scholarly journals Effect of Imidocarb Application on Oxidative DNA Damage Caused by Anaplasmosis

2021 ◽  
Vol 9 (12) ◽  
pp. 2308-2311
Author(s):  
Ahmet Cihat Öner ◽  
Adnan Ayan
Keyword(s):  
Dna Damage ◽  
Comet Assay ◽  
Dna Fragmentation ◽  
Oxidative Dna Damage ◽  
Clinical Signs ◽  
Tail Length ◽  
Assay Method ◽  
Control Group ◽  
Tail Moment ◽  
Before And After

This study was aimed to evaluate DNA fragmentation by using Comet assay in naturally infected sheep with Anaplasmosis before and after treatment with the Comet method, which shows DNA damage specifically. In the study, blood samples were collected from 10 Anaplosmosis infected and 10 healthy sheep. The anaplosmosis was diagnosed by clinical signs and symptoms. The infection was confirmed by Giemsa staining. The blood was collected from control group and infected group before and after the treatment, from the vena jugularis with the appropriate method. The DNA fragmentation was checked by using the Comet assay of blood cells. The data were analysed throught ANNOVA one-way. The result showed higher DNA fragmentation in sick animals diagnosed with anaplasmosis; tail length and tail moment values were found to be statistically significantly higher than the control group. When the data obtained after imidocarb (IMD) application were compared with obtained during the disease, a decreased DNA damage and tail moment was determined, however, these values higher than control. In this study, DNA damage and the extent of this damage were investigated by the Comet assay method using a healthy control group before and after treatment in animals with Anaplasmosis. When the findings obtained from the study were evaluated, it was seen that Anaplasma agents caused DNA damage and with the imidocarb application given for treatment, DNA damage was reduced and results close to healthy individuals were obtained.

Assessment of Antioxidant Effect of Beta-Glucan on the Whole Blood Oxidative DNA Damage with the Comet Assay in Colorectal Cancer

2021 ◽  
Vol 14 ◽  
Author(s):  
Necla Benlier ◽  
Nilay Uçar ◽  
Eda Öğüt ◽  
Havva Yeşil Çinkir ◽  
Mustafa Yildirim ◽  
...  
Keyword(s):  
Colorectal Cancer ◽  
Dna Damage ◽  
Comet Assay ◽  
Whole Blood ◽  
Oxidative Dna Damage ◽  
Tail Length ◽  
Antioxidant Effect ◽  
Control Group ◽  
Tail Moment ◽  
Beta Glucan

Objective: The present study aims to evaluate the antioxidant effect of beta glucan on oxidative DNA damage by comet assay. Methods: A total of 19 adult females and males diagnosed with stage 3-4 colorectal cancer and a control group of 20 age-matched healthy subjects were enrolled in the study. Blood samples of the participants were analyzed using Comet Assay for the parameters of DNA damage. Results: Significantly increased DNA damage was observed in patients versus control group as indicated by greater values of tail moment, tail percent DNA and tail length. Following incubation with β-glucan, a substantial reduction was found in the aforementioned parameters of DNA damage. Comet assay revealed significant levels of endogenous DNA damage in patients as shown by remarkable increases in the tail moment, the percentage of DNA in the tail and the tail length values, in comparison with the control group. Following treatment of fresh whole blood with β-glucan incubation, DNA damages were significantly reduced but lower values were observed after β-glucan incubation in the patient group versus control group. Conclusion: β-Glucan was found to reduce DNA damage substantially in colorectal cancer patients and show antimutagenic effects. Our results suggested that dietary β-glucan intake might be important in the genesis of colorectal cancer tumors.

scholarly journals Assessment of Cytogenetic Damage and Cholinesterases’ Activity in Workers Occupationally Exposed to Pesticides in Zamora-Jacona, Michoacan, Mexico

2021 ◽  
Vol 18 (12) ◽  
pp. 6269
Author(s):  
Rafael Valencia-Quintana ◽  
Rosa María López-Durán ◽  
Mirta Milić ◽  
Stefano Bonassi ◽  
Ma. Antonieta Ochoa-Ocaña ◽  
...  
Keyword(s):  
Dna Damage ◽  
Comet Assay ◽  
Whole Blood ◽  
Pesticide Exposure ◽  
Smoking Habit ◽  
Tail Length ◽  
Exposure Period ◽  
Control Group ◽  
Tail Moment ◽  
Cholinesterase Activities

