New functions of classical hormone α-melanophore-stimulating hormone

Autor: Tonosaki, Yoshikazu, Sugiura, Yasuo, Roubos, Eric W.
Jazyk: angličtina
Rok vydání: 2007
Předmět:
Zdroj: 弘前医学. 59:S202-S209
ISSN: 0439-1721
Popis: application/pdf
It is well-known that α-melanophore-stimulating hormone (α-MSH) release from the amphibian pars intermedia( PI) depends on the light condition of the animal’s background. In the present study, we present two new functions of α-MSH in amphibians and mammals. In Xenopus laevis, we show that temperatures below 8 ℃ stimulate α-MSH secretion of the PI and skin darkening, with a maximum at 5 ℃, under regulation of the hypothalamus rule, independently from the illumination state of the background. The cold-induced α-MSH release of the PI was inhibited by neuropeptide-Y-producing suprachiasmatic-melanotrope-inhibiting neurons in the ventrolateral area of the suprachiasmatic nucleus but increasely in thyrotropin-releasing-hormene-containing neurons of the magnocellular nucleus. It is known that intracerebroventricular( ICV) administration of a low dose of interleukin-1β( IL-1β) induces hyperalgesia in rat and that this eff ect can be inhibited by α-MSH. To identify the part of the brain that is aff ected by hyperalgesiainducing IL-1β and the site of α-MSH concerned, we have examined Fos expression in the brain in response to ICV microinjection of α-MSH and/or IL-1β. Following injection of 10 pg IL-1β, hyperalgesia was induced and Fos became expressed in the paraventricular nucleus( PVN) of the hypothalamus and in the arcuate nucleus( ARC), which contains α-MSH-producing neurons. ICV co-injection of IL-1β ・ with 30 ng α-MSH fully inhibited both hyperalgesia and Fos expression in the PVN and the ARC. We conclude that PVN neurons are activated by hyperalgesic IL-1β and propose that this eff ect is abolished by α-MSH released from the ARC but not from the pituitary gland.
弘前医学. 59(Suppl.), 2007, p.S202-S209
Databáze: OpenAIRE