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Erschienen in: Diabetologia 10/2003

01.10.2003 | Article

Increased expression of NAD(P)H oxidase subunits, NOX4 and p22phox, in the kidney of streptozotocin-induced diabetic rats and its reversibity by interventive insulin treatment

verfasst von: T. Etoh, T. Inoguchi, MD, M. Kakimoto, N. Sonoda, K. Kobayashi, J. Kuroda, H. Sumimoto, H. Nawata

Erschienen in: Diabetologia | Ausgabe 10/2003

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Abstract

Aim/hypothesis

An increased production of reactive oxygen species (ROS) could contribute to the development of diabetic nephropathy. NAD(P)H oxidase might be an important source of ROS production in kidney as reported in blood vessels. In this study, we show the increased expression of essential subunits of NAD(P)H oxidase, NOX4 and p22phox, in the kidney of diabetic rats.

Methods

The levels of mRNA of both NOX4 and p22phox were evaluated in kidney from streptozotocin-induced diabetic rats and age-matched control rats at 4 and 8 weeks after onset of diabetes by Northern blot analysis. The localization and expression levels of these components and 8-hydroxy-deoxyguanosine (8-OHdG), which is a marker of ROS-induced DNA damage, were also evaluated by immunostaining.

Results

The levels of both NOX4 and p22phox mRNA were increased in the kidney of diabetic rats as compared with control rats. Immunostaining analysis showed that the expression levels of NOX4 and p22phox were clearly increased in both distal tubular cells and glomeruli from diabetic rats. Both the localization and the expression levels of these components were in parallel with those of 8-OHdG. Interventive insulin treatment for 2 weeks completely restored the increased levels of these components in the diabetic kidney to control levels in parallel with those of 8-OHdG.

