It is impossible to remove methylmercury (MeHg) from biological systems because MeHg is found throughout our environment in many fresh and salt water fish. The consumption of fish is important to human nutrition and health. The mechanism of MeHg neurotoxicity must be understood to minimize adverse exposure consequences. The dissertation objective was to: 1) compare mechanisms of MeHg neurotoxicity between animals exposed as adults and those exposed during gestation, and 2) develop an in vitro test model of in vivo MeHg exposure. Total mercury (Hg) levels in tissue / cells were determined by combustion / trapping / atomic absorption. Cell death was determined by Fluoro-Jade histochemical staining and activated caspase 3 immunohistochemistry for in vivo studies, and Trypan blue exclusion, lactate dehydrogenase activity, and cytotoxicity assays for in vitro studies. Mitochondrial membrane potential (MMP), intracellular calcium ion concentration ([Ca2+]i), and production of reactive oxygen species (ROS) were determined using fluorescence microscopy or microplate reader assays. Young adult C57Bl/6 mice were exposed to a total dose of 0, 1.0, or 5.0 mg/kg body weight MeHg divided over postnatal days (P)35 to 39. Pregnant female mice were exposed to a total does of 0, 0.1, or 1.0 mg/kg body weight MeHg divided over gestational days (G)8 to 18. SY5Y cells were exposed to 0, 0.01, 0.1, or 1.0 ?M MeHg or HgCl2 for 24, 48, or 72 hours. Total Hg in brains of young adult mice, mouse pups, and SY5Y cells accumulated in a dose-dependent manner. Cell death increased in SY5Y cells exposed to the highest concentrations of MeHg and HgCl2 used in this study. Cell death increased in the molecular and granule cerebellar cell layers of young adult mice exposed to the highest doses of MeHg used in this study. P0 mouse pups showed no increase in cell death within the cerebellum following MeHg exposure. Cerebella of mice at P10 exhibited decreased dying cells only in the external germinal layer. Low concentrations of MeHg affected MMP in both in vivo and in vitro studies, but did not result in decreased MMP typically associated with higher MeHg concentrations. [Ca2+]i was increased throughout the in vivo experiments in an age- , sexand brain region-dependent manner. Generation of ROS was decreased in both in vivo and in vitro studies with both the MeHg and HgCl2 (in vitro) treatments. In summary, low and moderate MeHg exposure, both in vivo and in vitro, altered mitochondrial function, Ca2+ homeostasis, and ROS differently than what is reported in the literature for higher MeHg exposure concentrations. SY5Y cells were sensitive to low-levels of MeHg and HgCl2 and responded similarly to cells in the whole animal studies, thus making SY5Y cells realistic candidates for mechanistic MeHg studies. Cell culture and whole animal neuronal functional studies at chronic low-level MeHg exposure are limited. These data suggest that low-levels of MeHg may affect neuronal function. Therefore, further chronic low-level MeHg neuronal functional studies are warranted.

