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1.
Izv Akad Nauk Ser Biol ; (6): 645-52, 2013.
Article in Russian | MEDLINE | ID: mdl-25518549

ABSTRACT

The response of ejaculated bovine spermatozoa to gold nanoparticles was studied by the standard method of nuclear chromatin decondensation in vitro. After the treatment of semen samples with a hydrosol containing gold nanoparticles with an average diameter of 3.0 nm and a concentration of 1 x 10(15) particles/mL, the ability of sperm nuclei to decondense in the presence of sodium dodecyl sulfate (SDS) and dithiothreitol (DTT) dramatically changed compared to the control. The frequencies of gametes with nondecondensed ("intact"), partially decondensed, and completely decondensed nuclei correlated as 40 : 32 : 28% and 0 : 36 : 64% in the experiment and the control, respectively. Moreover, the appearance of a sufficiently large number of gametes with destructed and almost completely destroyed nuclei was noticed in the spermatozoa treated with gold nanoparticles. This article suggests the putative mechanisms of action of ultrasmall gold nanoparticles on the structural and functional integrity of the deoxyribonucleoprotein (DNP) complex of mature male gametes.


Subject(s)
Chromatin/drug effects , Gold/adverse effects , Metal Nanoparticles/adverse effects , Spermatozoa/drug effects , Animals , Cattle , Cell Nucleus , Gold/administration & dosage , Male , Metal Nanoparticles/administration & dosage , Particle Size , Spermatozoa/cytology
2.
Izv Akad Nauk Ser Biol ; (3): 279-87, 2012.
Article in Russian | MEDLINE | ID: mdl-22834311

ABSTRACT

The response of the mouse male germ cells exposed to gold nanoparticles (approximately 2.5 nm) was studied. Our investigation demonstrates that treatment with Au nanoparticles for four days does not impair the architecture of the spermatogenic epithelium. Cytogenetic evaluation using micronucleus assay showed that gold nanoparticles can affect the chromosomes of early primary spermatocytes. However, gold nanoparticles did not induce chromosome abnormalities in spermatogonial stem cells. Further, the cauda epididymal sperm was isolated on the 14th day after treatment and was incubated in SDS solution (Na sodium dodecyl) and then in a solution containing DTT (dithiothreitol) to induce nuclear chromatin decondensation. Observations showed that after four days of treatment of spermiogenic (postmeiotic) cells with gold nanoparticles the decondensation process had no differences from the control. On the contrary, in the experiment with the same cells and period of fixation but with a single exposure to gold nanoparticles, the number of mature gametes with totally decondensed nuclei reached 100% as opposed to 44% in the controls.


Subject(s)
Gold/pharmacology , Metal Nanoparticles , Spermatogenesis/drug effects , Spermatogonia/drug effects , Animals , Chromatin/drug effects , Dithiothreitol/pharmacology , Epididymis/cytology , Epididymis/drug effects , Epithelium/drug effects , Male , Mice , Mice, Inbred C57BL , Sodium Dodecyl Sulfate/pharmacology
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