Cardiotoxicity and lung toxicity in male rats induced by long-term exposure to iron oxide and silver nanoparticles

Abstract

Engineered nanoparticles (NPs) have been increasingly used in numerous fields over the last decade. In particular, iron oxide NPs (Fe₂O₃NPs) and silver NPs (AgNPs) have contributed to the current increase in NP usage. However, the possible side effects of increased NP exposure remain not fully elucidated. The present study aimed to assess the toxic effects of Fe₂O₃NPs and AgNPs, both individually and in combination, on the heart and lungs of male rats. To evaluate the in vivo NP toxic effects, the experimental animals were orally administered with Fe₂O₃NPs (5 mg/kg) and/or AgNPs (50 mg/kg). Animals were treated every day for 79 days. The results demonstrated that at the molecular level, Fe₂O₃NPs and AgNPs caused marked DNA base oxidation as indicated by the elevated DNA content of 8-hydroxy-2⁻deoxyguanosine in the heart and lungs. Fe₂O₃NPs and/or AgNPs decreased paraoxonase 1, antioxidant enzymes, total antioxidant capacity, and reduced glutathione in heart and lung. A dose-dependent increase in production of creatine kinase, thiobarbituric acid-reactive substances, nitric oxide end products, tumor necrosis factor-α, interleukin-6 and lipid profiles was detected. Histological changes were also evident in heart and lung tissues. The two NPs demonstrated similar toxic effects for the majority of factors when co-supplemented. In conclusion, the present study identified that Fe₂O₃NPs and AgNPs, alone and in combination, induced cardiotoxicity and lung toxicity. Furthermore, findings demonstrated that there was a greater toxic effect due to administration of both NPs compared to individual administration. It was hypothesized that the toxic effects may be mediated through the induction of oxidative DNA damage, lipid peroxidation, shifting redox status, disrupted gene expression, and deregulation in cytokine production.

Introduction

Nanoparticles (NPs) and other nanomaterials have entered virtually all areas of everyday life which has raised concerns over their toxicity and other potential effects on the body. The biological effects of NPs are determined by various factors including particle size, shape and ability to interact with the surrounding tissue (1).

Metal nanoparticles have widespread applications. Of these, iron oxide NPs (Fe₂O₃NPs) and silver NPs (AgNPs) are the most prominent. Fe₂O₃NPs are found in the environment as particulate matter originating from air pollution and volcanic eruptions. Fe₂O₃NPs particles can also be generated by traffic, industry and power station emissions. In addition, they are purposely chemically synthesised for a wide variety of applications (2). Similarly, AgNPs are widespread in the environment due to various different industries. Specifically, AgNPs are of interest due to their unique properties (e.g. the size and shape affecting its optical, electrical, and magnetic properties), meaning that they have roles in antimicrobial applications, biosensor materials, composite fibers, cryogenic superconducting materials, cosmetic products and electronic components (3). AgNPs have been predominately utilized for the development of medicines, drug delivery systems, and medical device coatings. An increase in AgNP usage has led to greater concentrations of NPs in the atmosphere and general environment. The most concerning element is their ability to infiltrate groundwater and soil, which are the greatest avenues of exposure. Ingested Fe₂O₃NPs and AgNPs can be translocated into the bloodstream and distributed throughout vital organs such as the heart, liver, kidney, brain and lungs (4), raising concerns about their acute and chronic toxic effects.

There is a compelling body of evidence that addresses the toxicological effects of Fe₂O₃NPs and AgNPs on animal cells and tissues (5,6). NPs may cause inflammation, cytokine production, cytoskeletal changes, altered vesicular trafficking, oxidative stress, apoptosis and changes in gene expression and cell signalling (1). Toxicity is further heightened by the metallic nature of Fe₂O₃NPs and AgNPs. It has been reported that silver ions (Ag⁺) are released from AgNPs in aqueous environments (7) and a study also demonstrated that the cytotoxicity of AgNPs was eliminated after Ag⁺ was chelated by a thiol ligand (8). Furthermore, Fe₂O₃NPs release free iron, which induces reactive oxygen species (ROS) production through the Fenton reaction process.

The toxicities of Fe₂O₃NPs and AgNPs are well documented; however, the effects of simultaneous co-exposure to both NPs remain uninvestigated, therefore the present study aimed to address this issue. Rats were subchronically exposed to Fe₂O₃NPs and AgNPs, as well as to a combination of both, for 79 days and the effects on different organs were assessed. The present study focused on the toxic effects with regards to the lungs and heart, as the role of NP exposure in the development of cardiovascular diseases is of particular concern in nanotoxicology. The aims were to determine the cardiotoxicity and lung toxicity of long-term Fe₂O₃NPs and AgNPs exposure, alone and in combination, and also to investigate the different mechanisms that may be involved, including oxidative stress, oxidative DNA damage, and dysregulated cytokine production.

