Tempone reduces renal dysfunction and injury mediated by oxidative stress of the rat kidney.

N. Patel, P. K. Chatterjee, B. E. Chatterjee, S. Cuzzocrea, I. Seranio, Paul Anthony James Brown, Keith Nicol Stewart, H. Mota-Filipe, C. Thiemermann

Research output: Contribution to journalArticle

18 Citations (Scopus)

Abstract

Here we investigate the effects of the stable, water-soluble nitroxyl radical, TEMPONE, on renal dysfunction and injury caused by ischemia/reperfusion (I/R) of the rat kidney in vivo. TEMPONE significantly improved both glomerular and tubular function (serum urea, creatinine, creatinine clearance, and fractional excretion of Na+) in a dose-dependent manner and significantly attenuated the reperfusion-injury associated with I/R (urinary N-acetyl-beta-D-glucosaminidase, aspartate aminotransferase, assessment of renal histology). TEMPONE also markedly reduced the immunohistochemical evidence of the formation of nitrotyrosine and poly(ADP-ribose), indicating reduction of nitrosative and oxidative stress, respectively. The latter was reflected in vitro, where TEMPONE significantly reduced cellular injury of primary cultures of rat renal proximal tubular (PT) cells caused by hydrogen peroxide in a dose-dependent manner. Importantly, in contrast to its in vivo metabolite TEMPOL (which also provided protective effects against renal I/R and oxidative stress of PT cells), TEMPONE reduced renal dysfunction and injury without causing a significant reduction in blood pressure upon administration. These results suggest, for the first time, that TEMPONE can reduce the renal dysfunction and injury caused by I/R and the injury caused to PT cells by oxidative stress without producing the adverse cardiovascular effects observed when using other nitroxyl radicals. (C) 2002 Elsevier Science Inc.

Original languageEnglish
Pages (from-to)1575-1589
Number of pages14
JournalFree Radical Biology and Medicine
Volume33
Issue number11
DOIs
Publication statusPublished - 2002

Keywords

  • TEMPONE
  • TEMPOL
  • renal
  • kidney
  • proximal tubule
  • ischemia/reperfusion
  • reperfusion injury
  • reactive oxygen species
  • oxidative stress
  • nitrotyrosine
  • nitrosative stress
  • poly(ADP-ribose)
  • poly(ADP-ribose) polymerase
  • free radicals
  • ISCHEMIA-REPERFUSION INJURY
  • PERMEABLE RADICAL SCAVENGER
  • SUPEROXIDE-DISMUTASE MIMICS
  • SYNTHASE KNOCKOUT MICE
  • NITRIC-OXIDE
  • PEROXYNITRITE FORMATION
  • NITROXIDE ANTIOXIDANTS
  • WARM ISCHEMIA
  • ORGAN INJURY
  • IN-VIVO

Cite this

Patel, N., Chatterjee, P. K., Chatterjee, B. E., Cuzzocrea, S., Seranio, I., Brown, P. A. J., ... Thiemermann, C. (2002). Tempone reduces renal dysfunction and injury mediated by oxidative stress of the rat kidney. Free Radical Biology and Medicine, 33(11), 1575-1589. https://doi.org/10.1016/S0891-5849(02)01116-4

Tempone reduces renal dysfunction and injury mediated by oxidative stress of the rat kidney. / Patel, N.; Chatterjee, P. K.; Chatterjee, B. E.; Cuzzocrea, S.; Seranio, I.; Brown, Paul Anthony James; Stewart, Keith Nicol; Mota-Filipe, H.; Thiemermann, C.

In: Free Radical Biology and Medicine, Vol. 33, No. 11, 2002, p. 1575-1589.

Research output: Contribution to journalArticle

Patel, N, Chatterjee, PK, Chatterjee, BE, Cuzzocrea, S, Seranio, I, Brown, PAJ, Stewart, KN, Mota-Filipe, H & Thiemermann, C 2002, 'Tempone reduces renal dysfunction and injury mediated by oxidative stress of the rat kidney.', Free Radical Biology and Medicine, vol. 33, no. 11, pp. 1575-1589. https://doi.org/10.1016/S0891-5849(02)01116-4
Patel, N. ; Chatterjee, P. K. ; Chatterjee, B. E. ; Cuzzocrea, S. ; Seranio, I. ; Brown, Paul Anthony James ; Stewart, Keith Nicol ; Mota-Filipe, H. ; Thiemermann, C. / Tempone reduces renal dysfunction and injury mediated by oxidative stress of the rat kidney. In: Free Radical Biology and Medicine. 2002 ; Vol. 33, No. 11. pp. 1575-1589.
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AU - Patel, N.

