Tanaka M, Sotomatsu A, Yoshida T, Hirai S
Department of Neurology, Gunma University School of Medicine, Japan.
Neurosci Lett. 1995 Jan 2;183(1-2):116-9. doi: 10.1016/0304-3940(94)11128-6.
Membrane lipid peroxidation has been suggested to participate in the nigral degeneration of Parkinson's disease. In the present study, we demonstrate that bromocriptine inhibits lipid peroxidation in phospholipid liposomes induced by dopa and iron complexes. Because this lipid peroxidation is not mediated by active oxygen species, antioxidant properties of bromocriptine do not seem to be derived from radical scavenging effects in our experimental conditions. Bromocriptine had no scavenging effect on superoxide produced by hypoxanthine-xanthine oxidase when determined by the chemiluminescence assay using MCLA, a Cypridina luciferin analog, as a probe.
膜脂质过氧化作用被认为参与了帕金森病的黑质变性过程。在本研究中,我们证明溴隐亭可抑制由多巴和铁复合物诱导的磷脂脂质体中的脂质过氧化作用。由于这种脂质过氧化作用不是由活性氧介导的,在我们的实验条件下,溴隐亭的抗氧化特性似乎并非源于自由基清除作用。当使用一种海萤荧光素类似物MCLA作为探针,通过化学发光测定法检测时,溴隐亭对次黄嘌呤 - 黄嘌呤氧化酶产生的超氧化物没有清除作用。