Datensatz

Zusammenfassung

One of the main problems in systems biology is to obtain information on signal processing between interconnected groups of neurons in highly distributed networks. The recently introduced technique of
manganese (Mn2+) enhanced MRI (MEMRI) to study neuronal connectivity in vivo opens the possibility to these studies. However, several drawbacks exist that challenge its applicability. High Mn2+ concentrations
produce cytotoxic effects that can perturb the circuits under study. In the other hand, the MR signal is proportional to the Mn2+ concentration in tissue and thus, significant amounts of Mn2+ are required to produce detectable contrast and reliable connectivity maps.
Here we attempt to optimize the MEMRI technique by preventing toxicity and improving the quality and
extension of the obtained connectivity maps.
The somatosensory cortex of male SD rats was stereotaxically injected with different Mn2+-containing
solutions. Total amount of injected Mn2+ ranged between 1 and 16 nmol and the injected volumes between 10
and 80 nL. Osmolarity and pH effects were investigated injecting pH buffered solutions of Mn2+ (pH 7.3 in
Tris-HCl buffer vs. 5.5 in H2O) at different concentration (0.05, 0.1 and 0.8 M MnCl2). Same amounts of
Mn2+ (8nmol) delivered to the tissue at different infusion rates were also compared. Following the injection,
T1-weighted MR imaging (250 mm isotropic resolution) was performed in a 7T scanner at different time
points. Fifteen days after the injection animals were sacrificed and brains processed for histology. Nissl
staining as well as GFAP and NeuN immunohistochemistry (selective staining for astrocytes and neurons,
respectively) were performed in the brain sections to examine cellular toxicity.
All injections produced connectivity maps consistent with the known anterograde projections of SI cortex
based on classical neuronal tract-tracing techniques. Our results show that pH buffered solution improve the
effectiveness of MEMRI, increasing T1 contrast in the projection sites. In addition, injections of pH buffered
and isotonic solutions of 50 and 100 mM MnCl2 yielded more extensive connectivity maps, in particular, ipsiand
contra-lateral corticocortical connections were evident in all animal injected with those solutions but not
with the more usual MEMRI protocol (0.8M MnCl2 in H2O). Hypertonic and non-buffered solutions
containing 8nmol Mn2+ resulted in neuronal death and astrogliosis in extensive areas around the injection
point. In sharp contrast, no neuronal toxicity was observed with injections containing up to 8nmol of Mn2+ in
isotonic solutions of up to 100 mM MnCl2 and pH 7.3. Slow infusion rates demonstrated also to be
advantageous and permitted application of larger amounts of Mn2+ without toxic effects, resulting in better T1
contrast in the low density projection fields. Any sign of toxicity was observed in any condition in the
projection fields.
We conclude that refined protocols for MEMRI improve the quality and extension of connectivity maps and
preserves tissue viability, assuring the application of this technique in longitudinal experiments.