Department of Molecular and Cellular Physiology, University of Cincinnati College of Medicine, 231 Albert Sabin Way, Cincinnati, OH 45267-0576, USA.
Cell Biochem Biophys. 2013 May;66(1):53-63. doi: 10.1007/s12013-012-9406-6.
In clinical trials, methadone, but not morphine, appeared to prevent beneficial effects of lubiprostone, a ClC-2 Cl(-) channel activator, on opioid-induced constipation. Effects of methadone and morphine on lubiprostone-stimulated Cl(-) currents were measured by short circuit current (Isc) across T84 cells. Whole cell patch clamp of human ClC-2 (hClC-2) stably expressed in HEK293 cells and in a high expression cell line (HEK293EBNA) as well as human CFTR (hCFTR) stably expressed in HEK293 cells was used to study methadone and morphine effects on recombinant hClC-2 and hCFTR Cl(-) currents. Methadone but not morphine inhibited lubiprostone-stimulated Isc in T84 cells with half-maximal inhibition at 100 nM. Naloxone did not affect lubiprostone stimulation or methadone inhibition of Isc. Lubiprostone-stimulated Cl(-) currents in hClC-2/HEK293 cells, but not forskolin/IBMX-stimulated Cl(-) currents in hCFTR/HEK293 cells, were inhibited by methadone, but not morphine. HEK293EBNA cells expressing hClC-2 showed time-dependent, voltage-activated, CdCl2-inhibited Cl(-) currents in the absence (control) and the presence of lubiprostone. Methadone, but not morphine, inhibited control and lubiprostone-stimulated hClC-2 Cl(-) currents with half-maximal inhibition at 100 and 200-230 nM, respectively. Forskolin/IBMX-stimulated hClC-2 Cl(-) currents were also inhibited by methadone. Myristoylated protein kinase inhibitor (a specific PKA inhibitor) inhibited forskolin/IBMX- but not lubiprostone-stimulated hClC-2 Cl(-) currents. Methadone caused greater inhibition of lubiprostone-stimulated currents added before patching (66.1 %) compared with after patching (28.7 %). Methadone caused inhibition of lubiprostone-stimulated Cl(-) currents in T84 cells and control; lubiprostone- and forskolin/IBMX-stimulated recombinant hClC-2 Cl(-) currents may be the basis for reduced efficacy of lubiprostone in methadone-treated patients.
在临床试验中,美沙酮而非吗啡似乎可预防氯通道激活剂鲁比前列酮对阿片类药物引起的便秘的有益作用。通过 T84 细胞的短路电流(Isc)测量美沙酮和吗啡对鲁比前列酮刺激的 Cl(-)电流的影响。使用全细胞膜片钳技术,研究美沙酮和吗啡对稳定表达于人肾上皮细胞(HEK293)中的人 ClC-2(hClC-2)和高表达细胞系(HEK293EBNA)以及稳定表达于人 CFTR(hCFTR)的 HEK293 细胞中的重组 hClC-2 和 hCFTR Cl(-)电流的影响。美沙酮而非吗啡抑制 T84 细胞中鲁比前列酮刺激的 Isc,半最大抑制浓度为 100 nM。纳洛酮不影响鲁比前列酮的刺激或美沙酮对 Isc 的抑制作用。美沙酮抑制 hClC-2/HEK293 细胞中的鲁比前列酮刺激的 Cl(-)电流,但不抑制福司可林/IBMX 刺激的 Cl(-)电流,而吗啡则没有这种作用。表达 hClC-2 的 HEK293EBNA 细胞在无(对照)和存在鲁比前列酮的情况下显示出时间依赖性、电压激活、CdCl2 抑制的 Cl(-)电流。美沙酮而非吗啡抑制对照和鲁比前列酮刺激的 hClC-2 Cl(-)电流,半最大抑制浓度分别为 100 nM 和 200-230 nM。福司可林/IBMX 刺激的 hClC-2 Cl(-)电流也被美沙酮抑制。肉豆蔻酰化蛋白激酶抑制剂(一种特异性 PKA 抑制剂)抑制福司可林/IBMX 但不抑制鲁比前列酮刺激的 hClC-2 Cl(-)电流。美沙酮在加样前(66.1%)对鲁比前列酮刺激电流的抑制作用大于加样后(28.7%)。美沙酮抑制 T84 细胞和对照中的鲁比前列酮刺激的 Cl(-)电流;鲁比前列酮和福司可林/IBMX 刺激的重组 hClC-2 Cl(-)电流可能是鲁比前列酮在美沙酮治疗患者中疗效降低的基础。