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Dive into the research topics where Michał Oczkowski is active.

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Featured researches published by Michał Oczkowski.


Journal of Applied Toxicology | 2012

Time‐dependent biodistribution and excretion of silver nanoparticles in male Wistar rats

K. Dziendzikowska; Joanna Gromadzka-Ostrowska; Anna Lankoff; Michał Oczkowski; A. Krawczyńska; J. Chwastowska; M. Sadowska-Bratek; E. Chajduk; M. Wojewódzka; Maria Dusinska; M. Kruszewski

Silver nanoparticles (AgNPs) are the most commonly used nanoparticles owing to their antimicrobial properties. The motivation of the present study was (1) to analyze the effect of silver particle size on rat tissue distribution at different time points, (2) to determine the accumulation of AgNPs in potential rat target organs, (3) to analyze the intracellular distribution of AgNPs and (4) to examine the excretion of AgNPs by urine and feces. AgNPs were characterized by dynamic light scattering (DLS), zeta potential measurements, BET surface area measurements, transmission and scanning electron microscopy. AgNPs (20 and 200 nm) were administered intravenously (i.v.) to male Wistar rats at a dose of 5 mg kg–1 of body weight. Biological material was sampled 24 h, 7 and 28 days after injection. Using inductively coupled plasma‐mass spectrometry (ICP‐MS) and transmission electron microscopy (TEM) it was observed that AgNPs translocated from the blood to the main organs and the concentration of silver in tissues was significantly higher in rats treated with 20 nm AgNPs as compared with 200 nm AgNPs. The highest concentration of silver was found in the liver after 24 h. After 7 days, a high level of silver was observed in the lungs and spleen. The silver concentration in the kidneys and brain increased during the experiment and reached the highest concentration after 28 days. Moreover, the highest concentration of AgNPs was observed in the urine 1 day after the injection, maintained high for 14 days and then decreased. The fecal level of silver in rats was the highest within 2 days after AgNPs administration and then decreased. Copyright


Toxicology and Applied Pharmacology | 2016

Progressive effects of silver nanoparticles on hormonal regulation of reproduction in male rats.

K. Dziendzikowska; Agata Krawczyńska; Michał Oczkowski; Tomasz Królikowski; K. Brzóska; Anna Lankoff; M. Dziendzikowski; T. Stępkowski; M. Kruszewski; Joanna Gromadzka-Ostrowska

The growing use of silver nanoparticles (AgNPs) in various applications, including consumer, agriculture and medicine products, has raised many concerns about the potential risks of nanoparticles (NPs) to human health and the environment. An increasing body of evidence suggests that AgNPs may have adverse effects of humans, thus the aim of this study was to investigate the effects of AgNPs on the male reproductive system. Silver particles (20nm AgNPs (groups Ag I and Ag II) and 200nm Ag sub-micron particles (SPs) (group Ag III)) were administered intravenously to male Wistar rats at a dose of 5 (groups Ag I and Ag III) or 10 (group Ag II) mg/kg of body weight. The biological material was sampled 24h, 7days and 28days after injection. The obtained results revealed that the AgNPs had altered the luteinising hormone concentration in the plasma and the sex hormone concentration in the plasma and testes. Plasma and intratesticular levels of testosterone and dihydrotestosterone were significantly decreased both 7 and 28days after treatment. No change in the prolactin and sex hormone-binding globulin concentration was observed. Exposure of the animals to AgNPs resulted in a considerable decrease in 5α-reductase type 1 and the aromatase protein level in the testis. Additionally, expression analysis of genes involved in steroidogenesis and the steroids metabolism revealed significant down-regulation of Star, Cyp11a1, Hsd3b1, Hsd17b3 and Srd5a1 mRNAs in AgNPs/AgSPs-exposed animals. The present study demonstrates the potential adverse effect on the hormonal regulation of the male reproductive function following AgNP/AgSP administration, in particular alterations of the sex steroid balance and expression of genes involved in steroidogenesis and the steroids metabolism.


Environmental Toxicology and Pharmacology | 2017

Proinflammatory effects of diesel exhaust particles from moderate blend concentrations of 1st and 2nd generation biodiesel in BEAS-2B bronchial epithelial cells—The FuelHealth project

Tonje Skuland; Magne Refsnes; Pål Magnusson; Michał Oczkowski; Joanna Gromadzka-Ostrowska; Marcin Kruszewski; Remigiusz Mruk; Oddvar Myhre; Anna Lankoff; Johan Øvrevik

