Abstract
Abstract: Neuronal loss in Huntington's disease (HD) is seen first in the neostriatum. It has been suggested that impaired metabolism underlies this degeneration, as striatal vulnerability to excitotoxicity is increased by metabolic compromise. At 12 weeks of age, a transgenic mouse carrying the HD mutation (R6/2 line) has been shown to have an increased vulnerability to the mitochondrial toxin 3‐nitropropionic acid (3‐NP). However, in contrast, younger R6/2 mice appear to be less vulnerable than wild‐type (WT) mice to the excitotoxins kainic acid and quinolinic acid (QA). In this study, we examine the possibility that the sensitivity of R6/2 mice to 3‐NP might be age dependent. We treated young, symptomatic R6/2 mice with 3‐NP and found that despite their progressive neurological phenotype, they were not more susceptible to 3‐NP intoxication than their WT littermates. Further, fewer R6/2 than WT mice developed striatal lesions. We suggest that compensatory mechanisms exist in the R6/2 mouse brain that protect it against the toxic effect of the transgene and coincidentally protect against exogenous toxins such as 3‐NP, QA, and kainic acid. The existence of similar compensatory mechanisms may explain why, in humans, HD is a late‐onset disorder, despite early expression of the genetic mutation.
References
34
Referenced
41
10.1038/321168a0
10.1523/JNEUROSCI.13-10-04181.1993
10.1073/pnas.120166397
10.1046/j.1471-4159.1998.71062642.x
10.1111/j.1750-3639.1999.tb00216.x
10.1523/JNEUROSCI.19-08-03248.1999
10.1073/pnas.95.11.6480
10.1098/rstb.1999.0449
/ Philos. Trans. R. Soc. Lond. [B] / Altered brain neurotransmitter receptor expression in transgenic mouse models of Huntington's disease gene. by Cha J. (1999)10.1126/science.7901908
10.1016/S0896-6273(00)81035-1
10.1016/S0092-8674(00)80513-9
10.1098/rstb.1999.0448
10.1016/S0896-6273(00)81022-3
10.1111/j.1365-2990.1982.tb00306.x
10.1007/BF00691103
10.1073/pnas.96.15.8727
- HarperP.(1996)Huntington's Disease. Saunders London.
10.1016/S0896-6273(00)80764-3
10.1016/0092-8674(93)90585-E
/ Cell / A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes. by Huntington's Disease Collaborative Research G (1993)10.2337/diabetes.48.3.649
10.1002/1531-8249(199912)46:6<842::AID-ANA6>3.0.CO;2-O
10.1523/JNEUROSCI.19-23-10428.1999
10.1017/S0317167100032212
10.1016/S0092-8674(00)81369-0
10.1016/S0361-9230(00)00238-0
10.1016/S0896-6273(00)80943-5
{'key': 'e_1_2_6_29_2', 'first-page': '1518', 'volume': '2', 'author': 'Pearse A.G.E.', 'year': '1972', 'journal-title': 'Histochemistry: Theoretical and Applied'}
/ Histochemistry: Theoretical and Applied by Pearse A.G.E. (1972)10.1016/S0166-2236(99)01415-0
10.1523/JNEUROSCI.18-23-10116.1998
10.1046/j.1471-4159.1999.721773.x
10.1016/S0092-8674(00)81743-2
10.1002/1531-8249(200001)47:1<80::AID-ANA13>3.0.CO;2-K
10.1093/hmg/8.5.839
10.1097/00005072-199805000-00001
Dates
Type | When |
---|---|
Created | 22 years, 5 months ago (March 12, 2003, 1:48 a.m.) |
Deposited | 1 year, 10 months ago (Oct. 29, 2023, 10:20 a.m.) |
Indexed | 1 month, 4 weeks ago (July 7, 2025, 1:25 a.m.) |
Issued | 24 years, 10 months ago (Nov. 1, 2000) |
Published | 24 years, 10 months ago (Nov. 1, 2000) |
Published Online | 23 years, 8 months ago (Jan. 4, 2002) |
Published Print | 24 years, 10 months ago (Nov. 1, 2000) |
@article{Hickey_2000, title={Mice Transgenic for the Huntington’s Disease Mutation Are Resistant to Chronic 3‐Nitropropionic Acid‐Induced Striatal Toxicity}, volume={75}, ISSN={1471-4159}, url={http://dx.doi.org/10.1046/j.1471-4159.2000.0752163.x}, DOI={10.1046/j.1471-4159.2000.0752163.x}, number={5}, journal={Journal of Neurochemistry}, publisher={Wiley}, author={Hickey, Miriam A. and Morton, A. Jennifer}, year={2000}, month=nov, pages={2163–2171} }