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Eur J Pharmacol ; 498(1-3): 59-69, 2004 Sep 13.
Artigo em Inglês | MEDLINE | ID: mdl-15363976

RESUMO

The effect of ligand pretreatment on human 5-hydroxytryptamine2C (5-HT2C) receptors was examined in CHO cells expressing high (CHO-1C7; 67+/-3 pmol/mg) or low (CHO-1C19; 72+/-10 fmol/mg) levels of the receptor. Seventy-two hours pretreatment of CHO-1C7 cells with various ligands did not affect receptor expression. Pretreatment with inverse agonists enhanced 5-HT-mediated inositol phosphate accumulation with no change in constitutive receptor activity. The enhanced agonist responsiveness was inversely correlated with the intrinsic activity of the pretreatment ligand. Seventy-two hours of pretreatment with the weak agonist, 5-methoxygramine, caused an elevation in constitutive activity but no alteration in 5-HT-mediated signaling. In CHO-1C19 cells, 24 but not 72 h of pretreatment with the inverse agonist mianserin enhanced 5-HT-mediated signaling, with no effect on basal signaling; pretreatment with 5-methoxygramine had no significant effect. These findings highlight differences in the pattern of chronic regulation of 5HT2C receptor signaling between high and low receptor expression levels in a common cellular background.


Assuntos
Ergolinas/metabolismo , Indofenol/análogos & derivados , Receptor 5-HT2C de Serotonina/metabolismo , Algoritmos , Análise de Variância , Animais , Ligação Competitiva/efeitos dos fármacos , Células CHO , Membrana Celular/efeitos dos fármacos , Membrana Celular/metabolismo , Clorpromazina/farmacologia , Cricetinae , Cricetulus , Relação Dose-Resposta a Droga , Humanos , Indóis/farmacologia , Indofenol/farmacologia , Fosfatos de Inositol/metabolismo , Cinética , Ligantes , Lisurida/farmacologia , Mianserina/farmacologia , Ensaio Radioligante , Receptor 5-HT2C de Serotonina/genética , Ritanserina/farmacologia , Serotonina/farmacologia , Antagonistas da Serotonina/farmacologia , Agonistas do Receptor de Serotonina/farmacologia , Trítio , Triptaminas/farmacologia
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