Page C R, MacInnis A J
J Parasitol. 1975 Apr;61(2):281-90.
Three species of cestodes, Hymenolepis diminuta, H. citelli, and H. microstoma, were shown to transport nucleosides by a mediated process. In H. diminuta the Ki values of various competitive inhibitors led to the conclusion that at least 2 different loci are involved in the transport of nucleosides. One of these loci has greater specificity for the purine nucleosides, the other for pyrimidine nucleosides. No significant difference was observed in their affinity for ribo- or deoxyribonucleosides, although thymidine was slightly less effective as an inhibitor of ribonucleosides than was uridine. Transport by the pyrimidine nucleoside locus was stimulated by thymine, but not by hypoxanthine, whereas transport by the purine nucleoside locus was stimulated by hypoxanthine but not by thymine. Preloading the worms with thymine gave less stimulation of transport than did the presence of eoxgenous modulator. Efflux of previously accumulated nucleoside was not blocked by the presence of exogenous modulator. The presence of exgenous thymine enhanced the incorporation of uridine into the nonextractable pool. Thymine also stimulated uracil transport in H. citelli, but not in H. microstoma, and had no effect on uridine transport in either of these species. The results of transport and modulator studies on H. diminuta grown in hamsters were not different from the results with worms grown in rats indicating that the regulatory effects observed were an inherent function of the parasite and not the host.
三种绦虫,即微小膜壳绦虫、鼠膜壳绦虫和小口膜壳绦虫,被证明可通过介导过程转运核苷。在微小膜壳绦虫中,各种竞争性抑制剂的Ki值表明,核苷转运至少涉及2个不同位点。其中一个位点对嘌呤核苷具有更高的特异性,另一个对嘧啶核苷具有更高的特异性。尽管胸腺嘧啶作为核糖核苷抑制剂的效果略低于尿苷,但它们对核糖核苷或脱氧核糖核苷的亲和力没有显著差异。嘧啶核苷位点的转运受到胸腺嘧啶的刺激,但不受次黄嘌呤的刺激,而嘌呤核苷位点的转运受到次黄嘌呤的刺激,但不受胸腺嘧啶的刺激。用胸腺嘧啶预先加载蠕虫对转运的刺激作用小于外源性调节剂的存在。外源性调节剂的存在不会阻止先前积累的核苷的流出。外源性胸腺嘧啶的存在增强了尿苷掺入不可提取池的能力。胸腺嘧啶还刺激了鼠膜壳绦虫中尿嘧啶的转运,但未刺激小口膜壳绦虫中尿嘧啶的转运,并且对这两种绦虫中尿苷的转运均无影响。对在仓鼠中生长的微小膜壳绦虫进行的转运和调节剂研究结果与在大鼠中生长的蠕虫的结果没有差异,这表明观察到的调节作用是寄生虫的固有功能,而非宿主的功能。