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Scientific Reports volume 13, Article number: 22011 (2023 ) Cite this article Mdpe
Diverse applications of nanoparticles due to their unique properties has rapidly increased human exposure to numerous nanoparticles such as calcium hydroxide (Ca(OH)2), calcium titanate (CaTiO3), and yttrium oxide (Y2O3) nanoparticles almost in all aspect of daily life. However, very limited data are available on the effect of these nanoparticles on genomic DNA integrity and inflammation induction in the gastric tissues. Hence, this study estimated the effect of Ca(OH)2, CaTiO3, or/and Y2O3 nanoparticles multiple oral administration on the genomic DNA damage and inflammation induction in the mice gastric tissues. A suspension containing 50 mg/kg b.w of Ca(OH)2, CaTiO3, or Y2O3 nanoparticles were given orally to male mice separately or together simultaneously three times a week for two consecutive weeks. Multiple oral administration of Ca(OH)2 nanoparticles led to significant elevations in DNA damage induction and ROS generation, in contrast to the non-significant changes observed in the level of induced DNA damage and generated ROS after administration of CaTiO3 or Y2O3 nanoparticles separately or in combination with Ca(OH)2 nanoparticles. Oral administration of Ca(OH)2 nanoparticles alone also highly upregulated INOS and COX-2 genes expression and extremely decreased eNOS gene expression. However, high elevations in eNOS gene expression were detected after multiple administration of CaTiO3 and Y2O3 nanoparticles separately or together simultaneously with Ca(OH)2 nanoparticles. Meanwhile, non-remarkable changes were noticed in the expression level of INOS and COX-2 genes after administration of CaTiO3 and Y2O3 nanoparticles separately or simultaneously together with Ca(OH)2 nanoparticles. In conclusion: genomic DNA damage and inflammation induced by administration of Ca(OH)2 nanoparticles alone at a dose of 50 mg/kg were mitigated by about 100% when CaTiO3 and Y2O3 nanoparticles were coadministered with Ca(OH)2 nanoparticles until they reached the negative control level through altering the expression level of eNOS, INOS and COX-2 genes and scavenging gastric ROS. Therefore, further studies are recommended to investigate the toxicological properties of Ca(OH)2, CaTiO3 and Y2O3 nanoparticles and possibility of using CaTiO3 and Y2O3 nanoparticles to mitigate genotoxicity and inflammation induction by Ca(OH)2 nanoparticles.
Cristina Simó, Meritxell Serra-Casablancas, ... Samuel Sánchez
Minju Sim, Chong-Su Kim, … Dong-Mi Shin
Michael J. Mitchell, Margaret M. Billingsley, … Robert Langer
Nanoparticles are materials that range in size from 1 to 100 nm and have novel size-dependent properties that differ from those of the same bulk materials. Thus nanomaterials are used in various applications including agricultural, environmental, biotechnology, waste disposal, industrial applications, and many other products e.g. electronics, clothes, optics, cosmetics, food, engineering and medicine1,2,3.
For example, nanoparticles of calcium hydroxide (Ca(OH)2) or slaked lime, are an inorganic chemical compound, widely used in various applications especially in food processing, wastewater treatment, cement, plastic production and dentistry4,5. Similarly, calcium titanate (CaTiO3) nanoparticles, a member of the metal titanate family, have sparked ongoing interest in both basic and applied material science and have recently been used in aquatic habitats to decompose contaminants, and are also used as a biomaterial to deliver calcium ions for osteoblasts differentiation, mineralization of bone marrow stem cells, and cells’ proliferation6,7. In addition, inorganic yttrium oxide (Y2O3) nanoparticles are a type of precious rare earth element that appears as a white powder and is frequently used in the production of microwave filters, cathode ray display panels, and plasma televisions, as an additive in paint, plastic and steel, as well as in biomedical applications including drug delivery, biosensors, bio-imaging, fluorescence imaging, and cancer treatments8,9.
