10 research outputs found

    Brain Mechanisms of Flavor Learning

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    Once the flavor of the ingested food (conditioned stimulus, CS) is associated with a preferable (e.g., good taste or nutritive satisfaction) or aversive (e.g., malaise with displeasure) signal (unconditioned stimulus, US), animals react to its subsequent exposure by increasing or decreasing ingestion to the food. These two types of association learning (preference learning vs. aversion learning) are known as classical conditioned reactions which are basic learning and memory phenomena, leading selection of food and proper food intake. Since the perception of flavor is generated by interaction of taste and odor during food intake, taste and/or odor are mainly associated with bodily signals in the flavor learning. After briefly reviewing flavor learning in general, brain mechanisms of conditioned taste aversion is described in more detail. The CSā€“US association leading to long-term potentiation in the amygdala, especially in its basolateral nucleus, is the basis of establishment of conditioned taste aversion. The novelty of the CS detected by the cortical gustatory area may be supportive in CSā€“US association. After the association, CS input is conveyed through the amygdala to different brain regions including the hippocampus for contextual fear formation, to the supramammillary and thalamic paraventricular nuclei for stressful anxiety or memory dependent fearful or stressful emotion, to the reward system to induce aversive expression to the CS, or hedonic shift from positive to negative, and to the CS-responsive neurons in the gustatory system to enhance the responsiveness to facilitate to detect the harmful stimulus

    Attenuation of Food Intake by Fragrant Odors: Comparison between <em>Osmanthus fragrans</em> and Grapefruit Odors

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    Odors affect various physiological and mental activities. Previous studies in rats have shown that the odors of grapefruit and Osmanthus fragrans (OSM, fragrant tea olive) attenuate food intake, leading to a reduction in body weight gain, but it is not yet clear whether the causative mechanisms underlying these effects are the same for both odors. The first part of the present study revealed that grapefruit odor had no effect on the expression of feeding-related neuropeptides, in contrast to the previous finding that OSM odor suppresses orexigenic and activates anorexigenic neuropeptides in the hypothalamus of the rat. The second part revealed that OSM odor activated the parasympathetic nerve, in contrast to the previous finding demonstrating that grapefruit odor activates sympathetic nerve activity. The third part was performed to confirm the previous findings about the effects of OSM odor on appetitive reactions in humans. In human subjects, we found that continuous exposure to OSM odor attenuated appetite and consumption of snacks (cookies) and improved mood, when evaluated using the POMS (Profile of Mood States) data from university students. In conclusion, OSM odor attenuated appetite and decreased food intake in humans, and the underlying causative mechanisms differed from those mediating the effects of grapefruit odor, specifically in terms of the expression of hypothalamic feeding-related neuropeptides and autonomic nerve activity

    Clinical characteristics of HIV-1-infected patients with high levels of plasma interferon-Ī³: a multicenter observational study

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    Abstract Background Circulating interferon-Ī³ (IFN-Ī³) concentration may be sustained at a high level regardless of the initiation of antiretroviral therapy (ART) in some patients with HIV-1 infection. In the present study, we examined the clinical characteristics of HIV-1-infected patients with high levels of plasma IFN-Ī³. Methods The study subjects were patients infected with HIV-1 who were either naĆÆve to ART with CD4+ cell count >ā€‰200 cells/Ī¼L (nā€‰=ā€‰12), or had achieved viral suppression after ART for over a year (nā€‰=ā€‰188). The levels of plasma IFN-Ī³ and interleukin-6 (IL-6) were measured by the enzyme-linked immunosorbent assay. Patients were divided into high IFN-Ī³ and low IFN-Ī³ groups based on a cutoff level of 5ā€‰pg/mL. Results The high IFN-Ī³ group included 41 patients (21%). Compared to the patients on ART with low IFN-Ī³ levels, those on ART in the high IFN-Ī³ group were more likely to be younger than 50ā€‰years of age (Pā€‰=ā€‰0.0051) and less likely to have dyslipidemia (Pā€‰=ā€‰0.0476) or to be on a protease inhibitor (Pā€‰=ā€‰0.0449). There was no significant difference between groups in the median increase of CD4+ cell counts from the initiation of ART for up to 3ā€‰years. However, after 4ā€‰years, the increase in CD4+ cell counts was significantly lower in the high IFN-Ī³ group compared with that in the low IFN-Ī³ group. There were no such significant differences between patients with low and high (>ā€‰2ā€‰pg/mL) levels of plasma IL-6. Conclusion We concluded that HIV-1-infected patients with high levels of circulating IFN-Ī³ did not have a higher rate of comorbidities related to immune activation. However, they exhibited lower CD4+ cell count recovery after 4ā€‰years of being on ART. This deficit could be a consequence of persistent immune activation
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