Vetter A E, O'Grady S M
Department of Veterinary Pathobiology, University of Minnesota, St. Paul 55108, USA.
Am J Physiol. 1997 Jul;273(1 Pt 1):C67-76. doi: 10.1152/ajpcell.1997.273.1.C67.
The purpose of this study was to investigate the regulation of electrolyte transport across the porcine endometrium by gastrin-releasing peptide (GRP) and substance P (SP). Luminal addition of GRP, neuromedin B (NMB), SP, or neurokinin A(NKA) to mucosal tissues mounted in Ussing chambers produced a multiphasic change in short-circuit current (Isc) characterized by an initial rapid increase and subsequent decrease in current. A similar response was obtained after addition of ionomycin or thapsigargin to the tissues. The Isc response to the peptides or Ca ionophore was inhibited by pretreatment of the tissues with luminal amiloride or benzamil. GRP and SP were more potent [50% effective concentration (EC50) of 3 nM] than NMB or NKA (EC50 values of 46 and 26 nM, respectively) in producing the decrease in Isc. Pretreatment with the GRP receptor antagonist 3-Phe-His-Trp-Ala-Val-D-Ala-His-D-Pro-psi Phe-NH2 blocked the Isc response to GRP and NMB but not to SP or NKA, whereas the NMB receptor antagonist D-Nal-[Cys-Try-D-Trp-Orn-Val-Cys]-Nal-NH2 was ineffective in inhibiting the Isc response to any of the peptides. In contrast, pretreatment of the tissue with the nonpeptide SP receptor antagonist CP-99,994 blocked the Isc response to SP and NKA but not to GRP or NMB. Experiments with amphotericin B-permeabilized tissues showed that GRP, SP, ionomycin, and thapsigargin increased current through an outwardly rectifying K conductance located on the apical membrane of the cells. The K-to-Na selectivity ratio of this conductance was calculated to be 2.5:1. These experiments showed that GRP and SP, acting through different receptors, produced an increase in K efflux through a Ca-dependent K conductance present in the apical membrane of surface endometrial epithelial cells. In addition, immunohistochemistry data showed that GRP-like immunoreactivity was localized to surface and glandular epithelial cells, whereas GRP receptor antibody labeling was observed in both epithelial and stromal cells. These results suggest that GRP functions as both an autocrine and paracrine regulatory peptide in the endometrium.
本研究的目的是探究胃泌素释放肽(GRP)和P物质(SP)对猪子宫内膜电解质转运的调节作用。向安装在尤斯灌流小室中的黏膜组织管腔添加GRP、神经介素B(NMB)、SP或神经激肽A(NKA),会使短路电流(Isc)产生多相变化,其特征为电流先快速增加,随后下降。向组织中添加离子霉素或毒胡萝卜素后也获得了类似的反应。用管腔氨氯吡咪或苄甲咪预处理组织可抑制对这些肽或钙离子载体的Isc反应。在使Isc下降方面,GRP和SP比NMB或NKA更有效[50%有效浓度(EC50)分别为3 nM],而NMB或NKA的EC50值分别为46和26 nM。用GRP受体拮抗剂3 - Phe - His - Trp - Ala-Val - D - Ala - His - D - Pro - ψPhe - NH2预处理可阻断对GRP和NMB的Isc反应,但不影响对SP或NKA的反应,而NMB受体拮抗剂D - Nal - [Cys - Try - D - Trp - Orn - Val - Cys] - Nal - NH2在抑制对任何一种肽的Isc反应方面均无效。相反,用非肽类SP受体拮抗剂CP - 99,994预处理组织可阻断对SP和NKA的Isc反应,但不影响对GRP或NMB的反应。两性霉素B通透组织的实验表明,GRP、SP、离子霉素和毒胡萝卜素通过增加位于细胞顶端膜上的外向整流钾通道的电流来增加电流。该通道的钾钠选择性比率经计算为2.5:1。这些实验表明,GRP和SP通过不同受体起作用,通过存在于子宫内膜表面上皮细胞顶端膜上的钙依赖性钾通道增加钾外流。此外,免疫组织化学数据显示,GRP样免疫反应性定位于表面和腺上皮细胞,而在GRP受体抗体标记中在上皮细胞和基质细胞中均观察到。这些结果表明,GRP在子宫内膜中既作为自分泌调节肽又作为旁分泌调节肽发挥作用。