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1.
Neuroscience Bulletin ; (6): 841-852, 2019.
Artigo em Inglês | WPRIM (Pacífico Ocidental) | ID: wpr-776474

RESUMO

Isolation rearing (IR) enhances aggressive behavior, and the central serotonin (5-hydroxytryptamine, 5-HT) system has been linked to IR-induced aggression. However, whether the alteration of central serotonin is the cause or consequence of enhanced aggression is still unknown. In the present study, using mice deficient in central serotonin Tph2 and Lmx1b, we examined the association between central serotonin and aggression with or without social isolation. We demonstrated that central serotonergic neurons are critical for the enhanced aggression after IR. 5-HT depletion in wild-type mice increased aggression. On the other hand, application of 5-HT in Lmx1b mice inhibited the enhancement of aggression under social isolation conditions. Dopamine was downregulated in Lmx1b mice. Similar to 5-HT, L-DOPA decreased aggression in Lmx1b mice. Our results link the serotoninergic system directly to aggression and this may have clinical implications for aggression-related human conditions.

2.
Neuroscience Bulletin ; (6): 156-164, 2018.
Artigo em Inglês | WPRIM (Pacífico Ocidental) | ID: wpr-777082

RESUMO

Peripheral itch stimuli are transmitted by sensory neurons to the spinal cord dorsal horn, which then transmits the information to the brain. The molecular and cellular mechanisms within the dorsal horn for itch transmission have only been investigated and identified during the past ten years. This review covers the progress that has been made in identifying the peptide families in sensory neurons and the receptor families in dorsal horn neurons as putative itch transmitters, with a focus on gastrin-releasing peptide (GRP)-GRP receptor signaling. Also discussed are the signaling mechanisms, including opioids, by which various types of itch are transmitted and modulated, as well as the many conflicting results arising from recent studies.


Assuntos
Animais , Humanos , Potenciais de Ação , Analgésicos Opioides , Farmacologia , Prurido , Metabolismo , Patologia , Células Receptoras Sensoriais , Metabolismo , Medula Espinal , Patologia , Transmissão Sináptica , Fisiologia
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