Abstract
The ultrastructural changes following a single intracisternal injection of 6-OHDA were studied in the intermediolateral nucleus of the monkey spinal cord. Post-operative survival periods ranged from 20 hours to 14 days. At all stages, only boutons containing clear, round vesicles (R-boutons) and those containing dense-cored vesicles (DCV-boutons) underwent degeneration. Boutons containing flattened vesicles (F-boutons) appeared to be unaffected. Changes were seen even at 20 hours after injection and these were confined to R-boutons only. The changes included an initial swelling and crowding of the vesicles, followed by an increase in the electron density of the axoplasm. The latter change was most marked on the second post-operative day and by the third day, most of the electron-dense profiles were glia-engulfed. By the third day, also, many unmyelinated and, occasionally, myelinated axons showed accumulations of mitochondria, membrane-bound tubular profiles and electron-dense bodies. Many astrocytic processes also showed accumulation of tubular profiles. From the fifth day onwards, few degenerating R-boutons were encountered but DCV-boutons containing swollen vesicles, with or without their dense cores, were obvious. Unmyelinated and, occasionally, myelinated axons and astrocytic processes containing tubular elements still continued to be seen. By the fourteenth post-operative day, degenerating profiles were rarely observed. The probable significance of these findings has been discussed in the light of recent anatomical and biochemical studies.
Full text
PDF










Images in this article
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Bartholini G., Richards J. G., Pletscher A. Dissociation between biochemical and ultrastructural effects of 6-hydroxydopamine in rat brain. Experientia. 1970;26(2):142–144. doi: 10.1007/BF01895541. [DOI] [PubMed] [Google Scholar]
- Bloom F. E., Algeri S., Groppetti A., Revuelta A., Costa E. Lesions of central norepinephrine terminals with 6-OH-dopamine: biochemistry and fine structure. Science. 1969 Dec 5;166(3910):1284–1286. doi: 10.1126/science.166.3910.1284. [DOI] [PubMed] [Google Scholar]
- Bloom F. E., Hoffer B. J., Siggins G. R. Studies on norepinephrine-containing afferents to Purkinje cells of art cerebellum. I. Localization of the fibers and their synapses. Brain Res. 1971 Feb 5;25(3):501–521. doi: 10.1016/0006-8993(71)90457-4. [DOI] [PubMed] [Google Scholar]
- Chiba T., Kato M. Synaptic structures and quantification of catecholaminergic axons in the nucleus tractus solitarius of the rat: possible modulatory roles of catecholamines in baroreceptor reflexes. Brain Res. 1978 Aug 4;151(2):323–338. doi: 10.1016/0006-8993(78)90888-0. [DOI] [PubMed] [Google Scholar]
- Chung K., LaVelle F. W., Wurster R. D. Ultrastructure of HRP-identified sympathetic preganglionic neurons in cats. J Comp Neurol. 1980 Mar 1;190(1):147–155. doi: 10.1002/cne.901900110. [DOI] [PubMed] [Google Scholar]
- Galabov P., Davidoff M. On the vegetative network of guinea pig thoracic spinal cord. Histochemistry. 1976 Jun 28;47(3):247–255. doi: 10.1007/BF00489966. [DOI] [PubMed] [Google Scholar]
- Hökfelt T., Ungerstedt U. Specificity of 6-hydroxydopamine induced degeneration of central monoamine neurones: an electron and fluorescence microscopic study with special reference to intracerebral injection on the nigro-striatal dopamine system. Brain Res. 1973 Oct 12;60(2):269–297. doi: 10.1016/0006-8993(73)90791-9. [DOI] [PubMed] [Google Scholar]
- Kapeller K., Mayor D. An electron microscopic study of the early changes proximal to a constriction in sympathetic nerves. Proc R Soc Lond B Biol Sci. 1969 Mar 11;172(1026):39–51. doi: 10.1098/rspb.1969.0010. [DOI] [PubMed] [Google Scholar]
- Kostrzewa R. M., Jacobowitz D. M. Pharmacological actions of 6-hydroxydopamine. Pharmacol Rev. 1974 Sep;26(3):199–288. [PubMed] [Google Scholar]
- Lorden J. F., Oltmans G. A., Dawson R., Jr, Callahan M. Evaluation of the non-specific effects of catecholamine and serotonin neurotoxins by injection into the medial forebrain bundle of the rat. Pharmacol Biochem Behav. 1979 Jan;10(1):79–86. doi: 10.1016/0091-3057(79)90172-2. [DOI] [PubMed] [Google Scholar]
- Réthelyi M. Cell and neuropil architecture of the intermedio-lateral (sympathetic) nucleus of cat spinal cord. Brain Res. 1972 Nov 13;46:203–213. doi: 10.1016/0006-8993(72)90016-9. [DOI] [PubMed] [Google Scholar]
- Smolen A. J., Ross L. L. The bulbospinal monoaminergic system of the chick: degeneration in the sympathetic nucleus following surgical and chemical lesions. Brain Res. 1978 Jan 6;139(1):153–159. doi: 10.1016/0006-8993(78)90067-7. [DOI] [PubMed] [Google Scholar]
- Sotelo C., Javoy F., Agid Y., Glowinski J. Injection of 6-hydroxydopamine in the substantia nigra of the rat. I. Morphological study. Brain Res. 1973 Aug 30;58(2):269–290. doi: 10.1016/0006-8993(73)90001-2. [DOI] [PubMed] [Google Scholar]
- Tan C. K., Wong W. C. An ultrastructural study of the synaptic glomeruli in the intermediolateral nucleus of the rat. Experientia. 1975 Feb 15;31(2):201–203. doi: 10.1007/BF01990706. [DOI] [PubMed] [Google Scholar]
- Uretsky N. J., Iversen L. L. Effects of 6-hydroxydopamine on catecholamine containing neurones in the rat brain. J Neurochem. 1970 Feb;17(2):269–278. doi: 10.1111/j.1471-4159.1970.tb02210.x. [DOI] [PubMed] [Google Scholar]
- Wong W. C., Tan C. K. Degeneration in the adult rat spinal cord following systemic treatment with 6-hydroxydopamine. Electron microscopic study. Experientia. 1974 Dec 15;30(12):1455–1459. doi: 10.1007/BF01919692. [DOI] [PubMed] [Google Scholar]
- Wong W. C., Tan C. K. The fine structure of the intermediolateral nucleus of the spinal cord of the monkey (Macaca fascicularis). J Anat. 1980 Mar;130(Pt 2):263–277. [PMC free article] [PubMed] [Google Scholar]












