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从秀丽代尔草中分离出的一种异戊烯基黄酮的线粒体毒性和抗氧化活性

Mitochondrial toxicity and antioxidant activity of a prenylated flavonoid isolated from Dalea elegans.

作者信息

Elingold Igal, Isollabella M Paula, Casanova Marta B, Celentano Ana M, Pérez Cristina, Cabrera José Luis, Diez Roberto A, Dubin Marta

机构信息

Centro de Estudios Farmacológicos y Botánicos (CEFYBO), Facultad de Medicina, UBA-CONICET, Paraguay 2155, piso 16, Buenos Aires, Argentina.

出版信息

Chem Biol Interact. 2008 Feb 15;171(3):294-305. doi: 10.1016/j.cbi.2007.10.005. Epub 2007 Oct 25.

DOI:10.1016/j.cbi.2007.10.005
PMID:18078919
Abstract

The prenylated flavanone 2'-4'-dihidroxy-5'-(1" '-dimethylallyl)-6-prenylpinocembrin) (6PP), isolated from the roots of Dalea elegans, shows antimicrobial activity. The aim of this study was to evaluate mitochondrial toxicity and antioxidant properties of 6PP. Addition of micromolar concentrations of 6PP to rat liver mitochondria, stimulated O2 uptake in state 4 and inhibited it in state 3 when malate-glutamate was the respiratory substrate, and inhibited O2 uptake in state 3 when succinate was the substrate. Highest concentration of 6PP also inhibited O2 uptake in state 4 in the latter case; in both conditions, respiratory control index values were decreased. This flavanone collapsed the mitochondrial membrane potential in a concentration-dependent manner. 6PP also inhibited F0F1-ATPase activity in coupled mitochondria and in submitochondrial particles. In the latter, this compound also inhibited NADH oxidase and succinate dehydrogenase activities. HEp-2 cells were incubated for 24 h with 6PP in presence or absence of 0.5% albumin. As measured by reduction of the mitochondrial-related probe MTT, in the albumin-free condition, 6PP was cytotoxic in a concentration-dependent manner; on the other hand, albumin decreased 6PP effect. In addition, in rat liver microsomes 6PP: (1) inhibited the enzymatic lipid peroxidation, (2) exhibited significant scavenging activity, measured by DPPH reduction assay and (3) demonstrated significant antioxidant activity by decreasing the reduction of Mo(VI) to Mo(V). We suggest that 6PP impairs the hepatic energy metabolism by acting as mitochondrial uncoupler and by inhibiting enzymatic activities linked to the respiratory chain. 6PP also exerts both antioxidant and antiradical activities. Due to its cytotoxicity, this molecule, and its future structure developments, can be considered as a potentially promising therapeutic agent, for instance in cancer chemotherapy.

摘要

从秀丽代儿茶根部分离得到的异戊烯基黄酮2'-4'-二羟基-5'-(1'''-二甲基烯丙基)-6-异戊烯基松属素(6PP)具有抗菌活性。本研究旨在评估6PP的线粒体毒性和抗氧化特性。向大鼠肝线粒体中添加微摩尔浓度的6PP,当苹果酸-谷氨酸作为呼吸底物时,刺激了状态4下的氧气摄取并抑制了状态3下的氧气摄取;当琥珀酸作为底物时,抑制了状态3下的氧气摄取。在后者情况下,6PP的最高浓度也抑制了状态4下的氧气摄取;在两种情况下,呼吸控制指数值均降低。这种黄酮以浓度依赖的方式使线粒体膜电位崩溃。6PP还抑制了偶联线粒体和亚线粒体颗粒中的F0F1-ATP酶活性。在后者中,该化合物还抑制了NADH氧化酶和琥珀酸脱氢酶活性。在有或没有0.5%白蛋白存在的情况下,将HEp-2细胞与6PP孵育24小时。通过线粒体相关探针MTT的还原测量,在无白蛋白条件下,6PP具有浓度依赖性细胞毒性;另一方面,白蛋白降低了6PP的作用。此外,在大鼠肝微粒体中,6PP:(1)抑制酶促脂质过氧化,(2)通过DPPH还原测定显示出显著的清除活性,(3)通过降低Mo(VI)到Mo(V)的还原显示出显著的抗氧化活性。我们认为,6PP通过作为线粒体解偶联剂并抑制与呼吸链相关的酶活性来损害肝脏能量代谢。6PP还具有抗氧化和抗自由基活性。由于其细胞毒性,该分子及其未来的结构改进可被视为一种潜在的有前景的治疗剂,例如在癌症化疗中。

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