Surface characterization, electrochemical properties and in vitro biological properties of Zn-deposited TiO2 nanotube surfaces

In this work, to improve antibacterial, biocompatible and bioactive properties of commercial pure titanium (cp-Ti) for implant applications, the Zn-deposited nanotube surfaces were fabricated on cp-Ti by using combined anodic oxidation (AO) and physical vapor deposition (PVD-TE) methods. Homogenous elemental distributions were observed through all surfaces. Moreover, Zn-deposited surfaces exhibited hydrophobic character while bare Ti surfaces were hydrophilic. Due to the biodegradable behavior of Zn on the nanotube surface, Zn-deposited nanotube surfaces showed higher corrosion current density than bare cp-Ti surface in SBF conditions as expected. In vitro biological properties such as cell viability, ALP activity, protein adsorption, hemolytic activity and antibacterial activity for Gram-positive and Gram-negative bacteria of all surfaces were investigated in detail. Cell viability, ALP activity and antibacterial properties of Zn-deposited nanotube surfaces were significantly improved with respect to bare cp-Ti. Moreover, hemolytic activity and protein adsorption of Zn-deposited nanotube surfaces were decreased. According to these results; a bioactive, biocompatible and antibacterial Zn-deposited nanotube surfaces produced on cp-Ti by using combined AO and PVD techniques can have potential for orthopedic and dental implant applications

Detection of lipid peroxidation and cytotoxicity induced by aluminium (Al) and cobalt (Co) ions in barbunia root tip cells

WOS: 000281449200018PubMed: 21387918The aim of this study was to investigate the cytotoxic effects of different concentrations of Aluminium (Al) and Cobalt (Co) heavy metal ions on Phaseolus vulgaris L. cv. Barbunia (Fabaceae) root tips. We used the germination percentage (GP), root length (RL), weight gain (WG) and micronucleus (MN) frequency as indicators of cytotoxicity, and correlated these data with statistical parameters. Additionally to the cytogenetic analysis, lipid peroxidation and DNA analyses were performed in root tips of barbunia seeds treated with Al and Co metals. The seeds were divided into five groups as control, Al and Co treatment groups. They were treated with 25 and 50 ppm doses of Al and Co during 7 days. The results indicated that there was an alteration in the GP, RL, WG and MN frequency depending on the treatment dose in the seeds exposed to Al and Co metal ions when compared with the controls. Al and Co metal ions at both the doses significantly reduced the GP, RL and WG in seeds of all the treatment groups. The highest GP was observed in seeds of the control group (in proportion as 96%). 25 and 50 ppm doses of Co and Al caused 30, 50 and 42, 64% decrease of seed germination, respectively In the control group, the final weights of all the seeds increased about 1.31 g when compared to initial weight. The mean RL of control seeds were measured as 3.71 cm at the end of experimental period. In Co and Al groups, the final weights of seeds increased about 0.34 g and 0.19 g according to initial weight at 50 ppm dose, respectively But, Al and Co ions caused a dose-dependent increase in the frequency of MN. The highest frequency of MN was observed at 50 ppm dose of Al and least frequency of MN was observed at 25 ppm dose of Co. Besides, 25 and 50 ppm concentrations of Al and Co significantly enhanced the lipid peroxidation and caused an increase in malondialdehyde (MDA) levels at both the doses. In roots treated with 25 and 50 ppm doses of Al, the increase of MDA was about 62 and 136% according to control, respectively In Co-treated roots, the increase of MDA was about 31 and 91% according to the control at 25 and 50 ppm doses, respectively The investigated parameters (except MN and MDA) were higher in the seeds exposed to Co than the seeds treated with Al. Moreover, it was observed that the yields of DNA in the seeds treated with Al and Co metals were lower than recorded in the controls. Hence, DNA yields exposed to Al and Co were run ahead on agarose gel according to the control group. The results of the present study indicate that Al and Co metal ions have toxic effects on barbunia root tip cells, and the selected parameters such as the GP, RL, WG, MN and MDA are very sensitive and useful biomarkers for biomonitoring these effects

Protective effects of beta-carotene against ammonium sulfate toxicity: Biochemical and histopathological approach in mice Model

