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Huxtable, Clive R. R.
  Mannoside storage and axonal dystrophy in sensory neurones of swainsonine-treated rats: Morphogenesis of lesions / C. R. Huxtable; P. R. Dorling
  En: Acta Neuropathol. -- Vol. 68, no. 1 (1985). -- Berlin : Springer, 1985

  Disponible en http://www.springerlink.com/content/t9240715627620j1/

  Summary Young rats were treated with swainsonine for up to 200 days at a dose rate that restricted neuronal mannoside storage to neurones not protected by the blood/brain barrier. In lumbar dorsal root ganglion neurones, mannoside storage in the cell body developed in parallel to dystrophic changes at the extremities of peripherally and centrally directed axons. The dystrophic process involved the accumulation of autophagic structures. In the CNS, axonal dystrophy was confined to areas receiving long processes from affected neurones. The results suggest that axonal dystrophy is a direct consequence of the lysosomal storage process in parent cell bodies. The possible relationship of axonal dystrophy to neuronal lysosomal function is discussed.
  ISSN: 00016322

  1. MORFOLOGIA ANIMAL; 2. MORFOGENESIS; 3. ROEDORES; 4. RATA; 5. NEURONAS; 6. DISTROFIA; 7. LESIONES; 8. MUSCULOS; 9. EXPERIMENTACION; 10. SEPARATAS I. Dorling, P. R.

  (6) Inv.: 03-R03020 S.T.: S-616.091 HUX ej.1
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03-R03020 S-616.091 HUX ej.1

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Huxtable, Clive R. R.
Mannoside storage and axonal dystrophy in sensory neurones of swainsonine-treated rats: Morphogenesis of lesions / C. R. Huxtable; P. R. Dorling
En: Acta Neuropathol. -- Vol. 68, no. 1 (1985). -- Berlin : Springer, 1985

Disponible en http://www.springerlink.com/content/t9240715627620j1/

Summary Young rats were treated with swainsonine for up to 200 days at a dose rate that restricted neuronal mannoside storage to neurones not protected by the blood/brain barrier. In lumbar dorsal root ganglion neurones, mannoside storage in the cell body developed in parallel to dystrophic changes at the extremities of peripherally and centrally directed axons. The dystrophic process involved the accumulation of autophagic structures. In the CNS, axonal dystrophy was confined to areas receiving long processes from affected neurones. The results suggest that axonal dystrophy is a direct consequence of the lysosomal storage process in parent cell bodies. The possible relationship of axonal dystrophy to neuronal lysosomal function is discussed.
ISSN: 00016322

1. MORFOLOGIA ANIMAL; 2. MORFOGENESIS; 3. ROEDORES; 4. RATA; 5. NEURONAS; 6. DISTROFIA; 7. LESIONES; 8. MUSCULOS; 9. EXPERIMENTACION; 10. SEPARATAS I. Dorling, P. R.

(6) Inv.: 03-R03020 S.T.: S-616.091 HUX ej.1
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