Pesticides have been considered as potential chemical mutagens; however, little is known about toxic and genotoxic effects during pesticide application in Zamora-Jacona, Michoacan State in Mexico. This study sought to determine DNA damage and cholinesterase activities inhibitions in 54 agricultural workers exposed to complex mixtures of pesticides vs. control group (26 individuals) using Comet assay in peripheral whole blood, micronucleus (MN) test in oral mucosa cells, Cytokinesis-blocked MN assay in lymphocytes (L-CBMNcyt) and measuring AChE and BChE activities in whole blood and plasma samples, respectively. Exposed subjects demonstrated significantly elevated levels of primary (Comet assay: tail intensity, tail length, tail moment, Olive tail moment) and permanent DNA damage (MN assay: in blood/buccal cells; frequencies of nuclear buds, binucleated cells, cells with condensed chromatin, karyorrhexis, pyknosis, and karyolysis). However, inhibition of cholinesterase activities (AChE and BChE) was not observed in the workers. Confounding factors including sex, age, BMI, working exposure period, protection level, smoking habit (cigarettes per day units), alcohol consumption (weekly), medication, were considered in the analysis. These combined techniques demonstrated usefulness in the health hazards risks pesticide exposure assessment and suggested the need for periodic monitoring together with the education and the training of occupational workers for the safe application of potentially harmful pesticides.

scholarly journals The Effect of Ellagic Acid on Paraoxanase - 1 Activity and DNA Damage in Acute Exercise

2019 ◽  
pp. 1-7
Author(s):  
Ersan Kara ◽  
Funda Karabağ Çoban ◽  
Mustafa Akıl ◽  
Recep Liman ◽  
İbrahim Hakkı Ciğerci
Keyword(s):  
Dna Damage ◽  
Ellagic Acid ◽  
Oxidative Dna Damage ◽  
Acute Exercise ◽  
Paraoxonase 1 ◽  
Assay Method ◽  
Control Group ◽  
Control Groups ◽  
Experimental Animals

The purpose of this study was to evaluate the correlation between exhaustive and intensive exercise with changes in paraoxonase-1 enzyme activity, oxidative DNA damage and the role of ellagic acid against possible damage. The study was carried out on 32 male and adult Spraque - Dawley rats at the Experimental Animal Research and Research Center of Afyon Kocatepe University. The experimental animals were equally divided into four groups. Swimming exercises were performed as acute exercises for once and experimental animals are made to swim in groups including two rats following the completion of the study and before the decapitation. At the end of the experiment, obtained blood samples; Paraoxonase-1 (PON-1), Malondialdehyde (MDA) and 8-HydroxyGuanine (8-OhdG) levels were measured to determine DNA damage and DNA damage was assessed by Comet Assay method. As a result, PON-1 levels in rats with intense swimming training were found to be significantly lower (p <0.05) than the control group. MDA and (8-OhdG) levels were significantly higher in the swimming group than in the control group (p <0.05). As to the DNA damage determination by COMET analysis, DNA damage was observed in the swimming groups according to the control groups. When the ellagic acid groups were compared with the swimming groups, there was a significant increase in PON-1 levels, and the levels of MDA and (8-OhdG) were significantly lower than the swimming groups. The DNA damage was also found to be low in these groups.

Oxidative DNA Damage and NOX4 Levels in Children with Undescended Testes

2019 ◽  
Vol 29 (06) ◽  
pp. 545-550 ◽  
Author(s):  
Veli Avci ◽  
Kemal Ayengin ◽  
Hamit Hakan Alp
Keyword(s):  
Dna Damage ◽  
Oxidative Dna Damage ◽  
Nicotinamide Adenine Dinucleotide Phosphate ◽  
Assay Method ◽  
Enzyme Linked Immunosorbent Assay ◽  
Control Group ◽  
Chromatography Method ◽  
Risk Of Malignancy ◽  
Healthy Control ◽  
Liquid Chromatography Method

