Literature DB >> 1893983

Grafting of fetal substantia nigra to striatum reverses behavioral deficits induced by MPTP in primates: a comparison with other types of grafts as controls.

J R Taylor1, J D Elsworth, R H Roth, J R Sladek, T J Collier, D E Redmond.   

Abstract

Fetal substantia nigra (SN) cells were transplanted into the caudate nucleus (CN) of four vervet monkeys (Cercopithecus aethiops sabaeus) that had been treated with 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP). MPTP treatment appears to produce a syndrome similar to that observed in patients with idiopathic Parkinson's disease. Normal and parkinsonian behaviors were quantitated by trained observers 5 days/week. Twenty-eight behaviors based on previous factor analyses were individually scored and rated. Parkinsonian signs included freezing, head and limb tremor, difficulty in eating, delayed initiation of movement, poverty of movement, tremor that stopped with intention, decreased response to threats, and lying immobile in the cage. These signs were combined to give an overall rating of parkinsonism. A summary measure of 'normal' healthy behavior was also examined, including such behaviors as yawning, scratching, self-grooming, shifting, and eating. Overall ratings of parkinsonism increased and those of healthy behavior decreased after MPTP. In the 4 monkeys grafted with fetal SN cells into the CN, behavior returned to pre-treatment levels by the time of sacrifice (2, 5, or 7.5 months after grafting). Three control subjects were transplanted with either SN cells into an inappropriate brain site (cortex) or inappropriate, non-dopaminergic, cells (cerebellar) into the CN. Subjects were also compared with three control animals that did not receive MPTP but received cryopreserved or fresh SN and other cells into the CN. Only MPTP-treated subjects that received SN cells into the CN showed evidence of a reversal of the MPTP syndrome after transplantation. In addition, grafting in animals that were not MPTP-treated did not appear to affect behavior. This paper reports the specific behavioral effects of severe MPTP toxicity that were or were not reversed after transplantation and suggests that only fetal SN cells grafted into the CN may be able to reverse behavioral deficits in MPTP-treated monkeys.

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Year:  1991        PMID: 1893983     DOI: 10.1007/bf00229411

Source DB:  PubMed          Journal:  Exp Brain Res        ISSN: 0014-4819            Impact factor:   1.972


  47 in total

1.  Transplantation of fetal neurons in primates.

Authors:  J R Sladek; D E Redmond; R H Roth
Journal:  Clin Res       Date:  1988-04

2.  Reconstruction of the nigrostriatal dopamine pathway by intracerebral nigral transplants.

Authors:  A Björklund; U Stenevi
Journal:  Brain Res       Date:  1979-11-30       Impact factor: 3.252

3.  Injury of nigral neurons exposed to 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine: a tyrosine hydroxylase immunocytochemical study in monkey.

Authors:  C A Kitt; L C Cork; F Eidelberg; T H Joh; D L Price
Journal:  Neuroscience       Date:  1986-04       Impact factor: 3.590

4.  Survival and growth of fetal catecholamine neurons transplanted into primate brain.

Authors:  J R Sladek; T J Collier; S N Haber; R H Roth; D E Redmond
Journal:  Brain Res Bull       Date:  1986-12       Impact factor: 4.077

5.  Improvements in MPTP-induced object retrieval deficits and behavioral deficits after fetal nigral grafting in monkeys.

Authors:  J R Taylor; J D Elsworth; R H Roth; T J Collier; J R Sladek; D E Redmond
Journal:  Prog Brain Res       Date:  1990       Impact factor: 2.453

6.  Selective loss of subpopulations of ventral mesencephalic dopaminergic neurons in the monkey following exposure to MPTP.

Authors:  J S Schneider; A Yuwiler; C H Markham
Journal:  Brain Res       Date:  1987-05-12       Impact factor: 3.252

7.  Disturbance of sequential movements in patients with Parkinson's disease.

Authors:  R Benecke; J C Rothwell; J P Dick; B L Day; C D Marsden
Journal:  Brain       Date:  1987-04       Impact factor: 13.501

8.  MPTP primate model of Parkinson's disease: a mechanographic and electromyographic study.

Authors:  D Doudet; C Gross; P Lebrun-Grandie; B Bioulac
Journal:  Brain Res       Date:  1985-05-27       Impact factor: 3.252

9.  Hemiparkinsonism in monkeys after unilateral internal carotid artery infusion of 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP).

