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Sökning: WFRF:(Hellstrand Monika 1955) > Dopamine D(2) recep...

Dopamine D(2) receptor-induced COX-2-mediated production of prostaglandin E(2) in D(2)-transfected Chinese hamster ovary cells without simultaneous administration of a Ca(2+)-mobilizing agent.

Hellstrand, Monika, 1955 (författare)
Gothenburg University,Göteborgs universitet,Institutionen för fysiologi och farmakologi, Avdelningen för farmakologi,Institute of Physiology and Pharmacology, Dept of Pharmacology
Eriksson, Elias, 1956 (författare)
Gothenburg University,Göteborgs universitet,Institutionen för fysiologi och farmakologi, Avdelningen för farmakologi,Institute of Physiology and Pharmacology, Dept of Pharmacology
Nilsson, Christer, 1953 (författare)
Gothenburg University,Göteborgs universitet,Institutionen för fysiologi och farmakologi, Avdelningen för farmakologi,Institute of Physiology and Pharmacology, Dept of Pharmacology
 (creator_code:org_t)
2002
2002
Engelska.
Ingår i: Biochemical pharmacology. - 0006-2952. ; 63:12, s. 2151-8
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • We have earlier demonstrated that dopamine stimulates the liberation of the prostaglandin E(2) (PGE(2)) precursor, arachidonic acid, in Chinese hamster ovary cells transfected with the rat dopamine D(2) receptor (long isoform), also without concomitant administration of a Ca(2+)-releasing agent [Nilsson et al., Br J Pharmacol 1998;124:1651-8]. In the present report, we show that dopamine, under the same conditions, also induces a concentration-dependent increase in the production of PGE(2), with a maximal effect of 235% at approximately 100 microM, and with an EC(50) of 794 nM. The effect was counteracted by the D(2) antagonist eticlopride, pertussis toxin, the inhibitor of intracellular Ca(2+) release TMB-8, incubation in Ca(2+)-free experimental medium, and PKC desensitization obtained by chronic pretreatment with the phorbol ester TPA. It was also antagonized by the non-specific cyclooxygenase (COX) inhibitor, indomethacin, and by the selective COX-2 inhibitor, NS-398, but not by the specific COX-1 inhibitor, valeryl salicylate. Both the non-specific phospholipase A(2) inhibitor, quinacrine, and an inhibitor of cPLA(2) and iPLA(2), AACOF3, counteracted the effect; in contrast, a selective iPLA(2) inhibitor, BEL, and a selective sPLA(2) inhibitor, TAPC, were ineffective. No effects of dopamine were obtained in control cells mock-transfected with the p3C vector only. The results reinforce previous assumptions that dopamine may interact with eicosanoid metabolism by means of D(2) receptor activation, and implicate an involvement of cPLA(2) and COX-2 in this effect. It is suggested that measurement of dopamine-induced PGE(2) production may serve as a convenient way to study D(2) receptor function in vitro.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Farmakologi och toxikologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Pharmacology and Toxicology (hsv//eng)

Nyckelord

Animals
Arachidonic Acids
pharmacology
CHO Cells
Calcium
metabolism
Calcium Channel Blockers
pharmacology
Cricetinae
Cyclooxygenase 2
Dinoprostone
biosynthesis
Dopamine
pharmacology
Dopamine Antagonists
pharmacology
Drug Interactions
Enzyme Inhibitors
pharmacology
Gallic Acid
analogs & derivatives
pharmacology
Indomethacin
pharmacology
Isoenzymes
metabolism
Naphthalenes
pharmacology
Nitrobenzenes
pharmacology
Phosphatidylcholines
pharmacology
Prostaglandin-Endoperoxide Synthases
metabolism
Pyrones
pharmacology
Quinacrine
pharmacology
Receptors
Dopamine D2
genetics
metabolism
Salicylamides
pharmacology
Salicylates
pharmacology
Sulfonamides
pharmacology
Tetradecanoylphorbol Acetate
pharmacology
Transfection

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