Materials and methods

Tested compounds and doses

Fe₂O₃NPs (spherical; 50 nm particle size; 50–245 m²/g surface area) and AgNPs (spherical; 50 nm particle size; 5.0 m²/g surface area) were purchased from Sigma-Aldrich (Merck KGaA). Fe₂O₃NPs and AgNPs were dispersed in distilled water by sonication for 30 sec to form suspensions before use at doses of 5 mg/ml and 50 mg/ml, respectively. The hydrodynamic size distribution of each NP in suspension was determined by dynamic light scattering using a Zetasizer Nano ZS (Malvern Instruments, Ltd.). Szalay et al (9) and Sharma et al (10) were consulted to determine the appropriate dosage of Fe₂O₃NPs (5 mg/kg/day) and AgNPs (50 mg/kg/day).

In vivo study and experimental groups

Forty adult male Wistar rats weighing 160–170 g at 5–6 months of age were used in the present study. Animals were provided by the Faculty of Medicine of Alexandria University. Rats had free access to tap water and a basal diet, which were provided ad libitum. Following two weeks of acclimation, animals were divided into 4 equal groups (n=10): Group 1 served as the control, group 2 was administered with Fe₂O₃NPs (5 mg/kg) by oral gavage, group 3 was administered with AgNPs (50 mg/kg) by oral gavage, and group 4 was administered with a combination of Fe₂O₃NPs (5 mg/kg) and AgNPs (50 mg/kg) by oral gavage. The rats were dosed with Fe₂O₃NPs and AgNPs every day for 79 days with this time period selected to cover two reproductive cycles of spermatogonia to study the reproductive toxicity (unpublished data). No signs of stress were observed in rats from any of the experimental groups during the study period.

All experimental procedures, animal handling, sampling, and scarification were performed in accordance with the Guide for the Care and Use of Laboratory Animals, 8th edition (National Research Council 2011) and were approved by the Research Ethical Committee of the Medical Research Institute of Alexandria University. All efforts were made to minimise the rats' suffering during the experimental period.

Blood sample collection and tissue preparation

On day 79 of the experimental period, all animals were sacrificed by cervical dislocation under anaesthesia (ketamine 100 mg/kg and xylazine 10 mg/kg intraperitoneally) in accordance with the literature (11). The final body weight was <200 g. There were no signs of toxicity at the stated doses of anaesthetic agents. Blood samples were collected in test tubes containing heparin as an anticoagulant and placed immediately on ice. The blood samples were centrifuged at 860 × g for 20 min to separate the plasma. The plasma was kept at −80°C until the experimental parameters were measured and analysed. The hearts and lungs were immediately removed and washed with chilled saline solution (0.9%) followed by the removal of the adhering fat and connective tissues. Then each tissue was divided for the following experiments: DNA isolation for 8-hydroxy-2⁻deoxyguanosine (8-OHdG) assessment, DNA fragmentation, RNA isolation for gene expression analysis, histological analysis and finally for ELISA.

Tissue homogenization

Heart and lung tissue was minced and homogenised (10%, w/v), separately, in ice-cold sucrose buffer (0.25 M) in a Potter-Elvehjem type homogeniser. The homogenates were then centrifuged at 10,000 × g for 20 min at 4°C, to pellet the cell debris. The supernatant was collected and stored at −80°C for analysis.

Index of oxidative DNA damage measured by 8-OHdG assay

A widely accepted sensitive marker of oxidative DNA damage and oxidative stress is 8-OHdG. The determination of DNA damage using 8-OHdG began with the isolation of genomic DNA using a DNeasy kit (Qiagen Inc.) following the manufacturer's instructions. The concentration was determined using Nanodrop. DNA was briefly digested then 5 µg/µl (total DNA 200 µg) was incubated with 100 units of DNase I (Bio Basic, Inc) in 40 µl Tris/hydrochloric acid 10 mM and 10 µl of 0.5 M MgCl₂ (final concentration of 20 mM) at 37°C for 1 h. The pH of the reaction mixture was then lowered with the addition of 15 µl of 0.5 M sodium acetate (pH 5.1), 10 µl of nuclease P1 (Bio Basic, Inc.) and 30 µl of 10 mM ZnSO₄, and the mixture was incubated for 1 h. After readjusting the pH with 100 µl of 0.4 M Tris/HCl (pH 7.8) and 20 µl alkaline phosphatase (Bio Basic, Inc.), the samples were incubated at 37°C for 30 min then boiled for 10 min. The resultant DNA hydrolysate was used for experimentation using the 8-OH-dG ELISA kit (cat. no. ab201734; Abcam) according to the manufacturer's protocol.

p53 and cytokine assessment using ELISA

The homogenates of heart and lung tissues were used for the determination of p53 (cat. no. ELR-p53-1; RayBiotech, Inc.), tumor necrosis factor-alpha (TNF-α; cat. no. ab100785) and interleukin-6 (IL-6; cat. no. ab100772) by using respective ELISA kits (Abcam) according to the manufacturer instructions.

