Literature DB >> 27073628

Establishment and identification of a hypoxia-ischemia brain damage model in neonatal rats.

Dan Yao1, Weiran Zhang1, Xue He1, Jinhu Wang2, Kewen Jiang3, Zhengyan Zhao1.   

Abstract

The present study was designed to set up a reliable model of severe hypoxia-ischemia brain damage (HIBD) in neonatal rats and several methods were used to identify whether the model was successful. A total of 40 healthy 7-day-old Sprague-Dawley rats were randomly divided into 2 groups: The sham-surgery group (n=18) and the HIBD model group (n=22). The HIBD model was produced according to the traditional Rice method. The rats were anesthetized with ethyl ether. The left common carotid artery (CCA) was exposed, ligated and cut. Following this, the rats were exposed to hypoxia in a normobaric chamber filled with 8% oxygen and 92% nitrogen for 2 h. In the sham-surgery group, the left CCA was exposed but was not ligated, cut or exposed to hypoxia. The neurobehavioral changes of the rats were observed in the 24 h after HIBD. The brains were collected after 72 h to observe the pathological morphological changes of the brain tissue. The behavioral ability and neurobehavioral changes were studied in each group. The water maze test was used for evaluating the learning-memory ability when the rats were 28 days old. Compared with the sham-surgery group, all the HIBD model rats had a lag of motor development. The rats had evident changes in anatomy and Nissl staining, and cognitive impairment was shown through the result of the water maze. Therefore, the model of HIBD in neonatal rats is feasible and provides a reliable model for subsequent studies.

Entities:  

Keywords:  Morris water maze; hypoxia-ischemic brain damage; model; neonatal rat

Year:  2016        PMID: 27073628      PMCID: PMC4812536          DOI: 10.3892/br.2016.610

Source DB:  PubMed          Journal:  Biomed Rep        ISSN: 2049-9434


  19 in total

1.  Fetal cerebral and peripheral circulatory responses to hypoxia after nitric oxide synthase inhibition.

Authors:  A P Harris; S Helou; C A Gleason; R J Traystman; R C Koehler
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2.  Xenon provides short-term neuroprotection in neonatal rats when administered after hypoxia-ischemia.

Authors:  John Dingley; James Tooley; Helen Porter; Marianne Thoresen
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Journal:  Pediatr Res       Date:  2005-02-17       Impact factor: 3.756

4.  Cerebral oxygenation during postasphyxial seizures in near-term fetal sheep.

Authors:  Hernan Gonzalez; Christian J Hunter; Laura Bennet; Gordon G Power; Alistair J Gunn
Journal:  J Cereb Blood Flow Metab       Date:  2005-07       Impact factor: 6.200

5.  Neonatal encephalopathy or hypoxic-ischemic encephalopathy? Appropriate terminology matters.

Authors:  Olaf Dammann; Donna Ferriero; Pierre Gressens
Journal:  Pediatr Res       Date:  2011-07       Impact factor: 3.756

Review 6.  Current management of the infant who presents with neonatal encephalopathy.

Authors:  Elena V Wachtel; Karen D Hendricks-Muñoz
Journal:  Curr Probl Pediatr Adolesc Health Care       Date:  2011 May-Jun

7.  Translating developmental time across mammalian species.

Authors:  B Clancy; R B Darlington; B L Finlay
Journal:  Neuroscience       Date:  2001       Impact factor: 3.590

8.  Vitamins E and C pretreatment prevents ovariectomy-induced memory deficits in water maze.

Authors:  Siomara C Monteiro; Cristiane Matté; Caren S Bavaresco; Carlos Alexandre Netto; Angela T S Wyse
Journal:  Neurobiol Learn Mem       Date:  2005-10-05       Impact factor: 2.877

9.  The neuropathology of hyperthermic seizures in the rat.

Authors:  W Jiang; T M Duong; N C de Lanerolle
Journal:  Epilepsia       Date:  1999-01       Impact factor: 5.864

10.  Developments of a water-maze procedure for studying spatial learning in the rat.

Authors:  R Morris
Journal:  J Neurosci Methods       Date:  1984-05       Impact factor: 2.390

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  3 in total

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2.  Quercetin alleviates neonatal hypoxic-ischemic brain injury by inhibiting microglia-derived oxidative stress and TLR4-mediated inflammation.

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3.  Human pluripotent stem cell-derived ectomesenchymal stromal cells promote more robust functional recovery than umbilical cord-derived mesenchymal stromal cells after hypoxic-ischaemic brain damage.

Authors:  Jiawei Huang; Kin Pong U; Fuyuan Yang; Zeyuan Ji; Jiacheng Lin; Zhihui Weng; Lai Ling Tsang; Tobias D Merson; Ye Chun Ruan; Chao Wan; Gang Li; Xiaohua Jiang
Journal:  Theranostics       Date:  2022-01-01       Impact factor: 11.600

  3 in total

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