Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Pivot Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Target Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Query: UNIPROT:P17174 (
aspartate aminotransferase
)
14,872
document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)
The use of serum
myosin light chain 1
(
MLC1
) in the diagnosis and treatment response of a patient with biopsy proven inflammatory myopathy is presented. A serum
MLC1
level was elevated at presentation despite a normal creatine phosphokinase level.
MLC1
levels more closely paralleled the clinical status than the
aspartate aminotransferase
and lactate dehydrogenase levels. The results suggest that
MLC1
levels may facilitate the early diagnosis and management of patients with inflammatory myopathy. Moreover, the excellent response of our patient to low dose prednisone might suggest that the results of treatment could be improved by early detection and institution of therapy.
...
PMID:Inflammatory myopathy--early diagnosis and management by serum myosin light chains measurements. 800 80
Since cardiac and skeletal myotoxicity affect the development of drug candidates, it is important to detect their toxicity at an early stage of drug development. For that purpose, in this study, the usefulness of several cardiac and skeletal myotoxic biomarkers in blood were evaluated using two rat models treated intraperitoneally with an acetylcholinesterase inhibitor carbofuran (CAF) or a synthetic catecholamine isoproterenol (ISO). The biomarkers assayed were fatty acid binding protein 3 (Fabp3),
myosin light chain 1
(
MLC1
), cardiac troponin I (cTnI), cardiac troponin T (cTnT),
aspartate transaminase
(
AST
), lactate dehydrogenase (LDH) and creatine kinase (CK). CAF and ISO treatment of rats induced greater increases in the levels of Fabp3,
MLC1
, cTnI and cTnT than in the levels of
AST
, LDH and CK. A kinetic analysis indicated that the levels of all of the biomarkers had returned to the basal level by 24h after drug administration. Pathological examination revealed lesions in the heart, mainly at the left ventricle and septum, in both CAF- and ISO-treated rats. CAF-treated rats showed widespread lesions of skeletal muscle that were independent of muscle fiber type, while in ISO-treated rats locoregional lesions were observed only in slow twitch muscle. Receiver operating characteristic curve analysis of the sensitivity of the tested biomarkers indicated that
MLC1
and cTnT were the most effective biomarkers of cardiotoxicity. For skeletal myotoxicity, Fabp3 and
MLC1
were the most effective biomarkers based on the specific tissue distribution of these proteins. Conversely, the rapid blood clearance of these markers should be taken into account when considering the use of these biomarkers.
...
PMID:Evaluation of the usefulness of biomarkers for cardiac and skeletal myotoxicity in rats. 1985 36