Pull I, McIlwain H
Biochem J. 1972 Dec;130(4):975-81. doi: 10.1042/bj1300975.
Adenine nucleotides of guinea-pig neocortical tissues were labelled by incubation with [(14)C]adenine and excess of adenine was then removed by superfusion with precursor-free medium. Adenine derivatives released from the tissue during continued superfusion, including a period of electrical stimulation of the tissue, were collected by adsorption and examined after elution and concentration. The stimulation greatly increased the (14)C output, and material collected during and just after stimulation had a u.v. spectrum which indicated adenosine to be a major component. The additional presence of inosine and hypoxanthine was shown by chromatography and adenosine was identified also by using adenosine deaminase. Total adenine derivatives released from the tissue during a 10min period of stimulation were obtained as hypoxanthine, after deamination and hydrolysis of adenosine and inosine, and amounted to 159nmol/g of tissue. This corresponded to the release of approx. 7pmol/g of tissue per applied stimulus. The hypoxanthine sample derived from superfusate hypoxanthine, inosine and adenosine was of similar specific radioactivity to the sample of inosine separated chromatographically, and each was of higher specific radioactivity than the adenine nucleotides obtained by cold-acid extraction of the tissue.
通过与[¹⁴C]腺嘌呤孵育标记豚鼠新皮质组织中的腺嘌呤核苷酸,然后用不含前体的培养基灌注去除过量的腺嘌呤。在持续灌注(包括对组织进行电刺激的一段时间)过程中从组织中释放的腺嘌呤衍生物,通过吸附收集,并在洗脱和浓缩后进行检测。电刺激极大地增加了¹⁴C的输出,在刺激期间及刚结束后收集的物质具有紫外光谱,表明腺苷是主要成分。通过色谱法显示了肌苷和次黄嘌呤的额外存在,并且也通过使用腺苷脱氨酶鉴定了腺苷。在刺激10分钟期间从组织中释放的总腺嘌呤衍生物,在腺苷和肌苷脱氨和水解后作为次黄嘌呤获得,每克组织为159nmol。这相当于每次施加刺激时每克组织释放约7pmol。来自灌注液次黄嘌呤、肌苷和腺苷的次黄嘌呤样品的比放射性与通过色谱法分离的肌苷样品相似,并且每个的比放射性都高于通过冷酸提取组织获得的腺嘌呤核苷酸。