Superparamagnetic iron oxide polyacrylic acid coated γ-Fe2O3 nanoparticles do not affect kidney function but cause acute effect on the cardiovascular function in healthy mice
Creators
- 1. Interdisciplinary Nanoscience Center, Aarhus University (Denmark)
- 2. Zoophysiology, Department of Biological Sciences, Aarhus University (Denmark)
- 3. Department of Biomedicine, Aarhus University (Denmark)
- 4. MR Research Center, Aarhus University Hospital, Aarhus University (Denmark)
- 5. Cardiovascular and Renal Research, Institute of Molecular Medicine, University of Southern Denmark (Denmark)
- 6. Physicochimie des Electrolytes, Colloïdes et Sciences Analytiques (PECSA) UMR 7195 CNRS-UPMC-ESPCI, 4 place Jussieu, 75252 Paris Cedex 05 (France)
- 7. Matière et Systèmes Complexes, UMR 7057 CNRS Université Denis Diderot Paris-VII, Bâtiment Condorcet, 10 rue Alice Domon et Léonie Duquet, 75205 Paris (France)
Description
This study describes the distribution of intravenously injected polyacrylic acid (PAA) coated γ-Fe2O3 NPs (10 mg kg−1) at the organ, cellular and subcellular levels in healthy BALB/cJ mice and in parallel addresses the effects of NP injection on kidney function, blood pressure and vascular contractility. Magnetic resonance imaging (MRI) and transmission electron microscopy (TEM) showed accumulation of NPs in the liver within 1 h after intravenous infusion, accommodated by intracellular uptake in endothelial and Kupffer cells with subsequent intracellular uptake in renal cells, particularly the cytoplasm of the proximal tubule, in podocytes and mesangial cells. The renofunctional effects of NPs were evaluated by arterial acid–base status and measurements of glomerular filtration rate (GFR) after instrumentation with chronically indwelling catheters. Arterial pH was 7.46 ± 0.02 and 7.41 ± 0.02 in mice 0.5 h after injections of saline or NP, and did not change over the next 12 h. In addition, the injections of NP did not affect arterial PCO2 or [HCO3−] either. Twenty-four and 96 h after NP injections, the GFR averaged 0.35 ± 0.04 and 0.35 ± 0.01 ml min−1 g−1, respectively, values which were statistically comparable with controls (0.29 ± 0.02 and 0.33 ± 0.1 ml–1 min–1 25 g–1). Mean arterial blood pressure (MAP) decreased 12–24 h after NP injections (111.1 ± 11.5 vs 123.0 ± 6.1 min−1) associated with a decreased contractility of small mesenteric arteries revealed by myography to characterize endothelial function. In conclusion, our study demonstrates that accumulation of superparamagnetic iron oxide nanoparticles does not affect kidney function in healthy mice but temporarily decreases blood pressure. -- Highlights: ► PAA coated γ-Fe2O3 nanoparticles were injected intravenously into healthy mice. ► We examine the distribution and physiological effects of nanoparticle accumulation. ► No effects of accumulation in kidney on acid-base status or GFR. ► Acute hypotension associated with decreased contractility of small vessels. ► We demonstrate physiological effects of PAA γ-Fe2O3 NP for medical purposes.
Availability note (English)
Available from http://dx.doi.org/10.1016/j.taap.2012.10.014Additional details
Identifiers
- DOI
- 10.1016/j.taap.2012.10.014;
- arXiv
- arXiv:1401.1847v1;
- PII
- S0041-008X(12)00456-5;
Publishing Information
- Journal Title
- Toxicology and Applied Pharmacology
- Journal Volume
- 266
- Journal Issue
- 2
- Journal Page Range
- p. 276-288
- ISSN
- 0041-008X
- CODEN
- TXAPA9
INIS
- Country of Publication
- United States
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 45037004
- Subject category
- S60: APPLIED LIFE SCIENCES;
- Descriptors DEI
- ARTERIES; BLOOD PRESSURE; CYTOPLASM; EXCRETION; FERRITES; HYPOTENSION; INJECTION; IRON OXIDES; LIVER; MICE; NANOSTRUCTURES; NMR IMAGING; RETICULOENDOTHELIAL SYSTEM; SUPERPARAMAGNETISM; TRANSMISSION ELECTRON MICROSCOPY; TUBULES; UPTAKE
- Descriptors DEC
- ANIMAL TISSUES; ANIMALS; BLOOD VESSELS; BODY; CARDIOVASCULAR SYSTEM; CELL CONSTITUENTS; CHALCOGENIDES; CLEARANCE; DIAGNOSTIC TECHNIQUES; DIGESTIVE SYSTEM; ELECTRON MICROSCOPY; FERRIMAGNETIC MATERIALS; GLANDS; INTAKE; IRON COMPOUNDS; KIDNEYS; MAGNETIC MATERIALS; MAGNETISM; MAMMALS; MATERIALS; MICROSCOPY; ORGANS; OXIDES; OXYGEN COMPOUNDS; RODENTS; TRANSITION ELEMENT COMPOUNDS; VERTEBRATES
Optional Information
- Copyright
- Copyright (c) 2012 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.