Authors:  K S Bankiewicz; E H Oldfield; C C Chiueh; J L Doppman; D M Jacobowitz; I J Kopin
Journal:  Life Sci       Date:  1986-07-07       Impact factor: 5.037

10.  Fetal neuronal grafts in monkeys given methylphenyltetrahydropyridine.

Authors:  D E Redmond; J R Sladek; R H Roth; T J Collier; J D Elsworth; A Y Deutch; S Haber
Journal:  Lancet       Date:  1986-05-17       Impact factor: 79.321

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  17 in total

1.  Large animal models are critical for rationally advancing regenerative therapies.

Authors:  Dustin R Wakeman; Andrew M Crain; Evan Y Snyder
Journal:  Regen Med       Date:  2006-07       Impact factor: 3.806

2.  Aged monkeys as a partial model for Parkinson's disease.

Authors:  P J Hurley; J D Elsworth; M C Whittaker; R H Roth; D E Redmond
Journal:  Pharmacol Biochem Behav       Date:  2011-05-18       Impact factor: 3.533

Review 3.  The immunological challenges of cell transplantation for the treatment of Parkinson's disease.

Authors:  Amanda L Piquet; Kala Venkiteswaran; Neena I Marupudi; Matthew Berk; Thyagarajan Subramanian
Journal:  Brain Res Bull       Date:  2012-04-11       Impact factor: 4.077

4.  Long distance directional growth of dopaminergic axons along pathways of netrin-1 and GDNF.

Authors:  C Zhang; Y Jin; K S Ziemba; A M Fletcher; B Ghosh; E Truit; D M Yurek; G M Smith
Journal:  Exp Neurol       Date:  2013-10-04       Impact factor: 5.330

5.  AAV2-mediated gene transfer of GDNF to the striatum of MPTP monkeys enhances the survival and outgrowth of co-implanted fetal dopamine neurons.

Authors:  J D Elsworth; D E Redmond; C Leranth; K B Bjugstad; J R Sladek; T J Collier; S B Foti; R J Samulski; K P Vives; R H Roth
Journal:  Exp Neurol       Date:  2008-02-15       Impact factor: 5.330

6.  Influence of cell preparation and target location on the behavioral recovery after striatal transplantation of fetal dopaminergic neurons in a primate model of Parkinson's disease.

Authors:  D E Redmond; A Vinuela; J H Kordower; O Isacson
Journal:  Neurobiol Dis       Date:  2007-08-28       Impact factor: 5.996

7.  Human neural stem cells survive long term in the midbrain of dopamine-depleted monkeys after GDNF overexpression and project neurites toward an appropriate target.

Authors:  Dustin R Wakeman; D Eugene Redmond; Hemraj B Dodiya; John R Sladek; Csaba Leranth; Yang D Teng; R Jude Samulski; Evan Y Snyder
Journal:  Stem Cells Transl Med       Date:  2014-04-17       Impact factor: 6.940

8.  Comparison of fetal mesencephalic grafts, AAV-delivered GDNF, and both combined in an MPTP-induced nonhuman primate Parkinson's model.

Authors:  D Eugene Redmond; Caleb R S McEntire; Joseph P Kingsbery; Csaba Leranth; John D Elsworth; Kimberly B Bjugstad; Robert H Roth; Richard J Samulski; John R Sladek
Journal:  Mol Ther       Date:  2013-08-05       Impact factor: 11.454

Review 9.  Cell-based therapies for Parkinson's disease: past, present, and future.

Authors:  Kathleen M Fitzpatrick; James Raschke; Marina E Emborg
Journal:  Antioxid Redox Signal       Date:  2009-09       Impact factor: 8.401

10.  Behavioral improvement in a primate Parkinson's model is associated with multiple homeostatic effects of human neural stem cells.

Authors:  D Eugene Redmond; Kimberly B Bjugstad; Yang D Teng; Vaclav Ourednik; Jitka Ourednik; Dustin R Wakeman; Xuejun H Parsons; Rodolfo Gonzalez; Barbara C Blanchard; Seung U Kim; Zezong Gu; Stuart A Lipton; Eleni A Markakis; Robert H Roth; John D Elsworth; John R Sladek; Richard L Sidman; Evan Y Snyder
Journal:  Proc Natl Acad Sci U S A       Date:  2007-06-22       Impact factor: 11.205

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