Pulmonary exposure to carbonaceous nanomaterials and sperm quality

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Pulmonary exposure to carbonaceous nanomaterials and sperm quality. / Skovmand, Astrid; Lauvas, Anna Jacobsen; Christensen, Preben; Vogel, Ulla; Hougaard, Karin Sorig; Goericke-Pesch, Sandra.

In: Particle and Fibre Toxicology, Vol. 15, 10, 2018.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Skovmand, A, Lauvas, AJ, Christensen, P, Vogel, U, Hougaard, KS & Goericke-Pesch, S 2018, 'Pulmonary exposure to carbonaceous nanomaterials and sperm quality', Particle and Fibre Toxicology, vol. 15, 10. https://doi.org/10.1186/s12989-018-0242-8

APA

Skovmand, A., Lauvas, A. J., Christensen, P., Vogel, U., Hougaard, K. S., & Goericke-Pesch, S. (2018). Pulmonary exposure to carbonaceous nanomaterials and sperm quality. Particle and Fibre Toxicology, 15, [10]. https://doi.org/10.1186/s12989-018-0242-8

Vancouver

Skovmand A, Lauvas AJ, Christensen P, Vogel U, Hougaard KS, Goericke-Pesch S. Pulmonary exposure to carbonaceous nanomaterials and sperm quality. Particle and Fibre Toxicology. 2018;15. 10. https://doi.org/10.1186/s12989-018-0242-8

Author

Skovmand, Astrid ; Lauvas, Anna Jacobsen ; Christensen, Preben ; Vogel, Ulla ; Hougaard, Karin Sorig ; Goericke-Pesch, Sandra. / Pulmonary exposure to carbonaceous nanomaterials and sperm quality. In: Particle and Fibre Toxicology. 2018 ; Vol. 15.

Bibtex

@article{3754e01c17ab4bd3a7998a2ece180c95,
title = "Pulmonary exposure to carbonaceous nanomaterials and sperm quality",
abstract = "BackgroundSemen quality parameters are potentially affected by nanomaterials in several ways: Inhaled nanosized particles are potent inducers of pulmonary inflammation, leading to the release of inflammatory mediators. Small amounts of particles may translocate from the lungs into the lung capillaries, enter the systemic circulation and ultimately reach the testes. Both the inflammatory response and the particles may induce oxidative stress which can directly affect spermatogenesis. Furthermore, spermatogenesis may be indirectly affected by changes in the hormonal milieu as systemic inflammation is a potential modulator of endocrine function. The aim of this study was to investigate the effects of pulmonary exposure to carbonaceous nanomaterials on sperm quality parameters in an experimental mouse model.MethodsEffects on sperm quality after pulmonary inflammation induced by carbonaceous nanomaterials were investigated by intratracheally instilling sexually mature male NMRI mice with four different carbonaceous nanomaterials dispersed in nanopure water: graphene oxide (18 μg/mouse/i.t.), Flammruss 101, Printex 90 and SRM1650b (0.1 mg/mouse/i.t. each) weekly for seven consecutive weeks. Pulmonary inflammation was determined by differential cell count in bronchoalveolar lavage fluid. Epididymal sperm concentration and motility were measured by computer-assisted sperm analysis. Epididymal sperm viability and morphological abnormalities were assessed manually using Hoechst 33,342/PI flourescent and Spermac staining, respectively. Epididymal sperm were assessed with regard to sperm DNA integrity (damage). Daily sperm production was measured in the testis, and testosterone levels were measured in blood plasma by ELISA.ResultsNeutrophil numbers in the bronchoalveolar fluid showed sustained inflammatory response in the nanoparticle-exposed groups one week after the last instillation. No significant changes in epididymal sperm parameters, daily sperm production or plasma testosterone levels were found.ConclusionDespite the sustained pulmonary inflammatory response, an eight week exposure to graphene oxide, Flammruss 101, Printex 90 and the diesel particle SRM1650b in the present study did not appear to affect semen parameters, daily sperm production or testosterone concentration in male NMRI mice.",
keywords = "Nanomaterials, Particles, Toxicity, Semen parameters, Pulmonary exposure, Computer-assisted sperm analysis, Inflammation",
author = "Astrid Skovmand and Lauvas, {Anna Jacobsen} and Preben Christensen and Ulla Vogel and Hougaard, {Karin Sorig} and Sandra Goericke-Pesch",
year = "2018",
doi = "10.1186/s12989-018-0242-8",
language = "English",
volume = "15",
journal = "Particle and Fibre Toxicology",
issn = "1743-8977",
publisher = "BioMed Central",