Lipid peroxidation assay

The process of lipid peroxidation results in the end product of malondialdehyde (MDA), therefore its quantification is generally used as a marker for lipid peroxidation activity. MDA levels were determined using thiobarbituric acid-reactive substances assay (12). In brief, the heart and lung tissues homogenates were heated with thiobarbituric acid at a low pH to produce a pink chromogen, which was analysed at a wavelength of 532 nm.

Nitric oxide (NOx) end products

The Griess reaction was used to determine the concentration of NOx end products, nitrite and nitrate, in the deproteinised heart and lung supernatants (13). The Griess reaction was supplemented with the reduction of nitrate to nitrite by nicotinamide-adenine dinucleotide phophate-dependent nitrate reductase. In brief, the first step required the diazotisation of sulphanilic acid with nitrite ions followed by the coupling of this product with diamine, resulting in a measurable pink metabolite, which was analysed at a wavelength of 540 nm.

Antioxidant determination

The total antioxidant capacity (TAC) and the activities of superoxide dismutase (SOD), glutathione peroxidase (GPX), glutathione S-transferase (GST) and catalase (CAT) in the tissue homogenates were measured using colorimetric kits (Bio-Diagnostic, Ltd.). Reduced glutathione (GSH) content was assessed after protein precipitation using a metaphosphoric acid reagent. The assay was based on the oxidation of GSH by 5,5′⁻dithiobis-(2-nitrobenzoic acid) (DTNB) to yield glutathione disulphide (GSSG) and 5-thio-2-nitrobenzoic acid (TNB). The rate of TNB formation was assessed at 412 nm and was proportional to the GSH amount present in the sample (14). The rate of formation of TNB was monitored by recording the change in the absorbance at 412 nm. The total GSH content in the samples was determined from a GSH standard curve. The results were subsequently expressed as nmol/g tissue by dividing the concentration of GSH in the sample by the total weight (g) of tissue used to prepare the sample.

Determination of paraoxonase (PON1) and creatine kinase-muscle/brain (CK-MB) activities in the heart

The PON1 enzyme activity in the heart was measured by applying the method of Mueller et al (15). The CK-MB was assayed using an ELISA kit (cat. no. K777; BioVision, Inc.).

Lipid profile assessment

Stored plasma samples were analysed for total lipids (cat. no. 8.05.36.0.0250; Atlas Medical UK), cholesterol (cat. no. 11805), triacylglycerol (TAG; cat. no. 11828) and high-density lipoprotein cholesterol (HDL-c; cat. no. 11557) using commercial kits (BioSystems S.A.). Very low-density lipoprotein-cholesterol (vLDL-c) was calculated by dividing the values of TAG by a factor of 5. Low-density lipoprotein-cholesterol (LDL-c) was determined by the following calculation: LDL-c=cholesterol-(HDL-c + vLDL-c). Rat Apolipoprotein B (ApoB) ELISA kit (cat. no. KT-7394; Kamiya Biomedical Company) was used for assessment of plasma level of ApoB. All assays were carried out in accordance with manufacturers' instructions.

Histological analysis of heart and lung

Heart and lung specimens were obtained from rats, and immediately fixed in 10% formalin for 18 h at room temperature before being treated with a conventional grade of alcohol and xylol, embedded in paraffin and sectioned at 4–6 mm thickness. The sections were stained with haematoxylin and eosin (H&E) in order to study the histopathological changes using a light microscope at a magnification of ×400 as previously described (16).

Statistical analysis

Results are expressed as mean ± standard error. All statistical analysis was carried out using the general linear model (SAS Institute, Inc.). Multiple comparisons were performed using one-way analysis of variance followed by Duncan's new multiple range test. To test for interactions between the individual treatments when given in combination, a factorial design test was used. P<0.05 was considered to indicate statistical significance.

Results

Levels of 8-OHdG increase in cardiac and lung tissue following exposure to NPs

A sensitive marker of oxidative DNA damage is 8-OHdG. Rats exposed to Fe₂O₃NPs and AgNPs alone or in combination displayed significantly higher levels of 8-OHdG in their cardiac and lung tissue compared with rats in the control group (Fig. 1). The rats exposed to Fe₂O₃NPs had higher cardiac and lung 8-OHdG contents compared with rats exposed to AgNPs (Fig. 1). The rats coexposed to both NPs exhibited markedly higher 8-OHdG contents in both cardiac (Fig. 1A) and lung (Fig. 1B) tissues compared with other groups.

Figure 1.

Content of 8-OHdG in control, Fe₂O₃NP-exposed group, AgNP-exposed group, and Fe₂O₃NP and AgNP-coexposed group. (A) Cardiac and (B) lung tissue 8-OHdG levels measured using ELISA. *P<0.05 vs. control group; ^#P<0.05 vs. Fe₂O₃NP-exposed group; ^$P<0.05 vs. AgNP-exposed group; ^&P<0.05 synergistic interactions when both NPs are combined using Factorial Design. 8-OHdG, 8-hydroxy-2′-deoxyguanosine; Fe₂O₃NP, iron oxide nanoparticle; AgNP, silver nanoparticle.

