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Synthesis and myocardial kinetics of N-13 and C-11 labeled branched-chain L-amino acids. [Dogs]

Journal Article · · J. Nucl. Med.; (United States)
OSTI ID:5009979

Glutamate dehydrogenase (GDH), immobilized on CNBr-activated Sepharose supports, was used with N-13 ammonia to aminate ..cap alpha..-ketoisocaproic acid (KIC), and ..cap alpha..-ketoisovaleric acid (KIV) to produce N-13-labeled branched-chain L-amino acids with radiochemical yields ranging from 29% to 35%. From kinetic and practical cosiderations, pH 7.5 to 8.0 was established to be optimal for the synthesis of N-13-labeled branched-chain-L-amino acids. Myocardial time-activity curves in dogs at control, during low-flow ischemia, reperfusion, and after transaminase inhibition following intracoronary bolus injection of the N-13 labeled amino acids were biexponential. Higher retention of N-13 activity was observed in ischemic segments both during low-flow ischemia (29.2%) and reperfusion (23.2%) when compared with controls (20.0%), (n-4). On the other hand, transaminase inhibition decreased residue fractions from 21.0% at control to 13.9% (n=4). The residual activity with L-(1-/sup 11/C)leucine allows for the calculation of protein synthesis rates.

Research Organization:
Univ. of California, Los Angeles; Scripps Clinic and Research Foundation, La Jolla, CA
OSTI ID:
5009979
Journal Information:
J. Nucl. Med.; (United States), Journal Name: J. Nucl. Med.; (United States) Vol. 24:10; ISSN JNMEA
Country of Publication:
United States
Language:
English

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