Keeling D J, Taylor A G, Smith P L
Gastrointestinal Research, SmithKline Beecham, The Frythe, Welwyn, U.K.
Biochim Biophys Acta. 1991 Nov 14;1115(1):42-8. doi: 10.1016/0304-4165(91)90009-6.
NPPB (5-nitro-2-(3-phenylpropylamino)benzoic acid) has been reported to block Cl- channels in isolated rabbit nephrons with high potency (IC50 = 80 nM). The effects of this compound on Cl(-)-mediated transport processes in intestinal tissues have been studied using agonist-stimulated short-circuit current (T84) in Ussing chamber experiments and 36Cl- fluxes in monolayers of a colonic cell line (T84). NPPB inhibited PGE1-stimulated Isc in rabbit distal colon and ileum at concentrations in the range 20 to 100 microM. However, NPPB at the same concentrations also inhibited glucose-stimulated Isc in rabbit ileum, suggesting that its effects were not restricted to those on Cl- transport. Consistent with this, exposure of rabbit distal colon to 100 microM NPPB was found to reduce endogenous ATP levels by 69%, implying that, at these concentrations, NPPB could impair active transport processes by an effect on cellular energy metabolism. Clear evidence for a direct effect of NPPB on epithelial chloride channels was found in studies on Cl- fluxes in T84 cell monolayers. NPPB inhibited VIP-stimulated Cl- uptake into T84 cells with an IC50 of 414 microM. NPPB (1 mM) also inhibited Cl- efflux from pre-loaded cells confirming its effect as a weak Cl- channel blocker in this system.
据报道,NPPB(5-硝基-2-(3-苯基丙基氨基)苯甲酸)能够高效阻断离体兔肾单位中的氯离子通道(IC50 = 80 nM)。在尤斯灌流室实验中,通过激动剂刺激的短路电流(T84)以及结肠细胞系(T84)单层中的36Cl-通量,研究了该化合物对肠道组织中氯离子介导的转运过程的影响。NPPB在20至100 microM的浓度范围内抑制了兔远端结肠和回肠中PGE1刺激的短路电流。然而,相同浓度的NPPB也抑制了兔回肠中葡萄糖刺激的短路电流,这表明其作用并不局限于对氯离子转运的影响。与此一致的是,发现兔远端结肠暴露于100 microM NPPB会使内源性ATP水平降低69%,这意味着在这些浓度下,NPPB可能通过影响细胞能量代谢来损害主动转运过程。在对T84细胞单层中的氯离子通量的研究中,发现了NPPB对上皮氯离子通道有直接作用的明确证据。NPPB抑制VIP刺激的氯离子摄取进入T84细胞,IC50为414 microM。NPPB(1 mM)也抑制了预加载细胞中的氯离子外流,证实了其在该系统中作为弱氯离子通道阻滞剂的作用。