Levels of p53, TNF-α, and IL-6 increase in cardiac and lung tissue following exposure to NPs

p53 controls the cell cycle to suppress the production of tumours, and acts as genome guard and as an inducer of apoptosis. TNF-α and IL-6 have important roles in tissue injury and oxidative stress. The results indicated that p53, TNF-α and IL-6 levels were significantly higher in heart and lung tissues of rats exposed to Fe₂O₃NPs and AgNPs (Fig. 2). Exposure to AgNPs caused the production of a significantly higher level of p53 in cardiac and lung tissues (Fig. 2A and B), and TNF-α in cardiac tissues (Fig. 2C) compared to the rats exposed to Fe₂O₃NPs. The amount of TNF-α present in lung tissues was lower in the rats exposed to AgNPs compared to the rats exposed to Fe₂O₃NPs. Regarding IL-6 levels (Fig. 2E and F), there was no significant difference in the tissues of rats exposed to Fe₂O₃NPs and AgNPs. The rats coexposed to both NPs demonstrated significantly higher p53, TNF-α, and IL-6 levels compared with the control rats or rats exposed to individual NPs (Fig. 2).

Figure 2.

Levels of inflammatory cytokines in control, Fe₂O₃NP-exposed group, AgNP-exposed group, and Fe₂O₃NP and AgNP-coexposed group. (A) Levels of p53 in rat cardiac and (B) lung tissues. (C) TNF-α levels in rat cardiac and (D) lung tissues. (E) Levels of IL-6 in rat cardiac and (F) lung tissues. *P<0.05 vs. control group; ^#P<0.05 vs. Fe₂O₃NP-exposed group; ^$P<0.05 vs. AgNP-exposed group; ^&P<0.05 synergistic interactions when both NPs are combined using Factorial Design. Fe₂O₃NP, iron oxide nanoparticle; AgNP, silver nanoparticle; TNF-α, tumor necrosis factor- α; IL, interleukin.

Lipid peroxidation and nitric oxide end products increase following exposure to NPs

NOx is a pleotropic molecule that serves an important role in cell signalling; however, at high concentrations it can act as a pro-oxidant leading to catastrophic cell damage. It has a short half-life, so upon analysis, it is typically identified as total nitrite and nitrate as these are both NOx end products. The male rats exposed to Fe₂O₃NPs and AgNPs demonstrated significantly higher tissues levels of thiobarbituric acid-reactive substances (TBARS) and NOx compared with the control rats (Table I). The rats exposed to AgNPs demonstrated significantly higher values of both TBARS and NOx in lung tissue and NOx in heart tissue compared with the rats exposed to Fe₂O₃NPs. The rats coexposed to both NPs exhibited a significant elevation in TBARS and NOx content in cardiac and lung tissues compared with all other groups (Table I).

Table I.

Heart and lung tissues levels of TBARS, NOx, GSH, SOD, CAT, GST, GPx and TAC of male rats exposed to Fe₂O₃NPs and AgNPs.

A, Heart tissues
	Experimental groups
Parameter	Control	Fe2O3NPs	AgNPs	Fe2O3NPs+AgNPs
TBARS (nmol/g tissue)	59.9±1.2	78.8±1.4a	87.5±3.4a,b	116.4±3.6a–d
NO (µmol/g tissue)	28.24±0.74	33.35±0.30a	40.78±2.5a,b	47.80±0.27a–c,e
GSH (nmol/g tissue)	5.0±0.20	3.7±0.27a	4.0±0.06a	3.3±0.14a,c
SOD (mU/mg protein)	38.3±2.2	24.3±1.6a	25.4±1.7a	16.2±0.8a,b,c,c
CAT (U/mg protein)	55.0±2.94	40.0±1.11a	38.0±1.88a	18.0±0.89a–d
GST (U/mg protein)	0.46±0.03	0.36±0.01a	0.32±0.02a	0.29±0.01a,b
GPX (mU/mg protein)	26.6±1.81	18.4±1.18a	17.1±1.29a	13.4±0.63a–c,e
TAC (µmol/g tissue)	21.50±0.10	17.27±0.31a	17.08±0.16a	14.14±0.12a–d
B, Lung tissues
	Experimental groups
Parameter	Control	Fe2O3NPs	AgNPs	Fe2O3NPs+AgNPs
TBARS (nmol/g tissue)	41.0±1.5	75.2±2.1a	70.6 ± 0.9a	89.5±2.7a–c,e
NO (µmol/g tissue)	36.6±1.73	51.8±0.81a	69.7±0.73a,b	75.6±0.57a–c
GSH (nmol/g tissue)	5.7±0.13	4.7±0.21a	4.4±0.24a	3.5±0.18a–c
SOD (mU/mg protein)	9.0±0.2	6.7±0.2a	7.2±0.1a	4.4±0.2a–d
CAT (U/mg protein)	42.9±0.85	28.5±1.16a	27.1±1.66a	15.5±0.87a–d
GST (U/mg protein)	0.57±0.02	0.44±0.01a	0.41±0.01a	0.35±0.02a–c
GPX (mU/mg protein)	33.8±0.844	25.1±0.976a	26.1±0.901a	18.6±0.879a–d
TAC (µmol/g tissue)	22.8±0.02	21.1±0.13a	18.7±0.07a,b	16.3±0.07a–c

