Restricted ablative lesions in motor portions of GPi in primates produce extensive loss of motor-related neurons and degeneration of the lenticular fasciculus

Experimental Neurology

Volumn 202, Issue 1, 2006, Pages 67-75

  Baron, Mark S ^a,b   Noonan, Jamie B ^c   Mewes, Klaus ^c  

^a Clinical Center   (United States)

^b VIRGINIA COMMONWEALTH UNIVERSITY SCHOOL OF MEDICINE   (United States)

^c EMORY UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

Ansa lenticularis; Deep brain stimulation; Globus pallidus; Lenticular fasciculus; Parkinson's disease; Subthalamic nucleus

Indexed keywords

ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; BEHAVIOR DISORDER; BRAIN DEPTH STIMULATION; COGNITIVE DEFECT; CONTROLLED STUDY; GLOBUS PALLIDUS; MOTOR DYSFUNCTION; NERVE CELL NECROSIS; NERVE CELL NETWORK; NERVE DEGENERATION; NERVE PROJECTION; NONHUMAN; PARKINSON DISEASE; PRIORITY JOURNAL; SUBTHALAMIC NUCLEUS;

ANIMALS; BRAIN INJURIES; BRAIN MAPPING; CATHETER ABLATION; EFFERENT PATHWAYS; FUNCTIONAL LATERALITY; GLOBUS PALLIDUS; MACACA MULATTA; MOTOR NEURONS; NERVE DEGENERATION; STAINING AND LABELING;

EID: 33748422195     PISSN: 00144886     EISSN: 10902430     Source Type: Journal    
DOI: 10.1016/j.expneurol.2006.05.014     Document Type: Article

References (40)

