The complementary and confirmatory insights offered by MDS were evaluated. Results from MDS of the relationship between indicators confirmed the closer relationship within sickness and within depression-like indicators (Fig. 6 left). Dimension 2 differentiated between Selleckchem Torin 1 sickness indicators (receiving positive coefficients) and depression-like indicators (receiving negative coefficients). Dimension 1 differentiated among the sickness indicators weight change (receiving positive coefficients) and activity (receiving negative coefficients). The overall consistency of results between the PCA and MDS analyses speaks to the strength of the relationships

among the behavioral indicators measured in this study. The slight differences between the relative coefficients in the PCA and MDS implementations is related to the PCA identification of the linear combination

of indicators that maximize the explained variance adjusted for all higher order combinations, meanwhile MDS preserved the distances between items while representing the items in a lower dimensional space. The results from MDS confirmed the distribution of mice within and between BCG-treatment groups observed in the PCA (Fig. 6 right). Mice from the BCG0 and BCG10 groups were located on either side of the two-dimensional Trichostatin A datasheet plot, meanwhile mice in the BCG5 group were located in-between. Multidimensional scaling analysis offered insights into the relative behavior of BCG10 mouse number 22 that clustered closer to the BCG0 group. Fig. 6 (right) demonstrates that this mouse was approximately half-way in between

group BCG10 and BCG0. Closer inspection of the indicators revealed that despite exhibiting levels of horizontal locomotor activity, rearing, forced swim immobility, and sucrose preference consistent with other mice in the BCG10 group, this mouse maintained weight during the trial. The unique combination of levels displayed by this mouse suggests the need to consider multiple sickness and depression-like Non-specific serine/threonine protein kinase indicators simultaneously and the need to measure additional mice. Linear discriminant analysis enabled a perfect discrimination of the mice among the corresponding BCG-treatment groups without miss-assignments. Leave-one-out cross validation confirmed these BCG-treatment class assignments. The coefficients of the behavioral indicators in the indices that discriminate between BCG10, BCG5 and BCG0 offered insights into the impact of indicators in the discrimination between BCG-treated and BCG0 but also within BCG-treated groups (Table 1). A linear trend was observed between the coefficient of the indicator and the BCG-treatment level in all except two behavior indicators. The linear trend consists on an increase (or decrease) in the coefficient with BCG-treatment level. This trend slightly departed for the forced swim immobility; however, the difference in coefficients between BCG-treatment levels was only 10%.