Hepatic and Extrahepatic Angiotensinogen Gene Expression in Rats with Acute Nephrotic Syndrome

References

• Frenk S, Antonowicks I, Craig J H, Metcoff J. Experimental nephrotic syndrome induced in rats by aminonucleoside: renal lesions and body electrolyte composition. Proc Soc Exp Biol Med 1955; 89: 424–427
   PubMed Web of Science ®Google Scholar
• Pedraza-ChaverrÍ J, Cruz C, Ibarra-Rubio ME, ChÁVez MT, Calleja C, Tapia E, Uribe MC, Romero L, PeÑA JC. Pathophysiology of experimental nephrotic syndrome induced by puromycin aminonucleoside in rats. I. The role of proteinuria, hypoproteinemia and renin-angiotensin-aldosterone system on the sodium retention. Rev invest Clin 1990; 42: 29–38
   PubMedGoogle Scholar
• Glassock R J, Cohen A H, Adler SG. Primary glomerular diseases. The Kidney, 5th ed., BM Brenner. W.B. Saunders, Philadelphia 1996; II: 1392–1497.
   Google Scholar
• Yayama K, Konishi K, Ohta A, Takano M, Ohtani R, Itoh N, Okamoto H. Elevation of plasma angiotensinogen in rats with experimentally induced nephrosis. Nephron 1993; 63: 89–93
   PubMedGoogle Scholar
• Pyo H J, Summer S N, Niederberger M, Kim JK, Schrier RW. Argininevasopressin gene expression in rats with puromycin-induced nephrotic syndrome. Am J Kidney Dis 1995; 25: 58–62
   Google Scholar
• Ricardo S D, Bertram J F, Ryan GB. Podocyte architecture in puromycin aminonucleoside-treated rats administered tungsten or allopurinol. Exp Nephrol 1995; 3: 270–279
   Google Scholar
• Ueda N, Baliga R, Shah S. Role of catalytic iron in an animal model of minimal change nephrotic syndrome. Kidney Int 1996; 49: 370–373
   PubMed Web of Science ®Google Scholar
• Bernard D B. Metabolic abnormalities in nephrotic syndrome: pathophysiology and complications. Contemporary Issues in Nephrology, Nephrotic Syndrome, JH Stein. Churchill Livingstone, New York 1982; 9: 85–20.
   Google Scholar
• Lewandowski A E, Liano WSL, Stinson-Fisher CA, Kenk JD, Jefferson LS. Effects of experimentally induced nephrosis on protein synthesis in rat liver. Am J Physiol 1988; 254: C634–C642
   Google Scholar
• Pedraza-ChaverrÍ J, Cruz C, ChÁVez MT, LÓPez A, Ibarra-Rubio ME, Tapia E, PeÑA JC. Pathophysiology of experimental nephrotic syndrome induced by puromycin aminonucleoside in rats. II. In vitro release of renin, angiotensinogen, and aldosterone. Rev Invest Clin 1990; 42: 120–126
   PubMedGoogle Scholar
• Pedraza-ChaverrÍ J, Cruz C, Ibarra-Rubio ME, HernÁNdez C, Tapia E, PeÑA JC. Urinary excretion of renin and angiotensinogen in nephrotic rats. Nephron 1991; 57: 106–108
   PubMedGoogle Scholar
• ArÉValo AE, Ibarra-Rubio ME, Cruz C, PeÑA JC, Pedraza-ChaverrÍ J. Angiotensin I converting enzyme activity in puromycin aminonucleoside-nephrotic syndrome. Clin Chim Acta 1990; 191: 175–184
   PubMed Web of Science ®Google Scholar
• Ohkubo H, Nakayama K, Tanaka T, Nakanishi S. Tissue distribution of rat angiotensinogen mRNA and structural analysis of its heterogeneity. J Biol Chem 1986; 261: 319–323
   PubMed Web of Science ®Google Scholar
• Campbell D J, Habener JF. Angiotensinogen gene is expressed and differentially regulated in multiple tissues of the rat. J Clin Invest 1986; 78: 31–39
   PubMed Web of Science ®Google Scholar
