Rühl A, Berezin I, Collins S M
Intestinal Disease Research Program, McMaster University Medical Centre, Hamilton, Ontario, Canada.
Gastroenterology. 1995 Dec;109(6):1852-62. doi: 10.1016/0016-5085(95)90752-1.
BACKGROUND & AIMS: Proinflammatory cytokines alter function in enteric nerves, but little is known about underlying mechanisms. This study was designed to investigate the roles of prostanoids and of macrophage-like cells in cytokine-induced suppression of [3H]norepinephrine release from rat myenteric plexus.
The release of 3H from jejunal longitudinal muscle-myenteric plexus preparations that had been loaded with [3H]norepinephrine was measured. Measurements of 3H release as well as concentrations of prostaglandin E2 and leukotriene were made in preparations exposed to interleukin 1 beta plus interleukin 6 and in the presence or absence of piroxicam, 5-lipoxygenase inhibitor MK886, cycloheximide, or cyclosporin A. An ultrastructural analysis was also performed to investigate the presence of macrophage-like cells in the myenteric plexus.
Interleukin 1 beta plus interleukin 6 suppressed 3H release and caused an increase in tissue prostaglandin E2 but not leukotriene E4. Piroxicam and cycloheximide but not MK886 attenuated the cytokine-induced increase in prostaglandin E2 and the suppression of [3H]norepinephrine release. Ultrastructural analysis showed macrophage-like cells in the plexus, and the cytokine effects were inhibited by cyclosporin A.
Prostanoids but not leukotrienes mediate the cytokine-induced suppression of norepinephrine release, and the results of this study suggest that macrophage-like cells are also involved.
促炎细胞因子可改变肠神经功能,但对其潜在机制知之甚少。本研究旨在探讨前列腺素和巨噬细胞样细胞在细胞因子诱导的大鼠肠肌间神经丛[3H]去甲肾上腺素释放抑制中的作用。
测定负载[3H]去甲肾上腺素的空肠纵行肌-肠肌间神经丛标本中3H的释放。在暴露于白细胞介素1β加白细胞介素6的标本中,在有或无吡罗昔康、5-脂氧合酶抑制剂MK886、放线菌酮或环孢素A的情况下,测量3H释放以及前列腺素E2和白三烯的浓度。还进行了超微结构分析,以研究肠肌间神经丛中巨噬细胞样细胞的存在情况。
白细胞介素1β加白细胞介素6抑制3H释放,并导致组织前列腺素E2增加,但白三烯E4未增加。吡罗昔康和放线菌酮可减弱细胞因子诱导的前列腺素E2增加和[3H]去甲肾上腺素释放的抑制,而MK886则无此作用。超微结构分析显示神经丛中有巨噬细胞样细胞,环孢素A可抑制细胞因子的作用。
前列腺素而非白三烯介导细胞因子诱导的去甲肾上腺素释放抑制,本研究结果表明巨噬细胞样细胞也参与其中。