L’évolution de la denture des vertébrés est un sujet majeur et des plus intéressants en biologie développementale évolutive (évo-dévo). Dans ce domaine, la souris Mus musculus est traditionnellement l’animal modèle utilisé. La denture de la souris inclus quatre incisives à croissance continue et douze molaires présentant une organisation caractéristique de leurs cuspides. Le réseau moléculaire régulant le développement de ces deux types de dents est très spécifique.La cascade ERK-MAPK est impliquée lors de différentes étapes du développement dentaire. Une étude comparée du phénotype des molaires de souris mutantes pour des gènes activés à différents points de la cascade a démontré l’existence d’un phénotype caractéristique, à savoir la présence d’une dent surnuméraire en position mésiale des rangées de molaires, ainsi que la présence d’anomalie dans le nombre et la forme de certaines cuspides. Parmi ces caractères présents chez les mutants, certains rappellent des caractères ancestraux présents uniquement chez des rongeurs fossiles. Ceci appuie le rôle que la cascade ERK-MAPK a pu jouer au cours de l’évolution de la denture chez les rongeurs. En travaillant sur une lignée transgénique sur-exprimant un inhibiteur de cette cascade, j’ai pu perfectionner notre connaissance du rôle des gènes de la famille Fgf dans les processus de mise en place des centres de signalisation dentaire et de minéralisation de l’émail.Si l’on considère les incisives à croissance continue, la denture de la souris est dynamique à l’échelle de la vie d’un individu. Réalisant un suivi des incisives supérieures d’une cohorte de souris au cours de leur vieillissement, j’ai pu préciser la chronologie d’apparition de défauts liés au vieillissement. Ces défauts apparaissent sur les incisives à partir de six mois, et le plus fréquent est le développement d’un sillon visible sur l’émail de l’incisive. J’ai enfin utilisé des techniques de séquençage de nouvelle génération (NGS) pour comprendre les bases moléculaires du vieillissement des niches de cellules souches des incisives. Ce faisant, j’ai détecté des changements dans les profils d’expression de gènes régulant le maintien des cellules souches, la prolifération cellulaire et le métabolisme. La présence d’un sillon apparaît corrélée à une forte réponse immunitaire détectée dans les tissus dentaires, ce qui constitue une perspective d’étude majeure dans le but d’achever la caractérisation du vieillissement des cellules souches dentaires. / The evolution of the vertebrate dentition is among the most exciting topics in the evo-devo field, with particular attention being drawn to the mouse model. The mouse dentition includes four ever-growing incisors and twelve molars with a specific cusp pattern. Incisors and molars develop according to a tightly regulated molecular network.The ERK-MAPK cascade is involved at various stages of tooth development. Molar tooth phenotype comparisons in mutant mice for genes acting at various levels of the cascade highlighted a dental phenotype signature, which consists in the presence of a supernumerary tooth and shared cusp pattern defects. Some of these recall characters present in fossil rodents, supporting the ERK-MAPK as a good candidate to explain some evolutionary trends of the rodent dentition. By working on a mouse line over-expressing one of this pathway inhibitor in the oral epithelium, I perfect our understanding of Fgf gene role in specifying signaling center formation at the right stage, and in achieving correct mineralization.When considering evergrowing incisors, mouse dentition is also dynamic at the lifetime scale. I monitored the ageing process of the mouse upper incisors, and provided a chronology of occurrence of the variety of age-related defects display. These defects are set up from the six months on, the most frequent abnormality being the presence of an enamel groove along the surface of the incisor. Using Next Generation Sequencing technologies, I detected transcriptomic changes in the stem cell niches affecting cell proliferation and metabolism, as well as the stem cell niche functioning. The correlation found between the groove occurrence and a large immune response in dental tissues expands our concern for dental stem cell ageing.

Indiana University-Purdue University Indianapolis (IUPUI) / Multiple lines of High Alcohol Preferring (HAP) mice were selectively bred for their intake of 10% ethanol (v/v) during 24-h daily access over a four-week period, with the highest drinking lines exhibiting intakes in excess of 20 g/kg/day. Drinking rhythms and corresponding blood ethanol concentrations (BEC) of the highest drinking HAP lines to those of the C57BL/6J (B6) inbred strain. Adult male and female crossed HAP (cHAP), HAP1 and B6 mice had free-choice access to 10% ethanol and water for 3 weeks prior to bi-hourly assessments of intake throughout the dark portion of a reverse 12:12 light dark cycle. In another cohort of cHAP mice, the same procedure was used to assess bi-hourly ethanol intake, and blood samples were taken across the day to look at the pattern of accumulation in these mice. Finally, considering the high level of intake by cHAP mice, we were interested in assessing whether metabolic and functional tolerance develop following chronic free-choice access, which were assessed using 2.0 and 1.75 g/kg challenge doses of 20% ethanol, respectively. cHAP and HAP1 mice maintained an excessive level of intake throughout the dark portion of the cycle, accumulating mean BEC levels of 261.5 + 18.09 and 217.9 + 25.02 mg/dl at 7-8 hours following lights off, respectively. B6 mice drank comparatively modestly, and did not accumulate high BEC levels (53.63 + 8.15 mg/dl). In the cHAP cohort, mean BECs were 112.47 + 19.91 at 2 hours after lights off, 189.00 + 27.40 at 6 hours after lights off, 193.80 + 29.66 at 10 hours after lights off, and 89.68 + 22.19 at 2 hours after lights on. Further, following 3 weeks of ethanol access, cHAP mice had a faster rate of ethanol metabolism and fewer hind slips than water-only exposed mice (ps < .05). In conclusion, the excessive free-choice drinking demonstrated by the HAP1 and cHAP lines, as well as the pattern of sustained high BECs in cHAP mice, challenge the notion that rodents will not reliably and voluntarily sustain ethanol intake at pharmacologically relevant levels. These results suggest that the highest drinking HAP lines may provide a unique opportunity for modeling the excessive intake that has been observed in alcohol-dependent individuals. Further, we observed that cHAP mice develop both metabolic and functional tolerance to the ataxic effects of ethanol following 3 weeks of free-choice access. Together, these findings support HAP mice as translational rodent model of alcoholism, and provide rationale for exploration of the predisposing factors for excessive consumption, as well as the development of physiological, behavioral, and toxicological outcomes following alcohol exposure.

