Dietary arginine alters time of symptom onset in Huntington’s disease transgenic mice
Autor: | Daniela Watts, A. Wallace Deckel, Ilana Abeles, Paige Volmer, Zhige Yan, Jonathan Covault, Ronald E. Weiner, Keith A. Gary, Daniel Sasso, Nurit Schmerler |
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Rok vydání: | 2000 |
Předmět: |
Blood Glucose
Genetically modified mouse medicine.medical_specialty Time Factors Arginine Ratón Mice Transgenic Biology Nitric oxide Mice chemistry.chemical_compound Huntington's disease Internal medicine Weight Loss medicine Animals Molecular Biology Movement Disorders General Neuroscience Neurodegeneration Brain medicine.disease Pathophysiology Diet Huntington Disease Endocrinology Cerebral blood flow chemistry Cerebrovascular Circulation Tyrosine Neurology (clinical) Developmental Biology |
Zdroj: | Brain Research. 875:187-195 |
ISSN: | 0006-8993 |
DOI: | 10.1016/s0006-8993(00)02640-8 |
Popis: | Recent neuroimaging studies reported complex changes in cerebral blood flow (CBF) in early-staged Huntington's disease (HD) patients. Deckel and co-workers [Deckel and Duffy, Brain Res. (in press); Deckel and Cohen, Prog. Neuro-Psychopharmacol. Biol. Psychiatry 24 (2000) 193; Deckel et al., Neurology 51 (1998) 1576; Deckel et al., J. Nucl. Med. 41 (2000) 773] suggested that these findings might be accounted for, in part, by alterations in cerebral nitric oxide (NO) and its byproduct, peroxynitrite. The current experiment tested this hypothesis by altering NO levels via manipulations of dietary L-arginine (ARG), the dietary precursor of NO, in mice transgenic for HD. Seventy-one mice were assigned at 12 weeks of age to one of three isocaloric diets that varied in their content of ARG. These diets included: (a) 0% ARG, (b) 1.2% ARG (i.e. typical mouse chow), or (c) 5% ARG. The 5% ARG diets in HD mice accelerated the time of onset of body weight loss (P0.05) and motor impairments (P0.05), and increased resting CBF in HD relative to control (P0.05). Conversely, the 0% ARG diet demonstrated no loss of body weight and had no changes in CBF relative to controls. However, the 0% ARG HD group continued to show significant deficits on motor testing (P0. 05). The 1.2% ARG HD group showed reduced body weight loss, better motor functioning, and fewer changes in CBF compared to the 5% ARG HD group. Immunocytochemistry analysis found greater deposition of nitrotyrosine in the cortex, and vasculature, of HD+ mice, 5% and 1. 2%0% arginine diets. When collapsed across all conditions, CBF inversely correlated (P0.05) both with the body weight and motor changes suggesting that changes in CBF are associated with behavioral decline in HD mice. Collectively, these findings indicate that dietary consumption of the NO precursor ARG has a measurable, but complex, effect on symptom progression in HD transgenic mice, and implicates NO in the pathophysiology of HD. |
Databáze: | OpenAIRE |
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