Investigation of lithium distribution in the rat brain ex vivo using lithium‐7 magnetic resonance spectroscopy and imaging at 17.2 T

Lithium is the first‐line mood stabilizer for the treatment of patients with bipolar disorder. However, its mechanisms of action and transport across the blood–brain barrier remain poorly understood. The contribution of lithium‐7 magnetic resonance imaging (7Li MRI) to investigate brain lithium distribution remains limited because of the modest sensitivity of the lithium nucleus and the expected low brain concentrations in humans and animal models. Therefore, we decided to image lithium distribution in the rat brain ex vivo using a turbo‐spin‐echo imaging sequence at 17.2 T. The estimation of lithium concentrations was performed using a phantom replacement approach accounting for B1 inhomogeneities and differential T1 and T2 weighting. Our MRI‐derived lithium concentrations were validated by comparison with inductively coupled plasma‐mass spectrometry (ICP‐MS) measurements ([Li]MRI = 1.18[Li]MS, R = 0.95). Overall, a sensitivity of 0.03 mmol/L was achieved for a spatial resolution of 16 μL. Lithium distribution was uneven throughout the brain (normalized lithium content ranged from 0.4 to 1.4) and was mostly symmetrical, with consistently lower concentrations in the metencephalon (cerebellum and brainstem) and higher concentrations in the cortex. Interestingly, low lithium concentrations were also observed close to the lateral ventricles. The average brain‐to‐plasma lithium ratio was 0.34 ± 0.04, ranging from 0.29 to 0.39. Brain lithium concentrations were reasonably correlated with plasma lithium concentrations, with Pearson correlation factors ranging from 0.63 to 0.90. Lithium is the first‐line mood stabilizer treatment of bipolar disorder. Use of Lithium‐7 magnetic resonance imaging to investigate brain lithium distribution remains limited due to the modest sensitivity of the lithium nucleus and the expected low concentrations in the brain. We worked at 17.2 T to image lithium distribution in the rat brain ex vivo. Our results were validated by comparison to the lithium concentrations obtained using inductively coupled plasma‐mass spectrometry.