AU - Chatterjee, P. K.

AU - Chatterjee, B. E.

AU - Cuzzocrea, S.

AU - Seranio, I.

AU - Brown, Paul Anthony James

AU - Stewart, Keith Nicol

AU - Mota-Filipe, H.

AU - Thiemermann, C.

PY - 2002

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N2 - Here we investigate the effects of the stable, water-soluble nitroxyl radical, TEMPONE, on renal dysfunction and injury caused by ischemia/reperfusion (I/R) of the rat kidney in vivo. TEMPONE significantly improved both glomerular and tubular function (serum urea, creatinine, creatinine clearance, and fractional excretion of Na+) in a dose-dependent manner and significantly attenuated the reperfusion-injury associated with I/R (urinary N-acetyl-beta-D-glucosaminidase, aspartate aminotransferase, assessment of renal histology). TEMPONE also markedly reduced the immunohistochemical evidence of the formation of nitrotyrosine and poly(ADP-ribose), indicating reduction of nitrosative and oxidative stress, respectively. The latter was reflected in vitro, where TEMPONE significantly reduced cellular injury of primary cultures of rat renal proximal tubular (PT) cells caused by hydrogen peroxide in a dose-dependent manner. Importantly, in contrast to its in vivo metabolite TEMPOL (which also provided protective effects against renal I/R and oxidative stress of PT cells), TEMPONE reduced renal dysfunction and injury without causing a significant reduction in blood pressure upon administration. These results suggest, for the first time, that TEMPONE can reduce the renal dysfunction and injury caused by I/R and the injury caused to PT cells by oxidative stress without producing the adverse cardiovascular effects observed when using other nitroxyl radicals. (C) 2002 Elsevier Science Inc.

AB - Here we investigate the effects of the stable, water-soluble nitroxyl radical, TEMPONE, on renal dysfunction and injury caused by ischemia/reperfusion (I/R) of the rat kidney in vivo. TEMPONE significantly improved both glomerular and tubular function (serum urea, creatinine, creatinine clearance, and fractional excretion of Na+) in a dose-dependent manner and significantly attenuated the reperfusion-injury associated with I/R (urinary N-acetyl-beta-D-glucosaminidase, aspartate aminotransferase, assessment of renal histology). TEMPONE also markedly reduced the immunohistochemical evidence of the formation of nitrotyrosine and poly(ADP-ribose), indicating reduction of nitrosative and oxidative stress, respectively. The latter was reflected in vitro, where TEMPONE significantly reduced cellular injury of primary cultures of rat renal proximal tubular (PT) cells caused by hydrogen peroxide in a dose-dependent manner. Importantly, in contrast to its in vivo metabolite TEMPOL (which also provided protective effects against renal I/R and oxidative stress of PT cells), TEMPONE reduced renal dysfunction and injury without causing a significant reduction in blood pressure upon administration. These results suggest, for the first time, that TEMPONE can reduce the renal dysfunction and injury caused by I/R and the injury caused to PT cells by oxidative stress without producing the adverse cardiovascular effects observed when using other nitroxyl radicals. (C) 2002 Elsevier Science Inc.

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KW - PERMEABLE RADICAL SCAVENGER

KW - SUPEROXIDE-DISMUTASE MIMICS

KW - SYNTHASE KNOCKOUT MICE

KW - NITRIC-OXIDE

KW - PEROXYNITRITE FORMATION

KW - NITROXIDE ANTIOXIDANTS

KW - WARM ISCHEMIA

KW - ORGAN INJURY

KW - IN-VIVO

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DO - 10.1016/S0891-5849(02)01116-4

M3 - Article

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EP - 1589

JO - Free Radical Biology and Medicine

JF - Free Radical Biology and Medicine

SN - 0891-5849

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