Squadrito F, Altavilla D, Squadrito G, Campo G M, Arlotta M, Quartarone C, Minutoli L, Ferlito M, Saitta A, Caputi A P
Institute of Pharmacology, School of Medicine, University of Messina, Italy.
Eur J Pharmacol. 1998 Nov 13;361(1):101-8. doi: 10.1016/s0014-2999(98)00705-5.
Selectin-mediated leucocyte accumulation is implicated in the pathogenesis of splanchnic artery occlusion. Sulfatide is recognized by P-selectin and blocks this adhesion molecule. We investigated the effects of sulfatide in rats subjected to splanchnic artery occlusion shock. Anaesthetized rats, subjected to total occlusion of the superior mesenteric artery and the coeliac trunk for 45 min developed severe shock resulting in death within 85-90 min after the release of occlusion. Sham operated animals were used as controls. Splanchnic artery occlusion shocked rats had marked hypotension, enhanced levels of tumor necrosis factor-alpha (TNF-alpha) in serum and macrophages, leucopenia and increased ileal leucocyte accumulation, studied by the means of myeloperoxidase activity. Furthermore, aortae from shocked rats showed marked hyporeactivity to phenylephrine (1 nM-10 microM), reduced responsiveness to acetylcholine (10 nM-10 microM) and an increased staining for P-selectin in the vasculature. In vivo administration of sulfatide (10 mg/kg, i.v., 5 min after occlusion of the splanchnic arteries) increased survival rate (90%, 4 h after splanchnic artery occlusion shock), enhanced mean arterial blood pressure, reduced serum TNF-alpha (37 +/- 11 U/ml vs. 398 +/- 18 U/ml), ameliorated leucopenia and reduced ileal myeloproxidase activity (1.2 +/- 0.4 U/g tissue vs. 8.2 +/- 0.8 U/g tissue). Aortae from splanchnic artery occlusion shocked rats treated with sulfatide exhibited a greater contractile response to phenylephrine and improved responsiveness to acetylcholine. Moreover sulfatide-treated rats showed a reduced staining for P-selectin in the aorta and in the superior mesenteric artery. Finally, passive immunization with specific monoclonal antibodies raised against P-selectin significantly protected from the lethality induced by splanchnic artery occlusion shock. Our results suggest that sulfatide protects against splanchnic artery occlusion shock.
选择素介导的白细胞聚集与内脏动脉闭塞的发病机制有关。硫苷脂可被P-选择素识别并阻断这种粘附分子。我们研究了硫苷脂对遭受内脏动脉闭塞性休克大鼠的影响。将麻醉的大鼠肠系膜上动脉和腹腔干完全闭塞45分钟后,会发生严重休克,在闭塞解除后85 - 90分钟内死亡。假手术动物用作对照。通过髓过氧化物酶活性研究发现,遭受内脏动脉闭塞性休克的大鼠有明显的低血压、血清和巨噬细胞中肿瘤坏死因子-α(TNF-α)水平升高、白细胞减少以及回肠白细胞聚集增加。此外,休克大鼠的主动脉对去氧肾上腺素(1 nM - 10 μM)反应明显减弱,对乙酰胆碱(10 nM - 10 μM)反应性降低,血管中P-选择素染色增加。在内脏动脉闭塞后5分钟静脉内给予硫苷脂(10 mg/kg)可提高存活率(内脏动脉闭塞性休克后4小时为90%),提高平均动脉血压,降低血清TNF-α(37 ± 11 U/ml对398 ± 18 U/ml),改善白细胞减少并降低回肠髓过氧化物酶活性(1.2 ± 0.4 U/g组织对8.2 ± 0.8 U/g组织)。用硫苷脂治疗的遭受内脏动脉闭塞性休克大鼠的主动脉对去氧肾上腺素表现出更大的收缩反应,对乙酰胆碱的反应性也有所改善。此外,硫苷脂治疗的大鼠主动脉和肠系膜上动脉中P-选择素染色减少。最后,用针对P-选择素的特异性单克隆抗体进行被动免疫可显著保护动物免受内脏动脉闭塞性休克诱导的致死作用。我们的结果表明硫苷脂可预防内脏动脉闭塞性休克。