All of these uses increase the risk of human intake of Ca(OH)2, Ca(OH)2 and Y2O3 nanoparticles together through contaminated food and water and medications. However, the ingestion extent and the potential risks posed by these nanoparticles exposure remain poorly studied, but the physical and chemical properties of nanoparticles are strongly influenced by their local microenvironment. The stomach is the most advanced and developed endocrine gland and the stomach diseases and their degree of severity vary. For example, gastritis is a term used to describe inflammation of the gastric mucosa, and can lead to cancer, dysplasia, and metaplasia. In developing nations, chronic gastritis is still a very frequent condition10. Consequently, all these necessitated studying the effect of Ca(OH)2, Ca(OH)2 and Y2O3 nanoparticles on the integrity of gastric tissues.
However, information is lacking on effect of Ca(OH)2, Ca(OH)2 and Y2O3 nanoparticles administration on the integrity of gastric tissues but few recent studies have been conducted on their genotoxicity and inflammation induction. For example, the study of Mohamed and her colleagues6 demonstrated the genetic safety of CaTiO3 nanoparticles towards normal human skin fibroblast (HSF) cells through the non-remarkable changes observed in the genomic DNA integrity, ROS generation and expression levels of apoptotic genes after HSF cells treatment with CaTiO3 nanoparticles. On the other hand, differential genotoxicity, apoptosis, mitochondrial DNA damage and inflammation induction by single oral administration of Ca(OH)2 nanoparticles have been demonstrated in various mice tissues: liver, brain, kidney, bone marrow, lung, heart and spleen11,12.
Therefore, the current study was done to estimate the possible DNA damage and inflammation induction by multiple oral administration of Ca(OH)2, CaTiO3, or/and Y2O3 nanoparticles in the gastric tissue of mice. That was conducted by performing alkaline comet assay to measure the genomic DNA integrity, and 2,7-dichlorofluorscein dye to detect the ROS production within gastric cells, along with quantitative real time PCR to quantify the expression level of COX-2, iNOS, and eNOS genes.
Powders of Ca(OH)2 nanoparticles were purchased from Nanotech Company (Giza, Egypt), while CaTiO3 and Y2O3 nanoparticles were purchased from Sigma Aldrich Company (St. Louis, MO, USA) with a particle size less than 100 nm. Characterization of Ca(OH)2, CaTiO3, and Y2O3 nanoparticles has been well conducted using transmission electron microscope (TEM), X-ray diffraction (XRD) and dynamic laser scattering (DLS) to confirm the purity and nan-size of dispersed nanoparticles6,11,13.
Forty five male Swiss webster mice aging 10–12 weeks and weighting 20–25 g were used in this study and were kept in the animal house at Zoology department, Faculty of Science, Cairo University under normal conditions of light/dark cycles and receiving standard diet pellets and water. Mice were left for 1 week before starting administration to be acclimatized with animal house condition.
The plan and experiments of this study were approved by the MSA University Research Ethics Committee. This study was reported according to ARRIVE guidelines and also Animal handling and experimentations were conducted in accordance with the Guidelines of the National Institutes of Health (NIH) regarding the care and use of animals for experimental procedures.
Nanopowders of Ca(OH)2, CaTiO3, or Y2O3 were weighted and suspended in deionized distilled water to prepare the appropriate dose. Suspension of tested nanoparticles were also ultrasonicated using the biologics ultrasonic homogenizer (Model 150VT) immediately prior to animal administration. For simultaneous administration of the three tested nanoparticles, a suspension containing 50 mg/kg of Ca(OH)2, CaTiO3, and Y2O3 nanoparticles with equal ratio 1:1:1 was prepared.
An acute toxicity test was done to determine the tested dose of Ca(OH)2, CaTiO2 and Y2O3 nanoparticles based on the Organization of Economic Cooperation and Development (OECD) quidelines-420. Twenty male mice were randomly divided into four groups, five mice each: a control group and three treated groups. The mice of the control group were orally given deionized distilled water, while, mice of the treated groups were orally given Ca(OH)2, CaTiO2 or Y2O3 nanoparticles at the dose level of 2000 mg/kg b.w. All mice of the four groups were monitored carefully for 24 h after given a single dose of nanoparticles and then observed daily for 14 days for any morphological sign or behavior of toxicity. The tested dose of the three used nanoparticles was calculated based the OECD guidelines-420 (fixed dose method) to be as 2.5% (50 mg/kg b.w) of the safety tested dose14,15.
