, 2002 and Uwano et al., 1995). In summary, MeAV projections are a subset of those arising from the MeAD and MePV. Their major outputs to the amygdalostriatal transition area and to the dorsomedial and central parts of the ventromedial hypothalamic nucleus suggest that the MeAV may play a role in orienting responses to chemosensory cues and defensive behaviors

elicited by the odor of predators. Part of the material examined in this study was collected from a large library of cases used in previous S3I-201 nmr investigations. The experiments were conducted on adult female Wistar albino rats weighing 170–210 g (n = 40). The animals were housed in groups of four in standard polypropylene cages with food and water ad libitum and maintained under controlled environmental conditions VE-821 clinical trial (21 ± 1 °C, 12-hour light–dark cycle with lights on at 6 am). The surgical procedures were performed under general anesthesia with a solution containing ketamine hydrochloride (Vetbrands, São Paulo, Brazil; 9 mg/100 g, i.p.) and xylazine (Vetbrands, São Paulo, Brazil; 1 mg/100 g, i.p.). Animal care and all the experimental protocols were approved by the local Animal Research

Committee and are in accordance with the U.S. National Institutes of Health Guidelines for the Care and Use of Laboratory Animals. Unilateral injections of PHA-L (Vector, Burlingame, CA; 2.5% in 0.1 M sodium phosphate buffer (PB), pH 7.4) were placed stereotaxically in different parts of the Me (n = 14) and of FG (Fluorochrome, Denver, CO; 2% in saline), in major targets of the Me,

including the lateral amygdaloid nucleus (n = 1), posterior basomedial amygdaloid nucleus (n = 2), amygdalostriatal transition area (n = 2), BST Liothyronine Sodium (n = 6), medial preoptic nucleus (n = 5), anterior hypothalamic nucleus (n = 5) or ventromedial hypothalamic nucleus (n = 5). The tracers were delivered by iontophoresis through a glass micropipette with an internal tip diameter of 10–15 μm for PHA-L and 20–25 μm for FG, by passing a positive-pulsed current, 7 s on/off intervals, set at 5 μA for 10–15 min with PHA-L, or at 1.5 μA for 5–10 min with FG. To reduce the leakage of tracer along the pipette track, the pipette was left in place for an additional 10–15 min period. After a survival of 10–14 days for PHA-L injections and 5–10 days for FG injections, the rats were deeply anesthetized and perfused transcardially by the aid of a peristaltic pump with a brief saline rinse followed by ice-cold 4% paraformaldehyde in 0.1 M PB (up to 500 ml for 30 min). Several hours later, the brains were removed from the skull, cryoprotected by overnight immersion in a 20% sucrose solution in PB at 4 °C and sectioned in the coronal plane at 40 μm into four series on a sliding microtome. One or two series of sections were processed by immunohistochemistry by using the avidin–biotin–peroxidase (ABC) technique.