Miñana M D, Portolés M, Jordá A, Grisolía S
J Neurochem. 1984 Dec;43(6):1556-60. doi: 10.1111/j.1471-4159.1984.tb06078.x.
Rats ingesting high doses of caffeine reproduce the self-destructive behaviour observed in the Lesch-Nyhan syndrome. This syndrome includes a deficit in hypoxanthine-guanine phosphoribosyltransferase. We have observed, however, that the activity of hypoxanthine-guanine phosphoribosyltransferase increases in direct proportion to the concentration of caffeine found in rat brain. It appears, therefore, that the caffeine model is not a true model for the Lesch-Nyhan syndrome, or alternatively, that the deficit in hypoxanthine-guanine phosphoribosyltransferase is coincidental and not a main key to the multifarious aspects of the syndrome, particularly the self-mutilation. The possibility that levels of dopamine are increased in the caffeine model are discussed as a basis for the destructive behaviour. We have found also that ingestion of large amounts of caffeine increases the activities in rat brain of adenosine deaminase, purine nucleoside phosphorylase, aspartate carbamoyl-transferase, dihydroorotase, and dihydroorotate oxidase.
摄入高剂量咖啡因的大鼠会重现莱施-奈恩综合征中观察到的自我毁灭行为。该综合征包括次黄嘌呤-鸟嘌呤磷酸核糖转移酶缺乏。然而,我们观察到,大鼠脑中次黄嘌呤-鸟嘌呤磷酸核糖转移酶的活性与咖啡因浓度成正比增加。因此,似乎咖啡因模型并非莱施-奈恩综合征的真实模型,或者说,次黄嘌呤-鸟嘌呤磷酸核糖转移酶缺乏是巧合,并非该综合征多方面表现的关键因素,尤其是自残行为。文中讨论了咖啡因模型中多巴胺水平升高作为破坏性行为基础的可能性。我们还发现,摄入大量咖啡因会增加大鼠脑中腺苷脱氨酶、嘌呤核苷磷酸化酶、天冬氨酸氨甲酰转移酶、二氢乳清酸酶和二氢乳清酸氧化酶的活性。