Twenty five male mice were randomly divided into five groups, with five mice in each group. Mice of group I (negative control) group were orally intake deionized distilled water, while mice of II, III, IV and V groups received oral suspension of Ca(OH)2, CaTiO2 or/and Y2O3 nanoparticles three times a week for two consecutive weeks. The mice of the five groups were then sacrificed by cervical dislocation and dissected to obtain stomach tissues which were washed with cold phosphate buffered saline (PBS) and stored at − 80° for further studies.
The level of ROS formation within gastric cells was determined based on the formation of a highly fluorescent compound dichlorofluoroscein as a result of the selective reaction between the 2,7-dichloroflurescin diacetate (DCFH-DA) and intracellular ROS16. A small portion of fresh stomach tissue (≈50 mg) was gently minced in cold PBS, then the cell suspension was mixed with DCFH-DA dye (20 mM), the mixture was incubated in the dark for 30 min, and then the cells were spread on slides for visualization under epi-fluorescent microscope at 200× magnification.
The effect of Ca(OH)2, CaTiO3, or/and Y2O3 NPs administration on the integrity of the gastric genomic DNA was studied using the alkaline Comet assay17 with minor modifications. The prepared slides were stained ethidium bromide, examined and photographed using an epi-fluorescent microscope at a magnification of 200× and finally fifty Comet nuclei were analyzed and scored using the scoring software TriTek Comet Score™ Freeware v1.5. The three comet parameters: tail length, % DNA in tail, and tail moment were used as an indicator for genomic DNA damage and presented as mean ± SD.
The gastric mRNA expression level of cyclooxygenase-2 (COX-2) and endothelial (eNOS) and inducible (iNOS) nitric oxide synthase genes was measured in the studied five groups using Real-time polymerase chain reaction (RT-PCR). To do that total gastric RNA was extracted using Thermo Scientific, USA’s GeneJET RNA Purification Kit, and reversely transcribed into complementary DNA using Revert Aid First Strand cDNA Synthesis Kit (Thermo Scientific, USA). A separate RT-PCR was conducted for each gene using SYBER Green master mix and the previously designed primers shown in Table 118,19,20 by the 7500 Fast system (Applied Biosystem 7500, Clinilab, Egypt). The expression level of theCOX-2, iNOS and eNOS genes were standardized against expression of the housekeeping ß-actin gene and the comparative Ct (ΔΔCt) method was utilized to calculate the genes expression. Results are displayed as mean ± SD.
The obtained results are presented as mean ± SD and were analyzed using the Statistical Package for the Social Sciences (SPSS 20). To determine the influence of Ca(OH)2, CaTiO2 or/and Y2O3 nanoparticles oral administration on the induction of DNA damage, intracellular ROS production and gene expression level, One-Way analysis of Variance (ANOVA) followed was carried out. Additionally, the homogenity between the five experimental groups were studied using Duncan's test.
Nanoparticles of Ca(OH)2, CaTiO3 and Y2O3 have been well characterized in our recent published studies6,11,13 and the XRD pattern, DLS analysis and TEM imaging revealed the purity of the purchased nanoparticles as well as the stability and well distribution of the suspended nanoparticles in deionized distilled water. The Zeta potential value of − 53.2 mV confirmed the stability and low aggregations of Y2O3 nanoparticles, while, the low Zeta potential values of dispersed Ca(OH)2 (2.48 mV) and CaTiO3 (− 3.38 mV) nanoparticles revealed low stability and high aggregations, consequently, suuspension of used nanoparticles were highly sonicated immediately prior administration to ensure well distribution of administered nanoparticles. The TEM imaging of nano-suspensions showed the spherical and polyhedral morphology of Ca(OH)2, CaTiO3 and Y2O3 nanoparticles, and also confirmed the well distribution of administered nanoparticles. The average particles' size of Ca(OH)2, CaTiO3 and Y2O3 nanoparticles was found to be 15.57, 88.79 and 14.00 nm, respectively6,11,13.
