Nowa wersja platformy, zawierająca wyłącznie zasoby pełnotekstowe, jest już dostępna.
Przejdź na https://bibliotekanauki.pl

PL EN


Preferencje help
Widoczny [Schowaj] Abstrakt
Liczba wyników
2006 | 62 | 07 | 827-829
Tytuł artykułu

Zawartosc zelaza w roznych typach oligodendrogleju w obszarze ciala modzelowatego i torebki wewnetrznej mozgowia szczurow

Warianty tytułu
EN
Iron content in various types of oligodendroglia in the corpus callosum and capsula interna of rat brains
Języki publikacji
PL
Abstrakty
EN
The aim of the study was to trace the content and location of iron in three types of oligodendrocytes in the corpus callosum and capsula interna of the brains of thirty-day old Wistar rats. The evaluation was achieved by Leo Omega 912 AB electron microscope, using the spectroscopy method of mapping iron ESI (Electron Spectroscopic Imaging). A variety within the iron content of the three different types of examined cells was indicated. The greatest accumulation of iron displayed dark oligodendrocytes, lesser - medium and the least - light oligodendrocytes. The paper discussed the relation between cytoplasm density and iron content in the studied types of oligodendroglia.
Wydawca
-
Rocznik
Tom
62
Numer
07
Strony
827-829
Opis fizyczny
s.827-829,rys.,bibliogr.
Twórcy
  • Akademia Rolnicza, ul.Akademicka 12, 20-033 Lublin
autor
autor
Bibliografia
  • 1.Aisen P.: The transferrin receptor and the release of iron from transferrin. Adv. Exp. Med. Biol. 1994, 356, 31-40.
  • 2.Beal M. F.: Mitochondrial dysfunction in neurodegenerative diseases. Biochim. Biophys. Acta 1998, 1366, 211-223.
  • 3.Beard J. L., Connor J. R., Jones B. C.: Iron in the brain. Nutr. Rev. 1993, 51, 157-170.
  • 4.Bjatmar C.: Oligodendroglial sheath in developing rat ventral funiculus and corpus callosum. J. Neurosci. 1996, 2, 85-88.
  • 5.Connor J. R., Menzies S. L., St Martin S. M., Mufson E. J.: Cellular distribution of transferrin, ferritin and iron in normal and aged human brains. J. Neurosci. Res. 1990, 27, 595-611.
  • 6.Connor J. R., Menzies S. L., St. Martin S. M., Mufson E. J.: A histochemical study of iron, transferrin and ferritin in Alzheimer's diseased brains. J. Neurosci. Res. 1992, 31, 75-83.
  • 7.Connor J. R., Menzies S. L.: Cellular management of iron in the brain. J. Neurol. Sci. 1995, 134, 33-44.
  • 8.Connor J. R., Menzies S. L.: Relationship of iron to oligodendrocytes and myelination. Glia 1996, 17, 83-93.
  • 9.Drayer B., Burger P., Hurwitz B., Dawson D., Cain J.: Reduced signal intensity on mr images of thalamus and putamen in multiple sclerosis: Increased iron content? A. M. J. Roentgenol. 1987, 149, 357-363.
  • 10.Erb G. L., Osterbur D. L., Le Vine S. M.: The distribution of iron in the brain: a phylogenetic analysis using iron histochemistry. Brain Res. 1996, 1-2, 120-128.
  • 11.Gould R. M., Freund C. M., Palmer F., Finstein D. L.: Messenger RNA's located in myelin sheath assembly sites. J. Neurochem. 2000, 75, 1834-1844.
  • 12.Hardy R. J., Lazzarini R. A., Colman D. R., Friedrich V. L.: Cytoplasmic and nuclear localization of myelin basic proteins reveals heterogenecity among oligodendrocytes. J. Neurosci. Res. 1996, 2, 246-257.
  • 13.Jellinger K. A.: The role of iron in neurodegeneration: Prospects for pharmacotherapy of Parkinson's disease. Drugs Aging 1999, 14, 115-140.
  • 14.Knapp P. E.: Proteolipid protein: Is it more than just a structural component of myelin? Dev. Neurosci. 1996, 18, 297-308.
  • 15.Larkin E. C., Rao A.: Importance of fetal and neonatal iron: Adequancy for normal development of central nervous system. Brain, Behaviour and Iron in the infant Diet. Springer Verlag New York 1999, 43-63.
  • 16.Leapman R. D.: Detecting single atoms of calcium and iron in biological structures by electrom energy-loss spectrum-imaging J. Microscopy 2003, 210, 1-5.
  • 17.Leeden R. W., Chakraborty G.: Cytokines, signal transduction and inflammatory demyelination: review and hypothesis. Neurochem. Res. 1998, 23, 277-289.
  • 18.Le Vine S. M., Macklin W. B.: Iron-enriched oligodendrocytes: A reexamination of their spatial distribution J. Neurosci. Res. 1990, 26, 508-512.
  • 19.Meneghini R.: Iron homeostasis, oxidative stress and DNA damage. Free Radical Biology Medicine 1997, 23, 783-792.
  • 20.Mori S., Leblond C. P.: Electron microscopic identification of three classes of oligodendrocytes and a preliminary study of their proliferative activity in the corpus callosum of young rats. J. Comp. Neurol. 1970, 139, 1-30.
  • 21.Moss T., Morgan E. H.: Transferin and transferrin receptor function in brain barrier systems. Cell Mol. Neurobiol. 2000, 1, 77-95.
  • 22.Reimer L.: Transmission electron microscopy. Physics of image formation and microanalysis. Springer Series in Optical Sciences. Berlin, Heidelberg, New York 1997, 36, 452-454.
  • 23.Roncagliolo M., Garrido M., Walter T., Peirano P., Lozoff B.: Evidence of altered central nervous system development in infants with iron deficiency anemia at 6 mo: Delayed maturation of auditory brainstem responses. Am. J. Clin. Nutr. 1998, 68, 683-690.
  • 24.Roskams A. J. I., Connor J. R.: Iron, transrerrin and ferritin in the rat brain during development and aging. J. Neurochem. 1994, 63, 709-716.
  • 25.Sato T.: A modified method for lead staining of thin sections. J. Electronomicroscop. 1968, 17, 158-159.
  • 26.Taylor E. M., Morgan E. H.: Developmental changes in transferrin and iron uptake by the brain in the rat. Dev. Brain Res. 1990, 55, 35-42.
  • 27.Thomson K. J., Shoham S., Connor J. R.: Iron and neurodegenerative disorders. Brain. Res. 2001, 55, 155-164.
  • 28.Wawrzyniak-Gacek A.: Location of various types of oligodendroglia and iron contained in it within the area of corpus callosum and capsula interna. Annales UMCS 2003, LVIII, 1-14.
  • 29.Youdim M. B. H.: Neuropharmacological and neurobiochemical aspects of iron deficiency, [w:] Dobbing J. (wyd.): Brain behavior and iron in the infant diet. Springer-Verlag London 1990, 8, 83-106.
Typ dokumentu
Bibliografia
Identyfikatory
Identyfikator YADDA
bwmeta1.element.agro-article-67c550b2-10ba-4a18-95a4-f90969ef3346
JavaScript jest wyłączony w Twojej przeglądarce internetowej. Włącz go, a następnie odśwież stronę, aby móc w pełni z niej korzystać.