首页> 外文期刊>The Journal of Physiology >Cyclic GMP-dependent relaxation of isolated rat renal glomeruli induced by extracellular ATP.
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Cyclic GMP-dependent relaxation of isolated rat renal glomeruli induced by extracellular ATP.

机译:细胞外ATP诱导的离体大鼠肾小球的循环GMP依赖性松弛。

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The relaxing effect of extracellular ATP on renal glomeruli has been investigated by applying ATP and its analogues to suspensions of angiotensin II-precontracted rat renal glomeruli. Based on changes of glomerular [3H]inulin space (GIS) the relaxation of glomeruli was analysed in the presence of agonists: ATP, ADP, AMP, UTP, 2-methylthio-ATP (P2Y agonist), beta,gamma-methylene-ATP (P2X agonist) and adenosine. ATP, 2-methylthio-ATP, ADP and UTP induced concentration-dependent relaxation whereas AMP, beta,gamma-methylene-ATP and adenosine had no effect. The rank order of relaxation potency was 2-methylthio-ATP > ATP > ADP > UTP. An inhibitor of constitutive nitric oxide synthase (NOS), Nomega-nitro-L-arginine (NNA) prevented the ATP-induced increased accumulation of L-citrulline and the relaxation effect of ATP. An inhibitor of the neuronal isoform of NOS, 7-nitroindazole, had no effect on the relaxation effect of ATP. The relaxing effect of ATP was prevented in the presence of inhibitors of cyclic guanylyl cyclase: methylene blue (MB) and the more specific inhibitor 1H-[1,2,4]oxadiazolo-[4,3-a]quinoxalin-1-one (ODQ). ATP stimulated an accumulation of cGMP that was diminished in the presence of MB. We indicated that extracellular ATP may relax the glomeruli via activation of P2Y receptors with the subsequent activation of the endothelial isoform of nitric oxide synthase and soluble guanylyl cyclase. We suggest that, based on the described mechanism, extracellular ATP may increase the filtration surface which, in turn, may influence the glomerular filtration rate.
机译:通过将ATP及其类似物应用于血管紧张素II预收缩的大鼠肾小球悬液中,已研究了细胞外ATP对肾小球的松弛作用。根据肾小球[3H]菊粉空间(GIS)的变化,分析了在以下激动剂存在下肾小球的松弛情况:ATP,ADP,AMP,UTP,2-甲硫基ATP(P2Y激动剂),β,γ-亚甲基-ATP (P2X激动剂)和腺苷。 ATP,2-甲硫基ATP,ADP和UTP引起浓度依赖性松弛,而AMP,β,γ-亚甲基ATP和腺苷则无作用。弛豫能力的等级顺序为2-甲硫基-ATP> ATP> ADP> UTP。组成型一氧化氮合酶(NOS)的抑制剂Nomega-nitro-L-精氨酸(NNA)阻止了ATP诱导的L-瓜氨酸的积累增加以及ATP的松弛作用。 NOS的神经元亚型的抑制剂7-硝基吲唑对ATP的舒张作用没有影响。在存在环状鸟苷基环化酶抑制剂:亚甲基蓝(MB)和更特异性的抑制剂1H- [1,2,4]恶二唑-[4,3-a]喹喔啉-1-酮的情况下,阻止了ATP的松弛作用(ODQ)。 ATP刺激了cGMP的积累,而MB的存在会减少该积累。我们表明,细胞外ATP可能通过激活P2Y受体并随后激活一氧化氮合酶和可溶性鸟苷酸环化酶的内皮同工型而使肾小球松弛。我们建议,基于所描述的机制,细胞外ATP可能会增加滤过表面,进而影响肾小球滤过率。

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