, 2012 and Wang et al., 2001): (BE = fresh weight of mushrooms/dry weight of substrate) × 100 Subsequently, the mushrooms were dried in an oven at 45 °C for the determination of their dry

weight. To determine the content of minerals, crude proteins and to evaluate the accessibility of Li, the dried mushrooms were ground using a knife mill and passed through a 2-mm sieve. Samples of 100 mg of dry mushrooms were milled and submitted to digestion with a mixture of nitric acid and perchloric acid (3:1, v:v) at 200 °C for 2 h (Tedesco, Gianello, Crizotinib concentration Bissani, Bohnen, & Volkweis, 1995). The levels of Li were determined using a flame photometer. The standard curve was prepared with the following concentrations of this element: 0.00; 0.09; 0.36; 0.72; 1.44; 1.80; 2.88; 3.60 and 9.00 mg L−1. The percentage of Li was calculated according to the formula: ConcentrationofLiindrymass(μgg-1)=[M]×DFDM×1000where, [M] = mineral concentration in mg L−1, DF = dilution

factor = 0.025, DM = dry mass of sample. The content of Fe, Zn, Cu, potassium (K), calcium (Ca), phosphorus (P), sulphur (S), lead (Pb), chromium (Cr), magnesium (Mg), aluminium (Al),, cadmium (Cd) and nickel (Ni) contained in the mushrooms were measured by inductively-coupled plasma optical emission spectrometry (Optima 3300 DV; Perkin Elmer, Waltham, MA), using specific standards for each mineral. The crude MEK inhibitor protein content was determined using the semimicro-Kjeldahl method (AOAC, 1996). The nitrogen content was multiplied by a factor of 4.38 to calculate

the percentage of crude protein (Kalac, 2009). The sequential extraction and in vitro methods were used to evaluate the accessibility of Li. We compared mushrooms grown in substrate enriched or not with LiCl (0 and 500 mg kg−1) and a psychiatric drug containing lithium carbonate (140.9 mg of Li per g of pill, as reported by the manufacturer). To evaluate the solubility of Li, 1 g of dried mushroom and also 1 g of the psychiatric drug pill were processed according to sequential extraction CHIR-99021 nmr methodology described by Ramos, Hernandez, and Gonzalez (1994) and modified by Ma and Rao (1997). After each successive extraction, the extracts were separated by centrifugation at 1500g for 10 min, and the supernatant was collected. The sediment obtained after each extraction was resuspended and again subjected to extraction to collect a new supernatant. This procedure was repeated until six fractions were obtained. We then conducted the analysis of dissolved Li using a flame photometer. The second method was the in vitro simulation of gastrointestinal digestion, with the purpose of predicting the accessibility of Li in the digestive tract ( Elless et al., 2000 and Glahn et al., 1998). For this, 250 mg of samples of both dried mushrooms and of the psychiatric drug were crushed. Next, the samples were centrifuged at 1500g for 10 min and filtered to obtain soluble extracts.