Effects of Agmatine on Contrast-Induced Nephropathy in Rats and Rabbits

Biol Pharm Bull. 2020;43(10):1556-1561. doi: 10.1248/bpb.b20-00405.

Abstract

Renal insufficiency secondary to contrast administration remains a prevalent and debilitating complication of angiographic procedures. Contrast-induced nephropathy (CIN) is a common clinical problem for which there is no effective medical treatment. However, agmatine has been shown to be effective against ischemia/reperfusion-induced acute kidney injury in rats, a similar condition to CIN. Our aim was to examine the protective effects of agmatine in a rat model of CIN and, based on those results, in a rabbit model of CIN. CIN in the rat model was induced by intravenous administration of indomethacin (10 mg/kg), Nω-nitro-L-arginine methyl ester (L-NAME) (10 mg/kg) and iopamidol (OYPALOMIN, 7.4 g iodine/kg) at 2 weeks after a unilateral nephrectomy. CIN in the rabbit model was induced by intrarenal arterial injection of only iopamidol (BYSTAGE, 4.8 g iodine/kg). Intravenous injection of agmatine (0.1 and 0.3 mmol/kg) did not attenuate the CIN-induced renal insufficiency in the rat model. Intravenous injection of agmatine (0.3 mmol/kg) attenuated the CIN-induced renal insufficiency in the rabbit model such as increases in blood urea nitrogen and plasma creatinine levels. Renal histological damage was also improved by the agmatine administration. The difference in effects of agmatine injection between CIN rats and CIN rabbits was caused by indomethacin and L-NAME administrations. These results indicate that agmatine prevents the development of CIN-induced renal insufficiency in rabbits, and the effect is accompanied by activation of nitric oxide synthase and subsequent increase of blood flow.

Keywords: agmatine; contrast-induced nephropathy; intrarenal arterial injection; iopamidol; rabbit.

MeSH terms

  • Acute Kidney Injury / chemically induced*
  • Acute Kidney Injury / drug therapy*
  • Acute Kidney Injury / enzymology
  • Agmatine / therapeutic use*
  • Animals
  • Contrast Media / toxicity*
  • Disease Models, Animal*
  • Dose-Response Relationship, Drug
  • Male
  • Nitric Oxide Synthase / metabolism
  • Rabbits
  • Rats
  • Rats, Sprague-Dawley
  • Treatment Outcome

Substances

  • Contrast Media
  • Agmatine
  • Nitric Oxide Synthase