Warianty tytułu
Języki publikacji
Abstrakty
Badania przeprowadzono na 180 szczurach szczepu Wistar/Hannower w trzech oddzielnych doświadczeniach E, E+C i C. W każdym z doświadczeń zwierzęta dzielono na sześć grup w zależności od sposobu ekspozycji i dodatku witaminy E i С w paszy standardowej. Zwierzęta z grup kontrolnych oraz grup II żywiono paszą standardową dla gryzoni „Murigran", natomiast z grup III-VI w zależności od doświadczenia paszą wzbogaconą witaminą E, E+C lub C. Zwierzęta z grup II-VI eksponowano na 1.0±0.4 mg 03/ m3 powietrza przez okres 5 tygodni, 8 godz. dziennie. Po zakończeniu doświadczeń pobierano od szczurów płuca, wykonywano homogenat tkanki płucnej oraz otrzymywano z niego supernatant. W tkance płucnej metodą chromatografii gazowej oznaczono procentowy udział frakcji jedno i wielonienasyconych kwasów tłuszczowych, w homogenacie tkanki płucnej oznaczono poziom fluorescencji frakcji lipidowej i wodnej produktów peroksydacji lipidów, poziom dialdehydu małonowego i witaminy С metodą spektrofotometryczną, natomiast w supernatancie homogenatu określono zawartość białka całkowitego. Wyniki poddano analizie statystycznej. Stwierdzono niekorzystny wpływ ozonu na płuca zwierząt przejawiający się nasileniem procesów peroksydacji lipidów. Wykazano celowość żywienia szczurów paszą wzbogacaną witaminą E i С w warunkach narażenia ich na wielokrotnie powtarzane ekspozycje na powietrze o zwiększonej koncentracji ozonu.
Three separate experiments (E, E+C and C) were carried out on 180 Wistar/Hannower rats. The rats were divided into six groups in each experiment depending on their exposure and the vitamin E and С supplement in the standard feed. The control animals and the rats from group II were fed the standard ŇMurigranÓ feed for rodents but animals in groups III— VI were fed feed enriched with vitamin E, E+C or C. The experimental animals from groups II-VI were exposed to 1.0ń0.4 mg 03/m3 air for 8 hours a day over 5 weeks. After the experiment, the rat lungs were separated, lung tissue was homogenised and supernatant was obtained. The gas chromatography technique was used to determine the share of mono- and polyunsaturated fatty acids in the lung tissue. The lipid and water percentage in the lipid peroxidation product fluorescence level, and the concentrations of malonyldialdehyde and vitamin С were determined with the use of the spectrophotometric technique. However, the total protein was determined in the homogenised lung tissue supernatant. The results were analysed statistically. A negative ozone influence on the rat lungs was observed resulting in the intensification of lipid peroxidation processes. Based on the experiments, it may be concluded that feeding animals with the feed supplemented with vitamins E and С is beneficial for rats when exposed to air with elevated ozone concentrations.
Słowa kluczowe
Wydawca
Rocznik
Tom
Strony
29-46
Opis fizyczny
s.29-46,rys.,tab.,bibliogr.
Twórcy
Bibliografia
- Abraham W., Delehunt L., Yerger L., Marchette В., Oliver W. 1984. Changes in airway permeability and responsiveness after exposure to ozone. Environ. Res. 34: 110-119.
- Banerjee S., Mudd J. 1992. Reaction of ozone with glycophorin in solution and in lipid vesicles. Arch. Biochem. Biophys. 295: 84-89.
- Barry В., Miller F., Crapo J. 1985. Effects of inhalation of 0,12 and 0,25 parts per milion ozone on the proximal alveolar region of juwenile and adult rats. Lab. Invest. 6: 692-704.
- Buettner G. 1993. The pecking order of free radicals and antioxidants: lipid peroxidation, a-tocopherol, and ascorbate. Arch. Biochem. Biophys. 300 (2): 535-543.
- Chow C., Tappel A. 1972. An enzymatic protective mechanism against lipid peroxidation damage to lungs of ozone-exposed rats. Lipids 7: 518-524.
- Chow C., Plopper C., Chin M., Dungworth D. 1981. Dietary vitamin E and pulmonary biochemical and morphological alterations of rats exposed to 0,1 ppm ozone. Environ. Res. 24: 315-324.
- Chow C., Plopper C., Dungworth D. 1979. Influence of dietary vitamin E on the lungs of ozone-exposed rats. Environ. Res. 20: 309-317.
- Dubick M., Critchfield J., Last J., Cross C., Rucker R. 1983. Ascorbic acid turnover in the mouse following acute ozone exposure. Toxicology 27: 301-313.
- Fletcher В., Dillard С., Tappel A. 1973. Measurement of fluorescent lipid peroxidation products in biological systems and tissues. Anal. Biochem. 52: 1-9.
- Fletcher В., Tappel A. 1973. Protective effects of dietary Error! Bookmark not defined.- tocopherol in rats exposed to toxic levels of ozone and nitrogen dioxide. Environ. Res. 6: 165-175.
- Folinsbee L., Bedi J., Horvath S. 1980. Respiratory responses in human repeatedly exposed to low concentrations of ozone. Am. Rev. Respir. Dis. 121: 431—439.
- Frei В., Stocker R., Ames В. 1988. Antioxidant defenses and lipid peroxidation in human plasma. Proc. Natl. Acad. Sci. 85: 9748-9752.
- Giamalva D., Church D., Pryor W. 1986. Kinetics of ozonation. 4. Reactions of ozone with alpha-tocopherol and oleate and linoleate esters in carbon tetrachloride and in aqueous micellar solvents. J. Am. Chem. Soc. 108: 6646-6651.