No morphological or behavioral sign of toxicity was observed while observing all mice in the control group and the three treated groups orally given 2000 mg/kg b.w of Ca(OH)2, CaTiO3 or Y2O3 nanoparticles and all mice were still healthy throughout the experimental period. Thus, the lethal half dose (LD50) of Ca(OH)2, CaTiO3 and Y2O3 nanoparticles was considered to be higher 2000 mg/kg according to the OECD-420 guidelines, and the tested dose of the three used nanoparticles in this study was calculated as 2½% (50 mg/kg body weight) of the LD50 Obtained from acute toxicity test.
As displayed in Fig. 1 oral administration of Ca(OH)2 nanoparticles (Group II) caused dramatic elevation in the generation of ROS within gastric cells, meanwhile, slight elevation was noticed in the ROS generated within gastric cells of mice orally given CaTiO3 nanoparticles (Group III) as visualized from the fluorescent green light emitted from the DCFH-DA stained cells compared to that emitted from the stained negative control cells (Group I). On contrary, oral administration of Y2O3 nanoparticles alone (Group IV) or in combination with Ca(OH)2 and nanoparticles (Group V) caused non observable changes in the ROS level generated within gastric cells of mice compared to the negative control ROS level (Fig. 1).
Level of ROS generated within the gastric cells of the negative control group and groups orally administered Ca(OH)2, CaTiO3 or/and Y2O3 nanoparticles.
Results of the alkaline Comet assay revealed a loss of genomic DNA stability in the gastric tissue of mice orally given Ca(OH)2 nanoparticles alone (Group II) as manifested by statistically significant elevations in tail length (p < 0.001) and tail moment (p < 0.01) compared to the negative control (Group I) values as seen in Table 2. On the other hand, non-remarkable changes (p > 0.05) in the measured parameters of genomic DNA damage: tail length, %DNA in tail and tail moment were noticed in the gastric tissues of mice orally given CaTiO3 (Group III) and Y2O3 (Group IV) nanoparticles separately or with Ca(OH)2 nanoparticles (Group V) as shown in Table 2. Representative examples for the scored comet nuclei with intact and damaged DNA are displayed in Fig. 2.
Representative photos for the scored comet intact with intact and damaged DNA regardless treatment.
Gastric genes expression analysis using RT-PCR demonstrated that multiple oral administration of Ca(OH)2 nanoparticles (Group II) caused statistically significant elevations (p < 0.001) in the gastric iNOS and COX-2 genes expression, but it is caused non-significant decrease (p > 0.05) in the iNOS gene expression compared to the negative control expression levels (Table 3). Meanwhile, multiple oral administration of CaTiO3 (Group III) and Y2O3 (Group IV) nanoparticles separately or simultaneously with Ca(OH)2 nanoparticles (Group V) caused remarkable high elevations the gastric eNOS gene expression and non-significant changes in the gastric iNOS and COX-genes expression compared to their expression level in the negative control group as shown in Table 3.
The exponential increase in the applications and utilization of Ca(OH)2, CaTiO3 and Y2O3 nanoparticles in intensive industrial, medical and food applications highly increase their production and environmental release causing their high accumulation in many environmental compartments such as air, water, and soil and even in food. Consequently, attention has been paid to study the potential risks of these nanoparticles on human health particularly gastrointestinal risks3. Unfortunately the biological effects and genotoxicity of orally intake Ca(OH)2, CaTiO3 or/and Y2O3 nanoparticles on gastric tissues are poorly understanding. Therefore, the present study was done to estimate the genomic instability and inflammation induction by Ca(OH)2, CaTiO3 or/and Y2O3 nanoparticles in the gastritis of mice.
In this study Ca(OH)2, CaTiO3 and Y2O3 nanoparticles were orally administered to mice because oral intake of nanoparticles is a main route of Ca(OH)2, CaTiO3 and Y2O3 nanoparticles exposure due their wide uses in food and other products, along with the potential for unintentional ingestion from environmental contamination such as contaminated water and food. Upon oral ingestion, nanoparticles disperse and penetrate the gastric tissues attacking proteins, lipids, carbohydrates and DNA3,11,12,21.