Acar, Ali/0000-0001-8617-2206WOS: 000446677000001PubMed: 30300052In this study, the protective role of beta-carotene against ammonium sulfate-induced toxicity has been evaluated in Mus musculus var. albino mice, along with biochemical and histopathological parameters. Some biochemical parameters such as aspartate transaminase (AST), alanine transaminase (ALT), blood urea nitrogen (BUN), creatinine and oxidative stress parameters, malondialdehyde (MDA), and glutathione (GSH) levels in kidney and liver tissues were investigated. The mice were randomly divided into six groups. Group I received intraperitoneal injections of 0.9% NaCl; group II received orally administered 250 mg kg(-1) bw beta-carotene, group III received orally administered 500 mg kg(-1) bw beta-carotene; group IV received 320 mg kg(-1) bw ammonium sulfate; group V was given 250 mg kg(-1) bw beta-carotene +320 mg kg(-1) of bw ammonium sulfate; and group VI received orally administered 500 mg kg(-1) of bw beta-carotene +320 mg kg(-1) of bw ammonium sulfate. As a result, it was determined that the ammonium sulfate treatment causes significant changes in the biochemical and oxidative stress parameters and also in histological examinations. In group IV, significant increases in ALT, AST, BUN, MDA, and creatinine levels, and a significant decrease in GSH levels were observed compared with control group. In histopathological examinations, different pathological findings such as proteinaceous deposits, thickening of basement membrane, hyaline cast in kidney tissue and stellate cell, karyomegaly, and binucleated cells in liver tissue were observed. beta-carotene treatment in group V and VI ameliorated the elevated levels of liver enzymes and improved oxidative stress and histopathological findings, and so, it could be concluded that beta-carotene offered remarkable protection against ammonium sulfate-induced toxicity

In vivo epiclorohidrine toxicity: cytogenetic, biochemical, physiological, and anatomical evidences

yalcin, emine/0000-0002-5280-5375WOS: 000477591700027PubMed: 31154645In this study, the toxic effects of epiclorohidrine (ECh) were investigated in vivo by Allium test. The toxic effects have been investigated in terms of physiological, cytogenetic, anatomical, and biochemical aspects. The changes in germination percentage, weight gain, and root length were investigated as physiological parameter; micronucleus (MN), mitotic index (MI), and chromosomal abnormality (CA) frequencies were as cytogenetic parameter. Oxidative stress indicators such as superoxide dismutase (SOD), catalase (CAT), and malondialdehyde (MDA) were analyzed for biochemical changes and also damages in root tip cells were evaluated as anatomical parameter. It was determined that germination percentage, weight gain, root length, and MI decreased; MN and CA frequencies were increased with the increase of ECh treatment dose. ECh treatment caused significant increase in SOD and CAT enzyme activities and MDA levels and these results indicated a stress formation. A variety of anatomical changes and damages were observed in the root tip cells induced by ECh. In conclusion, the toxic effects of ECh on A. cepa which is a model of eucaryotic cell were investigated in a multi-directional way and serious toxic effects of ECh treatment were determined

Aneugenic, clastogenic, and multi-toxic effects of diethyl phthalate exposure

DEMIRTAS, Guray/0000-0002-3853-5524; yalcin, emine/0000-0002-5280-5375WOS: 000514845700075PubMed: 31853848Diethyl phthalate (DEP) is a compound which is used in many industrial fields, especially in cosmetic sector and causes contamination in air, water, and soil due to its widespread usage. In this study, the potential toxic effects of DEP were investigated by using physiological, anatomical, biochemical, and cytogenetic parameters in Allium cepa. The micronucleus (MN) test specifically aimed to elucidate the aneugenic and clastogenic effects of DEP. Physiological effects were determined by germination percentage, root length, weight gain parameters, and cytogenetic effects were investigated by mitotic index (MI) and chromosomal abnormality (CA) test. Malondialdehyde (MDA) level, catalase (CAT), and superoxide dismutase (SOD) activities were investigated as oxidative damage indicators and structural changes were investigated with anatomical cross sections. For this purpose, Allium cepa bulbs were divided into four groups as control and application groups and the application groups were germinated with 1.0, 2.2, and 4.4 mu M DEP for 72 h. As a result, it was determined that germination percentage, weight gain and root length decreased, CA frequency, MDA level, SOD, and CAT activities were increased in DEP-treated groups when compared with the control group. DEP has been found to induce CA in root tip cells such as fragment, chromosome bridge, c-mitosis, sticky chromosome, and unequal chromatin distribution. When MN formations induced by DEP application were examined, both large-scale and small-scale MNs were determined. MN formation in both sizes indicates that DEP has both clastogenic and aneugenic effects. And also, it was found that DEP application caused structural changes and especially anatomic damages such as necrosis in 4.4 mu M DEP application. As a result, it was found that DEP caused various toxic effects depending on the dose and that A. cepa test material was a useful indicator in determining these effects

Royal Jelly (Honey Bee) Is a Potential Antioxidant Against Cadmium-Induced Genotoxicity and Oxidative Stress in Albino Mice

