Lu Songmin, Yang Heming, Song Shuangming, Liu Jiancang, Li Ping, Wan Zhihong, Jia Houjun
Research Institute of Surgery, Daping, Chongqing 400042, China.
Chin J Traumatol. 1998 Nov 15;1(1):32-36.
To elucidate the effects of lipopolysaccharide (LPS), phospholipase A(2) (PLA(2)) and oxygen free radical (OFR) on proton transmembrane translocation and H(+)-ATPase. METHODS: The normal rats were sacrificed for preparetion liver mitochondria and submitochondrial particles for experiments in vitro. Submitochondrial particles were incubated with LPS (100 &mgr;g/mL), PLA(2) (10 u/mL) and FeSO(4)/Vit C (30/90 &mgr;mol/L) at 30 degrees C for 30 min. The proton translocation of submitochondrial particles (SMPs) were assayed with the fluorescent probe ACMA (9-amino-6-chloro-2 methoxya cridine). The mitochondria were incubated with different concentration of LPS, PLA(2) and FeSO(4)/Vit C. The H(+)-ATPase, PLA(2) and malondialdehyde (MDA) were assayed. RESULTS: The fluorescent quenching of ACMA and H(+)-ATPase activity in high dose was significantly decreased after treatment with LPS, PLA(2), FeSO(4)/Vit C (P<0.05). The mitochondrial PLA(2) activity and MDA content were significantly increased after treatment with LPS (P<0.01). CONCLUSIONS: FeSO(4)/Vit C in low dose causes increases H(+)-ATPase activity. LPS, PLA(2), FeSO(4)/Vit C might be the important factors changing H(+)-ATPase and proton translocation across the membrane.
阐明脂多糖(LPS)、磷脂酶A2(PLA2)和氧自由基(OFR)对质子跨膜转运及H(+)-ATP酶的影响。方法:处死正常大鼠以制备肝线粒体及亚线粒体颗粒用于体外实验。将亚线粒体颗粒与LPS(100μg/mL)、PLA2(10U/mL)和FeSO4/Vit C(30/90μmol/L)在30℃孵育30分钟。用荧光探针ACMA(9-氨基-6-氯-2-甲氧基吖啶)检测亚线粒体颗粒(SMPs)的质子转运。将线粒体与不同浓度的LPS、PLA2和FeSO4/Vit C孵育。检测H(+)-ATP酶、PLA2和丙二醛(MDA)。结果:用LPS、PLA2、FeSO4/Vit C处理后,ACMA的荧光猝灭及高剂量时的H(+)-ATP酶活性显著降低(P<0.05)。用LPS处理后线粒体PLA2活性及MDA含量显著增加(P<0.01)。结论:低剂量的FeSO4/Vit C可使H(+)-ATP酶活性增加。LPS、PLA2、FeSO4/Vit C可能是改变H(+)-ATP酶及质子跨膜转运的重要因素。