• Richoux J P, Cordonnier J L, Bouhnik J, Clauser E, Corvol P, Menard J, et al. Immunocytochemical localization of angiotensinogen in rat liver and kidney. Cell Tissue Res 1983; 233: 439–451
   PubMedGoogle Scholar
• Kunapuli S P, Kumar A. Molecular cloning of human angiotensinogen cDNA and evidence for the presence of its mRNA in rat heart. Circ Res 1987; 60: 786–790
   PubMed Web of Science ®Google Scholar
• Lindpaintner K, Ganten D. The cardiac renin-angiotensin system: an appraisal of present experimental and clinical evidence. Circ Res 1991; 68: 905–921
   PubMed Web of Science ®Google Scholar
• Lynch K R, Hawelu-Johnson CL, Guyenet PG. Localization of brain angiotensinogen mRNA by hybridization histochemistry. Mol Brain Res 1987; 2: 149–158
   Google Scholar
• Genain C P, Van Loon GR, Kotchen TA. Distribution of renin activity and angiotensinogen in rat brain: effects of dietary sodium chloride intake on brain renin. J Clin Invest 1985; 76: 1939–1945
   Google Scholar
• Ganten D, Schelling P, Vecsei P, Ganten U. Iso-renin extrarenal origin: the tissue angiotensinogenase systems. Am J Med 1976; 60: 760–772
   PubMed Web of Science ®Google Scholar
• Dzau V J. Circulating versus local renin-angiotensin system in cardiovascular homeostasis. Circulation 1988; 77: 14–113
   Google Scholar
• Mendelsohn Fso. Angiotensin II: evidence for its role as an intrarenal hormone. Kidney Int 1982; 22: S78–S81
   Google Scholar
• Schunkert H, Ingelfinger J R, Dzau VJ. Evolving concepts of intrarenal renin–angiotensin system in health and disease: contributions of molecular biology. Renal Physiol Biochem 1991; 14: 146–154
   Google Scholar
• Mulrow P J. Adrenal renin: a possible local regulator of aldosterone production. Yale J Biol Med 1989; 62: 503–510
   Google Scholar
• Ganong W F. The brain angiotensin system. Annu Rev Physiol 1984; 46: 17–31
   PubMed Web of Science ®Google Scholar
• Kunapuli S P, Benedict C R, Kumar A. Tissue specific hormonal regulation of the rat angiotensinogen gene expression. Arch Biochem Biophys 1987; 254: 642–646
   PubMed Web of Science ®Google Scholar
• Ingelfinger J R, Pratt R E, Ellison K E, Dzau VJ. Sodium regulation of angiotensinogen mRNA expression in rat kidney cortex and medulla. J Clin Invest 1986; 78: 1311–1315
   PubMed Web of Science ®Google Scholar
• GÓMez RA, Cassis L, Lynch KR, Chevalier RL, Wilfong N, Carey RM, Peach MJ. Fetal expression of the angiotensinogen gene. Endocrinology 1988; 123: 2298–2302
   PubMed Web of Science ®Google Scholar
• Keuneke C, Yacullo R, Sugiura Mall G, Metzeger R, Ganten D. Converting enzyme inhibitors differentially affect expression of genes of the renin angiotensin system. Clin Exp Hypertens 1995; 17: 551–574
   PubMed Web of Science ®Google Scholar
• Ibarra-Rubio ME, Pedraza-ChaverrÍ J, Panduro A. Differential regulation in the expression of hepatic genes in nephrotic and pair-fed rats. Nephron 1993; 65: 119–124
   PubMedGoogle Scholar
• Thabet M A, Challa A, Chan W, Liu F, Hintz R L, Chan JCM. Insulin like growth factor and growth hormone receptor in nephrotic rats. Am J Physiol 1994; 266: E102–E106
   Google Scholar
• Iwao H, Fukui K, Kim S, Nakayama K, Ohkubo H, Nakanishi S, Youichi A. Sodium balance effects on renin, angiotensinogen, and atrial natriuretic polypeptide mRNA levels. Am J Physiol 1988; 255: E129–E136