^aP<0.05 vs. control group

^bP<0.05 vs. Fe₂O₃NP-exposed group

^cP<0.05 vs. AgNP-exposed group

^dP<0.05 synergistic interactions when both NPs are combined using Factorial Design

^eP<0.05 additive interactions when both NPs are combined using Factorial Design. TBARS, thiobarbituric acid-reactive substances; NOx, nitric oxide end products; GSH, glutathione; SOD, superoxide dismutase; CAT, catalase; GST, glutathione S-transferase; GPx, glutathione peroxidase; TAC, total antioxidant capacity; Fe₂O₃NPs, iron oxide nanoparticles; AgNPs, silver nanoparticles.

Antioxidant levels decrease following exposure to NPs

The antioxidant parameters detected in the present study included GSH, which represents 90% of the reducing power of the cell, and antioxidant enzymes SOD, CAT, GPX, and GST, and TAC. Exposure to Fe₂O₃NPs or AgNPs caused a significant decline in the heart and lung antioxidant parameters compared with the levels found in control rats. (Table I) When comparing rats exposed to Fe₂O₃NPs and the group exposed to AgNPs the only significant difference was a significantly lower level of TAC in the lung tissues of rats exposed to AgNPs. Of note, rats coexposed to both NPs had significantly lower levels of all antioxidant parameters compared with control rats and also rats exposed to single NPs only (Table I).

PON1 and creatine kinase-MB (CK-MB) levels in cardiac and lung tissue decrease following exposure to NPs

PON1 enzyme is a major antiatherosclerotic component of HDL and has an important role in reducing atherosclerosis. PON1 levels in plasma and heart tissues were significantly lower in rats exposed to Fe₂O₃NPs or AgNPs compared with control rats (Fig. 3A and B). However, there was no significant difference in PON1 levels between the rats exposed to Fe₂O₃NPs or AgNPs. Coexposure to both NPs caused a significant decline in the plasma and cardiac levels of PON1 compared with the control group and rats exposed to single NPs only (Fig. 3A and B).

Figure 3.

PON1 and CK-MB levels in control, Fe₂O₃NP-exposed group, AgNP-exposed group, and Fe₂O₃NPs and AgNP-coexposed group. (A) Levels of PON1 in cardiac tissue and (B) in plasma. (C) Activity of CK-MB in cardiac tissues and (D) in plasma. *P<0.05 vs. control group; ^#P<0.05 vs. Fe₂O₃NPs exposed group; ^$P<0.05 vs. AgNPs exposed group; ^&P<0.05 synergistic interactions when both NPs are combined using Factorial Design. PON1, paraoxonase; CK-MB, creatine kinase-muscle/brain; Fe₂O₃NP, iron oxide nanoparticle; AgNP, silver nanoparticle.

CK-MB is an important cardiac marker used to assist diagnoses of myocardial infarction. The activity of CK-MB was significantly elevated in the cardiac tissues and plasma of rats exposed to Fe₂O₃NPs or AgNPs (Fig. 3C and D). AgNPs exposure caused significantly higher plasma activity of CK-MB than exposure to Fe₂O₃NPs. Coexposure to both NPs significantly elevated the activity of CK-MB in plasma and cardiac tissues by >3-fold (Fig. 3C and D).

Lipid profile parameters

The plasma levels of total lipid, triglycerides, cholesterol, LDL-c, vLDL-c and ApoB of rats exposed to Fe₂O₃NPs or AgNPs were significantly higher compared with control rats. The total lipids, LDL-c and ApoB were significantly higher in the rats exposed to AgNPs compared with those exposed to Fe₂O₃NPs, whilst the other lipid profile parameters demonstrated no significant difference between the two groups (Table II). There were significantly lower levels of HDL-c in the rats exposed to either Fe₂O₃NPs or AgNPs compared with the control group. The rats coexposed to both NPs displayed significantly higher levels of all lipid profile parameters, with the exception of HDL-c which displayed significantly lower levels, compared with the control rats and rats exposed to single NPs only (Table II).

Table II.

Plasma total lipid, triglyceride, cholesterol, LDL-c, vLDL-c, HDL-C, and ApoB of male rats exposed to Fe₂O₃NPs and AgNPs.