Biodiesel fuel fuels are introduced at an increasing extent as a more carbon-neutral alternative to reduce CO2-emissions, compared to conventional diesel fuel. In the present study we have investigated the impact of increasing the use of 1st generation fatty acid methyl ester (FAME) biodiesel from current 7% blend (B7) to 20% blend (B20), or by increasing the biodiesel content by adding 2nd generation hydrotreated vegetable oil (HVO) based biodiesel (SHB; Synthetic Hydrocarbon Biofuel) on toxicity of diesel exhaust particles (DEP) in an in vitro system. Human bronchial epithelial BEAS-2B cells were exposed for 4 and 20h to DEP from B7, B20 and SHB at different concentrations, and examined for effects on gene expression of interleukin 6 (IL-6), CXCL8 (IL-8), CYP1A1 and heme oxygenase-1 (HO-1). The results show that both B20 and SHB were more potent inducers of IL-6 expression compared to B7. Only B20 induced statistically significant increases in CXCL8 expression. By comparison the rank order of potency to induce CYP1A1 was SHB>B7>B20. No statistically significant difference were observed form HO-1 expression, suggesting that the differences in cytokine responses were not due to oxidative stress. The results show that even moderate increases in biodiesel blends, from 7% to 20%, may increase the proinflammatory potential of emitted DEP in BEAS-2B cells. This effect was observed for both addition of 1st generation FAME and 2nd generation HVO biodiesel.


Inhalation Toxicology | 2017

No adverse lung effects of 7- and 28-day inhalation exposure of rats to emissions from petrodiesel fuel containing 20% rapeseed methyl esters (B20) with and without particulate filter – the FuelHealth project

Pål Magnusson; Michał Oczkowski; Johan Øvrevik; Małgorzata Gajewska; Jacek Wilczak; Jacek Biedrzycki; K. Dziendzikowska; Dariusz Kamola; Tomasz Królikowski; Marcin Kruszewski; Anna Lankoff; Remigiusz Mruk; Gunnar Brunborg; Christine Instanes; Joanna Gromadzka-Ostrowska; Oddvar Myhre

Abstract Increased use of biofuels raises concerns about health effects of new emissions. We analyzed relative lung health effects, on Fisher 344 rats, of diesel engine exhausts emissions (DEE) from a Euro 5-classified diesel engine running on petrodiesel fuel containing 20% rapeseed methyl esters (B20) with and without diesel particulate filter (DPF). One group of animals was exposed to DEE for 7 days (6 h/day), and another group for 28 days (6 h/day, 5 days/week), both with and without DPF. The animals (n = 7/treatment) were exposed in whole body exposure chambers. Animals breathing clean air were used as controls. Genotoxic effects of the lungs by the Comet assay, histological examination of lung tissue, bronchoalveolar lavage fluid (BALF) markers of pulmonary injury, and mRNA markers of inflammation and oxidative stress were analyzed. Our results showed that a minor number of genes related to inflammation were slightly differently expressed in the exposed animals compared to control. Histological analysis also revealed only minor effects on inflammatory tissue markers in the lungs, and this was supported by flow cytometry and ELISA analysis of cytokines in BALF. No exposure-related indications of genotoxicity were observed. Overall, exposure to DEE with or without DPF technology produced no adverse effects in the endpoints analyzed in the rat lung tissue or the BALF. Overall, exposure to DEE from a modern Euro 5 light vehicle engine run on B20 fuel with or without DPF technology produced no adverse effects in the endpoints analyzed in the rat lung tissue or the BALF.


Alcoholism and Drug Addiction | 2014

Wpływ występujących w piwie związków polifenolowych na organizm – przegląd literatury

Aleksandra Kołota; Michał Oczkowski; Joanna Gromadzka-Ostrowska

Abstract The long term health consequences of alcoholic beverage drinking are related primarily to the unfavourable influence of ethyl alcohol on the organism, which contributes to an increased risk of the development of various diseases. It is obvious that the excessive drinking of alcoholic beverages, including beer, has a negative impact on health, but it must be emphasised that compounds of hops are characterised by a multidirectional influence, including a health-related properties. Hop is a valuable source of polyphenolic compounds, which were classified into several structural groups characterised by various biological activities. Studies concerning bioactive substances present in beer, indicate that certain flavonoid compounds derived from hop are characterised by antioxidant, anti-inflammatory, anti-cancer, antiangiogenic or estrogenic properties. Due to these properties, it is important to determine the potential applicability of selected polyphenol compounds. Examination of their effects on the human body, as well as understanding the mechanisms of this influence will allow the development of methods for using these compounds in natural adjuvant treatment. The aim of the study was to characterise the main flavonoids found in beer – xanthohumol, isoxanthohumol and 8-prenylnaringenin and specify their multidirectional impact on the human body based on the literature.


