Sharshar Tarek, Gray Francoise, Lorin de la Grandmaison Geoffroy, Hopkinson Nicholas S, Ross Ewen, Dorandeu Anne, Orlikowski David, Raphael Jean-Claude, Gajdos Philippe, Annane Djillali
Service de Réanimation Médicale, Hôpital Raymond Poincaré, Faculté de Médecine Paris, Ile de France Ouest, Garches, France.
Lancet. 2003 Nov 29;362(9398):1799-805. doi: 10.1016/s0140-6736(03)14899-4.
Results of experimental and clinical studies have shown that septic shock is associated with cardiovascular autonomic failure. Thus, we aimed to investigate the existence of ischaemia and apoptosis within the cerebral autonomic centres that control the cardiovascular system in patients with septic shock.
In a prospective cohort study, we did post-mortem examinations of supraoptic and paraventricular nuclei, cerebral amygdala, locus coeruleus, and medullary autonomic nuclei in 19 patients with septic shock, seven with non-septic shock and five who died suddenly from extracranial injury. Ischaemic and apoptotic neurons and microglial cells, and expression of tumour necrosis factor alpha (TNFalpha) and inducible nitric oxide synthase (iNOS) were scored.
Ischaemic, neuronal, and microglial apoptosis scores differed between groups (p=0.0007, p<0.0001, and p=0.0037, respectively) and were higher in patients with septic shock than in those with non-septic shock (p=0.0033, p=0.0005, and p=0.0235, respectively), and extra-cranial injury related deaths (p=0.0027, p=0.0007, and p=0.0045, respectively). There was little microglial activation and glial expression of TNFalpha. The scores for endothelial iNOS expression were different between the three groups (p<0.0001), and were higher in septic shock than in non-septic shock (p=0.0009) and than in extracranial injury related deaths (p=0.0007). Vascular expression of iNOS also correlated (Spearman tau=0.57) with autonomic-centre neuronal apoptosis in the combined septic and non-septic shock group.
Septic shock is associated with neuronal and glial apoptosis within the autonomic centres, which is strongly associated with endothelial iNOS expression.
实验和临床研究结果表明,感染性休克与心血管自主神经功能衰竭有关。因此,我们旨在研究感染性休克患者中控制心血管系统的脑自主神经中枢内是否存在缺血和细胞凋亡。
在一项前瞻性队列研究中,我们对19例感染性休克患者、7例非感染性休克患者和5例因颅外损伤突然死亡的患者进行了视上核、室旁核、脑杏仁核、蓝斑和延髓自主神经核的尸检。对缺血和凋亡的神经元及小胶质细胞,以及肿瘤坏死因子α(TNFα)和诱导型一氧化氮合酶(iNOS)的表达进行评分。
各组之间的缺血、神经元和小胶质细胞凋亡评分存在差异(分别为p = 0.0007、p < 0.0001和p = 0.0037),感染性休克患者的评分高于非感染性休克患者(分别为p = 0.0033、p = 0.0005和p = 0.0235),也高于与颅外损伤相关的死亡患者(分别为p = 0.0027、p = 0.0007和p = 0.0045)。小胶质细胞活化和TNFα的胶质表达很少。三组之间内皮iNOS表达评分不同(p < 0.0001),感染性休克组高于非感染性休克组(p = 0.0009),也高于与颅外损伤相关的死亡组(p = 0.0007)。在感染性和非感染性休克合并组中,iNOS的血管表达也与自主神经中枢神经元凋亡相关(Spearman tau = 0.57)。
感染性休克与自主神经中枢内的神经元和胶质细胞凋亡有关,这与内皮iNOS表达密切相关。