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创伤性脑损伤后给予褪黑素是否会影响细胞因子水平?

Does the administration of melatonin during post-traumatic brain injury affect cytokine levels?

机构信息

Afzalipour Faculty of Medical, Physiology Research Center, Institute of Neuropharmacology, Kerman University of Medical Sciences, Kerman, Iran.

Neuroscience Research Center, Institute of Neuropharmacology, Kerman University of Medical Sciences, Kerman, Iran.

出版信息

Inflammopharmacology. 2018 Aug;26(4):1017-1023. doi: 10.1007/s10787-017-0417-1. Epub 2017 Nov 20.

Abstract

Increased levels of inflammatory cytokines after traumatic brain injury (TBI) can lead to brain edema and neuronal death. In this study, the effect of melatonin on pro-inflammatory (IL-1ß, IL-6, and TNF-α) and anti-inflammatory (IL-10) cytokines following TBI was investigated considering anti-inflammatory effect of melatonin. Male Wistar rats were divided into five groups: Sham, TBI, TBI + VEH (vehicle), TBI + 5 mg dose of melatonin (MEL5), TBI + 20 mg dose of melatonin (MEL20). Diffuse TBI was induced by Marmarou method. Melatonin was administered 1, 24, 48 and 72 h after TBI through i.p. Brain water content and brain levels of pro-inflammatory (IL-1ß, IL-6 and TNF-α) and anti-inflammatory (IL-10) cytokines were measured 72 h after TBI. The IL-1ß levels decreased in the TBI + MEL5 and TBI + MEL20 groups in comparison to TBI + VEH group (p < 0.001). The levels of IL-6 and TNF-α also decreased in melatonin-treated groups compared to control group (p < 0.001). The amount of IL-10 decreased after TBI. But melatonin administration increased the IL-10 levels in comparison with TBI + VEH group (p < 0.001). The results showed that melatonin administration affected the brain levels of pro-inflammatory and anti-inflammatory cytokines involving in brain edema led to neuronal protection after TBI.

摘要

创伤性脑损伤 (TBI) 后炎症细胞因子水平升高可导致脑水肿和神经元死亡。在这项研究中,考虑到褪黑素的抗炎作用,研究了褪黑素对 TBI 后促炎 (IL-1ß、IL-6 和 TNF-α) 和抗炎 (IL-10) 细胞因子的影响。雄性 Wistar 大鼠分为五组:假手术组、TBI 组、TBI+VEH(载体)组、TBI+5mg 褪黑素 (MEL5) 组、TBI+20mg 褪黑素 (MEL20) 组。采用 Marmarou 法诱导弥漫性 TBI。TBI 后 1、24、48 和 72 小时通过腹腔内给予褪黑素。TBI 后 72 小时测量脑水含量和脑内促炎 (IL-1ß、IL-6 和 TNF-α) 和抗炎 (IL-10) 细胞因子水平。与 TBI+VEH 组相比,TBI+MEL5 和 TBI+MEL20 组的 IL-1ß 水平降低(p<0.001)。与对照组相比,褪黑素治疗组的 IL-6 和 TNF-α 水平也降低(p<0.001)。IL-10 水平在 TBI 后降低。但褪黑素给药与 TBI+VEH 组相比增加了 IL-10 水平(p<0.001)。结果表明,褪黑素给药影响脑水肿中涉及的促炎和抗炎细胞因子的脑水平,导致 TBI 后神经元保护。

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