Background Undescended testis (UDT) is a common urological disorder. Patients with UDT have a risk of malignancy and infertility. The development of these conditions may be due to oxidative stress mediated by reactive oxygen species. The aim of this study was to investigate the relationship between these parameters by detecting oxidative DNA damage (8-hydroxy 2 deoxyguanosine/106 deoxyguanosine), ischemia-modified albumin (IMA), malondialdehyde (MDA), and nicotinamide adenine dinucleotide phosphate oxidase 4 (NOX4) levels in children with UDT and healthy control group. Materials and Methods The blood samples were obtained from 30 patients with UDT and 40 healthy male subjects. The levels of oxidative DNA damage were detected by high-pressure liquid chromatography method. We used commercially available kits that use enzyme-linked immunosorbent assay method to measure IMA, MDA, and NOX4 levels. Results The levels of MDA, IMA, NOX4, and oxidative DNA damage in children with UDT were statistically significantly higher than control group. In addition, we found that the levels of NOX4, IMA, and oxidative DNA damage after 12 months of age was significantly higher than before 12 months of age. Conclusion We identified increased lipid peroxidation, oxidative DNA damage, IMA, and NOX4 levels in children with UDT. Delay in the treatment of UDT may cause oxidative damage. That is why, according to us the antioxidant treatment may be beneficial in children with UDT.

DNA damage in rat kidneys and liver upon subchronic exposure to single and combined ochratoxin A and citrinin

2019 ◽  
Vol 12 (2) ◽  
pp. 163-172 ◽  
Author(s):  
D. Rašić ◽  
D. Želježić ◽  
N. Kopjar ◽  
D. Kifer ◽  
M. Šegvić Klarić ◽  
...  
Keyword(s):  
Dna Damage ◽  
Comet Assay ◽  
Ochratoxin A ◽  
Oxidative Dna Damage ◽  
Tail Length ◽  
Alkaline Comet Assay ◽  
Male Wistar Rats ◽  
Induction Of Apoptosis ◽  
Dose Dependent ◽  
Rat Kidneys

The study aimed to check whether ochratoxin A (OTA) and citrinin (CIT) increase DNA damage in the kidney and liver of male Wistar rats (alkaline comet assay), clarify the oxidative nature of DNA damage (hOGG1-modified comet assay), and verify whether resveratrol (RSV) could ameliorate OTA+CIT-induced genotoxicity. Rats were treated orally with OTA (0.125 and 0.250 mg/kg bodyweight (bw)) and CIT (2 mg/kg bw), OTA+CIT combinations and OTA+CIT+RSV (0.250+2+20 mg/kg bw) for 21 days. Both alkaline and hOGG1-modified comet assay showed that DNA damage was more severe in rat kidneys than in liver following mycotoxin treatment. Alkaline comet assay revealed a higher intensity of DNA damage, particularly as measured by tail intensity in the kidneys. Both tail length and tail intensity were OTA dose-dependent, but in combined OTA+CIT treatment these values were similar to CIT alone and lower than in animals treated with single OTA, possibly due to induction of apoptosis. hOGG1-modified comet showed that OTA+CIT evoked greater oxidative DNA damage than single mycotoxins. RSV did not reduce DNA damage measured by alkaline comet assay, but hOGG1-modified comet showed that RSV ameliorated OTA+CIT genotoxicity in the kidneys. Apart from oxidative stress, other mechanisms of DNA damage are involved in OTA and CIT genotoxicity. In rat kidneys RSV can reduce but not overcome oxidative DNA damage induced by combined OTA and CIT.

scholarly journals Evaluation of DNA damage in tobacco associated human buccal cells using comet assay

2021 ◽  
Vol 94 (2) ◽  
pp. 214-219
Author(s):  
Shanmugam Mohanapriya ◽  
Thangadurai Maheswaran ◽  
Nalliapan Ganapathy ◽  
Thukanayakanpalayam Ragunathan Yoithappr ◽  
Janardhanam Dineshshankar ◽  
...  
Keyword(s):  
Dna Damage ◽  
Comet Assay ◽  
Oral Mucosa ◽  
Precancerous Lesions ◽  
Tail Length ◽  
Assay Method ◽  
Oral Lesions ◽  
Buccal Cells ◽  
Group I ◽  
Tobacco Usage