Conclusions/interpretation

This study provides evidence that NAD(P)H oxidase subunits, NOX4 and p22phox, were increased in the kidney of diabetic rats. Thus, NAD(P)H-dependent overproduction of ROS could cause renal tissue damage in diabetes. This might contribute to the development of diabetic nephropathy.
Literatur
1.
Zurück zum Zitat Baynes JW (1991) Role of oxidative stress in development of complications in diabetes. Diabetes 40:405–412PubMed Baynes JW (1991) Role of oxidative stress in development of complications in diabetes. Diabetes 40:405–412PubMed
2.
Zurück zum Zitat Williamson JR, Chang K, Frangos M et al. (1993) Hyperglycemic pseudohypoxia and diabetic complications. Diabetes 42:801–813PubMed Williamson JR, Chang K, Frangos M et al. (1993) Hyperglycemic pseudohypoxia and diabetic complications. Diabetes 42:801–813PubMed
3.
Zurück zum Zitat Brownlee M, Cerami A, Vlassara H (1988) Advanced glycosylation end products in tissue and the biochemical basis of diabetic complications. N Engl J Med 318:1315–1321PubMed Brownlee M, Cerami A, Vlassara H (1988) Advanced glycosylation end products in tissue and the biochemical basis of diabetic complications. N Engl J Med 318:1315–1321PubMed
4.
Zurück zum Zitat Spitaler MM, Graier WF (2002) Vascular targets of redox signaling in diabetes mellitus. Diabetologia 45:476–494CrossRef Spitaler MM, Graier WF (2002) Vascular targets of redox signaling in diabetes mellitus. Diabetologia 45:476–494CrossRef
5.
Zurück zum Zitat Ha H, Kim C, Son Y, Chung MH, Kim KH (1994) DNA damage in the kidneys of diabetic rats exhibiting microalbuminuria. Free Radic Biol Med 16:271–274PubMed Ha H, Kim C, Son Y, Chung MH, Kim KH (1994) DNA damage in the kidneys of diabetic rats exhibiting microalbuminuria. Free Radic Biol Med 16:271–274PubMed
6.
Zurück zum Zitat Kakimoto M, Inoguchi T, Sonta T et al. (2002) Accumulation of 8-hydroxy-2′-deoxyguanosine and mitochondrial DNA deletion in kidney of diabetic rats. Diabetes 51:1588–1595PubMed Kakimoto M, Inoguchi T, Sonta T et al. (2002) Accumulation of 8-hydroxy-2′-deoxyguanosine and mitochondrial DNA deletion in kidney of diabetic rats. Diabetes 51:1588–1595PubMed
7.
Zurück zum Zitat Tesfamariam B, Brown ML, Cohen RA (1992) Aldose reductase and myo-inositol in endothelial cell dysfunction caused by elevated glucose. J Pharmacol Exp Ther 263:153–157 Tesfamariam B, Brown ML, Cohen RA (1992) Aldose reductase and myo-inositol in endothelial cell dysfunction caused by elevated glucose. J Pharmacol Exp Ther 263:153–157
8.
Zurück zum Zitat Nishikawa T, Edelstein D, Du XL et al. (2000) Normalizing mitochondrial superoxide production blocks three pathways of hyperglycaemic damage. Nature 404:787–790PubMed Nishikawa T, Edelstein D, Du XL et al. (2000) Normalizing mitochondrial superoxide production blocks three pathways of hyperglycaemic damage. Nature 404:787–790PubMed
9.
Zurück zum Zitat Mohazzab KM, Kaminski PM, Wolin MS (1994) NADH oxidoreductase is a major source of superoxide anion in bovine coronary artery endothelium. Am J Physiol 266:H2568–H2572PubMed Mohazzab KM, Kaminski PM, Wolin MS (1994) NADH oxidoreductase is a major source of superoxide anion in bovine coronary artery endothelium. Am J Physiol 266:H2568–H2572PubMed
10.
Zurück zum Zitat Griedling KK, Minieri CA, Ollerenshaw JD, Alexander RW (1994) Angiotensin II stimulates NADH and NADPH oxidase activity in culured vascular smooth muscle cells. Circ Res 74:1141–1148PubMed Griedling KK, Minieri CA, Ollerenshaw JD, Alexander RW (1994) Angiotensin II stimulates NADH and NADPH oxidase activity in culured vascular smooth muscle cells. Circ Res 74:1141–1148PubMed
11.
Zurück zum Zitat Rajagopalan S, Kurz S, Munzel T et al. (1996) Angiotensin II-mediated hypertension in the rat increases vascular superoxide production via membrane NADH/NADPH oxidase activation. J Clin Invest 97:1916–1923PubMed Rajagopalan S, Kurz S, Munzel T et al. (1996) Angiotensin II-mediated hypertension in the rat increases vascular superoxide production via membrane NADH/NADPH oxidase activation. J Clin Invest 97:1916–1923PubMed
12.
Zurück zum Zitat Ushio-Fukai M, Zafari AM, Fukui T, Ishizuka N, Griendling KK (1996) p22phox is a critical component of the superoxide-generating NADH/NADPH oxidase system and regulates angiotensin II-induced hypertrophy in vascular smooth muscle cells. J Biol Chem 271:23317–23321CrossRefPubMed Ushio-Fukai M, Zafari AM, Fukui T, Ishizuka N, Griendling KK (1996) p22phox is a critical component of the superoxide-generating NADH/NADPH oxidase system and regulates angiotensin II-induced hypertrophy in vascular smooth muscle cells. J Biol Chem 271:23317–23321CrossRefPubMed
13.
