Boehm S, Huck S, Illes P
Institute of Neuropharmacology, University of Vienna, Austria.
Br J Pharmacol. 1995 Nov;116(5):2341-3. doi: 10.1111/j.1476-5381.1995.tb15075.x.
In rat cultured sympathetic neurones, UDP, UTP and ATP at micromolar concentrations triggered Ca(2+)-dependent and tetrodotoxin-sensitive [3H]-noradrenaline release. The overflow evoked by UTP or ATP was similar at 100 mumol l-1, the concentration used in all subsequent experiments. Pre-exposure of the neurones to 100 mumol l-1 UTP significantly reduced ensuing secretory effects of UTP but not of ATP. Conversely, pre-exposure to ATP diminished the overflow due to ATP but not that due to UTP. In the presence of 10 mumol l-1 pyridoxal-5'-phosphate or 30 mumol l-1 suramin, the secretory response to ATP was reduced, but the effect of UTP was unaltered. Zn2+ (10 mumol l-1) reduced the overflow triggered by UTP, but increased the overflow due to ATP. These results indicate the presence of separate receptors for pyrimidine nucleotides and for purine nucleotides which both trigger transmitter release.
在大鼠培养的交感神经元中,微摩尔浓度的UDP、UTP和ATP可触发依赖钙离子且对河豚毒素敏感的[3H]-去甲肾上腺素释放。在随后所有实验中所采用的100 μmol l-1浓度下,UTP或ATP诱发的溢出情况相似。将神经元预先暴露于100 μmol l-1的UTP下,会显著降低随后UTP的分泌效应,但不会降低ATP的分泌效应。相反,预先暴露于ATP会减少由ATP引起的溢出,但不会减少由UTP引起的溢出。在存在10 μmol l-1的磷酸吡哆醛或30 μmol l-1的苏拉明时,对ATP的分泌反应会降低,但UTP的效应未改变。Zn2+(10 μmol l-1)会减少UTP触发的溢出,但会增加ATP引起的溢出。这些结果表明存在分别针对嘧啶核苷酸和嘌呤核苷酸的受体,二者均可触发递质释放。