Offline consolidation of spatial memory: Do the cerebellar output circuits play a role? A study utilizing a Morris water maze protocol in male Wistar rats.

To address whether the cerebellum takes part to spatial memory consolidation related to navigation, male Wistar rats were trained daily (4 days), in a Morris water maze to found a submerged escape platform by use of distal cues (place training test). Retention of the allocentric map was evaluated in the probe test (without platform), before the place test. Bilateral shutdown of deep cerebellar nuclei was carried by infusion of the GABA-A agonist muscimol (0.25 µl at 1 µg/µl) immediately after each place test. Histology revealed a dorsal dentate nucleus (DDN) group, with muscimol diffusion confined to dentate nuclei, and a ventromedial/dentate nuclei (VMDN) group, with muscimol additionally involving fastigial, interpositus and vestibular nuclei. In the place test, Vehicle, DDN and VMDN groups reduced latency and distance to the platform over the 4 days and within the single day, indicative of efficient acquisition and working memory; navigational trajectories however differed in that, while Vehicle and DDN groups evolved to use direct paths, VMDN group indulged to navigate in proximity to the platform, suggesting an impairment in refining the spatial map. In the probe test VMDN, unlike Vehicle and DDN animals, failed to develop a preference for the quadrant where the platform was previously located, indicating a consolidation deficit. In conclusion, ventromedial cerebellar related structures may contribute to the process of consolidation of an allocentric spatial memory: their inactivation may have impaired the offline integration of idiothetic information with allothetic signals within the navigational network, leading to a coarse resolution map.

Bisphenol-A differently affects estrogen receptors-alpha in estrous-cycling and lactating female rats.

The effect of long-term exposure to bisphenol-A (BPA) on estrogen receptor-alpha (ER) immunoreactivity was studied in the medial preoptic area, arcuate nucleus and the ventromedial nucleus of the hypothalamus of estrous cycling and lactating female rats. Pregnant/lactating or estrous cycling rats were exposed to BPA (40 mg/Kg/day) or peanut oil. Lactating females showed fewer ER-immunoreactive cells than non-lactating females in the medial preoptic area and ventromedial nucleus of the hypothalamus. BPA induced an increase in ER-immunoreactive cells in the medial preoptic nucleus irrespective of lactation. BPA only induced a decrease in ER-immunoreactive cells in the arcuate nucleus of the lactating group; oil induced an increase in ER-immunoreactive cells in the lactating with respect to non-lactating group. The results demonstrate that exposure of adult females to BPA modifies the number of ERs.

Haloperidol treatment decreases nerve growth factor levels in the hypothalamus of adult mice.

1. In a first study different doses of haloperidol (0.6, 1.2, 2.5, 5, 10, or 20 mg/kg; intraperitoneally) were administered to adult male mice (CD-1 strain) and tested for their ability to induce catalepsy. 2. The minimal haloperidol dose inducing complete catalepsy was found to be the 10 mg/kg dose and selected for the second experiment. 3. Using an immunoenzymatic assay (ELISA) hypothalamic nerve growth factor (NGF) level was measured 20 or 180 min following haloperidol injection (10 mg/kg). 4. Haloperidol treatment decreased NGF levels in mouse hypothalamus and this effect did not differ at the two time points tested. 5. The role of hypothalamic NGF in stress-related events is discussed.

Serum NGF levels increase during lactation and following maternal aggression in mice.

In the present study, serum levels of nerve growth factor (NGF) were assessed in virgin and in lactating female CD-1 mice. In the case of the lactating females, NGF levels were assessed both under basal conditions and 60 and 180 min following a 10 min encounter with a male or a nonlactating female mouse. Basal serum NGF levels of lactating females were higher than those of virgin females but did not increase significantly above base after an aggressive encounter with a male or a female conspecific. Female intruders were attacked in a ritualized manner. In contrast, males received numerous bites to vulnerable regions of their body. A positive correlation was found between serum NGF levels and pattern of aggression in females confronting male conspecifics. Thus, in lactating mice, serum NGF levels following an aggressive encounter relate to the specific pattern of behavior the female uses to defend the offspring.

NGF effects on hot plate behaviors in mice.

Adult CD-1 male mice were injected intravenously with 2.5 micrograms/g of highly purified murine NGF and then assessed for hot plate responding (52 degrees C) at 15, 30, 60, 180, and 360 min (repeated test) or at 30, 60, or 360 min (single test, i.e., exposure to hot plate only once). Control animals received cytochrome c (2.5 micrograms/g). In the repeated test, NGF produced hyperalgesia, increasing the number of jumps (particularly at 30 and 60 min postinjection), while in the single test the pain reaction of NGF-treated animals remained unaffected. Sensitization of C-fibers in the periphery or release of bioactive mediators from mast cells may account for NGF-induced changes in nociception.