Matsui H, Murakami M, Wynns G C, Conroy C W, Mead A, Maren T H, Sears M L
Oshima Ophthalmological Institute, Fukuoka, Japan.
Exp Eye Res. 1996 Apr;62(4):409-17. doi: 10.1006/exer.1996.0046.
Carbonic anhydrase inhibitors (CAIs) lower intraocular pressure by reducing aqueous flow. It has been thought that this pharmacologic reduction of aqueous flow is mediated by the ciliary epithelium, but it is not known whether this cellular action is effected by inhibition of the membranal (CA IV) and/or cytosolic (CA II) carbonic anhydrases of the ciliary epithelium. The isolated ciliary epithelial bilayer maintains its anatomic and functional polarity and generates a transepithelial potential difference (TEP) in an Ussing type chamber. Depletion of HCO3-, accomplished either with an HCO3(-)-free solution bathing the epithelial bilayer, or, with addition of freely permeant CAIs to HCO3(-)-containing media, (from either the PE or NPE side of the bilayer) depolarizes the preparation. Addition of CAIs to an HCO3(-)-depleted preparation has no further effect, indicating the specific action of the CAIs. The CAI, 2-p-NH2 benzenesulfonamido-1,3,4,-thiadiazole-5-SO2NH2, linked to polybutadiene maleic acid yields an impermeant polymer of 20000 Da with no loss of activity. At 45 microM this impermeant polymer caused a 60% increase in the SCC, seen only when the compound was applied to the NPE side of the bilayer. This latter result indicates an effect from inhibition of CA IV in the basolateral membranes of the NPE. Thus there are probably two different cellular actions of CAIs upon the ciliary epithelium to reduce aqueous inflow, cytoplasmic and membranal. The action of NPE basolateral membranal CA IV is probably linked to the chloride/bicarbonate exchanger.
碳酸酐酶抑制剂(CAIs)通过减少房水生成来降低眼压。一直以来人们认为这种药物对房水生成的减少是由睫状体上皮介导的,但尚不清楚这种细胞作用是否是通过抑制睫状体上皮的膜性(CA IV)和/或胞质(CA II)碳酸酐酶来实现的。分离的睫状体上皮双层结构保持其解剖和功能极性,并在尤斯灌流室中产生跨上皮电位差(TEP)。用不含HCO3-的溶液冲洗上皮双层结构,或者向含HCO3-的培养基中添加可自由通透的CAIs(从双层结构的PE或NPE侧添加),使HCO3-耗尽,会使该制剂去极化。向HCO3-耗尽的制剂中添加CAIs没有进一步影响,这表明了CAIs的特异性作用。与聚丁二烯马来酸相连的CAI 2-p-NH2苯磺酰胺基-1,3,4-噻二唑-5-SO2NH2产生一种分子量为20000 Da的不可通透聚合物,且不失活。在45 microM时,这种不可通透聚合物使短路电流(SCC)增加了60%,只有当该化合物应用于双层结构的NPE侧时才会出现这种情况。后一结果表明是抑制了NPE基底外侧膜中的CA IV所致。因此,CAIs对睫状体上皮减少房水流入可能有两种不同的细胞作用,即胞质作用和膜作用。NPE基底外侧膜CA IV的作用可能与氯/碳酸氢根交换体有关。