WOS: 000273180900016PubMed: 20041783Cadmium (Cd) is a highly toxic heavy metal that induces genotoxic damage in the body. Besides, Cd induces oxidative damage in various tissues by altering antioxidant defence enzymes system. In this study, we investigated the protective role of royal jelly (RJ) on Cd-induced genotoxicity and oxidative stress in mice. For this aim, the micronucleus (MN) test in erythrocytes and exfoliated cells of buccal mucosa and the chromosome aberration (CA) test in bone marrow cells were applied. In addition, the levels of reduced glutathione (GSH) and malondialdehyde (MDA) were evaluated in the liver and kidneys. Thirty-six animals were divided into six groups: the control group received distilled water alone, whereas mice in the treatment groups received RJ alone (100 and 250 mg/kg of body weight), Cd alone (2 mg/kg of body weight), and RJ+Cd. Cd toxicity resulted in a significant (P<.05) increase in CAs, abnormal metaphase number, and MN formation. Cd also caused a decrease in mitotic index. Oral administration of RJ at two doses (100 and 250 mg/kg of body weight) showed significant (P<.05) suppression of mutagenic effects of Cd. Moreover, Cd-induced oxidative damage caused a significant decrease in GSH level and a significant increase in MDA level in the liver and kidneys. Treatment with two doses of RJ caused a significant recovery in antioxidant status of GSH and a significant inhibition of MDA production. It could be concluded that RJ has a protective role against Cd-induced genotoxicity and oxidative stress in mice, due to its antioxidant effects.Giresun UniversityGiresun UniversityThis study was supported by grants from the Giresun University Scientific Research Projects Department

The investigation of cytotoxic effects of refinery wastewater on root tip cells of Vicia faba L.

WOS: 000279598600014PubMed: 21186721The present study was carried out to evaluate the cytotoxic effects of refinery wastewater collected from different stations of the Kizilirmak river on Vicia faba L. root tip cells. For this aim, we used the germination percentage, root length, weight gain and micronucleus (MN) frequency as indicators of cytotoxicity. Additionally to the cytological analysis, DNA analyses were performed in root tips men stems of Vicia faba seeds treated with refinery wastewater. Heavy metal concentrations in the water samples were determined using atomic absorption spectrophotometer (AAS). The concentrations of heavy metals in the water were in the order of Pb>Zn>Fe>Cu>Ni>Cd>Hg. The highest germination percantage was observed in the control group (in proportion as 96%). Heavy metals in the water samples collected from Station I, II and III caused a decrease in the germination percentage as 48, 18 and 30%, respectively The highest root length and weight gain was observed in the control group at the end of the experimental period. The least root length and weight gain was observed in seeds treated with wastewater collected from Station I. In the control group, the weights of all the seeds increased about 4.089 when compared with initial weight. The root lengths of the control seeds were determined as 6.38 cm at the end of the experimental period. The weights of the seeds exposed to wastewaters obtained from Station I, II and III increased about 1.08, 3.03 and 2.01 g according to initial weight, respectively Microscopic examination of V faba root tip meristem cells showed that any example of the MN formation was not seen in the control group. The highest frequency of MN was observed in group treated with wastewater collected from Station land least frequency of MN was observed in group treated with wastewater collected from Station II. It was also observed that the yields of DNA in the seeds exposed to wastewater were lower than recorded in the controls. Hence, DNA yields exposed to wastewater were run ahead on agarose gel according to the control group. The results clearly indicate that refinery wastewater had important cytotoxic effects on V faba root tip cells. It was also observed that V faba seeds are very sensitive and useful biomarkers for monitoring these effects in waters contaminated with heavy metals

Protective effect of ginkgo biloba l. leaf extract against glyphosate toxicity in swiss albino mice

ORUC, Ertan/0000-0003-4234-8219WOS: 000295950000023PubMed: 21859351The aim of the present study was to investigate the protective role of Ginkgo biloba L. leaf extract against the active agent of Roundup herbicide (Monsanto, Creve Coeur, MO, USA). The Swiss Albino mice were randomly divided into six groups, with each group consisting of six animals: Group! (control) received an intraperitoneal injection of dimethyl sulfoxide (0.2 mL, once only), Group II received glyphosate at a dose of 50 mg/kg of body weight, Group III received G. biloba at a dose of 50 mg/kg of body weight, Group IV received G. biloba at a dose of 150 mg/kg of body weight, Group V received G. biloba (50 mg/kg of body weight) and glyphosate (50 mg/kg of body weight), and Group VI received G. biloba (150 mg/kg of body weight) and glyphosate (50 mg/kg of body weight). The single dose of glyphosate was given intraperitoneally. Animals from all the groups were sacrificed at the end of 72 hours, and their blood, bone marrow, and liver and kidney tissues were analyzed for aspartate aminotransferase (AST), alanine aminotransferase (ALT), blood urea nitrogen (BUN), creatinine, malondialdehyde (MDA), and glutathione (GSH) levels and the presence of micronucleus (MN), chromosomal aberrations (CAs), and pathological damages. The results indicated that serum AST, ALT, BUN, and creatinine levels significantly increased in mice treated with glyphosate alone compared with the other groups (P<.05). Besides, glyphosate-induced oxidative damage caused a significant decrease in GSH levels and a significant increase in MDA levels of the liver and kidney tissues. Moreover, glyphosate alone treated mice presented higher frequencies of CAs, MNs, and abnormal metaphases compared with the controls (P<.05). These mice also displayed a lower mean mitotic index than the controls (P<.05). Treatment with G. biloba produced amelioration in indices of hepatotoxicity, nephrotoxicity, lipid peroxidation, and genotoxicity relative to Group II. Each dose of G. biloba provided significant protection against glyphosate-induced toxicity, and the strongest effect was observed at a dose of 150 mg/kg of body weight. Thus, in vivo results showed that G. biloba extract is a potent protector against glyphosate-induced toxicity, and its protective role is dose-dependent

