Willemot J, Paton D M
Naunyn Schmiedebergs Arch Pharmacol. 1981 Sep;317(2):110-4. doi: 10.1007/BF00500064.
In the isolated rat vas deferens stimulated at 0.2 Hz, [14C]labelled 5'-AMP, 5'-ADP and 5'-ATP (10 microM) inhibited twitch responses, were broken down to [14C]adenosine in the medium and incorporated into [14C]adenine ribonucleotides in the tissue. Pretreatment of tissues with 6-(2-hydroxy-5-nitrobenzyl)-thioguanosine (NBTGR), a potent inhibitor of adenosine transport, potentiated the presynaptic inhibitory action of these 5' nucleotides and reduced their incorporation in [14C]adenine nucleotides, but did not alter the appearance of [14C]adenosine in the medium. A series of 2', 3' and 5'-substituted adenine nucleotides (10 microM) inhibited the twitch responses of the vas deferens stimulated at 0.2 Hz. This effect was potentiated by NBTGR. Addition of exogenous adenosine deaminase very significantly reduced the inhibitory actions of adenosine, 5'-AMP, 5'-ADP and 5'-ATP and also reduced those of 2', 5'-ADP, NAD+ and dePCoA. The inhibitory actions of the other 2', 3' and 5' adenine nucleotides studied were not altered by exogenous adenosine deaminase. These results indicated that the presynaptic inhibitory actions of 5'-AMP, 5'-ADP and 5'-ATP in rat vas deferens predominantly result from their prior hydrolysis to adenosine whereas the 2', 3' and 5'-substituted adenine nucleotides appear to act mainly directly to inhibit transmitter release.
在以0.2Hz频率刺激的离体大鼠输精管中,[14C]标记的5'-AMP、5'-ADP和5'-ATP(10微摩尔)抑制抽搐反应,在培养基中分解为[14C]腺苷,并在组织中掺入[14C]腺嘌呤核苷酸。用腺苷转运的强效抑制剂6-(2-羟基-5-硝基苄基)-硫代鸟苷(NBTGR)预处理组织,可增强这些5'核苷酸的突触前抑制作用,并减少它们掺入[14C]腺嘌呤核苷酸,但不改变培养基中[14C]腺苷的出现。一系列2'、3'和5'-取代的腺嘌呤核苷酸(10微摩尔)抑制以0.2Hz频率刺激的输精管的抽搐反应。NBTGR可增强这种作用。添加外源性腺苷脱氨酶可非常显著地降低腺苷、5'-AMP、5'-ADP和5'-ATP的抑制作用,也降低2',5'-ADP、NAD+和去磷酸辅酶A的抑制作用。所研究的其他2'、3'和5'腺嘌呤核苷酸的抑制作用不受外源性腺苷脱氨酶的影响。这些结果表明,大鼠输精管中5'-AMP、5'-ADP和5'-ATP的突触前抑制作用主要源于它们先水解为腺苷,而2'、3'和5'-取代的腺嘌呤核苷酸似乎主要直接作用于抑制递质释放。