Suzuki K, Mizuno Y, Yoshida M
Department of Neurology, Jichi Medical School, Tochigi-ken, Japan.
Neurosci Lett. 1988 Mar 21;86(1):105-8. doi: 10.1016/0304-3940(88)90191-7.
Effects of tetrahydroisoquinoline (TIQ) on mitochondrial respiration, NADH-ubiquinone oxidoreductase (complex I) activity and on adenosine triphosphate (ATP) synthesis were studied using mitochondria prepared from mouse brains. Tetrahydroisoquinoline significantly inhibited mitochondrial respiration supported by glutamate + malate, pyruvate + malate or alpha-ketoglutarate. Activity of complex I and synthesis of ATP were also significantly inhibited by TIQ. Mitochondrial respiration supported by succinate and subsequent ATP synthesis were not inhibited at all by 5 mM of TIQ. Our study has revealed a novel action of TIQ, which has been proposed as a candidate for an endogenous substance that may induce Parkinson's disease.
利用从小鼠大脑中制备的线粒体,研究了四氢异喹啉(TIQ)对线粒体呼吸、NADH-泛醌氧化还原酶(复合体I)活性以及三磷酸腺苷(ATP)合成的影响。四氢异喹啉显著抑制由谷氨酸+苹果酸、丙酮酸+苹果酸或α-酮戊二酸支持的线粒体呼吸。复合体I的活性和ATP的合成也被TIQ显著抑制。5 mM的TIQ对由琥珀酸支持的线粒体呼吸及随后的ATP合成完全没有抑制作用。我们的研究揭示了TIQ的一种新作用,TIQ已被提出作为一种可能诱发帕金森病的内源性物质的候选物。