Yoshida Toshihiko, Tanaka Makoto, Suzuki Yoko, Sohmiya Makoto, Okamoto Koichi
Department of Neurology, Gunma University School of Medicine, Showa-machi, Maebashi, Gunma 371-8511, Japan.
Neurosci Lett. 2002 Sep 13;330(1):1-4. doi: 10.1016/s0304-3940(02)00594-3.
We evaluated the effect of cabergoline on superoxide anion production by rat microglial cells using a 2-methyl-6-(p-methoxyphenyl)-3,7-dihydroimidazo[1, 2-a]pyrazin-3-one-dependent chemiluminescence assay. Cabergoline dose-dependently inhibited superoxide anion production by microglial cells stimulated with phorbol myristate acetate or opsonized zymosan, while it had no superoxide dismutase-like activity. We also studied the effects of cabergoline and alpha-tocopherol on thiobarbituric acid reactive substances formation in homogenized brain-tissue in rats. Cabergoline was stronger than alpha-tocopherol in inhibiting auto-oxidation. While cabergoline is commonly used to treat the motor dysfunction of Parkinson's disease, it may also be effective in inhibiting oxidative stress, a possible mechanism of dopaminergic neuronal degeneration in Parkinson's disease.
我们使用一种依赖于2-甲基-6-(对甲氧基苯基)-3,7-二氢咪唑并[1,2-a]吡嗪-3-酮的化学发光测定法,评估了卡麦角林对大鼠小胶质细胞超氧阴离子产生的影响。卡麦角林剂量依赖性地抑制了由佛波酯肉豆蔻酸酯或调理酵母聚糖刺激的小胶质细胞的超氧阴离子产生,而它没有超氧化物歧化酶样活性。我们还研究了卡麦角林和α-生育酚对大鼠脑组织匀浆中硫代巴比妥酸反应性物质形成的影响。在抑制自氧化方面,卡麦角林比α-生育酚更强。虽然卡麦角林通常用于治疗帕金森病的运动功能障碍,但它在抑制氧化应激方面可能也有效,氧化应激是帕金森病中多巴胺能神经元变性的一种可能机制。