   PubMed Web of Science ®Google Scholar
• Rosenberg M E, Chimielewski D, Hosteller TH. Effect of dietary protein on rat renin and angiotensinogen gene expression. J Clin Invest 1990; 85: 1144–1149
   PubMed Web of Science ®Google Scholar
• Lowry O H, Rosenbrought N J, Farr A L, Randall RJ. Protein determination with the Folin phenol reagent. J Biol Chem 1951; 193: 265–272
   PubMed Web of Science ®Google Scholar
• Pedraza-ChaverrÍ J, ZÚÑIga-Estarda A, Ibarra-Rubio ME, Cruz C, Tapia E, PeÑA JC. Productión de anticuerpos policlonales para la cuantificación del decapéptido angiotensina I por radioinmunoanálisis. Rev Invest Clin 1988; 40: 365–377
   PubMedGoogle Scholar
• Chomczynski P, Sacchi N. Single-step method of RNA isolation by acid guanidinium-thiocyanate-phenol-chloroform extraction. Anal Biochem 1987; 162: 156–159
   PubMed Web of Science ®Google Scholar
• Lynch K R, Simnad V I, Ben-Ari ET, Garrison JC. Localization of preangiotensinogen messenger RNA sequences in the rat brain. Hypertension 1986; 8: 540–543
   PubMed Web of Science ®Google Scholar
• Everett A D, Scott J, Wilfong N, Marino B, Rosenkranz R P, Inagami T, Gez RA. Renin and angiotensinogen expression during the evolution of diabetes. Hypertension 1992; 19: 70–78
   Google Scholar
• Liang K H, Oveisi F, Vaziri ND. Gene expression of hepatic cholesterol 7-alpha-hydroxylase in the course of puromycin-induced nephrosis. Kidney Int 1996; 49: 855–860
   Google Scholar
• Yamauchi A, Imai E, Noguchi T, Tanaka T, Yamamoto S, Mikami H, Fukuhara Y, Fuji M, Orita Y, Kamada T. Albumin gene transcription is enhanced in liver of nephrotic rats. Am J Physiol 1989; 254: E676–E679
   Google Scholar
• Pedraza-ChaverrÍ J, Huberman A. Actinomycin D blocks the hepatic functional albumin mRNA increase in aminonucleoside nephrotic rats. Nephron 1991; 59: 648–650
   PubMedGoogle Scholar
• Lewandowski A E, Liao WSL, Stinson-Fisher CA, Kenk JD, Jefferson LS. Effects of experimentally induced nephrosis on protein synthesis in rat liver. Am J Physiol 1988; 254: C634–C642
   Google Scholar
• Tarugi P, Calanmdra S, Chan L. Changes in apolipoprotein AI mRNA level in the liver of rats with nephrotic syndrome. Biochim Biophys Acta 1986; 686: 51–61
   Google Scholar
• Panduro A, CastrillÓN L, Pedraza-ChaverrÍ J, Vargas F, Ibarra-Rubio ME. Regulation of apolipoprotein A-I and E gene expression in liver and intestine of nephrotic and pair-fed rats. Nephron 1993; 65: 100–107
   PubMedGoogle Scholar
• Vaziri N D, Liang KH. Hepatic HMG-CoA reductase gene expression during the course of puromycininduced nephrosis. Kidney Int 1995; 48: 1979–1985
   Google Scholar
• Correa-Rotter R, Hostetter TH, Rosenberg ME. Renin and angiotensinogen gene expression in experimental diabetes mellitus. Kidney Int 1992; 41: 796–804
   Google Scholar
• Pratt R E, Zou W M, Naftilan A J, Ingelfinger J R, Dzau VJ. Altered sodium regulation of renal angiotensinogen mRNA in the spontaneously hypertensive rat. Am J Physiol 1989; 256: F469–F474
   PubMed Web of Science ®Google Scholar
• Cassis L A, Saye J A, Peach MJ. Location and regulation of rat angiotensinogen messenger RNA. Hypertension 1988; 11: 591–596
   PubMed Web of Science ®Google Scholar