Metabolome in Tibialis and Soleus Muscles in Wild-Type and <i>Pin1</i> Knockout Mice through High-Resolution Magic Angle Spinning <sup>1</sup>H Nuclear Magnetic Resonance Spectroscopy
2024
Valeria Righi | Martina Grosso | Renata Battini | Takafumi Uchida | Anna Gambini | Susanna Molinari | Adele Mucci
Skeletal muscles are heterogenous tissues composed of different myofiber types that can be classified as slow oxidative, fast oxidative, and fast glycolytic which are distinguished on the basis of their contractile and metabolic properties. Improving oxidative metabolism in skeletal muscles can prevent metabolic diseases and plays a protective role against muscle wasting in a number of neuromuscular diseases. Therefore, achieving a detailed understanding of the factors that regulate myofiber metabolic properties might provide new therapeutic opportunities for these diseases. Here, we investigated whether peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 (PIN1) is involved in the control of myofiber metabolic behaviors. Indeed, PIN1 controls glucose and lipid metabolism in a number of tissues, and it is also abundant in adult skeletal muscles; however, its role in the control of energy homeostasis in this tissue is still to be defined. To start clarifying this topic, we compared the metabolome of the tibialis anterior muscle (mainly glycolytic) and soleus muscle (oxidative) in wild-type and <i>Pin1</i> knockout mice with High-Resolution Magic Angle Spinning (HR-MAS) NMR on intact tissues. Our analysis reveals a clear demarcation between the metabolomes in the two types of muscles and allows us to decode a signature able to discriminate the glycolytic versus oxidative muscle phenotype. We also detected some changes in <i>Pin1</i>-depleted muscles that suggest a role for PIN1 in regulating the metabolic phenotype of skeletal muscles.
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