Zurück zum Zitat Warnholtz A, Nickenig G, Schulz E et al. (1999) Increased NADH-oxidase-mediated superoxide production in the early stages of atherosclerosis. Circulation 99:2027–2033PubMed Warnholtz A, Nickenig G, Schulz E et al. (1999) Increased NADH-oxidase-mediated superoxide production in the early stages of atherosclerosis. Circulation 99:2027–2033PubMed
14.
Zurück zum Zitat Azumi H, Inoue N, Takeshita S et al. (1999) Expression of NADH/NADPH oxidase p22phox in human coronay arteries. Circulation 100:1494–1498PubMed Azumi H, Inoue N, Takeshita S et al. (1999) Expression of NADH/NADPH oxidase p22phox in human coronay arteries. Circulation 100:1494–1498PubMed
15.
Zurück zum Zitat Barry-Lane PA, Patterson C, Merwe M van der et al. (2001) p47phox is required for atherosclerotic lesion progression in Apo E -/- mice. J Clin Invest 108:1513–1522CrossRefPubMed Barry-Lane PA, Patterson C, Merwe M van der et al. (2001) p47phox is required for atherosclerotic lesion progression in Apo E -/- mice. J Clin Invest 108:1513–1522CrossRefPubMed
16.
Zurück zum Zitat Sorescu D, Weiss D, Lassegue B et al. (2002) Superoxide production and expression of Nox family proteins in human atherosclerosis. Circulation 105:1429–1435CrossRefPubMed Sorescu D, Weiss D, Lassegue B et al. (2002) Superoxide production and expression of Nox family proteins in human atherosclerosis. Circulation 105:1429–1435CrossRefPubMed
17.
Zurück zum Zitat Fukui T, Ishizaka N, Rajagopalan S et al. (1997) p22phox mRNA expression and NADPH oxidase activity are increased in aortas from hypertensive rats. Circ Res 80:45–51PubMed Fukui T, Ishizaka N, Rajagopalan S et al. (1997) p22phox mRNA expression and NADPH oxidase activity are increased in aortas from hypertensive rats. Circ Res 80:45–51PubMed
18.
Zurück zum Zitat Inoguchi T, Li P, Umeda F et al. (2000) High glucose level and fatty acid atimulate reactive oxygen spieces production through protein kinase C-dependent activation of NAD(P)H oxidase in cultured vascular cells. Diabetes 49:1939–1945PubMed Inoguchi T, Li P, Umeda F et al. (2000) High glucose level and fatty acid atimulate reactive oxygen spieces production through protein kinase C-dependent activation of NAD(P)H oxidase in cultured vascular cells. Diabetes 49:1939–1945PubMed
19.
Zurück zum Zitat Hink U, Li H, Mollnau H et al. (2001) Mechanisms underlying endothelial dysfunction in diabetes mellitus. Circ Res 88:e14–e22PubMed Hink U, Li H, Mollnau H et al. (2001) Mechanisms underlying endothelial dysfunction in diabetes mellitus. Circ Res 88:e14–e22PubMed
20.
Zurück zum Zitat Kim YK, Lee MS, Son SM et al. (2002) Vascular NADH oxidase is involved in impaired endothelium-dependent vasodilation in OLETF rats, a model of type 2 diabetes. Diabetes 51:522–527PubMed Kim YK, Lee MS, Son SM et al. (2002) Vascular NADH oxidase is involved in impaired endothelium-dependent vasodilation in OLETF rats, a model of type 2 diabetes. Diabetes 51:522–527PubMed
21.
Zurück zum Zitat Guzik TJ, Mussa S, Gastaldi D et al. (2002) Mechanisms of increased vascular superoxide production in human diabetes mellitus. Circulation 105:1656–1662CrossRefPubMed Guzik TJ, Mussa S, Gastaldi D et al. (2002) Mechanisms of increased vascular superoxide production in human diabetes mellitus. Circulation 105:1656–1662CrossRefPubMed
22.
Zurück zum Zitat Laurent B, Ardaillou R (1986) Reactive oxygen species: production and role in the kidney. Am J Physiol 251:F765–F776PubMed Laurent B, Ardaillou R (1986) Reactive oxygen species: production and role in the kidney. Am J Physiol 251:F765–F776PubMed
23.
Zurück zum Zitat Ueda N, Kaushal GP, Shah SV (2000) Apoptotic mechanisms in acute renal failure. Am J Med 108:403–415CrossRefPubMed Ueda N, Kaushal GP, Shah SV (2000) Apoptotic mechanisms in acute renal failure. Am J Med 108:403–415CrossRefPubMed
24.
Zurück zum Zitat Griendling KK, Sorescu D, Ushio-Fukai M (2000) NAD(P)H oxidase-role in cardiovascular biology and disease. Circ Res 86:494–501PubMed Griendling KK, Sorescu D, Ushio-Fukai M (2000) NAD(P)H oxidase-role in cardiovascular biology and disease. Circ Res 86:494–501PubMed
25.
Zurück zum Zitat Geiszt M, Kopp JB, Varnai P, Leto TL (2000) Identification of Renox, an NAD(P)H oxidase in kidney. Proc Natl Acad Aci USA 97:8010–8014CrossRef Geiszt M, Kopp JB, Varnai P, Leto TL (2000) Identification of Renox, an NAD(P)H oxidase in kidney. Proc Natl Acad Aci USA 97:8010–8014CrossRef
26.
Zurück zum Zitat Shiose A, Kuroda J, Tsuruya K et al. (2001) A novel superoxide-producing NAD(P)H oxidase in kidney. J Biol Chem 276:1417–1423CrossRefPubMed Shiose A, Kuroda J, Tsuruya K et al. (2001) A novel superoxide-producing NAD(P)H oxidase in kidney. J Biol Chem 276:1417–1423CrossRefPubMed