- Giamalva D., Church D., Pryor W. 1985. A comparison of the rates of ozonation of biological antioxidants and oleate and linoleate esters. Biochem. Biophys. Res. Commun. 133: 773-779.
- Huang Y., Chang L., Miller F., Crapo J. 1989. Lung injury caused by ambient levels of ozone. J. Aerosol. Med. 2: 149-158.
- Ichinose Т., Sagai M. 1992. Combined exposure to N02, 03 and H2S04 - aerosol and lung tumor formation in rats. Toxicology 74: 173-184.
- Kleeberger S., Lewitt R., Zhang L. 1993. Susceptibility to ozone-induced inflammation. Am. J. Physiol. 264 (Lung Cell. Mol. Physiol. 8): L15-L20.
- Lippmann M. 1989a. Effects of ozone on respiratory function and structure. Annu. Rev. Public Health 10: 49-67.
- Lippmann M. 1989b. Health effects of ozone: a critical review. J. Air Pollut. Control Assoc. 39: 672-695.
- Lowry 0., Rosebrough A., Farr A., Randall R. 1951. Protein measurement with Folin phenol reagent. J. Biol. Chem. 193: 265-275.
- Marshall E. 1989. Clear air? Don't hold your breath. Science 244: 517-520.
- Matzen R. 1957. Effect of vitamin С and hydrocortisone on the pulmonary edema produced by ozone in mice. J. Appl. Physiol. 2: 105-109.
- McDonnell W., Horstman D., Hazucha М., Seal E., Haak D., Salaam S., House D. 1983. Pulmonary effects of ozone exposure during exercise: dose-response characteristics. J. Appl. Physiol. 54: 1345-1352.
- Menzel D. 1992. Antioxidant vitamins and prevention of lung disease. Ann. N.Y. Acad. Sci. 669: 141-155.
- Menzel D. 1994. The toxicity of air pollution in experimental animals and humans: the role of oxidative stress. Toxicol. Lett. 72: 269-277.
- Mustafa M., Elsayed N., Quinn C., Postlethwait E., Gardner D., Graham J. 1982. Comparison of pulmonary biochemical effects of low level ozone exposure on mice and rats. J. Toxicol. Environ. Health 9: 857-865.
- Mustafa М., Elsayed N., von Dohlen F., Hassett С., Postlethwait е., Quinn C., Graham J., Gardner D. 1984. Comparison of biochemical effects of nitrogen dioxide, ozone and their combination in mouse lung. I. Intermittent exposures. Toxicol. Appl. Pharmacol. 72: 82-93.
- Nambu Z., Ichikawa I., Yokoyama E. 1991. Neutral sugar accumulation in lung lavage fluid following ozone exposure - a sensitive indicator of ozone-induced pulmonary damage. Toxicol. Ind. Health 7 (5/6): 465-471.
- Nikula K., Wilson D., Giri S., Plopper C., Dungworth D. 1988. The response of the rat tracheal epithelium to ozone exposure - injury, adaptation and repair. Am. J. Pathol. 131: 373-384.
- Peisker K. 1964. A rapid semi-micro method for preparation of methyl esters from triglycerides using chloroform, methanol and sulphric acid. J. Am. Oil Sci. 41: 87-89.
- Pryor W. 1991a. Can vitamin E protect us against the pathological effects of ozone in smog? Am. J. Clin. Nutr. 53: 702-722.
- Pryor W. 1991b. The antioxidant nutrients and disease prevention - what do we know and what do we need to find out? Am. J. Clin. Nutr. S 53: 391-393.
- Pryor W., Church D. 1991. Aldehydes, hydrogen peroxide and organic radicals as mediators of ozone toxicity. Free Radic. Biol. Med. 11: 41-46.
- Pryor W., Das B, Church D. 1991. The ozonation of unsaturated fatty acids: aldehydes and hydrogen peroxide as products and possible mediators of ozone toxicity. Chem. Res. Toxicol. 4 (3): 341-348.
- Pryor W., Wang K., Bermudez E. 1992. Cholesterol ozonation products as biomarkers for ozone exposure in rats. Biochem. Biophys. Res. Commun. 188 (2): 618-623.
- Pryor W. 1993. Ozone in all its splendor. J. Lab. Clin. Med. 122: 483-486.
- Roe J., Kuether C. 1943. Technique for determination of ascorbic acid in whole blood and urine through 2,4 dinitrophenylohydrazine deriváte of dehydroascorbic acid. J. Biol. Chem. 147: 399-408.
- Sagai M., Ichinose T. 1991. Biochemical effects of combined gases of nitrogen dioxide and ozone. IV. Changes of lipid peroxidation and antioxidative protective systems in rat lungs upon life span exposure. Toxicology 66: 121-132.
- Ward A., Till O., Hatherill J., Annersley Т., Kunkel R. 1985. Systematic complement activation, lung injury and products of lipid peroxidation. J. Clin. Invest. 76: 517-527.
- Zieliński H., Jakubowski K. 1997. Wpływ zwiększonej zawartości ozonu w powietrzu na wybrane wskaźniki biochemiczne, hemotologiczne i immunologicne u szczurów w warunkach podawania w paszy zróżnicowanych dawek witaminy E i С. 1 Wpływ zwiększonej zawartości ozonu w powietrzu na wybrane wskaźniki odpornościowe. Acta Acad. Agricult. Tech. Olst., Veterinaria, 25: 15-28.
Typ dokumentu
Bibliografia
Identyfikatory
Identyfikator YADDA
bwmeta1.element.agro-article-a1103e27-7983-49a2-b7a0-c50fdcf15ce4