Tubular and Glomerular L-Arginine Transport (Uptake and Transporters) and the Nitric Oxide Synthases in Ischemic Acute Renal Failure (iARF) in Streptozotocin-Induced Diabetic Rats (STZ-DM)

REFERENCES

• Bonventre JV. Mechanisms of ischemic acute renal failure. Kidney Int. 1993; 43: 1160–1178
   PubMed Web of Science ®Google Scholar
• Maessen JG. Reperfusion injury in the kidney. Pathophysiology of Reperfusion Injury, DL Das. CRC Press, Boca Raton, Fla. 1993; 79–100
   Google Scholar
• Peffella MA, Edell ES, Lrowka MJ, et al. Endothelium derived relaxing factor in pulmonary and renal circulations during hypoxia. Am J Physiol. 1992; 263: R45–R50
   Google Scholar
• Adnot S, Raffestin B, Eddahibi S, et al. Loss of endothelium relaxant activity in the pulmonary circulation of rats exposed to chronic hypoxia. J Clin Invest. 1991; 85: 155–162
   Google Scholar
• Van Benthyysen KM, McMurtry IF, Horwitz LD. Reperfusion after acute coronary occlusion in dogs impairs endothelium-dependent relaxation to acetylcholine and augments contractile reactivity in vitro. J Clin Invest. 1987; 79: 265–274
   Google Scholar
• Conger JD, Robinette JB, Scherier RW. Smooth muscle calcium and endothelium derived relaxing factor in the abnormal vascular responses of acute renal failure. J Clin Invest. 1988; 82: 532–537
   PubMed Web of Science ®Google Scholar
• Baylis C, Harton P, Engels K. Endothelial derived relaxing factor controls renal hemodynamics in the normal rat kidney. J Am Soc Nephrol. 1990; 1: 875
   PubMed Web of Science ®Google Scholar
• Brezis M, Heyman SN, Dinour D, et al. Role of nitric oxide in renal medullary oxygenation: Studies in isolated and intact rat kidneys. J Clin Invest. 1991; 88: 390
   PubMed Web of Science ®Google Scholar
• Conger J, Robinette J, Villar A, et al. Increased nitric oxide synthase activity despite lack of response to endothelium-dependent vasodilators in postischemic acute renal failure. J Clin Invest. 1995; 96: 631–638
   PubMed Web of Science ®Google Scholar
• Goor Y, Peer G, Iaina A, et al. Nitric oxide in ischemic acute renal failure of streptozotocin diabetic rats. Diabetologia. 1996; 39: 1036–1040
   Google Scholar
• Maree A, Peer G, Schwartz D, et al. Role of nitric oxide in glycerol-induced acute renal failure in rats. Nephrol Dial Transplant. 1994; 9: 78–81
   PubMed Web of Science ®Google Scholar
• Schwartz D, Blum M, Peer G, et al. Role of nitric oxide (EDRF) in radiocontrast acute renal failure in rats. Am J Physiol. 1994; 267: F374–F379
   PubMedGoogle Scholar
• Yu L, Gengaro PE, Niederberger M, et al. Nitric oxide: A mediator in tubular hpoxia/reoxygenation injury. Proc Natl Acad Sci USA. 1994; 91: 1691–1695
   PubMed Web of Science ®Google Scholar
• Persleni T, Noiri E, Bahou W, Goligorsky MS. Antisense oligodeoxynucleotide to inducible NO synthase rescue epithelial cells from oxidative stress injury. Am J Physiol. 1996; 270: F971–F977
   Google Scholar
• Lipton SA, Choi YB, Pan ZH, et al. A redox-based mechanism for the neuroprotective and neurodestructive effects of nitric oxide and related nitroso-compounds. Nat Lond. 1993; 364: 626–632
   PubMed Web of Science ®Google Scholar
• Beasley D, Schwartz JH, Brenner BM. Interleukin-1 induces prolonged L-arginine dependent cyclinc guanosine monophosphate and nitrite production in rat vascular smooth muscle cells. J Clin Invest. 1991; 87: 602–608
   PubMed Web of Science ®Google Scholar
