Adenosine A1 receptor down-regulation in mothers and fetal brain after caffeine and theophylline treatments to pregnant rats

被引:56
作者
León, D [1 ]
Albasanz, JL [1 ]
Ruíz, MA [1 ]
Fernández, M [1 ]
Martín, M [1 ]
机构
[1] Univ Castilla La Mancha, Fac Quim, Area Bioquim, Ctr Reg Invest Biomed, E-13071 Ciudad Real, Spain
关键词
A(1) receptor; caffeine; down-regulation; rat brain; theophylline;
D O I
10.1046/j.1471-4159.2002.01008.x
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Pregnant rats were treated daily with 1 g/L of caffeine or theophylline in their drinking water during pregnancy and the effect of these methylxanthines on adenosine A(1) receptor was assayed using binding and reverse transcription polymerase chain reaction (RT-PCR) assays in brains from both mothers and full-term fetuses. In plasma membranes from pregnant rat brain, caffeine and theophylline caused a significant decrease in total receptor numbers, of the same order in both cases (30%), with no significant changes on receptor affinity. The effect of these adenosine receptor antagonists on plasma membranes from fetal brains was more marked, being detected at approximately 50% of the total receptors detected in control conditions. However, in this tissue, a significant increase in the receptor affinity, of the same order in both cases, was also detected after antagonist administration. No significant variation on the potency of caffeine and theophylline as antagonists was detected after treatments in mothers; however, higher affinities were detected in fetuses. A decrease in the total receptor numbers in fetal brain was associated with an increase in the mRNA coding A(1) receptor, as determined by RT-PCR assays, not having detected any mRNA difference in maternal brain. No variation in the levels of mRNA coding A(2A) receptor was detected in any case. These results suggest that maternal caffeine or theophylline intake modulates adenosine A(1) receptor, causing a down-regulation of adenosine A(1) receptor in brain in both mothers and fetuses.
引用
收藏
页码:625 / 634
页数:10
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