Szabó G, Kovács G L, Székeli S, Baláspiri L, Telegdy G
Acta Physiol Hung. 1987;69(1):115-22.
Earlier it was found that oxytocin (OXT) treatment inhibited the development of tolerance to ethanol. In the present study the possibility was investigated whether the effect of OXT on ethanol tolerance was related to peptide fragments derived from the C-terminal part of the molecule. The actions of different doses of the C-terminal tripeptide (prolyl-leucyl-glycinamide, PLG) and of a synthetic dipeptide derivative (Z-prolyl-D-leucine, Z-Pro-D-Leu) on the development of tolerance to the hypothermic effect of ethanol in CFLP mice were therefore investigated. Peptide treatment did not affect body temperature in ethanol-naive animals. The acute effects (hypothermia, sleeping time) of a single ethanol injection were also unaffected by these peptides. In contrast, both PLG and Z-Pro-D-Leu inhibited the development of tolerance to the hypothermic effect of ethanol. Accordingly, it might be speculated that a sequence active in affecting ethanol tolerance is located in the C-terminal part of the OXT molecule.
早期研究发现,催产素(OXT)治疗可抑制对乙醇耐受性的发展。在本研究中,对OXT对乙醇耐受性的影响是否与该分子C末端衍生的肽片段有关进行了调查。因此,研究了不同剂量的C末端三肽(脯氨酰 - 亮氨酰 - 甘氨酰胺,PLG)和一种合成二肽衍生物(Z - 脯氨酰 - D - 亮氨酸,Z - Pro - D - Leu)对CFLP小鼠乙醇低温效应耐受性发展的作用。肽处理对未接触过乙醇的动物体温没有影响。单次注射乙醇的急性效应(体温过低、睡眠时间)也不受这些肽的影响。相反,PLG和Z - Pro - D - Leu均抑制了对乙醇低温效应耐受性的发展。因此,可以推测,影响乙醇耐受性的活性序列位于OXT分子的C末端部分。