• Iyengar R, Stuehr DJ, Marletta MA. Macrophage synthesis of nitrite, nitrate and N-nitrosamines precursors and role of the respiratory burst. Proc Natl Acad Sci USA. 1987; 84: 6369–6373
   PubMed Web of Science ®Google Scholar
• Hattori Y, Kasai K, Gross SS. Cationic amino acid transporter gene expression in cultured vascular smooth muscle cells and in rats. Am J Physiol. 1999; 276: H2020–H2028
   Google Scholar
• Albritton LM, Tseng L, Scadden D, Cunningham JM. A putative murine ecotropic retrovirus receptor gene encodes a multiple membrane-spanning protein and confers susceptibility to virus infection. Cell. 1989; 57: 659–666
   PubMed Web of Science ®Google Scholar
• Kim JW, Closs EI, Albritton LM, Cunningham JM. Transport of cationic amino acids by the mouse ecotropic retrovirus receptor. Nature. 1991; 352: 725–728
   PubMedGoogle Scholar
• Wang H, Lavanaugh MP, North RA, Labat D. Cell surface receptor for the ecotropic murine retroviruses is a basic amino acid. Nature. 1991; 352: 729–731
   PubMed Web of Science ®Google Scholar
• Low BC, Grigor MR. Angiotensin II stimulated system y+and cationic amino acid transporter gene expression I cultured vascular smooth muscle cells. J Biol Chem. 1995; 270: 27577–27583
   Google Scholar
• Howokawa H, Wawamura T, Lobayyashi S, et al. Cloning and characterization of a brain-specific cationic amino acid transporter. J Biol Chem. 1997; 272: 8717–8722
   Google Scholar
• Ito K, Groudine M. A new member of a cationic amino acid transporter family is preferentially expressed in adult mouse brain. J Biol Chem. 1997; 272: 26780–26786
   PubMedGoogle Scholar
• Wu F, Cholew AB, Mattson DL. Characterization of L-arginine transporters in rat renal inner medullary collecting duct. Am J Physiol. 2000; 278: R1506–R1512
   Google Scholar
• Schwartz IF, Schwartz D, Traskonov M, et al. L-arginine transport is augmented through up-regulation of tubular CAT-2 mRNA in ischemic acute renal failure in rats. Kidney Int. 2002; 62: 1700–1706
   Google Scholar
• Mauer MS. Structural-functional correlations of diabetic nephropathy. Kidney Int. 1994; 45: 612–622
   PubMed Web of Science ®Google Scholar
• Keynan S, Hirshberg B, Levin-Iaina N, et al. Renal nitric oxide production during the early phase of experimental diabetes mellitus. Kidney Int. 2000; 58: 740–747
   PubMed Web of Science ®Google Scholar
• Schwartz IF, Iaina A, Benedict Y, et al. Augmented arginine uptake through modulation of cationic amino acid transporter-1, increases GFR in diabetic rats. Kidney Int. 2004; 65: 1311–1319
   Google Scholar
• Gazzola GC, Dall'Asta V, Franchi-Gazzola R, White MF. The cluster-trey method for rapid measurement of solute fluxes in adherent cultured cells. Anal Biochem. 1981; 115: 368–374
   PubMed Web of Science ®Google 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
• Kilbourn RG, Griffith OW. Overproduction of nitric oxide in cytokine-mediated and septic shock. J Natl Cancer Inst. 1992; 84: 827–831
   PubMed Web of Science ®Google Scholar
• Durante W, Liao L, Iftikhar I, et al. Differential regulation of L-arginine transport and nitric oxide production by vascular smooth muscle and endothelium. Circ Res. 1996; 78: 1075–1082
   Google Scholar
• Bredt DS, Hwang PM, Glatt CE, et al. Cloned and expressed NOS structurally resembles cytochrome P-450 reductase. Nature. 1991; 351: 714–718
   PubMed Web of Science ®Google Scholar