Browse > Article
http://dx.doi.org/10.5352/JLS.2004.14.6.975

The Effects of EGEE on the Morphometry in the Thickness and Histogenesis of Rat Cerebral Cortex During Developmental Phase  

Lee Eung-Hee (Department of Biology, Graduate School, Pusan National University)
Jeong Gil-Nam (Department of Biology, Graduate School, Pusan National University)
Jo Gi-Jin (Department of Biology, Graduate School, Pusan National University)
Jo Un-Bock (Department of Biology, Graduate School, Pusan National University)
Publication Information
Journal of Life Science / v.14, no.6, 2004 , pp. 975-985 More about this Journal
Abstract
This study attempts to investigate the developmental alterations of rat cerebral cortex, and the effects of EGEE on the developmental cerebral cortex in the prenatal, postnatal and adults were examined by morphological methods and H-E staining was used for the histological changes. In the case of injection of EGEE, at 14 day of fetal phase, parietal cortex was thickest $(95{\pm}12.7\;{\mu}m)$ but, it was thinner than in the control group $(102{\pm}14.0\;{\mu}m)$ and, occipital cortex $(57{\pm}10.5\;{\mu}m)$ compared with other cortexes was the thinnest in fetal phase. In the suckling phase, each cortex grew thick quickly but, after weanning phase, the growth of the cortex slowed and the thickness of cortex was similar to that of cortex in the adult phase. At 105 day after birth, the parietal cortex was thickest $(934{\pm}21.6\;{\mu}m)$ but, decreased compared with control group $(1113{\pm}19.0\;{\mu}m)$. When EGEE was injected in intraperitoneal of rat, the number of neuroblasts per unit area was largest $(207.7{\pm}11.4/10^{-2}\;mm$ at the mantle layer of parietal cortex at 14 day of fetal phase but, decreased compared with control group $(224.2{\pm}13.8/10^{-2}\;mm$ , and the size was largest $(7.5{\pm}1.3\;{\mu}m)$ at the ependymal cell layer of occipital cortex at 3 day after birth but, decreased compared with control group $(9.0{\pm}1.2\;{\mu}m)$. Simillar to control group, the number of granular cells and pyramidal cells were largest at the II and III layer of parietal cortex, but decreased during developmental phase. The size was largest at the IV and V layer of occipital cortex but it was decreased compared with control group. When EGEE was injected in intraperitoneal of rat, the cerebral cortex from fetal phase to 3 day after birth has differentiated into the 3 layers; ependymal, mantle and marginal layer, but empty cisternaes or vacoules in the cerebral cortexes and the condensed phases of neuroblasts were appeared. From 5 day after birth, it has differentiated into the 4 layers; molecular, external granular, mixed layer of internal granular, external and internal pyramidal cells and multiformal layer but, empty cisternaes or vacoules in the granular and pyramidal cell layers were appeared and the number per unit area of neuron was decreased. In the cerebral cortex of the weaning and adult phases, division of cell layers was not clear and empty cisternae was formed in the cortex with the cells in external granular and pyramidal cell layers, was magnified or condensed around blood vessels of neurons.
Keywords
EGEE; Developmental Cerebral cortex; Neuroblast; Granular cell; Pyramidal cell;
Citations & Related Records
연도 인용수 순위
  • Reference
1 Svalander, P. C., M. Hjortberg, K. O. Gronvik and B. O. Nilsson. 1989. Mouse blastocyst surface expression of galactose-containing epitopes coinciding with trophoblast differentiation. Cell Differ. Dev. 26(3), 191-200   DOI   ScienceOn
2 Takeuchi, Y. and N. Hisanaga. 1977. The neurotoxicity of toluene; EGG changes in rats exposed to various concentrations. British J. Indust. Med. 34, 314-324
3 Terry, R. D., R. DeTeresa and L. A. Hansen. 1987. Neocortical cell counts in normal human adult aging. Ann. Neurol. 21(6), 530-539   DOI   ScienceOn
4 Thomaidou, D., M. C. Mione, J. F. Cavanagh and J. G. Parnavelas. 1997. Apoptosis and its relation to the cell cycle in the developing cerebral cortex. J. Neurosci. 17(3), 1075- 1085
