Pereira Marcy Lancia, D'ancona Carlos Arturo Levi, Rojas-Moscoso Julio Alejandro, Ramos Antonio Celso Saragossa, Monica Fabiola Zakia, Antunes Edson
Departamento de Cirurgia, Faculdade de Ciências Médicas - UNICAMP, Campinas, SP, Brasil.
Departamento de Urologia, Faculdade de Ciências Médicas - UNICAMP, Campinas, SP, Brasil.
Int Braz J Urol. 2017 Mar-Apr;43(2):356-366. doi: 10.1590/S1677-5538.IBJU.2015.0441.
To investigate the lower urinary tract changes in mice treated with L-NAME, a non-selective competitive inhibitor of nitric oxide synthase (NOS), or aminoguanidine, a competitive inhibitor of inducible nitric oxide synthase (iNOS), after 5 weeks of partial bladder outlet obstruction (BOO), in order to evaluate the role of constitutive and non-constitutive NOS in the pathogenesis of this experimental condition.
C57BL6 male mice were partially obstructed and randomly allocated into 6 groups: Sham, Sham + L-NAME, Sham + aminoguanidine, BOO, BOO + L-NAME and BOO + aminoguanidine. After 5 weeks, bladder weight was obtained and cystometry and tissue bath contractile studies were performed.
BOO animals showed increase of non-voiding contractions (NVC) and bladder capacity, and also less contractile response to Carbachol and Electric Field Stimulation. Inhibition of NOS isoforms improved bladder capacity and compliance in BOO animals. L-NAME caused more NVC, prevented bladder weight gain and leaded to augmented contractile responses at muscarinic and electric stimulation. Aminoguanidine diminished NVC, but did not avoid bladder weight gain in BOO animals and did not improve contractile responses.
It can be hypothesized that chronic inhibition of three NOS isoforms in BOO animals leaded to worsening of bladder function, while selective inhibition of iNOS did not improve responses, what suggests that, in BOO animals, alterations are related to constitutive NOS.
研究在部分膀胱出口梗阻(BOO)5周后,用一氧化氮合酶(NOS)的非选择性竞争性抑制剂L - 精氨酸甲酯(L - NAME)或诱导型一氧化氮合酶(iNOS)的竞争性抑制剂氨基胍处理的小鼠下尿路变化,以评估组成型和非组成型NOS在这种实验条件发病机制中的作用。
将C57BL6雄性小鼠进行部分梗阻,并随机分为6组:假手术组、假手术 + L - NAME组、假手术 + 氨基胍组、BOO组、BOO + L - NAME组和BOO + 氨基胍组。5周后,获取膀胱重量,并进行膀胱测压和组织浴收缩研究。
BOO动物显示无排尿收缩(NVC)增加和膀胱容量增加,并且对卡巴胆碱和电场刺激的收缩反应也较小。抑制NOS同工型可改善BOO动物的膀胱容量和顺应性。L - NAME导致更多的NVC,阻止膀胱重量增加,并导致毒蕈碱和电刺激时收缩反应增强。氨基胍减少了NVC,但未避免BOO动物的膀胱重量增加,也未改善收缩反应。
可以推测,在BOO动物中慢性抑制三种NOS同工型会导致膀胱功能恶化,而选择性抑制iNOS并未改善反应,这表明在BOO动物中,改变与组成型NOS有关。