The results of the current study demonstrated the non-genotoxic effects of CaTiO3 or Y2O3 nanoparticles through non-significant changes in the tail length, %DNA in tail and tail moment noticed after multiple oral administrations of CaTiO3 or Y2O3 nanoparticles separately. Similarly, recent studies have shown that CaTiO3 and Y2O3 nanoparticles are non-genotoxic on normal human skin fibroblast (HSF) and retinal epithielial-1 (REP1) cells, respectively, through non-remarkable changes in the genomic DNA integrity after cells treatment with CaTiO3 or Y2O3 nanoparticles6,13.
Based on the results obtained from RTPCR, the demonstrated safety of CaTiO3 and Y2O3 nanoparticles on gastric genomic DNA may result from the marked overexpression of the gastric eNOS gene noticed after administration of CaTiO3 or Y2O3 nanoparticles because overexpression of the eNOS gene maintains the integrity of the gastric tissue by regulating gastric blood flow and stimulating the synthesis and secretion of gastric mucus besides reducing ROS formation22. Accordingly, the observed non-significant changes in the gastric ROS generation level and the expression level of the studied pro-inflammatory mediators (iNOS and COX-2 genes) revealed the absence of inflammation and oxidative stress induction after administration of CaTiO3 or Y2O3 nanoparticles and could also be attributed to the above mentioned marked upregulation of gastric eNOS gene expression.
Surveying ROS generation within gastric tissues using 2,7 DCFH-DA demonstrated marked over ROS generation after oral administration of Ca(OH)2 nanoparticles that disrupt homeostasis and induce oxidative stress consistent with the reported oxidative stress induction through high ROS generation in mice given orally a single dose of Ca(OH)2 nanoparticles11,12. High ROS generation and oxidative stress induction unbalance cell membrane permeability and cause many pathological conditions such as genomic DNA damage, neurodegenerative disorders, inflammation, and cancer6,23,24.
Induction of genomic DNA damage by chronic Ca(OH)2 nanoparticles administration was manifested in this study by the remarkable high elevations in the gastric DNA damage indicating parameters measured by the alkaline Comet assay. Ongoing with the genotoxicity of Ca(OH)2 nanoparticles demonstrated in previous studies, this genotoxic effect can be attributed to the aforementioned over-ROS production within the gastric tissues of mice given orally Ca(OH)2 nanoparticles alone11,12.
Inflammation occurs naturally in response to various injurious agents such as the infectious pathogens and toxins. However, persistent exposure to inflammatory agents induces chronic inflammation through disruption of the immune system causing many diseases such as rheumatoid arthritis, chronic gastritis atherosclerosis, diabetes, septic shock, chronic hepatitis and inflammatory neurodegenerative diseases25. Once toxins and pathogens induce high ROS generation and DNA damage, inflammation is induced leading to cellular malfunction, excessive secretion of inflammatory cytokines and mediators, tissue degenerative changes and metabolic complications25,26.
Inflammation induction after Ca(OH)2 nanoparticles administration was demonstrated in this study through the marked elevations observed in the expression level of the gastric iNOS and COX-2 genes and may result from the noticed high ROS generation within the gastric tissue of mice orally administered Ca(OH)2 nanoparticles alone. Consistent with previous studies besides high generation of ROS, significant elevations in the iNOS gene expression seen after Ca(OH)2 nanoparticles lead to over-production of harmful nitric oxide that reacts with superoxide anions forming reactive nitrogen species (RNS). Accordingly elevations in the ROS and RNS generation stimulate upregulation of the pro-inflammatory mediator COX-2 inducing sever inflammation12,27,28.
Extensive uses of Ca(OH)2, CaTiO3 and Y2O3 nanoparticles in various applications increase their environmental release and accumulation in contaminated water, soil and food, which together increases the risk of human exposure to these nanoparticles3 and necessitates studying the genotoxic effect of simultaneous exposure to Ca(OH)2, CaTiO3 and Y2O3 nanoparticles. Accordingly, the effect of Ca(OH)2, CaTiO3 and Y2O3 nanoparticles coadministration on the gastric genomic DNA integrity and inflammation induction was also estimated in the current study.
