ascorbic-acid and Hyperoxaluria--Primary

Topics: Ascorbic Acid; Diet; Glyoxylates; Humans; Hyperoxaluria; Hyperoxaluria, Primary; Intestinal Absorption; Kidney; Metabolism, Inborn Errors; Oxalates

Topics: Adolescent; Ascorbic Acid; Biochemical Phenomena; Biochemistry; Child; Classification; Diet; Genetics, Medical; Glycine; Glycolates; Humans; Hyperoxaluria, Primary; Infant; Kidney Calculi; Metabolic Diseases; Metabolism; Nephrocalcinosis; Oxalates; Pathology; Terminology as Topic; Uremia; Urine; Vitamin B 6 Deficiency

We have previously reported that hyperoxalemia can be aggravated by vitamin C supplementation in regular hemodialysis patients. The present study was undertaken to examine the validity of this observation in an experimental setting. Fifty five-sixths nephrectomized rats were divided into two groups: 30 rats were allowed free access to water containing 8 mg/ml of vitamin C (100-160 mg/100 g/24 h) and the remainder given tap water without vitamin C. The serum creatinine increased and the Hct decreased gradually; however, there was no difference between the two groups. Plasma vitamin C, oxalate and urinary oxalate levels were higher in the vitamin -treated group than the nontreated rats. Histological examination revealed glomerular and interstitial fibrosis and round cell infiltration as well as tubular cyst formation. Oxalate deposits in renal tubules were found only in vitamin C-treated rats with advanced renal failure. Nontreated animals with equally advanced renal impairment showed no oxalate deposits. These results confirm our previous clinical findings that vitamin C supplementation aggravates the secondary oxalosis of chronic renal failure.

Topics: Animals; Ascorbic Acid; Hyperoxaluria, Primary; Kidney Failure, Chronic; Kidney Tubules; Male; Nephrectomy; Oxalates; Oxalic Acid; Rats; Rats, Inbred Strains

Topics: Ascorbic Acid; Humans; Hyperoxaluria, Primary; Metabolism; Oxalates; Urine