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Healthou_Creatine supplementation does not affect kidney function in an animal model with pre‐existing renal failure
  1. Norbert H. Lameire 2

+Author Affiliations

  1. 1Laboratory of Clinical Chemistry and
  2. 2Renal Division, Department of Internal Medicine, University Hospital Ghent and
  3. 3Department of Physiology and Physiopathology, Ghent University, Ghent, Belgium
  • Received June 24, 2002.
  • Accepted September 12, 2002.

Abstract

Background. Creatine is widely used as an ergogenic substance among athletes. Safety of prolonged creatine intake has been questioned, based upon case reports and animal data. We investigated the effect of prolonged creatine ingestion on renal function in animals with normal kidney function or pre‐existing kidney failure, respectively.

Methods. Male Wistar rats were randomly allocated to four experimental groups: (i) sham‐operated, control diet; (ii) sham‐operated, creatine‐supplemented diet (2% w/w (0.9±0.2 g creatine/kg body weight/day)); (iii) two‐thirds nephrectomized, control diet; and (iv) two‐thirds nephrectomized, creatine supplemented diet. Glomerular filtration rate was determined using inulin and creatinine clearance, together with albumin excretion, urea clearance, muscle and serum creatine and serum cystatin C concentrations.

Results. In contrast to previous reports, no detrimental effects of creatine supplementation on the renal function indices were observed in two‐thirds nephrectomized or sham‐operated animals. No differences were observed in inulin (0.28±0.08 vs 0.25±0.08 ml/min/100 g; P=NS) or creatinine clearance rates. Serum cystatin C concentration, urinary protein excretion, and albumin and urea clearance were comparable between creatine‐supplemented and control‐diet fed animals in both sham‐operated and two‐thirds nephrectomized animals. Serum creatine and intramuscular total creatine concentrations were higher in creatine‐supplemented groups (P<0.05).

Conclusions. Creatine supplementation at a dosage of 2% w/w for 4 weeks does not impair kidney function in animals with pre‐existing renal failure or in control animals.

Key words

 

from source:http://ndt.oxfordjournals.org/content/18/2/258.short


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