1. Alexander G.E., and Crutcher M.D. Functional architecture of basal ganglia circuits: neural substrates of parallel processing. Trends Neurosci. 13 (1990) 266-271
2. Alterman R.L., Shils J.L., Gudesblatt M., and Tagliati M. Immediate and sustained relief of levodopa-induced dyskinesias after dorsal relocation of a deep brain stimulation lead. Case report. Neurosurg. Focus 17 (2004) 39-42
3. Baron M.S., Sidibé M., DeLong M.R., and Smith Y. Course of motor and associative pallidothalamic projections in monkeys. J. Comp. Neurol. 429 (2001) 490-501
4. Baron M.S., Wichmann T., Ma D., and DeLong M.R. Effects of transient focal inactivation of the basal ganglia in parkinsonian primates. J. Neurosci. 22 (2002) 592-599
5. Benabid A.L., Benazzouz A., and Pollack P. Mechanisms of deep brain stimulation. Mov. Dis. 17 (2002) S73-S74
6. Boraud T., Bezard E., Bioulec B., and Gross C. High frequency stimulation of the internal globus pallidus GPi. simultaneously improves parkinsonian symptoms and reduces the firing frequency of GPi neurons in the MPTP-treated monkey. Neurosci. Lett. 215 (1996) 17-20
7. DeLong M.R. Activity of pallidal neurons during movement. J. Neurophysiol. 34 (1971) 414-427
8. DeOlmos J.S., Beltramino C., and Lorenzo S.D.O.D. Use of an amino-cupric-silver technique for the detection of early and semiacute neuronal degeneration cause by neurotoxicants, hypoxia, and physical trauma. Neurotoxicol. Teratol. 16 (1994) 545-561
9. Follett K.A. Comparison of pallidal and subthalamic deep brain stimulation for the treatment of levodopa-induced dyskinesias. Neurosurg. Focus 17 (2004) 14-19
10. Gross R.E., Lombardi W.J., Lang A.E., Duff J., Hutchison W.D., Saint-Cyr J.A., Tasker R.R., and Lozano A.M. Relationship of lesion location to clinical outcome following microelectrode-guided pallidotomy for Parkinson's disease. Brain 122 (1999) 405-416
11. Hariz M.I. Correlation between clinical outcome and size and site of the lesion in computed tomography guided thalamotomy and pallidotomy. Stereotact. Funct. Neurosurg. 54-55 (1990) 172-185
12. Holsheimer J., Demeulemeester H., Nuttin B., and de Sutter P. Identification of the target neuronal elements in electrical deep brain stimulation. Eur. J. Neurosci. 12 (2000) 4573-4577
13. Hoover J.E., and Strick P.L. The organization of cerebellar and basal ganglia outputs to primary motor cortex as revealed by retrograde transneuronal transport of herpes simplex virus type 1. J. Neurosci. 19 (1999) 1446-1463
14. Iacono R.P., Carlson J.D., Mohamed A.S., and Kuniyoshi S.M. Reversal of levodopa failure syndrome by posteroventral-ansa pallidotomy. Adv. Neurol. 80 (1999) 619-622
15. Kim R., Nakano K., Jayaraman A., and Carpenter M.B. Projections of the globus pallidus and adjacent structures: an autoradiographic study in the monkey. J. Comp. Neurol. 169 (1976) 263-290
16. Krack P., Pollak P., Limousin P., Hoffmann D., Benazzouz A., Le Bas J.F., Koudsie A., and Benabid A.L. Opposite motor effects of pallidal stimulation in Parkinson's disease. Ann. Neurol. 43 (1998) 180-192
17. Krauss J.K., Desaloms J.M., Lai E.C., King D.E., Jankovic J., and Grossman R.G. Microelectrode-guided posteroventral pallidotomy for treatment of Parkinson's disease: postoperative magnetic resonance imaging analysis. J. Neurosurg. 87 (1997) 358-367
18. Kuo J.-S., and Carpenter M.B. Organization of pallidothalamic projections in the rhesus monkey. J. Comp. Neurol. 151 (1973) 201-236
19. Lehman R.M., Mezrich R., Sage J., and Goldbe L. Peri- and postoperative magnetic resonance imaging localization of pallidotomy. Stereotact. Funct. Neurosurg. 62 (1994) 61-70
20. Liu X., Aziz T.Z., and Bain P.G. Intraoperative monitoring of motor symptoms using surface electromyography during stereotactic surgery for movement disorders. J. Clin. Neurophysiol. 22 (2005) 183-191
21. Lombardi W.J., Gross R.E., Trepanier L.L., Lang A.E., Lozano A.M., and Saint-Cyr J.A. Relationship of lesion location to cognitive outcome following microelectrode-guided pallidotomy for Parkinson's disease: support for the existence of cognitive circuits in the human pallidum. Brain 123 (2000) 746-758
22. Lozano A.M., and Eltahawy H. How does DBS work?. Suppl. Clin. Neurophysiol. 57 (2004) 733-736
23. Mitrofanis J. Some certainty for the "zone of uncertainty"? Exploring the function of the zona incerta. Neuroscience 130 (2005) 1-15
24. Nambu A., Takada M., Inase M., and Tokuno H. Dual somatotopical representations in the primate subthalamic nucleus: evidence for ordered but reversed body-map transformations from the primary motor cortex and the supplementary motor area. J. Neurosci. 16 (1996) 2671-2683
25. Okun M.S., and Vitek J.L. Lesion therapy for Parkinson's disease and other movement disorders: update and controversy. Mov. Disord. 19 (2004) 375-389
26. Parent A. Carpenter's Human Neuroanatomy. 9th ed. (1996), Williams and Wilkins, Philadelphia
27. Parent M., and Parent A. The Pallidofugal motor fiber system in primates. Parkinsonism Relat. Disord. 10 (2004) 203-211
28. Parent M., Martin L., and Parent A. Two types of projection neurons in the internal pallidum of primates: single-axon tracing and three-dimensional reconstruction. J. Comp. Neurol. 439 (2001) 162-175
29. Patil A.A., Hahn F., Sierra-Rodriguez J., Traverse J., and Wang S. Anatomical structures in the Leksell pallidotomy target. Stereotact. Funct. Neurosurg. 70 (1998) 32-37
30. Ranck J.B. Which elements are excited in electrical stimulation of mammalian central nervous system: a review. Brain Res. 98 (1975) 417-440
31. Ranson S.W., and Ranson M. Pallidofugal fibers in the monkey. AMA Arch. Neurol. Psychiatry 42 (1939) 1059-1067
32. Saint-Cyr J.A., Hoque T., Pereira L.C., Dostrovsky J.O., Hutchison W.D., Mikulis D.J., Abosch A., Sime E., Lang A.E., and Lozano A.M. Localization of clinically effective stimulating electrodes in the human subthalamic nucleus on magnetic resonance imaging. J. Neurosurg. 97 (2002) 1152-1166
33. Sidibé M., Bevan M.D., Bolam J.P., and Smith Y. Efferent connections of the internal globus pallidus in the squirrel monkey: I. Topography and synaptic organization of the pallidothalamic projection. J. Comp. Neurol. 382 (1997) 323-347
34. Trepanier L.L., Kumar R., Lozano A.M., Lang A.E., and Saint-Cyr J.A. Neuropsychological outcome of GPi pallidotomy and GPi or STN deep brain stimulation in Parkinson's disease. Brain Cogn. 42 (2000) 324-347
35. Vitek J.L., Bakay R.A.E., Hashimoto T., Kaneoke Y., Mewes K., Zhang J.Y., Rye D., Starr P., Baron M., Turner R., and DeLong M.R. Microelectrode-guided pallidotomy: technical approach and its application for medically intractable Parkinson's disease. J. Neurosurg. 88 (1998) 1027-1043
36. Voges J., Volkmann J., Allert N., Lehrke R., Koulousakis A., Freund H.J., and Sturm V. Bilateral high-frequency stimulation in the subthalamic nucleus for the treatment of Parkinson disease: correlation of therapeutic effect with anatomical electrode position. Neurosurgery 96 (2002) 269-279
37. Volkmann J., Herzog J., Kopper F., and Deuschl G. Introduction to the programming of deep brain stimulators. Mov. Disord. 17 Suppl. 3 (2002) S181-S187
38. Winters W., Kado W., and Adey W. A Stereotaxic Brain Atlas for Macaca Nemestrina (1969), University of California Press, Berkeley
39. Yelnik J., Damier P., Demeret S., Gervais D., Bardinet E., Bejjani B.P., Francois C., Houeto J.L., Arnule I., Dormont D., Galanaud D., Pidoux B., Cornu P., and Agid Y. Localization of stimulating electrodes in patients with Parkinson disease by using a three-dimensional atlas-magnetic resonance imaging coregistration method. J. Neurosurg. 99 (2003) 89-99
40. Yoshida S.I., Nambu A., and Jinnai K. The distribution of the globus pallidus neurons with input from various cortical areas in the monkeys. Brain Res. 611 (1993) 170-174