D'Or Institute for Research and Education, Rio de Janeiro, Brazil ; Lab. Immunopharmacology, Instituto Oswaldo Cruz, Fundação Oswaldo Cruz (FIOCRUZ), Rio de Janeiro, Brazil.
Lab. Neurobiology of Memory, Instituto de Bioquímica Médica, Universidade Federal do Rio de Janeiro (UFRJ), Rio de Janeiro, Brazil ; National Center for Bioimaging (CENABIO), Universidade Federal do Rio de Janeiro (UFRJ), Rio de Janeiro, Brazil.
PLoS One. 2014 Jan 8;9(1):e85009. doi: 10.1371/journal.pone.0085009. eCollection 2014.
When 5-lipoxygenase (5-LO) is inhibited, roughly half of the CNS effect of the prototypic endocannabinoid anandamide (AEA) is lost. Therefore, we decided to investigate whether inhibiting this enzyme would influence physiological functions classically described as being under control of the endocannabinoid system. Although 5-LO inhibition by MK-886 reduced lipoxin A4 levels in the brain, no effect was found in the elevated plus maze (EPM), even at the highest possible doses, via i.p. (10 mg/kg,) or i.c.v. (500 pmol/2 µl) routes. Accordingly, no alterations in anxiety-like behavior in the EPM test were observed in 5-LO KO mice. Interestingly, aged mice, which show reduced circulating lipoxin A4 levels, were sensitive to MK-886, displaying an anxiogenic-like state in response to treatment. Moreover, exogenous lipoxin A4 induced an anxiolytic-like profile in the EPM test. Our findings are in line with other reports showing no difference between FLAP KO or 5-LO KO and their control strains in adult mice, but increased anxiety-like behavior in aged mice. We also show for the first time that lipoxin A4 affects mouse behavior. In conclusion, we propose an age-dependent relevancy of endogenous 5-LO derivatives in the modulation of anxiety-like behavior, in addition to a potential for exogenous lipoxin A4 in producing an anxiolytic-like state.
当 5-脂氧合酶(5-LO)被抑制时,典型内源性大麻素大麻素(AEA)的大约一半的中枢神经系统作用就会丧失。因此,我们决定研究抑制这种酶是否会影响经典地被描述为受内源性大麻素系统控制的生理功能。尽管 MK-886 抑制 5-LO 降低了大脑中的脂氧素 A4 水平,但通过腹腔内(10 mg/kg)或脑室内(500 pmol/2 µl)途径,即使在最高可能剂量下,在高架十字迷宫(EPM)中也未发现任何作用。因此,在 EPM 测试中,5-LO KO 小鼠的焦虑样行为没有发生改变。有趣的是,年龄较大的小鼠表现出循环脂氧素 A4 水平降低,对 MK-886 敏感,表现出焦虑样状态。此外,外源性脂氧素 A4 在 EPM 测试中诱导出抗焦虑样特征。我们的研究结果与其他报道一致,即 FLAP KO 或 5-LO KO 与其对照品系在成年小鼠中没有差异,但在老年小鼠中表现出焦虑样行为增加。我们还首次表明脂氧素 A4 会影响小鼠行为。总之,我们提出内源性 5-LO 衍生物在调节焦虑样行为方面存在年龄依赖性相关性,此外外源性脂氧素 A4 具有产生抗焦虑样状态的潜力。