Jackson M J, Jones D A, Harris E J
Biosci Rep. 1984 Jul;4(7):581-7. doi: 10.1007/BF01121915.
Chloropromazine, mepacrine, tetracaine, dibucaine, chloroquine, and procaine have been shown to inhibit the iron- and ascorbate-induced lipid peroxidation of skeletal-muscle homogenates in vitro. These compounds are known to be inhibitors of phospholipase activity, but they were also found to be effective in blocking free-radical-mediated damage to lipids in denatured homogenates, to linoleate suspensions, and to glutamic acid solutions where phospholipase activity was not a relevant factor. The inhibitory action did not appear to be related to any iron-binding activity of the compounds.
氯丙嗪、阿的平、丁卡因、布比卡因、氯喹和普鲁卡因已被证明在体外可抑制铁和抗坏血酸诱导的骨骼肌匀浆脂质过氧化。已知这些化合物是磷脂酶活性的抑制剂,但还发现它们能有效阻断自由基介导的对变性匀浆、亚油酸酯悬浮液和谷氨酸溶液中脂质的损伤,而在这些体系中磷脂酶活性并非相关因素。抑制作用似乎与这些化合物的任何铁结合活性无关。