Kato Haruto, Kawaguchi Masahiko, Inoue Satoki, Hirai Katsuji, Furuya Hitoshi
Department of Anesthesiology, Nara Medical University, Kashihara City, Nara, Japan.
Anesth Analg. 2009 Jan;108(1):288-95. doi: 10.1213/ane.0b013e318187bb93.
Proinflammatory cytokines increase in cerebrospinal fluid (CSF) after subarachnoid hemorrhage (SAH). Recent evidence suggested that beta-adrenoceptor antagonist could reduce proinflammatory cytokines. We conducted the present study to examine whether beta-adrenoceptor antagonists would reduce proinflammatory cytokine concentrations after SAH in rats.
In Experiment 1, to investigate the time course of interleukin-6 (IL-6) and tumor necrosis factor-alpha (TNF-alpha), rats were randomized into groups: 1, 3, 6, and 12 h after SAH or sham operation. CSF and blood samples were obtained at each time point. In Experiment 2, to investigate the effects of beta-adrenoceptor antagonists on the IL-6 and TNF-alpha concentrations, rats were randomized into groups: 1) control group: SAH + normal saline, 2) propranolol group: SAH + propranolol, 3) metoprolol group: SAH + metoprolol, and 4) butoxamine group: SAH + butoxamine (beta(2)-adrenoceptor antagonist). CSF and blood samples were obtained 6 h after SAH. IL-6 and TNF-alpha concentrations in samples were measured.
In Experiment 1, CSF IL-6 concentrations in the SAH groups increased markedly and peaked at 6 h after SAH, whereas CSF TNF-alpha concentrations in the SAH groups were consistently low. In Experiment 2, CSF IL-6 concentrations in the propranolol and butoxamine groups were significantly lower compared with those in the control group (P < 0.01 and P < 0.05 for each group). Plasma IL-6, CSF TNF-alpha, and plasma TNF-alpha concentrations were comparable in all four groups.
CSF IL-6 concentrations increased in the acute stage of SAH and beta-adrenoceptor antagonists with a beta(2)-adrenoceptor blocking action suppressed this elevation of IL-6 concentrations after SAH in rats.
蛛网膜下腔出血(SAH)后,脑脊液(CSF)中的促炎细胞因子会增加。最近的证据表明,β-肾上腺素能受体拮抗剂可以降低促炎细胞因子水平。我们进行了本研究,以检验β-肾上腺素能受体拮抗剂是否能降低大鼠SAH后促炎细胞因子的浓度。
在实验1中,为研究白细胞介素-6(IL-6)和肿瘤坏死因子-α(TNF-α)的时间进程,将大鼠随机分为SAH或假手术后1、3、6和12小时组。在每个时间点采集脑脊液和血液样本。在实验2中,为研究β-肾上腺素能受体拮抗剂对IL-6和TNF-α浓度的影响,将大鼠随机分为以下几组:1)对照组:SAH + 生理盐水;2)普萘洛尔组:SAH + 普萘洛尔;3)美托洛尔组:SAH + 美托洛尔;4)布托沙明组:SAH + 布托沙明(β₂-肾上腺素能受体拮抗剂)。SAH后6小时采集脑脊液和血液样本。测量样本中IL-6和TNF-α的浓度。
在实验1中,SAH组脑脊液中IL-6浓度显著升高,并在SAH后6小时达到峰值,而SAH组脑脊液中TNF-α浓度一直较低。在实验2中,普萘洛尔组和布托沙明组脑脊液中IL-6浓度显著低于对照组(每组P < 0.01和P < 0.05)。所有四组血浆IL-6、脑脊液TNF-α和血浆TNF-α浓度相当。
SAH急性期脑脊液中IL-6浓度升高,具有β₂-肾上腺素能受体阻断作用的β-肾上腺素能受体拮抗剂可抑制大鼠SAH后IL-6浓度的这种升高。