Following a stroke, normal usage of the impaired limb guides spontaneous recovery across many months or even years; however, recovery is rarely complete. Pre-clinical tools are needed to investigate stroke-induced cortical reorganization over long periods. This thesis aims to characterize stroke impairment and spontaneous recovery in parallel with a battery of behaviour tasks in a mouse model of focal stroke. Young adult Thy1-ChR2 mice were implanted with a transcranial window over the intact skull permitting cortex visualization and enabling longitudinal assessments with light-based motor mapping and intrinsic signal optical imaging. Furthermore, mice were tested on sensorimotor behavioural tasks in parallel to the mapping experiments. These experiments allowed for the quantification of impairments in the sensorimotor cortex and forelimb function while identifying regions within the sensorimotor cortex that show re-mapping associated with behavioural recovery. Following primary motor cortex-stroke induction, both sensory and motor map impairments occurred. Sensory map transient impairments recovered within the same atlas-defined regions two weeks after a primary motor cortex stroke as identified by intrinsic signal optical imaging. In contrast, motor forelimb recovery was observed four weeks after the stroke in the peri-infarct region, the supplemental motor cortex, and the contralesional motor cortex. This recovery was identified through a combination of analyses, including changes in the mapped area and the amplitude of evoked forelimb movements using light-based motor mapping. Behavioural recovery occurred four to six weeks post-stroke, depending on the sensitivity of the task in forelimb impairment. Additionally, the contralesional hemisphere and forelimb did not show impairment acutely but evoked forelimb amplitude was significantly increased by post-stroke week four for both forelimbs. As the first study to conduct within-animal longitudinal spontaneous recovery sensory and motor map experiments using bilateral forelimb and hemispheric representations, we show that 1) photothrombotic stroke impacts both forelimb representations pertained within the ipsilesional hemisphere in LBMM experiments, 2) recovery of the impaired forelimb occurs ipsilesionally and contralesionally and, 3) impairments from stroke observed through motor mapping are functionally relevant and precede behavioural recovery ranging from zero to two or more weeks depending on the motor cortex's involvement in the behavioural task.

No description available.