5 Yu, I. J., J. Y. Lee, Y. H. Chung, K. J. Kim, J. H. Han, G. Y. Cha, W. G, Chung, Y. N. Cha, J. D. Park, Y. M. Lee and Y. H. Moon. 1999. Coadministration of toluene and xylene antagonized the testicular toxicity but not the hematopoietic toxicity caused by ethylene glycol monoethyl ether in Sprague-Dawley rats. Toxicol.` Lett. 20;109(1-2), 11-20
6 마재준. 1988. Toluene 흡입에 의한 대뇌피질 myelin의 성상변화. 한양대 학교 석사학위논문
7 염영옥. 2003. Ethylene glycol monoethyl ether가 흰쥐 정소의 형태와 복합 당질의 lectin 결합 양상에 미치는 영향. 부산대학교 석사학위논문
8 한국산업안전공단. 1999. 산업안전보건법(셀로솔브, 인쇄업과 관련된 화학물질자료)
9 Foster, P. M., D. M. Creasy and T. J. Foster. 1984. Testicular toxicity produced by ethylene glycol momoethyl and monoethyl ethers in the rat. Environ. Health Perspect 57, 207-217   DOI   ScienceOn
10 Hanaway, J. 1967. Formation and differentiation of the external granular layer of the chick cerebellum. J. Comp. Neurol. 131, 1-14.   DOI   ScienceOn
11 Jonsson, A. K., J. Pedersen and G. Steen. 1982. Ethoxyacetic acid and N-ethoxyacetylglycine ; Metabolite of ethoxyethanol (ethylcellosolve) in rats. Acta. Pharmacol. Toxicol. 50, 358-362   DOI   ScienceOn
12 Kim, Y. H., N. R. Lee, S. Tadashi, K. S. Kim, S. Y. Jeong, S. H. Park, C. R. Lee, H. K. Cheong and Y. H. Moon. 1999. Evaluation of exposure to ethylene glycol monoethyl ehter acetates and their possible hematological effects on shipyard painters. Occup. Environ. Med. 56(6), 378-382   DOI   ScienceOn
13 Kirazov, E., L. Kirazov and L. Venkov. 1989. Chanovs of soluble and membrane proteins of rat brain during preand postnatal development. Cellular & Molecular Biology 35(6), 643-656
14 McIntosh, N., R. L. Picetet, S. L. Kaplan and M. M. Grumbach. 1977. The developmental pattern of somatostain in the embryonic and fetal rat pancreas. Endocrinology 101, 825-829   DOI   ScienceOn
15 Melnick, R. L. 1984. Toxicities of ethylene glycol and ethylene glycol monoethyl ether in Fischer 344/N rats and B6C3F1 mice. Environ. Health Perspect 57, 147-55   DOI
16 Nelson, B. K. and W. S. Brightwell. 1984. Behavioral teratology of ethylene glycol monoethyl and monomethyl ethers. Environ. Health.' Perspect 57, 43-46   DOI
17 Barbee, S. J., J. B. Terrill, D. J. DeSousa and C. C. Conaway. 1984. Subchronic inhalation toxicology of ethylene glycol monoethyl ether in the rat and rabbit. Environ. Health Perspect 57, 157-163   DOI   ScienceOn
18 Caviness, V. S. and C. H. Yorke. 1976. Interhemispheric neocortical connections of the corpus callosum in the reeler mutant mouse: a study based on anterograde and retrograde methods. J. Comp. Neurol. 170(4), 449-459   DOI   ScienceOn
19 Nelson, B. K., W. S. Brightwell, J. V. Setzer and T. L. O'Donohue. 1984. Reproductive toxicity of the industrial solvent 2-Ethoxyethanol in rats and interactive effects of ethanol. Environ. Health Perspect 57, 255-259   DOI
20 Blaschke, A. J., K. Staley and J. Chun. 1996. Widespred programmed cell death in proliferative and postmitotic regions of the fetal cerebral cortex. Development 122, 1165-1174
21 Carpenter, K. L., C. E. Brabbs and M. J. Mitchinson. 1991. Oxygen radicals and atheroschschlerosis. Klin. Wochenschr. 69(21-23), 1039-1045   DOI   ScienceOn
22 Clarke, A. R. 1995. Murine models of neoplasia; functional analysis of the tumor suppressor genes Rb-1 and p53. Cancer Metastasis Rev. 14(2), 125-148   DOI   ScienceOn
23 Cheever, K. L., H. B. Plotnick, D. E. Richards and W. W. Weigel. 1984. Metabolism and excretion of 2-ethoxyethanol in the adult mle rat. Environ. Health Perspect 57, 241-248   DOI   ScienceOn
24 Chung, W. G., I. J. Yu, C. S. Park, K. H. Lee, H. K. Roh and Y. N. Cha. 1999. Decreased formation of ethoxyacetic acid from ethylene glycol monoethyl ether and reduced atrophy of testes in male rats upon combined administration with toluene and xylene. Toxicol. Lett. 104(1-2), 143-150   DOI   ScienceOn
25 Dupouy, J. P., A. Chatelain and M. P. Dubois. 1983. Normal development of cells with somatostatin immunoreactivity in the pancreas and duodenum of the rat fetus and newborn. Cell Tiss. Res. 231, 463-468
26 Andrew, F. D. and B. D. Hardin. 1984. Developmental effects after inhalation exposure of gravid rabbits and rats to ethylene glycol monoethyl ether. Environ. Health Perspect 57, 13-23   DOI