Abstract |
The content of 3-methylhistidine (3-MH) and 1-methylhistidine (1-MH) was measured in muscle biopsy specimens from 13 normal controls, 19 patients with Duchenne muscular dystrophy, 8 limb-girdle disease patients, and 23 disease controls with different forms of muscular pathology. 3-MH and 1-MH concentrations in normal human muscle did not appear to be influenced by sex, body weight, and age, at least for subjects in the 10--60 year age group examined. Skeletal muscle 1-MH levels did not significantly differ from mean control values in any of the pathologies investigated. In the patient population examined, the mean 3-MH level per unit of noncollagen protein (NCP) was significantly lower than normal in Duchenne dystrophy only, the reduction being related to disease severity. The significantly lower concentrations of 3-MH in muscle of Duchenne patients indicate the importance of measuring 3-MH in diseased muscle to obtain reliable estimates of the myofibrillar protein catabolic rate.
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Authors | E Mussini, F Cornelio, F Dworzak, L Cotellessa, L Morandi, L Colombo, G De Ponte, F Marcucci |
Journal | Muscle & nerve
(Muscle Nerve)
1983 Jul-Aug
Vol. 6
Issue 6
Pg. 423-9
ISSN: 0148-639X [Print] United States |
PMID | 6621612
(Publication Type: Comparative Study, Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Methylhistidines
- Muscle Proteins
- 1-methylhistidine
- Histidine
- 3-methylhistidine
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Topics |
- Adolescent
- Adult
- Child
- Child, Preschool
- Female
- Histidine
(analogs & derivatives)
- Humans
- Infant
- Male
- Methylhistidines
(metabolism)
- Middle Aged
- Muscle Proteins
(metabolism)
- Muscles
(metabolism)
- Muscular Atrophy
(metabolism)
- Muscular Diseases
(metabolism)
- Muscular Dystrophies
(metabolism)
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