La lutte contre les rongeurs est souvent un enjeu majeur dans les agroécosystèmes. Nous avons conduit une étude comparative dans des plantations de palmiers à huile dans les provinces de Riau et de Bangka en Indonésie. Dans les deux zones, des chouettes ont été introduites pour la lutte contre les rats ; toutefois, à Riau les rats sont maintenus à des niveaux de population acceptables sans recours au raticide, tandis qu’à Bangka les dégâts des rats sont très importants et l’usage de raticide intensif. Nous avons comparé ce deux systèmes en terme d’abondance et/ou de régime alimentaire de deux prédateurs, chouettes et petits carnivores. D’après nos résultats, les petits carnivores sont beaucoup plus abondants dans les plantations à Riau qu’à Bangka, et le chat léopard (Prionailurus bengalensis) est absent à Bangka tandis que cette espèce domine à Riau. Nos résultats suggèrent également que la prédation sur les rats par les chouettes et les petits carnivores serait moindre à Bangka qu’à Riau. D’une manière générale, cette étude confirme l’hypothèse selon laquelle les petits carnivores, notamment les chats léopard, joueraient un rôle important dans la lutte contre les rats en palmeraies. Par ailleurs, nous avons analysé la distribution spatiale des petits carnivores en plantation. Nos résultats suggèrent que, bien que l’habitat palmeraie soit largement utilisé la nuit par certains petits carnivores comme le chat leopard, qui y trouve une abondante ressource alimentaire, la plupart des espèces sont dépendantes de la forêt. Les gestionnaires des palmeraies devraient adapter leurs pratiques, afin de favoriser les petits carnivores dans une perspective de lutte contre les rats. / Rodent pest control is often a major issue in agroecosystems. We conducted a 3-year comparative study (2010-2012) in oil palm plantations in Riau and Bangka provinces, in Indonesia: in both areas barn owls have been introduced for rat control, and were at least as abundant in Bangka plantations than in Riau, but in Riau rat populations have been maintained at an acceptable level without the use of rodenticide, whereas in Bangka intensive rodenticide applications did not prevent high levels of rat damage. We compared these two contrasting systems in terms of predator community (barn owls and small carnivores) abundance and/or diet. We found that small carnivores were much more abundant in Riau plantations than in Bangka, and that the leopard cat (Prionailurus bengalensis) was the dominant species in Riau while absent from Bangka. Our results on diet suggested that rat prey intake from barn owls and from the small carnivore community would be less in Bangka plantations than in Riau. Broadly, our results suggest that small carnivores, notably the leopard cat, play an important role in rodent control. In addition, we investigated spatial distribution of small carnivores within the oil palm habitat. Our results support the hypothesis that, although the oil palm may be habitable for some small carnivore species such as the leopard cat, where they supposedly forage at night, most species still need forest for their survival in oil palm landscapes. Oil palm plantations managers should adapt agricultural practices and land-use to enhance small carnivores, with the view to improve rodent control.

Indiana University-Purdue University Indianapolis (IUPUI) / Losing a job or a significant other are examples of incentive shifts that result in negative emotional reactions. The occurrence of negative life events is associated with increased drinking, and alleviation of negative emotions has been cited as a drinking motive for individuals with problematic drinking patterns (Keyes et al., 2011; Adams et al., 2012). Further, there is evidence that certain genotypes drink alcohol in response to stressful negative life events (Blomeyer et al., 2008; Covault et al., 2007). It is possible that shared genetic factors contribute to both alcohol drinking and emotional reactivity, but there is a critical need for this relationship to be understood. The first aim of this proposal will use an incentive downshift paradigm to address whether emotional reactivity is elevated in mice predisposed to drink alcohol. The second aim of this proposal will address if reactivity to an incentive shift can result in rash action using a differential reinforcement of low rates of responding task, and whether this response is also associated with a predisposition for high drinking. The third aim of this proposal will investigate if experimenter administered ethanol reduces contrast effects, and if an incentive shift increases ethanol consumption in a high drinking line. The overall goal of this proposal is to investigate whether reactivity to incentive shift is an important mechanism underlying alcohol drinking in these mice, and the role an incentive shift may play in producing rash action and influencing ethanol consumption.

No description available.

While task-based functional magnetic resonance imaging (fMRI) has helped us understand the functional role of many regions in the human brain, many diseases and complex behaviors defy explanation. Alternatively, if no task is performed, the fMRI signal between distant, anatomically connected, brain regions is similar over time. These correlations in “resting state” fMRI have been strongly linked to behavior and disease. Previous work primarily calculated correlation in entire fMRI runs of six minutes or more, making understanding the neural underpinnings of these fluctuations difficult. Recently, coordinated dynamic activity on shorter time scales has been observed in resting state fMRI: correlation calculated in comparatively short sliding windows and quasi-periodic (periodic but not constantly active) spatiotemporal patterns. However, little relevance to behavior or underlying neural activity has been demonstrated. This dissertation addresses this problem, first by using 12.3 second windows to demonstrate a behavior-fMRI relationship previously only observed in entire fMRI runs. Second, simultaneous recording of fMRI and electrical signals from the brains of anesthetized rats is used to demonstrate that both types of dynamic activity have strong correlates in electrophysiology. Very slow neural signals correspond to the quasi-periodic patterns, supporting the idea that low-frequency activity organizes large scale information transfer in the brain. This work both validates the use of dynamic analysis of resting state fMRI, and provides a starting point for the investigation of the systemic basis of many neuropsychiatric diseases.