Till sidans topp

Sidansvarig: Webbredaktion
Sidan uppdaterades: 2012-09-11 15:12

Tipsa en vän
Utskriftsversion

Dopamine D(2) receptor-in… - Göteborgs universitet Till startsida
Webbkarta
Till innehåll Läs mer om hur kakor används på gu.se

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.

Artikel i vetenskaplig tidskrift
Författare Monika Hellstrand
Elias Eriksson
Christer Nilsson
Publicerad i Biochemical pharmacology
Volym 63
Nummer/häfte 12
Sidor 2151-8
ISSN 0006-2952
Publiceringsår 2002
Publicerad vid Institutionen för fysiologi och farmakologi, Avdelningen för farmakologi
Sidor 2151-8
Språk en
Länkar www.ncbi.nlm.nih.gov/entrez/query.f...
Ämnesord 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
Ämneskategorier Farmakologi och toxikologi

Sammanfattning

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.

Sidansvarig: Webbredaktion|Sidan uppdaterades: 2012-09-11
Dela:

På Göteborgs universitet använder vi kakor (cookies) för att webbplatsen ska fungera på ett bra sätt för dig. Genom att surfa vidare godkänner du att vi använder kakor.  Vad är kakor?