17 research outputs found

    Glucagon-Like Peptide-1 and its Analogues Act in the Dorsal Raphe and Modulate Central Serotonin to Reduce Appetite and Body Weight.

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    Glucagon-like peptide-1 (GLP-1) and serotonin play critical roles in energy balance regulation. Both systems are exploited clinically as anti-obesity strategies. Surprisingly whether they interact in order to regulate energy balance is poorly understood. Here we investigated mechanisms by which GLP-1 and serotonin interact at the level of the CNS. Serotonin depletion impaired the ability of exendin-4, a clinically utilized GLP-1 analogue, to reduce body weight in rats, suggesting serotonin is a critical mediator of the energy balance impact of GLP-1R activation. Serotonin turnover and expression of 5HT2A and 5HT2C serotonin receptors in the hypothalamus were altered by GLP-1R activation. We demonstrate that 5HT2A, but surprisingly not 5HT2C, receptor is critical for weight-loss, anorexia and fat mass reduction induced by central GLP-1R activation. Importantly, central 5HT2A receptors are also required for peripherally injected liraglutide to reduce feeding and weight. Dorsal raphe (DR) harbors cell bodies of serotonin producing neurons that supply serotonin to the hypothalamic nuclei. We show that GLP-1R stimulation in DR is sufficient to induce hypophagia and increase electrical activity of the DR serotonin neurons. Finally our results disassociate brain metabolic and emotionality pathways impacted by GLP-1R activation. This study identifies serotonin as new critical neural substrate for GLP-1 impact on energy homeostasis, and expands the current map of brain areas impacted by GLP-1R activation.This research was funded by the Swedish Research Council (2014-2945 and 2013-7107), Novo Nordisk Foundation Excellence project grant, Ragnar Söderberg Foundation, Harald Jeanssons Stiftelse and Greta Jeanssons Stiftelse, and Magnus Bergvalls Stiftelse

    ICAR: endoscopic skull‐base surgery

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    The impact of the American mink (Neovison vison) on native vertebrates in mountainous streams in Central Spain

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    The American mink (Neovison vison) is responsible for the widespread decline of its prey species in the regions where it is an invasive species. The current expansion of the mink in the Iberian Peninsula has aroused concern among conservationists about its negative impact on the rich native fauna. However, evidence for this is still scarce, although there are several studies establishing a direct causal relationship between declining native species and the presence of the American mink. Thus, it is important to further investigate the responses of native species to the American mink in several habitats and locations to enhance our knowledge about the patterns of the effect of the mink in Spain, as well as to inform conservation actions. A field study of the impact of the American mink on a mountainous vertebrate community in central Spain is presented. We studied six species: two fish, one amphibian, one bird, and two mammals. The general results showed a species-specific sensitivity to mink presence, with the Mediterranean water shrew (Neomys anomalus) and the southern water vole (Arvicola sapidus) being the most affected because their ranges were significantly decreased after the introduction of the mink. Regarding the other species, neither their abundance nor range was apparently affected by the American mink. The predatory behavior of the mink and interactions with other carnivores could account for these results. These data aid in shedding light about the current impact of the mink on invaded areas of the Iberian Peninsula and highlight the variability of its effects, as well as the urgent need to establish a general program of control of the mink to avoid negative effects upon native prey communities. Furthermore, given the different responses of native species, we propose that measures to protect native species should be based on species-specific goals and attributes. © 2013 Springer-Verlag Berlin Heidelberg.Pablo García-Díaz, Valentín Arévalo, Rafael Vicente, Miguel Lizan
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