Benson R, Crowell B, Hill B, Doonquah K, Charlton C
Meharry Medical College, Department of Physiology, Nashville, TN 37208.
Neurochem Res. 1993 Mar;18(3):325-30. doi: 10.1007/BF00969090.
L-dopa, the major treatment for Parkinson's disease (PD), depletes S-adenosyl-L-methionine (SAM). Since SAM causes PD-like symptoms in rodents, the decreased efficacy of chronic L-dopa administered to PD patients may result from a rebound increase in SAM via methionine adenosyl transferase (MAT), which produces SAM from methionine and ATP. This was tested by administering intraperitoneally saline, or L-dopa to mice and assaying for brain MAT activity. As compared to controls, L-dopa (100 mg/kg) treatments of 1 and 2 times per day for 4 days did not significantly increase MAT activity. However, treatments of 3 times per day for 4 and 8 days did significantly increase the activity of MAT by 21.38% and 28.37%, respectively. These results show that short interval, chronic L-dopa treatments significantly increases MAT activity, which increases the production of SAM. SAM may physiologically antagonize the effects of L-dopa and biochemically decrease the concentrations of L-dopa and dopamine. Thus, an increase in MAT may be related to the decreased efficacy of chronic L-dopa therapy in PD.
左旋多巴是治疗帕金森病(PD)的主要药物,它会消耗S-腺苷-L-甲硫氨酸(SAM)。由于SAM在啮齿动物中会引发类似PD的症状,因此长期给PD患者服用左旋多巴疗效降低,可能是由于通过甲硫氨酸腺苷转移酶(MAT)使SAM反弹增加所致,该酶可利用甲硫氨酸和ATP生成SAM。通过给小鼠腹腔注射生理盐水或左旋多巴,并检测脑内MAT活性对此进行了验证。与对照组相比,每天1次或2次、连续4天给予左旋多巴(100mg/kg)治疗,并未显著增加MAT活性。然而,每天3次、连续4天和8天的治疗,分别使MAT活性显著增加了21.38%和28.37%。这些结果表明,短间隔、长期左旋多巴治疗可显著增加MAT活性,进而增加SAM的生成。SAM可能在生理上拮抗左旋多巴的作用,并在生化层面降低左旋多巴和多巴胺的浓度。因此,MAT增加可能与长期左旋多巴治疗PD疗效降低有关。