27.
Zurück zum Zitat Parkos CA, Allen RA, Cochrane CG, Jesaitis AJ (1987) Purified cytochrome b from human granulocyte plasma membrane is comprised of two polypeptides with relative molecular weights of 91,000 and 22,000. J Clin Invest 80:732–742PubMed Parkos CA, Allen RA, Cochrane CG, Jesaitis AJ (1987) Purified cytochrome b from human granulocyte plasma membrane is comprised of two polypeptides with relative molecular weights of 91,000 and 22,000. J Clin Invest 80:732–742PubMed
28.
Zurück zum Zitat Suh YA, Arnold RS, Lassegue B et al. (1999) Cell transformation by the superoxide-generating oxidase Mox1. Nature 401:79–82CrossRefPubMed Suh YA, Arnold RS, Lassegue B et al. (1999) Cell transformation by the superoxide-generating oxidase Mox1. Nature 401:79–82CrossRefPubMed
29.
Zurück zum Zitat Merriwether DA, Clark AG, Ballinger SW et al. (1991) The structure of human mitochondrial DNA variation. J Mol Evol 33:543–555PubMed Merriwether DA, Clark AG, Ballinger SW et al. (1991) The structure of human mitochondrial DNA variation. J Mol Evol 33:543–555PubMed
30.
Zurück zum Zitat Ishii H, Jirousek MR, Koya D et al. (1996) Amelioration of vascular dysfunctions in diabetic rats by an oral PKC β inhibitor. Science 272:728–731PubMed Ishii H, Jirousek MR, Koya D et al. (1996) Amelioration of vascular dysfunctions in diabetic rats by an oral PKC β inhibitor. Science 272:728–731PubMed
31.
Zurück zum Zitat Inoguchi T, Battan R, Handler E, Sportsman JR, Heath W, King GL (1992) Preferential elevation of protein kinase C isoform βII and diacylglycerol levels in the aorta and heart of diabetic rats: differential reversibility to glycemic control by islet cell transplantation. Proc Natl Acad Sci USA 89:11059–11063PubMed Inoguchi T, Battan R, Handler E, Sportsman JR, Heath W, King GL (1992) Preferential elevation of protein kinase C isoform βII and diacylglycerol levels in the aorta and heart of diabetic rats: differential reversibility to glycemic control by islet cell transplantation. Proc Natl Acad Sci USA 89:11059–11063PubMed
32.
Zurück zum Zitat Shiba T, Inoguchi T, Sportsman JR, Heath WF, Bursell S, King GL (1993) Correlation of diacylglycerol level and protein kinase C activity in rat retina to retinal circulation. Am J Physiol 265:E783–E793PubMed Shiba T, Inoguchi T, Sportsman JR, Heath WF, Bursell S, King GL (1993) Correlation of diacylglycerol level and protein kinase C activity in rat retina to retinal circulation. Am J Physiol 265:E783–E793PubMed
33.
Zurück zum Zitat Koya D, King GL (1998) Protein kinase C activation and the development of diabetic complications. Diabetes 47:859–866PubMed Koya D, King GL (1998) Protein kinase C activation and the development of diabetic complications. Diabetes 47:859–866PubMed
34.
Zurück zum Zitat Swain SD, Helgerson SL, Davis AR, Nelson LK, Quinn MT (1997) Analysis of activation-induced conformational changes in p47phox using tryptophan flurescence spectroscopy. J Biol Chem 272:29502–29510CrossRefPubMed Swain SD, Helgerson SL, Davis AR, Nelson LK, Quinn MT (1997) Analysis of activation-induced conformational changes in p47phox using tryptophan flurescence spectroscopy. J Biol Chem 272:29502–29510CrossRefPubMed
35.
Zurück zum Zitat Benna JE, Dang PMC, Gaudry M et al. (1997) Phosphorylation of the respiratory burst oxidase sbunit p67phox during human neutrophil activation: regulation by protein kinase C-dependent and independent pathways. J Biol Chem 272:17204–17208CrossRefPubMed Benna JE, Dang PMC, Gaudry M et al. (1997) Phosphorylation of the respiratory burst oxidase sbunit p67phox during human neutrophil activation: regulation by protein kinase C-dependent and independent pathways. J Biol Chem 272:17204–17208CrossRefPubMed
36.
Zurück zum Zitat Akasaki T, Koga H, Sumimoto H (1999) Phosphoinositide 3-kinase-dependent and -independent activation of the small GTPase Rac2 in human neutrophils. J Biol Chem 274:18055–18059CrossRefPubMed Akasaki T, Koga H, Sumimoto H (1999) Phosphoinositide 3-kinase-dependent and -independent activation of the small GTPase Rac2 in human neutrophils. J Biol Chem 274:18055–18059CrossRefPubMed
Metadaten
Titel
Increased expression of NAD(P)H oxidase subunits, NOX4 and p22phox, in the kidney of streptozotocin-induced diabetic rats and its reversibity by interventive insulin treatment
verfasst von
T. Etoh
T. Inoguchi, MD
M. Kakimoto
N. Sonoda
K. Kobayashi
J. Kuroda
H. Sumimoto
H. Nawata
Publikationsdatum
01.10.2003
Verlag
Springer-Verlag
Erschienen in
Diabetologia / Ausgabe 10/2003
Print ISSN: 0012-186X
Elektronische ISSN: 1432-0428
DOI
https://doi.org/10.1007/s00125-003-1205-6

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