Environmental Toxicology and Pharmacology | 2018

The effects of 1st and 2nd generation biodiesel exhaust exposure on hematological and biochemical blood indices of Fisher344 male rats – The FuelHealth project

K. Dziendzikowska; Małgorzata Gajewska; Jacek Wilczak; Remigiusz Mruk; Michał Oczkowski; Ewa Żyła; Tomasz Królikowski; M. Stachoń; Johan Øvrevik; Oddvar Myhre; Marcin Kruszewski; M. Wojewódzka; Anna Lankoff; Joanna Gromadzka-Ostrowska

Diesel exhaust emissions (DEE), being one of the main causes of ambient air pollution, exert a detrimental effect on human health and increase morbidity and mortality related to cardiovascular and pulmonary diseases. Therefore, the objective of the present study was to investigate potential adverse effects of exhausts emissions from B7 fuel, the first-generation biofuel containing 7% of fatty acid methyl esters (FAME), and SHB20 fuel, the second-generation biofuel containing 20% FAME/hydrotreated vegetable oil (HVO), after a whole-body exposure with and without diesel particle filter (DPF). The experiment was performed on 95 male Fischer 344 rats, divided into 10 groups (8 experimental, 2 control). Animals were exposed to DEE (diluted with charcoal-filtered room air to 2.1-2.2% (v/v)) for 7 or 28 days (6 h/day, 5 days/week) in an inhalation chamber. DEE originated from Euro 5 engine with or without DPF treatment, run on B7 or SHB20 fuel. Animals in the control groups were exposed to clean air. Our results showed that the majority of haematological and biochemical parameters examined in blood were at a similar level in the exposed and control animals. However, exposure to DEE from the SHB20 fuel caused an increase in the number of red blood cells (RBC) and haemoglobin concentration. Moreover, 7 days exposure to DEE from SHB20 fuel induced genotoxic effects manifested by increased levels of DNA single-strand breaks in peripheral blood lymphocytes. Furthermore, inhalation of both types of DEE induced oxidative stress and caused imbalance of anti-oxidant defence enzymes. In conclusion, exposure to DEE from B7, which was associated with higher exposure to polycyclic aromatic hydrocarbons, resulted in decreased number of T and NK lymphocytes, while DEE from SHB20 induced a higher level of DNA single-strand breaks, oxidative stress and increased red blood cells parameters. Additionally, DPF technology generated increased number of smaller PM and made the DEE more reactive and more harmful, manifested as deregulation of redox balance.


Food & Function | 2015

The effect of low or high molecular weight oat beta-glucans on the inflammatory and oxidative stress status in the colon of rats with LPS-induced enteritis

Jacek Wilczak; Katarzyna Błaszczyk; Dariusz Kamola; Małgorzata Gajewska; Joanna Harasym; Małgorzata Jałosińska; Sylwia Gudej; Dominika Suchecka; Michał Oczkowski; Joanna Gromadzka-Ostrowska


Journal of Functional Foods | 2015

Antioxidative and anti-inflammatory effects of high beta-glucan concentration purified aqueous extract from oat in experimental model of LPS-induced chronic enteritis

Dominika Suchecka; Joanna Harasym; Jacek Wilczak; Małgorzata Gajewska; Michał Oczkowski; Sylwia Gudej; Katarzyna Błaszczyk; Dariusz Kamola; R. Filip; Joanna Gromadzka-Ostrowska


Food and Chemical Toxicology | 2015

Silver and titanium dioxide nanoparticles alter oxidative/inflammatory response and renin-angiotensin system in brain.

Agata Krawczyńska; K. Dziendzikowska; Joanna Gromadzka-Ostrowska; Anna Lankoff; Andrzej Przemysław Herman; Michał Oczkowski; Tomasz Królikowski; Jacek Wilczak; Maria Wojewódzka; Marcin Kruszewski


Pathophysiology | 2018

BENEFICIAL EFFECTS OF OAT β-GLUCANS ON THE LARGE INTESTINAL INFLAMMATION

K. Dziendzikowska; Ewa Żyła; Jacek Wilczak; Dariusz Kamola; Michał Oczkowski; Tomasz Królikowski; Małgorzata Gajewska; Joanna Harasym; Joanna Gromadzka Ostrowska

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Joanna Gromadzka-Ostrowska

Warsaw University of Life Sciences

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Anna Lankoff

Jan Kochanowski University

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K. Dziendzikowska

Warsaw University of Life Sciences

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Jacek Wilczak

Warsaw University of Life Sciences

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Tomasz Królikowski

Warsaw University of Life Sciences

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Marcin Kruszewski

Translational Research Institute

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Małgorzata Gajewska

Warsaw University of Life Sciences

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Remigiusz Mruk

Warsaw University of Life Sciences

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Johan Øvrevik

Norwegian Institute of Public Health

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Dariusz Kamola

Warsaw University of Life Sciences

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