In contrast to the demonstrated Ca(OH)2 nanoparticles induced genotoxicity, oral coadministration of CaTiO3 and Y2O3 nanoparticles simultaneously with Ca(OH)2 nanoparticles was non-genotoxic and did not cause any noticeable changes in the integrity of gastric genomic DNA as detected by the non-significant changes observed in the measured DNA damage indicating parameters: tail length, %DNA in tail and tail moment after administration of Ca(OH)2, CaTiO3 and Y2O3 nanoparticles. Recently, Y2O3 nanoparticles showed antioxidant capacity through scavenging free radicals, thus administration of Y2O3 nanoparticles prohibits the induction of oxidative stress by decreasing the level of intracellular ROS generation and enhancing the antioxidant status of the cell29,30. Accordingly, the non-genotoxic effect detected after coadministration of CaTiO3 and Y2O3 nanoparticles simultaneously with Ca(OH)2 nanoparticles may result from the antioxidant and free radicals scavenging abilities of Y2O3 nanoparticles which prohibit Ca(OH)2 nanoparticles induced ROS generation and DNA damage.
Our findings of significant elevations in the gastric eNOS gene expression and non-noticeable changes in the gastric ROS level and expression level of inflammatory iNOS and COX-2 genes after coadministration of Ca(OH)2, CaTiO3 and Y2O3 nanoparticles revealed the absence of inflammation and oxidative stress and also confirmed the previously reported antioxidant and free radicals scavenging capacity of Y2O3 nanoparticles because gastric eNOS overexpression decreases the formation of ROS and increases the expression of antioxidants such as superoxide dismutase and Heme-oxygenase-I22,29,30.
Based on the findings of this study, oral administration of Ca(OH)2 nanoparticles was genotoxic and disrupted the genomic DNA integrity through high ROS generation and overexpression of inflammatory iNOS and COX-2 genes. Conversely, oral administration of CaTiO3 and Y2O3 nanoparticles separately or together simultaneously with Ca(OH)2 nanoparticles was non-genotoxic and inhibited ROS overproduction and inflammation induction through upregulating eNOS gene expression that maintains on cell balance. Therefore, more in vivo and in vitro studies on the biological and toxic effects of Ca(OH)2, CaTiO3, or/and Y2O3 nanoparticles are recommended to understand their impact on human health.
The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.
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Many thanks to the Zoology Department at faculty of science Cairo University for hosting this project and providing us with required equipment needed to conduct the experiments.
Open access funding provided by The Science, Technology & Innovation Funding Authority (STDF) in cooperation with The Egyptian Knowledge Bank (EKB). The experiments of this study were partially funded by Faculty of Science Cairo University and Faculty of Biotechnology, October University for Modern Sciences and Arts (MSA) Egypt.
Zoology Department Faculty of Science, Cairo University, Giza, Egypt
Faculty of Biotechnology, October University for Modern Sciences and Arts, 6th of October City, Egypt
Salma H. Elbasiouni, Ahmed H. Farouk, Kirolls A. Nasif, Karima Nasraldin & Gehan Safwat
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H.R.H.M. designed the study, conducted the molecular experiments, wrote manuscript, and performed statistical analysis. A.H.F., S.H.E., and K.A.N. performed experimentations and wrote manuscript. G.S., K.N. and other authors reviewed the manuscript.
Correspondence to Hanan R. H. Mohamed.
The authors declare no competing interests.
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Mohamed, H.R.H., Elbasiouni, S.H., Farouk, A.H. et al. Alleviation of calcium hydroxide nanoparticles induced genotoxicity and gastritis by coadministration of calcium titanate and yttrium oxide nanoparticles in mice. Sci Rep 13, 22011 (2023). https://doi.org/10.1038/s41598-023-49303-x
DOI: https://doi.org/10.1038/s41598-023-49303-x
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