Aim and objective. To assess the DNA damage in tobacco associated human buccal cells using comet assay. Methods. The study included 75 study subjects, which were divided into 3 groups on the basis of tobacco usage. Group I - 25 individuals with no history of tobacco usage, Group II - 25 individuals with tobacco usage but without oral lesions and Group III - 25 individuals with tobacco associated oral lesions. Cytological smears collected from these individuals were used to assess the tobacco associated DNA damage by measuring the tail length in the comet assay method. Results. The average tail length was found to be 1.46 µm in the normal mucosa, 2.86 µm in tobacco users without oral lesions, 3.86 µm in the lesional sites of tobacco users and 3.67 µm in the non-lesional sites of these individuals. Factors like age, gender, duration and different forms of tobacco habit had their own impact on the oral mucosa. Conclusion. Comet assay helps assess the subclinical genetic changes of oral mucosa even before the clinical manifestations of the precancerous lesions appeared due to tobacco usage. Thus, comet assay may bloom out as a novel adjuvant tool for the prevention of oral cancer in the near future.

scholarly journals Evaluation of Genetic Damage in Oreochromis mossambicus Exposed to Selected Nanoparticles by Using Micronucleus and Comet Bioassays

2018 ◽  
Vol 76 (3) ◽  
pp. 115-124 ◽  
Author(s):  
Puthan Variyam Vidya ◽  
Kumari Chidambaran Chitra
Keyword(s):  
Dna Damage ◽  
Comet Assay ◽  
Micronucleus Test ◽  
Tail Length ◽  
Oreochromis Mossambicus ◽  
Control Group ◽  
Dependent Manner ◽  
Genetic Damage ◽  
Sublethal Concentrations

Abstract The purpose of the present study is to extend knowledge on the adverse effects of nanoparticles by evaluating genotoxicity as environmental risk assessment in Oreochromis mossambicus. Fish were exposed to sublethal concentrations of the selected nanoparticles, namely silicon dioxide (SiO2NPs-12mg/L), aluminium oxide (Al2O3NPs-4mg/L), titanium dioxide (TiO2NPs-16.4mg/L) and iron oxide (Fe3O4NPs-15mg/L) for short-term (24, 72 and 96 h) and long-term durations (15, 30 and 60 days). Genetic damages such as cytoplasmic, nuclear and DNA damage were measured in the erythrocytes of fish by using standard genotoxicity tests such as micronucleus test and comet assay. The frequencies of micronuclei along with nuclear and cytoplasmic abnormalities were scored and compared with the control group. The intensity of micronuclei along with other nuclear and cytoplasmic anomalies are found to be increased significantly (p<0.05) in time-dependent manner in all exposure groups when compared to the control group, thereby indicating chromosomal damage as a result of contact with nanoparticles. The tail length and percent of tail DNA within the comet significantly (p<0.05) increased in time-dependant manner after exposure to all nanoparticles, demonstrating an increase in DNA damage. Taken together, by using micronucleus test and comet assay, it is evident that the selected nanoparticles at sublethal concentrations induced genetic damage in Oreochromis mossambicus.

scholarly journals Investigating Genetic Damage in Peripheral Lymphocytes of Radiation Workers at Al-Tuwaitha Site in Iraq Using Four Genetic End-Points

2014 ◽  
Vol 8 (2) ◽  
pp. 5-10
Author(s):  
Amel J. Mutter ◽  
Abdulsahib K. Ali ◽  
Abdullah A. K. ◽  
Haider Y. L. ◽  
Ali H. F
Keyword(s):  
Comet Assay ◽  
Genetic Parameter ◽  
Tail Length ◽  
Control Group ◽  
Tail Moment ◽  
Genetic Damage ◽  
Peripheral Lymphocytes ◽  
Significant Difference ◽  
Radiation Workers ◽  
The Mean

