Inflammatory milieu as an early marker of kidney injury in offspring rats from diabetic mothers

Eur J Pharmacol. 2012 Aug 15;689(1-3):233-40. doi: 10.1016/j.ejphar.2012.05.024. Epub 2012 May 28.

Abstract

The present study investigated the early presence of inflammatory response in renal tissue of young offspring from diabetic mothers. The effect of L-arginine (L-arg) supplementation was also investigated. The offspring was divided into four groups: group CO (controls); group DO (diabetic offspring); group CA (CO receiving 2% L-arg solution) and group DA (DO receiving the 2% L-arg solution). Glycemia, arterial pressure and renal function were evaluated; gene and protein expression of pro-inflammatory cytokines were also measured. Blood pressure levels were significantly increased in 2 and 6 month-old DO rats, whereas L-arg administration caused a significant decrease in the DA group, at both ages. DO rats showed a significantly blunted glycemic response to exogenous insulin. In 2 month-old DO animals, renal protein expression of pro-inflammatory molecules was significantly increased. At six months of age, we also observed an increase in gene expression of pro-inflammatory molecules, whereas L-arg supplementation prevented this increase at both ages. Our data suggest that activation of inflammatory pathways is present early in the kidney of DO rats, and that L-arg can attenuate the expression of these markers of tissue inflammation. Our results also reinforce the concept that intrauterine environmental factors are a fundamental determinant in the development of metabolic and vascular diseases later in life.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acute Kidney Injury / diagnosis
  • Acute Kidney Injury / etiology
  • Acute Kidney Injury / pathology*
  • Animals
  • Arginine / administration & dosage
  • Arginine / toxicity
  • Biomarkers / metabolism
  • Diabetes Mellitus, Experimental / complications
  • Diabetes Mellitus, Experimental / diagnosis
  • Diabetes Mellitus, Experimental / pathology*
  • Early Diagnosis
  • Female
  • Inflammation Mediators / administration & dosage*
  • Inflammation Mediators / toxicity
  • Male
  • Pregnancy
  • Pregnancy Complications / diagnosis
  • Pregnancy Complications / etiology
  • Pregnancy Complications / pathology*
  • Prenatal Exposure Delayed Effects / diagnosis
  • Prenatal Exposure Delayed Effects / etiology
  • Prenatal Exposure Delayed Effects / pathology*
  • Random Allocation
  • Rats
  • Rats, Wistar

Substances

  • Biomarkers
  • Inflammation Mediators
  • Arginine