Casavola V, Guerra L, Reshkin S J, Jacobson K A, Murer H
Institute of General Physiology, University of Bari, Italy.
Mol Pharmacol. 1997 Mar;51(3):516-23.
The effect of adenosine on Na+/H+ exchange activity was examined in cultured A6 renal epithelial cells. Adenosine and its analogue N6-cyclopentyladenosine (CPA) had different effects on Na+/H+ exchange activity depending on the side of addition. Basolateral CPA induced a stimulation of Na+/H+ exchange activity that was completely prevented by preincubation with an A2A-selective antagonist, 8-(3-chlorostyryl)caffeine, whereas apical CPA induced a slight but significant inhibition of Na+/H+ exchange activity that was significantly reduced by the A1-receptor antagonist 1,3-dipropyl-8-cyclopentylxanthine. Protein kinase C activation may be involved in mediating the apical CPA inhibition of Na+/H+ exchange activity; this inhibition was prevented by the protein kinase C inhibitor calphostin C. Treatment with either forskolin or 8-bromo-cAMP significantly stimulated Na+/H+ exchange activity; only basolateral CPA addition induced an increase in cAMP level. These observations together with the finding that the CPA-dependent stimulation of exchange activity was prevented by the protein kinase A inhibitor H-89 support the hypothesis that basolateral CPA stimulates Na+/H+ exchange via adenylate cyclase/protein kinase A activation. Basolateral CPA also increased transepithelial Na+ transport, and this stimulation was prevented by the Na+/H+ exchange inhibitor HOE-694, suggesting that changes in pHi during hormone action can act as an intermediate in the second-messenger cascade.
在培养的A6肾上皮细胞中研究了腺苷对Na⁺/H⁺交换活性的影响。腺苷及其类似物N⁶-环戊基腺苷(CPA)对Na⁺/H⁺交换活性的影响取决于添加的一侧。基底外侧CPA诱导Na⁺/H⁺交换活性增强,预先用A₂A选择性拮抗剂8-(3-氯苯乙烯基)咖啡因孵育可完全阻断这种增强;而顶端CPA诱导Na⁺/H⁺交换活性轻微但显著抑制,A₁受体拮抗剂1,3-二丙基-8-环戊基黄嘌呤可显著减轻这种抑制。蛋白激酶C激活可能参与介导顶端CPA对Na⁺/H⁺交换活性的抑制;蛋白激酶C抑制剂钙泊三醇C可阻止这种抑制。用福斯可林或8-溴-cAMP处理均显著刺激Na⁺/H⁺交换活性;仅添加基底外侧CPA可诱导cAMP水平升高。这些观察结果以及蛋白激酶A抑制剂H-89可阻止CPA依赖性交换活性增强这一发现支持以下假说:基底外侧CPA通过腺苷酸环化酶/蛋白激酶A激活来刺激Na⁺/H⁺交换。基底外侧CPA还增加了跨上皮Na⁺转运,并且这种刺激被Na⁺/H⁺交换抑制剂HOE-694阻断,这表明激素作用期间细胞内pH值的变化可作为第二信使级联反应的中间环节。