Kennedy-Lydon Teresa, Crawford Carol, Wildman Scott S, Peppiatt-Wildman Claire M
Urinary System Physiology Unit, Medway School of Pharmacy, The Universities of Kent and Greenwich at Medway, Kent, United Kingdom.
Urinary System Physiology Unit, Medway School of Pharmacy, The Universities of Kent and Greenwich at Medway, Kent, United Kingdom
Am J Physiol Renal Physiol. 2015 Oct 1;309(7):F648-57. doi: 10.1152/ajprenal.00199.2015. Epub 2015 Jul 22.
We have previously shown that vasa recta pericytes are known to dilate vasa recta capillaries in the presence of PGE2 and contract vasa recta capillaries when endogenous production of PGE2 is inhibited by the nonselective nonsteroidal anti-inflammatory drug (NSAID) indomethacin. In the present study, we used a live rat kidney slice model to build on these initial observations and provide novel data that demonstrate that nonselective, cyclooxygenase-1-selective, and cyclooxygenase -2-selective NSAIDs act via medullary pericytes to elicit a reduction of vasa recta diameter. Real-time images of in situ vasa recta were recorded, and vasa recta diameters at pericyte and nonpericyte sites were measured offline. PGE2 and epoprostenol (a prostacyclin analog) evoked dilation of vasa recta specifically at pericyte sites, and PGE2 significantly attenuated pericyte-mediated constriction of vasa recta evoked by both endothelin-1 and ANG II. NSAIDs (indomethacin > SC-560 > celecoxib > meloxicam) evoked significantly greater constriction of vasa recta capillaries at pericyte sites than at nonpericyte sites, and indomethacin significantly attenuated the pericyte-mediated vasodilation of vasa recta evoked by PGE2, epoprostenol, bradykinin, and S-nitroso-N-acetyl-l-penicillamine. Moreover, a reduction in PGE2 was measured using an enzyme immune assay after superfusion of kidney slices with indomethacin. In addition, immunohistochemical techniques were used to demonstrate the population of EP receptors in the medulla. Collectively, these data demonstrate that pericytes are sensitive to changes in PGE2 concentration and may serve as the primary mechanism underlying NSAID-associated renal injury and/or further compound-associated tubular damage.
我们之前已经表明,已知直小血管周细胞在存在前列腺素E2(PGE2)时会使直小血管毛细血管扩张,而当非选择性非甾体抗炎药吲哚美辛抑制PGE2的内源性产生时,直小血管周细胞会使直小血管毛细血管收缩。在本研究中,我们使用活大鼠肾切片模型在这些初步观察的基础上进行深入研究,并提供新的数据,证明非选择性、环氧化酶-1选择性和环氧化酶-2选择性非甾体抗炎药通过髓质周细胞起作用,导致直小血管直径减小。记录了原位直小血管的实时图像,并离线测量了周细胞部位和非周细胞部位的直小血管直径。PGE2和依前列醇(一种前列环素类似物)特别在周细胞部位引起直小血管扩张,并且PGE2显著减弱了内皮素-1和血管紧张素II引起的周细胞介导的直小血管收缩。非甾体抗炎药(吲哚美辛>SC-560>塞来昔布>美洛昔康)在周细胞部位引起的直小血管毛细血管收缩明显大于非周细胞部位,并且吲哚美辛显著减弱了PGE2、依前列醇、缓激肽和S-亚硝基-N-乙酰-L-青霉胺引起的周细胞介导的直小血管血管舒张。此外,在用吲哚美辛灌注肾切片后,使用酶免疫测定法测量了PGE2的减少。另外,使用免疫组织化学技术来证明髓质中EP受体的数量。总的来说,这些数据表明周细胞对PGE2浓度的变化敏感,并且可能是与非甾体抗炎药相关的肾损伤和/或进一步的化合物相关的肾小管损伤的主要机制。