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New metallophamaceutic reduced renal injury induced by non-steroidal anti-inflammatory 1 1 Research performed at Laboratory of Experimental Surgery (LABCEX), Centro Universitário Christus (UNICHRISTUS), and Scientific Research and Teaching Institute (INPEC), Fortaleza-CE, Brazil. Part of Master degree thesis, Postgraduate Program in Minimally Invasive Technology and Health Simulation Area. Tutor: Prof. Marcio Wilker Soares Campelo.

Abstract

Purpose

To evaluate the effect of Rut-bpy (Cis-[Ru(bpy)2(SO3)(NO)]PF 6), a novel nitric oxide donor, able to modulate the histological changes caused by the NASID (meloxicam).

Methods

Wistar rats were assigned into three groups (n=6 rats/group): Sham group (saline solution), NSAID group (meloxicam - 15 mg/kg) and Rut-bpy group (100 mg/kg of Rut-bpy associated with 15mg/kg of meloxicam). At the end of experiments, kidneys were removed for histological study, fractal dimension and lacunarity in all animals.

Results

At the histological examination, all animals (six animals – 100 %) in the NSAID group had membrane thickening and other changes (necrosis, acute tubular congestion and vascular congestion); on the other hand, only one animal (16.6 %) of the Rut-bpy group had congestion. The fractal dimension and lacunarity were greater in the control and Rut-bpy group than in NSAIDs group (p<0.05).

Conclusion

Rut-bpy may prevent renal histological changes in rats caused by meloxicam.

Anti-Inflammatory Agents, Non-Steroidal; Kidney; Ruthenium; Rats

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