Protective effect of kombucha mushroom (KM) tea on phenol-induced cytotoxicity in albino mice

ORUC, Ertan/0000-0003-4234-8219WOS: 000281449200011PubMed: 21387911The present study was carried out to evaluate the protective role of kombucha mushroom (KM) tea on cytotoxicity induced by phenol (PHE) in mice. We used weight gain and micronucleus (MN) frequency as indicators of cytotoxicity, and supported these parameters with pathological findings. The animals were randomly divided into seven groups: (Group I) only tap water (Group II)1000 mu l kg(-1) b. wt KM-tea, (Group III) 35 mg kg(-1) body wt. PHE (Group IV) 35 mg kg(-1) body wt. PHE + 250 mu l kg(-1) b. wt KM-tea (Group V) 35 mg kg(-1) b. wt PHE + 500 mu l kg(-1) b. wt KM-tea (Group VI) 35 mg kg(-1) b. wt PHE + 750 mu l kg(-1) b. wt KM-tea, (Group VII) 35 mg kg(-1) b. wt PHE + 1000 mu l kg(-1) b. wt KM-tea, for 20 consecutive days by oral gavage. The results indicated that all KM-tea supplemented mice showed a lower MN frequency than erythrocytes in only PHE-treated group. There was an observable regression on account of lesions in tissues of mice supplemented with different doses of KM-tea in histopathological observations. In conclusion, the KM-tea supplementation decreases cytotoxicity induced by PHE and its protective role is dose-dependent.Scientific Researches Unit (BAB) of Giresun UniversityGiresun UniversityWe thank Dr. Perihan Guler, Faculty of Science and Art Faculty, Kirikkale University, Turkey, for starter culture of KM-tea. Besides, we thank Scientific Researches Unit (BAB) of Giresun University for financial support

The protective effect of royal jelly on chronic lambda-cyhalothrin toxicity: serum biochemical parameters, Lipid peroxidation, and genotoxic and histopathological alterations in Swiss Albino Mice

ORUC, Ertan/0000-0003-4234-8219WOS: 000295950000019PubMed: 21663479The present study was undertaken to investigate the protective effect of royal jelly (RJ) against toxicity induced by a synthetic pyrethroid insecticide, lambda-cyhalothrin (LCT), in Swiss albino mice. Animals were randomly divided into six groups of six animals each. The control group received distilled water alone, whereas mice in the treatment groups received RJ alone (100 or 250 mg/kg of body weight), LCT alone (668 ppm), or RJ + LCT for 21 days. All mice (100%) survived until the end of experiment and were sacrificed at the end of 24 hours. Blood, bone marrow, and liver and kidney tissues were analyzed for aspartate aminotransferase (AST), alanine aminotransferase (ALT), blood urea nitrogen (BUN), creatinine, malondialdehyde (MDA), and reduced glutathione (GSH) levels and micronucleus (MN) frequency, chromosomal aberrations (CAs), and pathological damages. Serum AST, ALT, BUN, and creatinine levels were elevated in mice treated with LCT alone compared with the other tested groups (P<.05). LCT-induced oxidative damage caused a significant decrease in GSH levels and a significant rise in MDA levels of liver and kidney tissues. LCT alone treated mice presented higher frequencies (P<.05) of MNs, CAs, and abnormal metaphases compared with the controls; moreover, the mitotic index was lower than in controls (P<.05). Oral treatment with RJ significantly ameliorated the indices of hepatotoxicity, nephrotoxicity, lipid peroxidation, and genotoxicity induced by LCT. Both doses of RJ tested provided significant protection against LCT-induced toxicity, and its strongest effect was observed at the dose level of 250 mg/kg of body weight. In vivo results suggest that RJ is a potent antioxidant against LCT-induced toxicity, and its protective effect is dose dependent