Superoxide dismutase restores the influence of nitric oxide on renal arterioles in diabetes mellitus

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Abstract

Experiments were performed to determine the influence of endogenous nitric oxide (NO) on basal arteriolar diameter in kidneys from diabetic rats and to evaluate the role of superoxide anions as modulators of NO activity under these conditions. Male Sprague-Dawley rats were injected with streptozotocin (STZ, 65 mg/kg iv) and received insulin via ip osmotic minipumps (3 U/kg per day). Sham rats received vehicle treatments. Videomicroscopy was used, in conjunction with the in vitro blood-perfused juxtamedullary nephron technique, to visualize renal afferent and efferent arterioles 2 wk after the onset of diabetes. Baseline afferent arteriolar inside diameter was greater in STZ (32 ± 2 μm) than in sham rats (24 ± 2 μm). Efferent arteriolar diameter did not differ between STZ (24 ± 2 μm) and sham rats (21 ± 1 μm). In kidneys from sham rats, N(ω)-nitro-L-arginine (L-NNA, an NO synthase inhibitor) decreased arteriolar diameters in a concentration-dependent manner, with 100 μM L-NNA significantly reducing both afferent (13 ± 2%) and efferent (11 ± 1%) diameters. In kidneys from STZ rats, 100 μM L-NNA reduced afferent and efferent diameters by only 3 ± 1 and 4 ± 1%, respectively, indicating a suppressed arteriolar influence of NO. In STZ kidneys treated with superoxide dismutase (SOD, 150 U/mL), afferent and efferent arteriolar L-NNA responses were restored to levels comparable to those of SOD-treated and untreated sham kidneys. These observations suggest that suppressed SOD activity reduces the tonic influence of NO on renal arterioles during the early stage of diabetes mellitus, perhaps through allowing the accumulation of NO-scavenging superoxide anions.

Original languageEnglish (US)
Pages (from-to)1559-1566
Number of pages8
JournalJournal of the American Society of Nephrology
Volume5
Issue number8
StatePublished - Jan 1 1995

Fingerprint

Arterioles
Superoxide Dismutase
Diabetes Mellitus
Nitric Oxide
Kidney
Superoxides
Video Microscopy
Nephrons
Streptozocin
Nitric Oxide Synthase
Sprague Dawley Rats
Arginine
Insulin

Keywords

  • N(ω)-nitro-L-arginine
  • afferent arteriole
  • efferent arteriole
  • endothelium-derived relaxing factor
  • superoxide anion

ASJC Scopus subject areas

  • Nephrology

Cite this

Superoxide dismutase restores the influence of nitric oxide on renal arterioles in diabetes mellitus. / Ohishi, K.; Carmines, Pamela K.

In: Journal of the American Society of Nephrology, Vol. 5, No. 8, 01.01.1995, p. 1559-1566.

Research output: Contribution to journalArticle

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abstract = "Experiments were performed to determine the influence of endogenous nitric oxide (NO) on basal arteriolar diameter in kidneys from diabetic rats and to evaluate the role of superoxide anions as modulators of NO activity under these conditions. Male Sprague-Dawley rats were injected with streptozotocin (STZ, 65 mg/kg iv) and received insulin via ip osmotic minipumps (3 U/kg per day). Sham rats received vehicle treatments. Videomicroscopy was used, in conjunction with the in vitro blood-perfused juxtamedullary nephron technique, to visualize renal afferent and efferent arterioles 2 wk after the onset of diabetes. Baseline afferent arteriolar inside diameter was greater in STZ (32 ± 2 μm) than in sham rats (24 ± 2 μm). Efferent arteriolar diameter did not differ between STZ (24 ± 2 μm) and sham rats (21 ± 1 μm). In kidneys from sham rats, N(ω)-nitro-L-arginine (L-NNA, an NO synthase inhibitor) decreased arteriolar diameters in a concentration-dependent manner, with 100 μM L-NNA significantly reducing both afferent (13 ± 2{\%}) and efferent (11 ± 1{\%}) diameters. In kidneys from STZ rats, 100 μM L-NNA reduced afferent and efferent diameters by only 3 ± 1 and 4 ± 1{\%}, respectively, indicating a suppressed arteriolar influence of NO. In STZ kidneys treated with superoxide dismutase (SOD, 150 U/mL), afferent and efferent arteriolar L-NNA responses were restored to levels comparable to those of SOD-treated and untreated sham kidneys. These observations suggest that suppressed SOD activity reduces the tonic influence of NO on renal arterioles during the early stage of diabetes mellitus, perhaps through allowing the accumulation of NO-scavenging superoxide anions.",
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