scholarly journals In vitro effects of single and binary mixtures of regulated mycotoxins and persistent organochloride pesticides on steroid hormone production in MA-10 Leydig cell line

2019 ◽  
Vol 60 ◽  
pp. 272-280 ◽  
Author(s):  
Ukpai A. Eze ◽  
John D. Huntriss ◽  
Michael N. Routledge ◽  
Yun Yun Gong
2007 ◽  
Vol 26 (5) ◽  
pp. 407-417 ◽  
Author(s):  
Katarzyna Augustowska ◽  
Zofia Magnowska ◽  
Maria Kapiszewska ◽  
Ewa L. Gregoraszczuk

The present study was conducted to define the action of a mixture obtained by the extraction and purification of real fly ash, on specific toxicity endpoints, such as hormonal secretion, CYP1A1 expression, DNA damage and cell apoptosis. JEG-3 cell line was exposed in vitro to different doses of 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) or Polychlorinated dibenzo-p-dioxin/Polychlorinated dibenzo-P-furan (PCDD/PCDF) mixture. Both TCDD and the mixture decreased hCG secretion, while inhibition of progesterone levels was noted only under the influence of TCDD. The changes in hormone production were not due to the action on cell viability. There were time-dependent differences in CYP1A1 expression in cells exposed to TCDD and PCDD/PCDF mixture. Both TCDD and PCDD/PCDF mixture did not induce the DNA damage, as evaluated by the comet assay. Significantly lower DNA migration from the head of comet into the comet tail was noted after the removal of reagents. The highest efficiency of this process was noted 4 h after the TCDD and 24 h after the PCDD/PCDF mixture removal. These results suggest that the DNA adducts and/or DNA—DNA cross-links were formed. Neither TCDD nor PCDD/PCDF mixture had any effect on cell apoptosis assessed by caspase-3 activity and Hoechst 33258. Taken together, these findings clearly indicate a weaker action of the mixture when compared with TCDD. However, in both cases, their action was not due to the induction of the DNA damage and subsequent cell apoptosis but due to a direct influence of these toxicants on placental hormone production. Human & Experimental Toxicology ( 2007) 26, 407—417


2020 ◽  
Vol 2020 ◽  
pp. 1-8
Author(s):  
Baofang Jin ◽  
Dalin Sun ◽  
Weihang Dong ◽  
Bing Chen ◽  
Weimin Deng ◽  
...  

Background. The testicular microcirculation was an important aspect of testicular physiology and it offered a stable environment for the transport of nutrients and secretary products in the testis. Yangjing capsule (YC), a traditional Chinese compound herbal prescription, has been proved as an effective drug to ameliorate spermatogenesis, promote testosterone synthesis in vivo, and cure spermatogenesis in clinical practice. Objective. This study was aimed at understanding the potential mechanisms of YC exerting angiogenic effects in the mouse spermatogenesis dysfunction model induced by cyclophosphamide (CP) and MLTC-1 cells. Materials and Methods. Balb/c mice were randomly divided into five groups: control, CP, CP plus YC (630 mg/kg), CP plus YC (1260 mg/kg), and CP plus YC (2520 mg/kg). After 30 days, mice were sacrificed and the expressions of endothelial marker CD34+, angiogenic marker VEGFA, VEGFR1, VEGFR2, and eNOS in the testes of the mice were examined; moreover, Leydig cell line MLTC-1 cells were cultured and treated with different concentrations of YC extracts (YCE), and the expressions of VEGFA, VEGFR1, VEGFR2, and eNOS, as well as the secretion of NO, were evaluated. Results. We observed that YC significantly increased the expressions of VEGFA, VEGFR1, VEGFR2, and eNOS in testes of CP-treated mice; moreover, YCE has led to increased expressions of VEGFA, VEGFR1, VEGFR2, and eNOS and secretion of NO in MLTC-1 in vitro. These data suggested that the YC might be an alternative treatment for the dysfunction of testicular microcirculation by promoting the angiogenesis in the testis.


2011 ◽  
Vol 60 (232) ◽  
pp. 1331-1334
Author(s):  
O.F. Smith ◽  
A.A. Ogunsola ◽  
A.O. Ladokun ◽  
T.A. Ajadi

2018 ◽  
Vol 282 ◽  
pp. 25-36 ◽  
Author(s):  
Venkatanaidu Karri ◽  
Vikas Kumar ◽  
David Ramos ◽  
Eliandre Oliveira ◽  
Marta Schuhmacher

Steroids ◽  
2008 ◽  
Vol 73 (3) ◽  
pp. 328-338 ◽  
Author(s):  
Chandrakesan Parthasarathy ◽  
Karundevi Balasubramanian
Keyword(s):  

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