Prasanna G, Dibas A, Hulet C, Yorio T
Department of Pharmacology, University of North Texas Health Science Center, Fort Worth, Texas 76107, USA.
J Pharmacol Exp Ther. 2001 Mar;296(3):966-71.
Endothelin-1 (ET-1), a potent vasoconstrictor, lowers intraocular pressure in mammals, either by enhancing the outflow of aqueous humor (AH) via the trabecular meshwork and Schlemm's canal or by reducing AH formation at the ciliary epithelium. Aqueous humor production occurs by passive diffusion of water coupled with active transport of ions, mainly involving Na(+):K(+):2Cl(-) cotransporter and Na(+)/K(+)-ATPase pump from serosal to aqueous side. Presently, we have evaluated the effects of ET-1 on Na(+):K(+):2Cl(-) cotransport and Na(+)/K(+)-ATPase activity in HNPE cells using (86)Rb(+) uptake. ET-1 (100 pM-100 nM) decreased mean (86)Rb(+) uptake by 15% during a 15-min uptake period. ET-1's effect was not prevented by BQ610, an ET(A) receptor antagonist, but was blocked by BQ788, an ET(B) receptor antagonist. ET-1's effect was mimicked by sarafotoxin, an ET(B) agonist. ET-1-induced reduction in (86)Rb(+) uptake was additive with bumetanide, a selective inhibitor of Na(+):K(+):2Cl(-) cotransporter but not with ouabain, a selective inhibitor of the Na(+)/K(+)-ATPase. ET-1 did not affect iberiotoxin-sensitive maxi K(+) channels. This suggests that ET-1-induced reduction in (86)Rb(+) uptake is mediated through the inhibition of the Na(+)/K(+)-ATPase via an ET(B)-like receptor. These findings are consistent with an ET-1 effect on active ion transport activity in HNPE cells that could explain the reduction in aqueous humor production and the lowering of intraocular pressure.
内皮素 -1(ET -1)是一种强效血管收缩剂,可通过增强房水(AH)经小梁网和施莱姆管的流出,或通过减少睫状体上皮细胞的房水生成来降低哺乳动物的眼压。房水生成是通过水的被动扩散以及离子的主动转运发生的,主要涉及从浆膜侧到房水侧的Na(+):K(+):2Cl(-)共转运体和Na(+)/K(+)-ATP酶泵。目前,我们使用(86)Rb(+)摄取评估了ET -1对人非色素睫状体上皮(HNPE)细胞中Na(+):K(+):2Cl(-)共转运和Na(+)/K(+)-ATP酶活性的影响。在15分钟的摄取期内,ET -1(100 pM - 100 nM)使平均(86)Rb(+)摄取减少了15%。ET(A)受体拮抗剂BQ610不能阻止ET -1的作用,但ET(B)受体拮抗剂BQ788可阻断其作用。ET(B)激动剂沙拉毒素可模拟ET -1的作用。ET -1诱导的(86)Rb(+)摄取减少与布美他尼(一种Na(+):K(+):2Cl(-)共转运体的选择性抑制剂)具有相加作用,但与哇巴因(一种Na(+)/K(+)-ATP酶的选择性抑制剂)没有相加作用。ET -1不影响iberiotoxin敏感的大电导钾通道。这表明ET -1诱导的(86)Rb(+)摄取减少是通过类似ET(B)受体抑制Na(+)/K(+)-ATP酶介导的。这些发现与ET -1对HNPE细胞中主动离子转运活性的作用一致,这可以解释房水生成减少和眼压降低的现象。