Transport of biotinylated dextran amine shows the spatial segregation of mechanosensory afferents in the nucleus tuberis anterior (TA) of a gymnotiform fish, Gymnotus cf. carapo. Only the intermediate subdivision of this nucleus receives projections from the lateral region of the ventral torus semicircularis (TSv), which represents the principal midbrain center for mechanosensory information processing, and from the ventral nucleus praeeminentialis, which receives collaterals of ascending second order mechanosensory fibers that emerge from the mechanosensory lateral line lobe. Considering this aspect, a rostrocaudal subdivision of the TA is proposed. The TA also receives input from regions subserving other sensory modalities, suggesting a role in multisensory interaction. Another important finding of this work consisted in the demonstration of reciprocal connections between the TA and the inferior lobe of the hypothalamus, which is known to receive gustatory, visual, and electrosensory input and is therefore considered a multisensory integration center involved in feeding and aggressive behavior. Furthermore, reciprocal connections between the TA and the preelectromotor central-posterior/prepacemaker complex may provide an access for the processed mechanosensory information to interact with the transient modulations of the electric organ discharge that accompany different behaviors.
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http://dx.doi.org/10.1002/cne.21413 | DOI Listing |
Front Nutr
December 2024
Department of Pathophysiology, School of Basic Medicine, Qingdao University, Qingdao, Shandong, China.
Objective: The ventral tegmental area (VTA), a pivotal hub in the brain's reward circuitry, receives inputs from the lateral hypothalamic area (LHA). However, it remains unclear whether melanin-concentrating hormone (MCH) and orexin-A (OX-A) neurons in the LHA exert individual or cooperative influence on palatable food consumption in the VTA. This study aims to investigate the modulatory role of MCH and OX-A in hedonic feeding within the VTA of high-fat diet (HFD) mice.
View Article and Find Full Text PDFJ Neurosci
January 2025
Laboratory of Reproductive Neurobiology, Hun-Ren Institute of Experimental Medicine, Budapest, 1083 Hungary;
While hypothalamic kisspeptin (KP) neurons play well-established roles in the estrogen-dependent regulation of reproduction, little is known about extrahypothalamic KP-producing (KP) neurons of the lateral septum. As established previously, expression in this region is low and regulated by estrogen receptor- and GABA receptor-dependent mechanisms. Our present experiments on knock-in mice revealed that transgene expression in the LS begins at P33-36 in females and P40-45 in males and is stimulated by estrogen receptor signaling.
View Article and Find Full Text PDFSleep Sci
December 2024
Departamento de Psicobiologia, Escola Paulista de Medicina, Universidade Federal de São Paulo, São Paulo, SP, Brazil.
Melanin-concentrating hormone (MCH) and hypocretins (Hcrt) 1 and 2 are neuropeptides synthesized in the lateral hypothalamic area by neurons that are critical in the regulation of sleep and wakefulness. Their receptors are located in the same cerebral regions, including the frontal cortex and hippocampus. The present study aimed to assess whether 96 hours of paradoxical sleep deprivation alters the functioning of the MCH and hypocretin systems.
View Article and Find Full Text PDFMol Psychiatry
December 2024
Peking University Sixth Hospital, Peking University Institute of Mental Health, NHC Key Laboratory of Mental Health (Peking University), National Clinical Research Center for Mental Disorders (Peking University Sixth Hospital), 100191, Beijing, China.
Sleep interacts reciprocally with the gut microbiota. However, mechanisms of the gut microbe-brain metabolic axis that are responsible for sleep behavior have remained largely unknown. Here, we showed that the absence of the gut microbiota can alter sleep behavior.
View Article and Find Full Text PDFNat Med
December 2024
Defitech Center for Interventional Neurotherapies (.NeuroRestore), CHUV/UNIL/EPFL, Lausanne, Switzerland.
A spinal cord injury (SCI) disrupts the neuronal projections from the brain to the region of the spinal cord that produces walking, leading to various degrees of paralysis. Here, we aimed to identify brain regions that steer the recovery of walking after incomplete SCI and that could be targeted to augment this recovery. To uncover these regions, we constructed a space-time brain-wide atlas of transcriptionally active and spinal cord-projecting neurons underlying the recovery of walking after incomplete SCI.
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