The present study aims to use the biological techniques in a genotoxicity assessment of DNA damage in peripheral lymphocytes of radiation workers at Al-Tuwaitha site due to decommissioning to radioactive contamination as a result of work during January 2010 to December 2011. The subjects were divided into two groups: (i) 85 workers from radiation workers at Al-Tuwaitha site; (ii) 50 controls were matched non-smoking and no alcohol drink. Fresh blood samples were collected from the workers and controls. Four genetic parameter were studied using the micronucleus (MN) test, nuclear division index (NDI) test, the comet assay and hypoxanthine guanine phosphoribosyl transferase (HPRT) mutation assay. The results of the MN test showed that the average of MN per cell (Mean ± SE) in workers were 0.025 ± 0.0016 MN/ cells, which were significantly higher than those 0.010 ± 0.0006 MN/ cells in controls P< 0.01. While, the results of NDI test the average of NDI (Mean ± SE) in workers were 1.154 ± 0.0089 when compared with the control 1.322 ± 0.0117, which were significant increase p<0.01. It was found in the comet assay that the mean tail length (Mean ± SE) of radiation workers and controls were 17.69 ± 0.23 µm and 14.05 ± 0.13 µm, respectively. There was a significant difference between radiation workers and controls for mean tail length P < 0.01, but the difference between the mean tail moment (Mean ± SE) 14.22 ±0.21 of workers and mean tail moment 12.96± 0.15 of controls was not significant P> 0.01. Mean while, the results of the average of mutation frequency for HPRT were no significant differences rate for radiation workers compared with the control group P> 0.01. In conclusion, the results of our experiment suggest that the accumulation of genetic damage is detectable in peripheral lymphocytes of radiation workers at Al-Tuwaitha site. Also, the current results of frequency MN and NDI within of normal values according of the technical report of International Atomic Energy Agency (IAEA) No. 405, 2001.

Basal damage and oxidative DNA damage in children with chronic kidney disease measured by use of the comet assay

2011 ◽  
Vol 725 (1-2) ◽  
pp. 22-28 ◽  
Author(s):  
Banu Aykanat ◽  
Gonca Cakmak Demircigil ◽  
Kibriya Fidan ◽  
Necla Buyan ◽  
Kaan Gulleroglu ◽  
...  
Keyword(s):  
Chronic Kidney Disease ◽  
Dna Damage ◽  
Kidney Disease ◽  
Comet Assay ◽  
Oxidative Dna Damage

scholarly journals Protection of sperm DNA against oxidative stress in vivo by accessory sex gland secretions in male hamsters

Reproduction ◽  
2002 ◽  
pp. 491-499 ◽  
Author(s):  
H Chen ◽  
MP Cheung ◽  
PH Chow ◽  
AL Cheung ◽  
W Liu ◽  
...  
Keyword(s):  
Dna Damage ◽  
Comet Assay ◽  
Prostate Gland ◽  
Single Strand ◽  
Ventral Prostate ◽  
Control Group ◽  
Dna Breakage ◽  
Accessory Glands ◽  
Sperm Dna ◽  
Epididymal Spermatozoa

Reactive oxygen species scavengers present in male accessory sex gland secretions might afford antioxidant protection to sperm DNA. This study was conducted to determine whether accessory sex gland secretions protect the genome and function of spermatozoa against oxidative damage in the uterus. Male golden hamsters were divided into four experimental groups: (i) all accessory sex glands removed; (ii) ampullary glands removed; (iii) ventral prostate gland removed and (iv) sham-operated controls. Ejaculated spermatozoa recovered from uteri 15-30 min after mating with experimental males and caput and cauda epididymal spermatozoa obtained from intact males were incubated in 0-20 mmol NADPH l(-1) for 2 h. These spermatozoa and untreated uterine spermatozoa were processed for two types of comet assay (single cell gel electrophoresis): alkaline comet assay (pH > 13) which revealed single-strand DNA breakage and neutral comet assay (pH 9) which revealed double-strand DNA breakage. In comparison with the sham-operated controls, spermatozoa that had not been exposed to accessory sex gland secretions had a higher incidence and more extensive single-strand DNA damage with increasing concentrations of NADPH. Spermatozoa from hamsters without ampullary glands and from hamsters without the ventral prostate glands were similar to those of the control group. After incubation with NADPH, the capacity of spermatozoa from hamsters without accessory glands and from sham-operated controls to fuse with oocytes in vitro was reduced. However, only hamsters without accessory glands showed a negative correlation between single-strand DNA damage and sperm-oocyte fusion. Cauda epididymal spermatozoa were less susceptible to NADPH treatment compared with caput epididymal spermatozoa. The results of the present study showed that male accessory sex gland secretions can preserve the integrity of the sperm genome.

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