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Kappa receptors pain modulation

There are various opioid receptors the three major classes of opioid receptors are mu (p), delta (5) and kappa (k) receptors. The p, receptor is the principal pain-modulating site in the CNS, mediating the action of morphine. There is considerable interest in the K receptor, which mediates a sedating analgesia with decreased addiction liability and respiratory depression and which allows for some structural flexibility. Unfortunately, the K receptor seems to be coupled to the sigma (a) receptor, which is implicated in psychotomimetic and dysphoric side effects. [Pg.352]

Abrahamsson C (2000) Neuropeptide Y1- and Y2-receptor-mediated cardiovascular effects in the anaesthetized guinea pig, rat, and rabbit. J Cardiovasc Pharmacol 36 451-8 Ackley MA, Hurley RW, Virnich DE et al (2001) A cellular mechanism for the antinociceptive effect of a kappa opioid receptor agonist. Pain 91 377-88 Aimone LD, Yaksh TL (1989) Opioid modulation of capsaicin-evoked release of substance P from rat spinal cord in vivo. Peptides 10 1127-31... [Pg.429]

Millan MJ (2002) Descending control of pain. Prog Neurobiol 66 355-474 Millan MJ, MiUan MH, Pilcher CW, Czlonkowski A, Herz A, Colpaert FC (1985) Spinal cord dynorphin may modulate nociception via a kappa-opioid receptor in chronic arthritic rats. Brain... [Pg.512]


See other pages where Kappa receptors pain modulation is mentioned: [Pg.52]    [Pg.467]    [Pg.104]    [Pg.381]    [Pg.297]    [Pg.493]    [Pg.356]    [Pg.1091]    [Pg.58]    [Pg.194]   
See also in sourсe #XX -- [ Pg.467 ]




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