}

RIS

TY - JOUR

T1 - Pulmonary exposure to carbonaceous nanomaterials and sperm quality

AU - Skovmand, Astrid

AU - Lauvas, Anna Jacobsen

AU - Christensen, Preben

AU - Vogel, Ulla

AU - Hougaard, Karin Sorig

AU - Goericke-Pesch, Sandra

PY - 2018

Y1 - 2018

N2 - BackgroundSemen quality parameters are potentially affected by nanomaterials in several ways: Inhaled nanosized particles are potent inducers of pulmonary inflammation, leading to the release of inflammatory mediators. Small amounts of particles may translocate from the lungs into the lung capillaries, enter the systemic circulation and ultimately reach the testes. Both the inflammatory response and the particles may induce oxidative stress which can directly affect spermatogenesis. Furthermore, spermatogenesis may be indirectly affected by changes in the hormonal milieu as systemic inflammation is a potential modulator of endocrine function. The aim of this study was to investigate the effects of pulmonary exposure to carbonaceous nanomaterials on sperm quality parameters in an experimental mouse model.MethodsEffects on sperm quality after pulmonary inflammation induced by carbonaceous nanomaterials were investigated by intratracheally instilling sexually mature male NMRI mice with four different carbonaceous nanomaterials dispersed in nanopure water: graphene oxide (18 μg/mouse/i.t.), Flammruss 101, Printex 90 and SRM1650b (0.1 mg/mouse/i.t. each) weekly for seven consecutive weeks. Pulmonary inflammation was determined by differential cell count in bronchoalveolar lavage fluid. Epididymal sperm concentration and motility were measured by computer-assisted sperm analysis. Epididymal sperm viability and morphological abnormalities were assessed manually using Hoechst 33,342/PI flourescent and Spermac staining, respectively. Epididymal sperm were assessed with regard to sperm DNA integrity (damage). Daily sperm production was measured in the testis, and testosterone levels were measured in blood plasma by ELISA.ResultsNeutrophil numbers in the bronchoalveolar fluid showed sustained inflammatory response in the nanoparticle-exposed groups one week after the last instillation. No significant changes in epididymal sperm parameters, daily sperm production or plasma testosterone levels were found.ConclusionDespite the sustained pulmonary inflammatory response, an eight week exposure to graphene oxide, Flammruss 101, Printex 90 and the diesel particle SRM1650b in the present study did not appear to affect semen parameters, daily sperm production or testosterone concentration in male NMRI mice.

AB - BackgroundSemen quality parameters are potentially affected by nanomaterials in several ways: Inhaled nanosized particles are potent inducers of pulmonary inflammation, leading to the release of inflammatory mediators. Small amounts of particles may translocate from the lungs into the lung capillaries, enter the systemic circulation and ultimately reach the testes. Both the inflammatory response and the particles may induce oxidative stress which can directly affect spermatogenesis. Furthermore, spermatogenesis may be indirectly affected by changes in the hormonal milieu as systemic inflammation is a potential modulator of endocrine function. The aim of this study was to investigate the effects of pulmonary exposure to carbonaceous nanomaterials on sperm quality parameters in an experimental mouse model.MethodsEffects on sperm quality after pulmonary inflammation induced by carbonaceous nanomaterials were investigated by intratracheally instilling sexually mature male NMRI mice with four different carbonaceous nanomaterials dispersed in nanopure water: graphene oxide (18 μg/mouse/i.t.), Flammruss 101, Printex 90 and SRM1650b (0.1 mg/mouse/i.t. each) weekly for seven consecutive weeks. Pulmonary inflammation was determined by differential cell count in bronchoalveolar lavage fluid. Epididymal sperm concentration and motility were measured by computer-assisted sperm analysis. Epididymal sperm viability and morphological abnormalities were assessed manually using Hoechst 33,342/PI flourescent and Spermac staining, respectively. Epididymal sperm were assessed with regard to sperm DNA integrity (damage). Daily sperm production was measured in the testis, and testosterone levels were measured in blood plasma by ELISA.ResultsNeutrophil numbers in the bronchoalveolar fluid showed sustained inflammatory response in the nanoparticle-exposed groups one week after the last instillation. No significant changes in epididymal sperm parameters, daily sperm production or plasma testosterone levels were found.ConclusionDespite the sustained pulmonary inflammatory response, an eight week exposure to graphene oxide, Flammruss 101, Printex 90 and the diesel particle SRM1650b in the present study did not appear to affect semen parameters, daily sperm production or testosterone concentration in male NMRI mice.

KW - Nanomaterials

KW - Particles

KW - Toxicity

KW - Semen parameters

KW - Pulmonary exposure

KW - Computer-assisted sperm analysis

KW - Inflammation

U2 - 10.1186/s12989-018-0242-8

DO - 10.1186/s12989-018-0242-8

M3 - Journal article

C2 - 29386028

VL - 15

JO - Particle and Fibre Toxicology

JF - Particle and Fibre Toxicology

SN - 1743-8977

M1 - 10

ER -

ID: 190433355