Staak S, Popov N, Matthies H
Institute of Pharmacology and Toxicology, Medical Academy, Magdeburg, GDR.
Biomed Biochim Acta. 1989;48(4):325-31.
As determined by the HPLC technique, injection of 1.85 mmoles/kg D-galactosamine caused strong alterations in the plasma level of cytidime. Thus, 2 h and 4 h after application of the amino sugar only 54% and 61%, respectively, of the normal values were measured, while an increase to 135% of controls was observed 24 h later. In contrast, intraperitoneal application of D-galactosamine had no influence on the plasma level of uridine. The activity of the enzyme, uridine kinase, in the hippocampal area of the rat brain was increased 2 h and 4 h after D-galactosamine treatment. The results are discussed in the light of behavioural findings in which intraperitoneally applied D-galactosamine at this dosage improves the retention performance of an acquired behaviour in the rat.
通过高效液相色谱(HPLC)技术测定,注射1.85毫摩尔/千克的D-半乳糖胺会导致胞嘧啶血浆水平发生显著变化。因此,在应用氨基糖2小时和4小时后,分别仅测得正常值的54%和61%,而在24小时后观察到增加至对照值的135%。相比之下,腹腔注射D-半乳糖胺对尿苷的血浆水平没有影响。在D-半乳糖胺处理后2小时和4小时,大鼠脑海马区的尿苷激酶活性增加。根据行为学研究结果对这些结果进行了讨论,在该研究中,以这种剂量腹腔注射D-半乳糖胺可改善大鼠后天习得行为的记忆保持表现。