1H and 31P magnetization transfer studies of hindleg muscle in wild-type and creatine kinase-deficient mice

• Published in: Magnetic resonance in medicine 2000-05, Vol.43 (5), p.657-664
• Main Authors: Kruiskamp, Marijn J., van Vliet, Gerard, Nicolay, Klaas
• Format: Article
• Language: English
• Subjects: (phospho)creatine; Biological and medical sciences; creatine kinase; Investigative techniques, diagnostic techniques (general aspects); magnetization transfer; Medical sciences; Osteoarticular system. Muscles; Radiodiagnosis. Nmr imagery. Nmr spectrometry; skeletal muscle; transgenic mice
• ISSN: 0740-3194; 1522-2594
• DOI: 10.1002/(SICI)1522-2594(200005)43:5<657::AID-MRM7>3.0.CO;2-1

The authors addressed the hypothesis that interactions with creatine kinase (CK) play a role in the off‐resonance magnetization transfer (MT) effect of creatine in skeletal muscle. Toward that aim, 1H MT studies were done on hindleg muscle in wild‐type mice and in transgenic mice, lacking cytoplasmic CK and/or mitochondrial CK. The 1H MT effect was essentially identical in wild‐type muscle and the two single CK knock‐out muscles, while moderately decreased in tissue lacking both CK isoforms. 31P‐NMR showed no off‐resonance 31P MT effect in skeletal muscle for PCr in any of the mice, while the enzymatic CK reaction flux was circa 0.2–0.3 sec−1 in the wild‐type muscle and in muscle deficient in mitochondrial CK. The CK enzyme flux was negligible in the other two CK knock‐outs. These data suggest that CK plays a minor role in the 1H MT effect of creatine. Irrespective of the underlying mechanism the creatine MT phenomenon probably has no significant consequences for the thermodynamic availability of total creatine to the CK reaction. Magn Reson Med 43:657–664, 2000. © 2000 Wiley‐Liss, Inc.