Chisari M, Salomone S, Laureanti F, Copani A, Sortino M A
Department of Experimental and Clinical Pharmacology, University of Catania, Italy.
J Neurochem. 2004 Dec;91(5):1171-9. doi: 10.1111/j.1471-4159.2004.02782.x.
The ability of activated glia to affect cerebral vascular tone has been evaluated using an in vitro experimental system in which basilar arteries were incubated with glial cultures activated by treatment with lipopolysaccharide (LPS). Vascular tone was measured with an isometric myograph. Contraction in response to high KCl and serotonin was reduced in arteries co-incubated for 24 h with LPS-activated glia, whereas the response to acetylcholine was not modified. The reduced contraction was prevented when the nitric oxide synthase (NOS) inhibitor L-N-nitro-arginine (L-NNA) was added throughout the whole incubation time (activation of glial cells with LPS + co-incubation of glial cells with cerebral arteries). Under these conditions, nitrite levels were drastically reduced. A reduced contraction to KCl was also observed after treatment of the cerebral vessel with sodium nitroprusside. In contrast, L-NNA added to the vessel did not modify the response to contracting stimuli and the expression of endothelial NOS was not modified in cerebral arteries pre-incubated with activated glia. These results suggest that activated glia, which finds an in vivo correlate in several neuropathological conditions, can contribute to changes of vascular tone by modifying the levels of nitric oxide (NO) to which the vessel is exposed.
已使用体外实验系统评估了活化胶质细胞影响脑血管张力的能力,在该系统中,将基底动脉与经脂多糖(LPS)处理而活化的胶质细胞培养物一起孵育。用等长肌动描记器测量血管张力。与LPS活化的胶质细胞共同孵育24小时的动脉中,对高钾和血清素的收缩反应降低,而对乙酰胆碱的反应未改变。在整个孵育期间添加一氧化氮合酶(NOS)抑制剂L-N-硝基精氨酸(L-NNA)(用LPS活化胶质细胞+胶质细胞与脑动脉共同孵育)时,可防止收缩反应降低。在这些条件下,亚硝酸盐水平大幅降低。用硝普钠处理脑血管后,对氯化钾的收缩反应也降低。相反,添加到血管中的L-NNA并未改变对收缩刺激的反应,且在与活化胶质细胞预孵育的脑动脉中,内皮型NOS的表达未改变。这些结果表明,活化胶质细胞在几种神经病理状态下在体内有相应的关联,它可通过改变血管所接触的一氧化氮(NO)水平来促成血管张力的变化。