Mixed-Function Oxygenases, Oxidative Stress, and Chromosomal Damage Measured in Lesser Scaup Wintering on the Indiana Harbor Canal

2000 ◽  
Vol 38 (4) ◽  
pp. 522-529 ◽  
Author(s):  
T. W. Custer ◽  
C. M. Custer ◽  
R. K. Hines ◽  
D. W. Sparks ◽  
M. J. Melancon ◽  
...  
2020 ◽  
Vol 13 (2) ◽  
pp. 137-143
Author(s):  
Abeer M. Rababa’h ◽  
Samah A. Hussein ◽  
Omar F. Khabour ◽  
Karem H. Alzoubi

Background: Methotrexate is an antagonist of folic acid that has been shown to be genotoxic to healthy body cells via induction of oxidative stress. Cilostazol is a phosphodiesterase III inhibitor and a potent antioxidant drug. Objectives: To evaluate the potential protective effect of cilostazol on methotrexate genotoxicity. Results: Methotrexate significantly increased the frequency of CAs and SCEs (p < 0.0001) as compared to control cultures. This chromosomal damage induced by methotrexate was considerably decreased by pretreatment of the cells with cilostazol (P < 0.01). Moreover, the results showed that methotrexate resulted in a notable reduction (P < 0.01) in cells kinetic parameters, the mitotic index (MI) and the proliferative index (PI). Similarly, cilostazol significantly reduced the mitotic index, which could be related to the anti-proliferative effect (P < 0.01). Conclusion: Methotrexate is genotoxic, and cilostazol could prevent the methotrexate-induced chromosomal damage with no modulation of methotrexate-induced cytotoxicity.


2021 ◽  
Vol 2021 ◽  
pp. 1-8
Author(s):  
Carla Nascimento ◽  
Milena Simões Peixoto ◽  
Luiz Fernando Fonte Boa ◽  
Caroline Coelho de Faria ◽  
Tulio Senna Fonseca Costa ◽  
...  

Obesity is usually linked to oxidative stress, which can lead to damage to biomolecules. The combination of aerobic and strength exercises seems to induce health benefits in obese individuals, but little is known about the effects of combined physical exercise on redox homeostasis and DNA damage in this population. Thus, the aim of the current study was to determine the effects of 16 weeks of combined physical exercise on biomarkers of oxidative stress and DNA damage in obese women. 17 obese women underwent 16 weeks of a combined physical training program, 3 times per week. Anthropometric and biochemical parameters, serum superoxide dismutase (SOD) and glutathione peroxidase activity, plasma 8-isoprostane levels, and DNA and chromosomal damage were evaluated before and after physical training. Combined physical exercise training decreased body weight ( 83.2 ± 9.6 vs. 80.2 ± 9.6  kg), body mass index ( 33.8 ± 3.6 vs. 32.6 ± 3.7  kg·m-2), body fat ( 40.2 ± 2.6 vs. 39.0 ± 3.2 %), and waist circumference ( 99.3 ± 9.4 vs. 94.1 ± 8.8  cm), while the fat-free mass was augmented ( 59.9 ± 2.9 vs. 60.7 ± 3.1  kg). Moreover, blood glucose reduced ( 113.5 ± 29.6 vs. 107.3 ± 28.9  mg/dL) along with high-density lipoprotein ( 54.6 ± 18.1 vs. 59.0 ± 18.8  mg/dL), TSH ( 2.1 ± 1.1 vs. 2.6 ± 1.2  mIU/mL), and free T4 ( 0.9 ± 0.1 vs. 1.12 ± 0.2  ng/dL) increase after physical exercise training. Plasma 8-isoprostane levels ( 17.24 ± 7.9 vs. 29.11 ± 17.44  pg/mL) and DNA damage ( 34.16 ± 7.1 vs. 45.96 ± 5.8 % DNA in tail) were also higher after physical training. No changes were observed in chromosomal damage levels. These results suggest that 16 weeks of combined exercise training 3 times per week is effective in reducing body fat but also increases oxidative stress and DNA damage in obese women.


Ecotoxicology ◽  
2017 ◽  
Vol 26 (10) ◽  
pp. 1392-1407 ◽  
Author(s):  
Thomas W. Custer ◽  
Christine M. Custer ◽  
Paul M. Dummer ◽  
Emilie Bigorgne ◽  
Elias M. Oziolor ◽  
...  

2008 ◽  
Vol 156 (3) ◽  
pp. 732-738 ◽  
Author(s):  
Kevin P. Kenow ◽  
David J. Hoffman ◽  
Randy K. Hines ◽  
Michael W. Meyer ◽  
John W. Bickham ◽  
...  

2017 ◽  
Vol 7 (1) ◽  
Author(s):  
Bilal Ahmed ◽  
Sourabh Dwivedi ◽  
Malik Zainul Abdin ◽  
Ameer Azam ◽  
Majed Al-Shaeri ◽  
...  

2020 ◽  
Vol 11 (10) ◽  
pp. 8547-8559
Author(s):  
Hongjing Zhao ◽  
Yu Wang ◽  
Mengyao Mu ◽  
Menghao Guo ◽  
Hongxian Yu ◽  
...  

Antibiotics are used worldwide to treat diseases in humans and other animals; most of them and their secondary metabolites are discharged into the aquatic environment, posing a serious threat to human health.


2019 ◽  
Vol 476 (24) ◽  
pp. 3705-3719 ◽  
Author(s):  
Avani Vyas ◽  
Umamaheswar Duvvuri ◽  
Kirill Kiselyov

Platinum-containing drugs such as cisplatin and carboplatin are routinely used for the treatment of many solid tumors including squamous cell carcinoma of the head and neck (SCCHN). However, SCCHN resistance to platinum compounds is well documented. The resistance to platinum has been linked to the activity of divalent transporter ATP7B, which pumps platinum from the cytoplasm into lysosomes, decreasing its concentration in the cytoplasm. Several cancer models show increased expression of ATP7B; however, the reason for such an increase is not known. Here we show a strong positive correlation between mRNA levels of TMEM16A and ATP7B in human SCCHN tumors. TMEM16A overexpression and depletion in SCCHN cell lines caused parallel changes in the ATP7B mRNA levels. The ATP7B increase in TMEM16A-overexpressing cells was reversed by suppression of NADPH oxidase 2 (NOX2), by the antioxidant N-Acetyl-Cysteine (NAC) and by copper chelation using cuprizone and bathocuproine sulphonate (BCS). Pretreatment with either chelator significantly increased cisplatin's sensitivity, particularly in the context of TMEM16A overexpression. We propose that increased oxidative stress in TMEM16A-overexpressing cells liberates the chelated copper in the cytoplasm, leading to the transcriptional activation of ATP7B expression. This, in turn, decreases the efficacy of platinum compounds by promoting their vesicular sequestration. We think that such a new explanation of the mechanism of SCCHN tumors’ platinum resistance identifies novel approach to treating these tumors.


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