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大鼠适度运动相关的超耐力诱导小脑氧化应激并损害反应性GFAP异构体谱。

Ultra-Endurance Associated With Moderate Exercise in Rats Induces Cerebellar Oxidative Stress and Impairs Reactive GFAP Isoform Profile.

作者信息

de Souza Raphael Fabricio, Augusto Ricielle Lopes, de Moraes Silvia Regina Arruda, de Souza Fabio Borges, Gonçalves Lílian Vanessa da Penha, Pereira Danielle Dutra, Moreno Gisele Machado Magalhães, de Souza Fernanda Maria Araujo, Andrade-da-Costa Belmira Lara da Silveira

机构信息

Laboratory of Neurophysiology, Department of Physiology and Pharmacology, Center of Biosciences, Federal University of Pernambuco, Recife, Brazil.

Postgraduate Program in Neuropsychiatry and Behavioral Sciences, Federal University of Pernambuco, Recife, Brazil.

出版信息

Front Mol Neurosci. 2020 Sep 2;13:157. doi: 10.3389/fnmol.2020.00157. eCollection 2020.

Abstract

Ultra-endurance (UE) race has been associated with brain metabolic changes, but it is still unknown which regions are vulnerable. This study investigated whether high-volume training in rodents, even under moderate intensity, can induce cerebellar oxidative and inflammatory status. Forty-five adult rats were divided into six groups according to a training period, followed or not by an exhaustion test (ET) that simulated UE: control (C), control + ET (C-ET), moderate-volume (MV) training and MV-ET, high-volume training (HV) and HV-ET. The training period was 30 (MV) and 90 (HV) min/day, 5 times/week for 3 months as a continuous running on a treadmill at a maximum velocity of 12 m/min. After 24 h, the ET was performed at 50% maximum velocities up to the animals refused to run, and then serum lactate levels were evaluated. Serum and cerebellar homogenates were obtained 24 h after ET. Serum creatine kinase (CK), lactate dehydrogenase (LDH), and corticosterone levels were assessed. Lipid peroxidation (LP), nitric oxide (NO), Interleukin 1β (IL-1β), and GFAP proteins, reduced and oxidized glutathione (GSH and GSSG) levels, superoxide dismutase (SOD) and catalase (CAT) activities were quantified in the cerebellum. Serum lactate concentrations were lower in MV-ET (∼20%) and HV-ET (∼40%) compared to the C-ET group. CK and corticosterone levels were increased more than ∼ twofold by HV training compared to control. ET increased CK levels in MV-ET vs. MV group ( = 0.026). HV induced higher LP levels (∼40%), but an additive effect of ET was only seen in the MV-ET group ( = 0.02). SOD activity was higher in all trained groups vs. C and C-ET ( < 0.05). CAT activity, however, was intensified only in the MV group ( < 0.02). The 50 kDa GFAP levels were enhanced in C-ET and MV-ET vs. respective controls, while 42 kDa (∼40%) and 39 kDa (∼26%) isoform levels were reduced. In the HV-ET group, the 50 KDa isoform amount was reduced ∼40-60% compared to the other groups and the 39 KDa isoform, increased sevenfold. LDH levels, GSH/GSSG ratio, and NO production were not modified. ET elevated IL-1β levels in the CT and MV groups. Data shows that cerebellar resilience to oxidative damage may be maintained under moderate-volume training, but it is reduced by UE running. High-volume training provoked systemic metabolic changes, cerebellar lipid peroxidation, and unbalanced enzymatic antioxidant resource. UE after high-volume training modified the GFAP isoform profile suggesting impaired astrocyte reactivity in the cerebellum.

摘要

超长耐力(UE)比赛与大脑代谢变化有关,但仍不清楚哪些区域易受影响。本研究调查了在啮齿动物中进行大量训练,即使是在中等强度下,是否会诱发小脑的氧化和炎症状态。45只成年大鼠根据训练期分为六组,之后进行或不进行模拟UE的力竭试验(ET):对照组(C)、对照组+ET(C-ET)、中等量(MV)训练组和MV-ET组、大量训练组(HV)和HV-ET组。训练期为每天30(MV)和90(HV)分钟,每周5次,持续3个月,在跑步机上以最大速度12米/分钟持续跑步。24小时后,以最大速度的50%进行ET,直至动物拒绝奔跑,然后评估血清乳酸水平。ET后24小时获取血清和小脑匀浆。评估血清肌酸激酶(CK)、乳酸脱氢酶(LDH)和皮质酮水平。在小脑中定量脂质过氧化(LP)、一氧化氮(NO)、白细胞介素1β(IL-1β)和GFAP蛋白、还原型和氧化型谷胱甘肽(GSH和GSSG)水平、超氧化物歧化酶(SOD)和过氧化氢酶(CAT)活性。与C-ET组相比,MV-ET组(约20%)和HV-ET组(约40%)的血清乳酸浓度较低。与对照组相比,HV训练使CK和皮质酮水平升高超过两倍。与MV组相比,ET使MV-ET组的CK水平升高(P = 0.026)。HV诱导更高的LP水平(约40%),但ET的叠加效应仅在MV-ET组中可见(P = 0.02)。与C组和C-ET组相比,所有训练组的SOD活性更高(P < 0.05)。然而,CAT活性仅在MV组中增强(P < 0.02)。与各自的对照组相比,C-ET组和MV-ET组中50 kDa的GFAP水平升高,而42 kDa(约40%)和39 kDa(约26%)同工型水平降低。在HV-ET组中,与其他组相比,50 KDa同工型的量减少约40 - 60%,39 KDa同工型增加了七倍。LDH水平、GSH/GSSG比值和NO产生未改变。ET使CT组和MV组的IL-1β水平升高。数据表明,在中等量训练下小脑对氧化损伤的恢复力可能得以维持,但UE跑步会使其降低。大量训练引发了全身代谢变化、小脑脂质过氧化以及酶促抗氧化资源失衡。大量训练后的UE改变了GFAP同工型谱,提示小脑星形胶质细胞反应性受损。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/534d/7492828/868bb34744ed/fnmol-13-00157-g001.jpg

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