Csaba G, Inczefi-Gonda A
Department of Biology, Semmeiweis University of Medicine, Budapest, Hungary.
Acta Physiol Hung. 1989;73(4):483-7.
A single neonatal insulin treatment decreased considerably the insulin binding capacity of erythrocytes in adult rats, by analogy of the behaviour of the hepatic insulin receptors in response to insulin exposure during the perinatal period, or during liver regeneration in adulthood. These observations substantitate earlier conclusions on the mechanism of imprinting and strongly suggest the universality of perinatal imprinting in living organisms. In vitro insulin exposure of the erythrocytes of adult rats depressed 48 h later the erythrocytic insulin binding capacity to a similar degree in individuals treated and not treated with insulin when newborn, from which it follows that neonatal exposure had no influence on erythrocytic response to later in vitro treatment. In the light of the present study the use of erythrocytes as model cells for imprinting studies deserves consideration.
单次新生期胰岛素治疗可显著降低成年大鼠红细胞的胰岛素结合能力,这与围产期或成年期肝脏再生过程中肝脏胰岛素受体对胰岛素暴露的反应行为类似。这些观察结果证实了早期关于印记机制的结论,并强烈提示围产期印记在生物体中的普遍性。成年大鼠红细胞在体外暴露于胰岛素48小时后,无论新生时是否接受胰岛素治疗,其红细胞胰岛素结合能力均受到类似程度的抑制,由此可见,新生期暴露对红细胞对后期体外治疗的反应没有影响。根据本研究,将红细胞用作印记研究的模型细胞值得考虑。