	Experimental groups
Parameter (mg/dl)	Control	Fe2O3NPs	AgNPs	Fe2O3NPs+AgNPs
Total lipid	505±9.0	610±14.8a	654±18.9a,b	706± 21.0a–d
Triglycerides	112.9±2.49	130.5±1.06a	134.8±1.17a	155.1±2.38a–c,e
Cholesterol	141.6±5.38	169.1±3.29a	182.6±3.10a	221.6±5.10a–d
LDL-c	50±6.9	88±6.9a	107±4.3a,b	157±7.1a–c,e
VLDL-c	23±0.5	26±0.5a	27±0.2a	31±0.5a–c
HDL-c	69±1.8	55±1.8a	48±1.9a	33±2.0a–d
ApoB	51±4.5	79± 4.5a	91±2.8a,b	127±4.6a–d

^aP<0.05 vs. control group

^bP<0.05 vs. Fe₂O₃NP-exposed group

^cP<0.05 vs. AgNP-exposed group

^dP<0.05 synergistic interactions when both NPs are combined using Factorial Design

^eP<0.05 additive interactions when both NPs are combined using Factorial Design. LDL-c, low density lipoprotein-cholesterol; vLDL-c, very low-density lipoprotein-cholesterol; HDL-C, high density lipoprotein-cholesterol; ApoB, Apolipoprotein B; Fe₂O₃NPs, iron oxide nanoparticles; AgNPs, silver nanoparticles.

Histological changes in rat lung and heart following exposure to NPs

The hearts of rats in the control group had normal myofiber cells with unaffected architectures (Fig. 4A), whilst rats exposed to Fe₂O₃NPs demonstrated effects of myocardial degeneration (Fig. 4B). Similarly, analysis of the rat heart tissue exposed to AgNPs (Fig. 4C) revealed fragmentation of sarcoplasm and degeneration changes in myocardial fibers. The heart tissues of the coexposed rats revealed loss of cross striation and also myocardial degeneration changes (Fig. 4D).

Figure 4.

Histological analysis of haematoxylin and eosin stained rat heart tissues of control, Fe₂O₃NP-exposed group, AgNP-exposed group, and Fe₂O₃NP and AgNP-coexposed group. (A) Control rats demonstrated normal myofiber cells and normal architecture. (B) Heart tissues of Fe₂O₃NP-exposed group revealed myocardial degeneration changes. (C) Heart of AgNP-exposed group revealed fragmentation of sacroplasm and degeneration changes in myocardial fibers. (D) Heart of the Fe₂O₃NP and AgNP-coexposed group revealed loss of cross striation and severe myocardial degeneration changes (magnification, ×400). Fe₂O₃NP, iron oxide nanoparticle; AgNP, silver nanoparticle.

The lung tissue of control rats demonstrated normal alveoli and bronchi lined mucous secreting columnar respiratory epithelium (Fig. 5A). However, the lung tissues belonging to rats exposed to Fe₂O₃NPs (Fig. 5B) demonstrated a moderate influx of polymorph, lymphocytes, and macrophages into perivascular tissue. Similarly, the lung tissues of rats administered with AgNPs (Fig. 5C) displayed an influx of polymorph, lymphocytes, and macrophages into the surrounding lung alveoli and perivascular cuff. The lung tissue from coexposed rats (Fig. 5D) demonstrate a moderate influx of polymorph, lymphocytes, and histiocytes into the surrounding perivascular tissue and surrounding bronchi. Semi-quantitative analysis was carried out on the heart and lung histology images of the different rat groups (Table III).

Figure 5.

Histological analysis of haematoxylin and eosin stained rat lung tissues of control, Fe₂O₃NP-exposed group, AgNP-exposed group, and Fe₂O₃NP and AgNP-coexposed group. (A) Lung of control rats revealed normal alveoli, bronchi lined mucous secreting columnar respiratory epithelium. (B) Lung of Fe₂O₃NP-exposed group demonstrated a moderate influx of polymorphs (green arrow), lymphocytes (red arrow) and macrophages (yellow arrow) into the perivascular tissue. (C) Lung of AgNP-exposed group demonstrated an influx of lymphocytes (red arrow) and histocytes (blue arrow) into the surrounding lung alveoli and perivascular cuff. (D) Lung of the Fe₂O₃NP and AgNP-co-exposed group demonstrated a moderate influx of polymorphs (green arrow), and lymphocytes (green arrow) into the surrounding perivascular tissue and bronchi (black arrow; magnification, ×400). Fe₂O₃NP, iron oxide nanoparticle; AgNP, silver nanoparticle.

Table III.

Semi-quantitative analysis of heart and lung histology of male rats exposed to Fe₂O₃NPs and AgNPs.

A, Heart tissue
	Experimental groups
Parameter (mg/dl)	Control	Fe2O3NPs	AgNPs	Fe2O3NPs+AgNPs
Loss of cross striation	−	++	+	+++
Fragmentation of sarcoplasm	−	++	+	+++
Cytoplasmic vacuolization in cardiac muscles	−	++	+	+++
Degenerative changes in myocardial fibers	−	++	++	+++
B, Lung tissue
	Experimental groups
Parameter (mg/dl)	Control	Fe2O3NPs	AgNPs	Fe2O3NPs+AgNPs
Extravasations of red blood cells into long parenchyma	−	++	+++	++++
Interstitial inflammation	−	++	++	++++
Alveolar wall thickening	−	++	+++	++++
Collapse of terminal bronchioles	−	++	+++	++++
Fibrosis	−	+	++	+++
Alveolar macrophages	−	++	+++	++++
Polymorphs infiltration	−	++	+++	++++

-, No change; +, mild change; ++, moderate change; +++, moderate to marked change; and ++++, marked change. Fe₂O₃NPs, iron oxide nanoparticles; AgNPs, silver nanoparticles.

