rats (~260 g). Thirty days later, these diabetic spontaneously hypertensive rats received ramipril by gavage 0.01 mg¡¤kg-1¡¤day-1 (D0.01, N = 14), 1 mg¡¤kg-1¡¤day-1 (D1, N = 9) or water (D, N = 11) for 15 days. Albumin and TGF-¦Â1 (24-h urine), direct arterial pressure, renal tissue angiotensin-converting enzyme activity (fluorometric assay), and GLUT1 and GLUT2 protein levels (Western blot, renal cortex) were determined. Glycemia and glycosuria were higher (P < 0.05) in the diabetic rats compared with controls, but similar between the diabetic groups. Diabetes in spontaneously hypertensive rats lowered renal tissue angiotensin-converting enzyme activity (40 percent), which was reduced further when higher ramipril doses were used. Diabetes associated with hypertension raised GLUT1 by 28 percent (P < 0.0001) and GLUT2 by 76 percent (P = 0.01), and both doses of ramipril equally reduced cortical GLUT1 (D vs D1 and vs D0.01, P ¡Ü 0.001). GLUT2 levels were reduced in D0.01 (P < 0.05 vs D). Diabetes increased urinary albumin and TGF-¦Â1 urinary excretion, but the 15-day ramipril treatment (with either dose) did not reduce them. In conclusion, ramipril is effective in lowering renal tissue angiotensin-converting enzyme activity, as well as blocking cortical GLUT1 overexpression, which may be beneficial in arresting the development of diabetic nephropathy.
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Full text: Available Index: LILACS (Americas) Main subject: Angiotensin-Converting Enzyme Inhibitors / Ramipril / Glucose Transporter Type 1 / Kidney Cortex Limits: Animals Language: English Journal: Braz. j. med. biol. res Journal subject: Biology / Medicine Year: 2008 Type: Article Affiliation country: Brazil Institution/Affiliation country: Fundação Universit¨¢ria de Cardiologia/BR / Universidade Federal do Rio Grande do Sul/BR / Universidade de São Paulo/BR

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Full text: Available Index: LILACS (Americas) Main subject: Angiotensin-Converting Enzyme Inhibitors / Ramipril / Glucose Transporter Type 1 / Kidney Cortex Limits: Animals Language: English Journal: Braz. j. med. biol. res Journal subject: Biology / Medicine Year: 2008 Type: Article Affiliation country: Brazil Institution/Affiliation country: Fundação Universit¨¢ria de Cardiologia/BR / Universidade Federal do Rio Grande do Sul/BR / Universidade de São Paulo/BR