Grion N, Repetto E M, Pomeraniec Y, Calejman C Martinez, Astort F, Sanchez R, Pignataro O P, Arias P, Cymeryng C B
Departmento de Bioquímica Humana, Facultad de Medicina, Universidad de Buenos Aires, Paraguay 2155 5, Buenos Aires C1121ABG, Argentina.
J Endocrinol. 2007 Jul;194(1):11-20. doi: 10.1677/JOE-06-0199.
The present study was designed to investigate the effect of lipopolysaccharide (LPS) on the expression levels and activities of the nitric oxide synthase (NOS) and heme oxygenase (HO) systems in the rat adrenal gland. Both enzymatic activities were significantly increased in this tissue after in vivo treatment with LPS. The concurrent induction of the HO-1, NOS-1, and NOS-2 gene products was also detected as both mRNAs and protein levels were augmented by this treatment in a time-dependent way. A significant interaction between both signaling systems was also demonstrated as in vivo blockage of NOS activity with N(G)-nitro-L-arginine methyl ester (L-NAME) resulted in a significant reduction in HO expression and activity levels, while an increase in NOS activity was observed when HO was inhibited by Sn-protoporphyrin IX (Sn-PPIX). As both NOS and HO activities have been previously involved in the modulation of adrenal steroidogenesis, we investigated the participation of these signaling systems in the adrenal response to LPS. Our results showed that acute stimulation of steroid production by ACTH was significantly increased when either NOS or HO activities were inhibited. We conclude that adrenal NOS and HO can be induced by a non-lethal dose of endotoxin supporting a modulatory role for these activities in the adrenal response to immune challenges.
本研究旨在探讨脂多糖(LPS)对大鼠肾上腺中一氧化氮合酶(NOS)和血红素加氧酶(HO)系统表达水平及活性的影响。体内给予LPS处理后,该组织中的两种酶活性均显著增加。同时还检测到HO-1、NOS-1和NOS-2基因产物的诱导,因为这种处理使mRNA和蛋白质水平均呈时间依赖性增加。两个信号系统之间也存在显著相互作用,因为用N(G)-硝基-L-精氨酸甲酯(L-NAME)体内阻断NOS活性会导致HO表达和活性水平显著降低,而当HO被锡原卟啉IX(Sn-PPIX)抑制时,NOS活性则会增加。由于NOS和HO活性先前均参与肾上腺类固醇生成的调节,我们研究了这些信号系统在肾上腺对LPS反应中的作用。我们的结果表明,当NOS或HO活性被抑制时,促肾上腺皮质激素(ACTH)对类固醇生成的急性刺激作用显著增强。我们得出结论,非致死剂量的内毒素可诱导肾上腺NOS和HO,支持这些活性在肾上腺对免疫挑战反应中的调节作用。