Cargando…

The Effect of Insulin Infusion on the Metabolites in Cerebral Tissues Assessed With Proton Magnetic Resonance Spectroscopy in Young Healthy Subjects With High and Low Insulin Sensitivity

OBJECTIVE: Insulin may play important roles in brain metabolism. Proton magnetic resonance spectroscopy ((1)H-MRS) of the central nervous system gives information on neuronal viability, cellular energy, and membrane status. To elucidate the specific role of insulin action in the brain, we estimated...

Descripción completa

Detalles Bibliográficos
Autores principales: Karczewska-Kupczewska, Monika, Tarasów, Eugeniusz, Nikołajuk, Agnieszka, Stefanowicz, Magdalena, Matulewicz, Natalia, Otziomek, Elżbieta, Górska, Maria, Strączkowski, Marek, Kowalska, Irina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Diabetes Association 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3747869/
https://www.ncbi.nlm.nih.gov/pubmed/23596182
http://dx.doi.org/10.2337/dc12-1437
Descripción
Sumario:OBJECTIVE: Insulin may play important roles in brain metabolism. Proton magnetic resonance spectroscopy ((1)H-MRS) of the central nervous system gives information on neuronal viability, cellular energy, and membrane status. To elucidate the specific role of insulin action in the brain, we estimated neurometabolites with (1)H-MRS and assessed their regulation by insulin infusion and their relationship with insulin sensitivity. RESEARCH DESIGN AND METHODS: We studied 16 healthy young men. (1)H-MRS was performed at baseline and after 240 min of euglycemic-hyperinsulinemic clamp. Voxels were positioned in the left frontal lobe, left temporal lobe, and left thalamus. The ratios of N-acetylaspartate (NAA), choline-containing compounds (Cho), myo-inositol, and glutamate/glutamine/γ-aminobutyric acid complex (Glx) to creatine (Cr) and nonsuppressed water signal were determined. The participants were divided into subgroups of high (high IS) and low (low IS) insulin sensitivity. RESULTS: Baseline neurometabolic substrates were not different between the groups. Insulin infusion resulted in an increase in frontal NAA/Cr and NAA/H(2)O and frontal and temporal Glx/Cr and Glx/H(2)O and a decrease in frontal Cho/Cr and temporal Cho/H(2)O and myo-inositol/H(2)O (all P < 0.05, except temporal Glx/H(2)O, P = 0.054, NS) in the high-IS, but not in the low-IS, group. Insulin sensitivity correlated positively with frontal NAA/Cr and NAA/H(2)O and temporal Glx/H(2)O and negatively with temporal myo-inositol/Cr and myo-inositol/H(2)O assessed during the second (1)H-MRS (all P < 0.05). CONCLUSIONS: Insulin might influence cerebral metabolites, and this action is impaired in subjects with low whole-body insulin sensitivity. Thus, our results provide a potential link between insulin resistance and altered metabolism of the central nervous system.