Discussion

Widespread medical and industrial NP applications increase the risk of human exposure to various NPs that may cause synergistic toxicities on internal organs. The cardiovascular and respiratory systems are of particular concern as they face the most interaction with NPs in medical processes and through general environmental exposure. The present study confirmed the cardiotoxicity and lung toxicity of both Fe₂O₃NPs and AgNPs, and also demonstrated their synergistic and additive effects in inducing these toxicities.

Damage to DNA is a fundamental example of cellular toxicity, and it is critical to identify damage caused by NPs as DNA damage is highly correlated with an increased risk of cancer. In the present study, 8-OHdG was employed as a sensitive indicator for oxidative DNA damage. Analysis demonstrated a significant 8-OHdG elevation in heart and lung tissues as a result of the exposure to Fe₂O₃NPs and AgNPs, with a even more prominent increase when rats were subjected to the combined NPs. Furthermore, NOx and TBARS were used as markers of lipid peroxidation with increased levels detected following exposure to NPs. The accumulation of these forms of oxidative damage results in DNA mutations and genotoxicity that may cause cell death (apoptotic or necrotic) or malignant transformation.

The ability of NPs to induce cell death is well documented (17). A previous study reported that AgNPs induces genotoxicity and cytotoxicity in cancer and normal cell lines, alters cell morphology, reduces cell viability, and causes oxidative stress in lung fibroblast and glioblastoma cells (18). AgNP-induced cytotoxicity may be partially caused by the direct action of Ag⁺ ions being released from AgNPs (19) and the subsequent enhanced generation of intracellular ROS and reactive nitrogen species (RNS), which are responsible for inducing oxidative and nitrosative damage. In turn, this results in lipid peroxidation of biological membranes, and elicits oxidative DNA and structural protein damage (20,21).

Previous nanotoxicity studies conducted with Fe₂O₃NPs have conclusively determined that the production of ROS is a major causal factor of cell death (22). Rate of uptake of Fe₂O₃NPs is mediated by the mononuclear phagocytic system via endocytosis and then degraded in the lysosomes. This releases the free iron from Fe₂O₃NPs, which affects the iron homeostasis (23). Free iron is then stored in the form of proteins, such as ferritin and haemosiderin, for further use in the body. However, when the iron storage capacity of these proteins is exceeded, iron overload occurs which triggers the production of ROS via the Fenton reaction. In accordance with the present results, many studies have documented the toxic effects of Fe₂O₃NPs resulting in cellular and DNA damage (9,22–25). Fe₂O₃NPs causes cell death, mitochondrial damage, and DNA damage in A549 cells (24). The genotoxic effects of Fe₂O₃NPs are mainly caused by the direct interaction with leached iron ions or various indirect factors, such as excessive ROS. The direct and indirect contact of Fe₂O₃NPs with DNA can affect the structure of DNA causing strand breaks, cross-linking, and oxidation of nucleotides as well as affecting DNA transcription and replication. In addition, Fe₂O₃NPs upregulate genes that are associated with endothelial layer integrity and lysosomal function (25).

A further effect of exposure to NPs is an elevated inflammatory response at the cellular level, as demonstrated by various studies (1,2,5,6,9,26). A large variety of soluble factors including ILs, TNF-α, ROS and RNS are inflammatory response factors that mediate inflammation. These inflammatory factors promote DNA damage such as chromosomal fragmentation, DNA point mutations, inhibition of DNA repair and formation of methylation patterns, that may lead to altered gene expression profiles and the formation of DNA adducts (26).

The present study confirmed the proinflammatory effects of Fe₂O₃NPs and AgNPs particularly when combined. For example, significantly higher levels of TNF-α and IL-6 in cardiac and lung tissues were detected. In accordance with these results, Zhu et al (6) reported that intravascular Fe₂O₃NPs induces endothelial system inflammation and dysfunction via either direct interaction with the endothelial monolayer or indirectly by releasing free iron, thus impacting the endothelial cells and provoking oxidative stress responses. Fe₂O₃NPs have evident intratracheal toxic effects as they cause specific pathomorphological damage in rat lungs and irreversible injury to the membranes of alveolar cells (9).

NPs are known to upregulate the transcription of various proinflammatory genes, including TNF-α, IL-1, IL-6, and IL-8, by activating NF-κB signaling. These sequential molecular and cellular events are known to cause oxidative stress, followed by severe cellular genotoxicity and then programmed cell death through activation of the JNK, p53 and NF-κB pathways. Fe₂O₃NP- and AgNP-induced inflammatory responses in murine tissues, such as the heart and lung have been well documented (27,28). It has also been documented that particle deposition in the lung causes recruitment of inflammatory cells that generate ROS, clastogenic factors, and cytokines either harming or stimulating resident lung cells (29).

