Suzuki Toshiyuki, Kikuchi Haruhisa, Ogura Masato, Homma Miwako K, Oshima Yoshiteru, Homma Yoshimi
Fukushima Medical University School of Medicine, Fukushima, 960-1295, Japan.
Graduate School of Pharmaceutical Sciences, Tohoku University, Sendai, 980-8678, Japan.
PLoS One. 2015 Feb 10;10(2):e0117088. doi: 10.1371/journal.pone.0117088. eCollection 2015.
Mitochondria play a key role in diverse processes including ATP synthesis and apoptosis. Mitochondrial function can be studied using inhibitors of respiration, and new agents are valuable for discovering novel mechanisms involved in mitochondrial regulation. Here, we screened small molecules derived from slime molds and other microorganisms for their effects on mitochondrial oxygen consumption. We identified Ppc-1 as a novel molecule which stimulates oxygen consumption without adverse effects on ATP production. The kinetic behavior of Ppc-1 suggests its function as a mitochondrial uncoupler. Serial administration of Ppc-1 into mice suppressed weight gain with no abnormal effects on liver or kidney tissues, and no evidence of tumor formation. Serum fatty acid levels were significantly elevated in mice treated with Ppc-1, while body fat content remained low. After a single administration, Ppc-1 distributes into various tissues of individual animals at low levels. Ppc-1 stimulates adipocytes in culture to release fatty acids, which might explain the elevated serum fatty acids in Ppc-1-treated mice. The results suggest that Ppc-1 is a unique mitochondrial regulator which will be a valuable tool for mitochondrial research as well as the development of new drugs to treat obesity.
线粒体在包括ATP合成和细胞凋亡在内的多种过程中发挥关键作用。可使用呼吸抑制剂来研究线粒体功能,新型试剂对于发现参与线粒体调节的新机制很有价值。在此,我们筛选了来自黏菌和其他微生物的小分子对线粒体氧消耗的影响。我们鉴定出Ppc-1是一种新型分子,它能刺激氧消耗且对ATP产生无不良影响。Ppc-1的动力学行为表明其作为线粒体解偶联剂的功能。对小鼠连续施用Ppc-1可抑制体重增加,对肝脏或肾脏组织无异常影响,也没有肿瘤形成的迹象。用Ppc-1处理的小鼠血清脂肪酸水平显著升高,而体脂含量保持较低。单次给药后,Ppc-1以低水平分布到个体动物的各种组织中。Ppc-1刺激培养中的脂肪细胞释放脂肪酸,这可能解释了用Ppc-1处理的小鼠血清脂肪酸升高的原因。结果表明,Ppc-1是一种独特的心线粒体调节剂,将成为线粒体研究以及开发治疗肥胖症新药的有价值工具。