Verhoef J, Prins A, Veldhuis H D, Witter A
J Neurochem. 1982 Apr;38(4):1135-8. doi: 10.1111/j.1471-4159.1982.tb05359.x.
Following subcutaneous injection of the tripeptide H-Pro-[3H]Leu-Gly-NH2 ([3H]PLG) in rats, the profile of intact peptide and its radioactively labeled metabolites was examined both in plasma and in brain tissue. [3H]PLG and metabolites were determined in trichloroacetic acid extracts by reverse-phase paired-ion HPLC. Maximal plasma levels of unmetabolized PLG were reached 6-8 min after administration, after which they decreased with an elimination half-life of 20 min. The uptake of [3H]PLG in the brain ranged from 0.0013% to 0.0017% of the administered dose per g tissue at 6-30 min following subcutaneous injection. After comparing these results with our previous findings with intravenous injection of [3H]PLG, it seemed likely that the subcutaneous route of administration might be more effective in eliciting CNS effects of PLG than the intravenous route of administration. The metabolite profiles in plasma and brain point to an initial cleavage of PLG at the NH2-terminal side and a very rapid degradation of the peptide intermediate H-Leu-Gly-NH2.
给大鼠皮下注射三肽H-Pro-[³H]Leu-Gly-NH₂([³H]PLG)后,在血浆和脑组织中检测完整肽及其放射性标记代谢物的情况。通过反相配对离子高效液相色谱法测定三氯乙酸提取物中的[³H]PLG及其代谢物。给药后6 - 8分钟达到未代谢PLG的血浆最高水平,之后其以20分钟的消除半衰期下降。皮下注射后6 - 30分钟,脑内[³H]PLG的摄取量为每克组织给药剂量的0.0013%至0.0017%。将这些结果与我们之前静脉注射[³H]PLG的研究结果相比较后,皮下给药途径似乎比静脉给药途径在引发PLG的中枢神经系统效应方面更有效。血浆和脑内的代谢物谱表明PLG在氨基末端侧首先发生裂解,并且肽中间体H-Leu-Gly-NH₂降解非常迅速。