Indices of oxidative damage on lipids and DNA molecules indicate that heart and lung tissues suffer oxidative stress damage not only as a result of increased ROS generation but also due to the impairment of the antioxidant mechanism caused by NP exposure. The present study demonstrated that Fe₂O₃NPs and AgNPs significantly hampered the main antioxidant processes in heart and lung tissues including levels of antioxidant enzymes SOD, GST, GPx, and CAT, TAC, and the GSH system. Therefore, a growing body of evidence, including the present findings, confirm the pro-oxidant effects of Fe₂O₃NPs and AgNPs (30,31).

Besides their general pro-oxidant and proinflammatory effects, Fe₂O₃NPs and AgNPs also induced specific metabolic alterations that may have important roles as atherogenic factors. PON1 is a hydrolytic enzyme with a wide range of substrates that is able to protect against lipid oxidation. The atheroprotective effects of PON1 are achieved through inhibition of LDL oxidation, reducing the risk of cardiovascular disease (32). The present results demonstrated that exposure to Fe₂O₃NPs and AgNPs alone or in combination caused depletion of PON1 in the plasma and heart tissues. The PON1 decline, together with the documented dyslipidemia including HDL-c decrease and elevation of triglycerides, cholesterol, LDL-c and total lipids, are strong atherogenic factors that predisposed the rats towards developing cardiovascular diseases. This risk is evidenced by the significant elevation of CK-MB plasma and cardiac activity as well as the histological abnormalities of cardiac tissues including myocardial congestion and degeneration. The increased activity of CK-MB in cardiac tissues due to Fe₂O₃NPs and AgNPs exposure may lead to disruption of the specific role of CK in the excitation-contraction mechanism. In addition, the high plasma activity of CK-MB is an indication of myocardial injury. In agreement with the present results, Nemmar et al (33) reported that Fe₂O₃NPs increases CK-MB levels in the heart and plasma tissues. Similarly, Shen et al (34) reported that Fe₂O₃NPs attack the myocardium muscles inducing myocardial iron overload, resulting in myocardial injury and deterioration of cardiac function via oxidative stress-mediated iron toxicity. Histology findings revealed myocyte apoptosis, inflammation, and fibrosis. Furthermore, Rathore et al (35) concluded that the heart muscle fibers treated with AgNPs demonstrated mild edema and separation of myofibrils. In addition, Adeyemi and Faniyan (36) documented that AgNPs cause inflammation, loss of cross striation with myocardial degeneration and cellular alteration in the cardiac tissue of male Wistar rats. Warheit et al (37) reported that in rat lungs exposed to Fe₂O₃NPs, the interstitium widened and was infiltrated with lymphocytes, macrophages, and plasma cells and fibrosis developed.

In summary, the present study determined the adverse effects of long-term exposure to Fe₂O₃NPs and AgNPs on the heart and lungs. Cardiotoxicity and lung toxicity were induced via different pathways including oxidative DNA modification, induction of inflammation, free radical generation, and inhibition of antioxidant mechanisms. In addition, NPs caused alterations in heart and lung histology and lipid profiles. Furthermore, the results evidently demonstrated that simultaneous co-exposure to Fe₂O₃NPs and AgNPs resulted in greater ramifications to the heart and lungs compared to the effect of individual NPs. The possible adverse effects on other rat organs coexposed to Fe₂O₃NPs and AgNPs will be further investigated with focus on the male reproductive system, liver and brain. In conclusion, the present findings raise concerns about the synergistic effects of different NPs in inducing chronic toxicity on the heart and lungs, and the impact this may have on the subsequent predisposition to cardiovascular and pulmonary diseases.

Glossary

Abbreviations

8-OHdG

8-hydroxy-2′-deoxyguanosine

TBARS

thiobarbituric acid-reactive substances

GSH

reduced glutathione

GST

glutathione S-transferase

SOD

superoxide dismutase

CAT

catalase

ROS

reactive oxygen species

GPX

glutathione peroxidase

LPO

lipid peroxidation

PON1

paraoxinase 1

vLDL

very low-density lipoprotein

ApoB

apolipoprotein B

CK

creatine kinase

HDL-c

high-density lipoprotein-cholesterol

NOx

nitric oxide

LDL

low-density lipoprotein

TL

total lipids

RNS

reactive nitrogen species

TAC

total antioxidant capacity

Funding

No funding received.

Availability of data and materials

The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.

Authors' contributions

MIY suggested the research topic, participated in the experimental design and contributed to the writing of the paper. AAA performed most experiments, carried out the statistical analysis of data and helped in the writing of the paper. MANK designed the experiments, performed the molecular experiments, and contributed to the writing and revising of the paper. All authors have read and approved the final paper.

Ethics approval and consent to participate

All experimental procedures, animal handling, sampling, and scarification were conducted in accordance with the Guide for the Care and Use of Laboratory Animals, 8th edition (National Research Council 2011) and were approved by the Research Ethical Committee of the Medical Research Institute, Alexandria University. All efforts were made to minimise the rats' suffering during the experimental period.

Patient consent for publication

Not applicable.

Competing interests

The authors declare that they have no competing interests.