1 ml/29 g body weight and samples of the parotid and submandibular glands were collected. The animals were then sacrificed with an overdose of the anaesthetic according to the ethical guidelines of the Brazilian College of Animal Experimentation (COBEA). The salivary gland samples were analysed by fluorescence microscopy for the observation of INS-R and ER-alpha. Frozen samples of the salivary glands

were cut into 12-μm thick sections and incubated in blocking solution for 1 h at room temperature for the blockade of nonspecific protein–protein binding sites. Next, the material was incubated for 1 h with the primary rabbit polyclonal antibody against ER-alpha (Santa Cruz Biotechnology, San Diego, CA, USA). The slides were then washed in phosphate buffered saline and incubated with the Rucaparib in vivo fluorescent conjugated Raf inhibitor secondary antibody (goat anti-rabbit, Santa Cruz Biotechnology, San Diego, CA, USA). The sections were mounted in 1,4-diazabicyclo[2.2.2]-octane (Sigma, St. Louis, MO, USA). For the evaluation of insulin receptors, a similar protocol was applied using a primary antibody against INS-R (Santa Cruz Biotechnology, San Diego, CA, USA) diluted in blocking solution. After incubation

with the primary antibody, the sections were washed in phosphate buffered saline and the secondary fluorescein-conjugated antibody (goat anti-rabbit, Santa Cruz Biotechnology, San Diego, CA, USA) diluted in blocking solution was applied. The sections were then washed in phosphate buffered saline and mounted in 1,4-diazabicyclo[2.2.2]-octane (Sigma, St. Louis, MO, USA). The specimens were examined under a TNI-06T-PL fluorescence microscope at the Department of Morphology and Basic Pathology, Faculty of Medicine of Jundiaí. The images were acquired using 10× and 40× objectives. Sections in which the primary antibody was omitted served as negative controls. The intensity of staining was scored as intense, moderate and mild according

to the intensity and distribution of immunoexpression of the cellular receptors in the tissue sections.12 and 45 Leukotriene-A4 hydrolase The mean glucose levels of untreated diabetic animals (group I) were ≥500 mg/dl. There was recovery of glucose levels in animals treated with insulin alone or combined with oestrogen, with mean levels of 190 mg/dl. These levels were similar to those of control animals (170 mg/dl). There was also a decrease of glucose levels in animals undergoing only oestrogen replacement therapy, with mean levels of 280 mg/dl. Mean blood oestrogen levels of groups III and IV (89.3 ± 18.2 pg/ml) were similar to that of the control group (group V) (93.8 ± 12.4 pg/ml). Mean oestrogen levels were 21.3 ± 7.2 pg/ml in animals of groups I and II. Group V showed intense expression of INS-R, mainly close to the acini and glandular ducts (Fig. 1A). Oestrogen receptor (ER-alpha) expression was mild and was localized in the nucleus of ductal cells (Fig. 1B and Table 1).