Expression of Translocator Protein in Early Brain Injury After Subarachnoid Hemorrhage in Mice
Copyright© by Editorial Board of Journal of Sichuan University (Medical Science Edition)..
OBJECTIVE: To evaluate the expression of translocator protein (TSPO) in brain tissue within 72 h after subarachnoid hemorrhage (SAH) in mice.
METHODS: Forty-four C57BL/6J mice were randomly divided into two groups, 17 in the Sham group and 27 in the SAH group. SAH mice model was performed by endovascular perforation as previously described with slight modifications. Sham group mice were performed by the same method but without piercing the blood vessels. Before and 6 h, 24 h, 48 h, 72 h after modeling, the two groups were scored with modified Garcia score for neurological function. At 6 h, 24 h, 48 h, 72 h after modeling, the mice were sacrificed. Sham group mice were sacrificed at 24 h after modeling. The expression of TSPO in brain tissue was evaluated by Western blot, positron emission tomography-computed tomography (PET-CT) and immunofluorescence staining. Fluorescent double staining was used to assess the relationship of TSPO and microglia.
RESULTS: The neurological function scores of the SAH group mice decreased with time and then increased. The expression of TSPO in the brain tissue increased first and then decreased with time, and there was a negative correlation between them (r=-0.615 6, P < 0.01). PET-CT showed that the tracer intake of mouse brain tissue after SAH was higher than that of Sham group, and the difference was statistically significant (P < 0.05). Immunofluorescence staining showed that TSPO increased in the parietal cortex and basal cortex of the SAH group. And fluorescent double staining suggested that TSPO colocalized with Iba-1 which was a specific marker of microglia.
CONCLUSIONS: In the early brain injury after SAH, the expression of TSPO in brain is widely increased, and the expression level increases first and then decreases. TSPO could participate in the activation of microglia and regulate the occurrence and development of brain injury after SAH.
Medienart: |
Artikel |
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Erscheinungsjahr: |
2019 |
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Erschienen: |
2019 |
Enthalten in: |
Zur Gesamtaufnahme - volume:50 |
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Enthalten in: |
Sichuan da xue xue bao. Yi xue ban = Journal of Sichuan University. Medical science edition - 50(2019), 4 vom: 21. Juli, Seite 500-505 |
Sprache: |
Chinesisch |
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Beteiligte Personen: |
Zhou, Jian [VerfasserIn] |
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Themen: |
Bzrp protein, mouse |
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Anmerkungen: |
Date Completed 14.11.2019 Date Revised 08.01.2020 published: Print Citation Status MEDLINE |
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Förderinstitution / Projekttitel: |
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PPN (Katalog-ID): |
NLM302483284 |
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LEADER | 01000naa a22002652 4500 | ||
---|---|---|---|
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100 | 1 | |a Zhou, Jian |e verfasserin |4 aut | |
245 | 1 | 0 | |a Expression of Translocator Protein in Early Brain Injury After Subarachnoid Hemorrhage in Mice |
264 | 1 | |c 2019 | |
336 | |a Text |b txt |2 rdacontent | ||
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500 | |a Date Revised 08.01.2020 | ||
500 | |a published: Print | ||
500 | |a Citation Status MEDLINE | ||
520 | |a Copyright© by Editorial Board of Journal of Sichuan University (Medical Science Edition). | ||
520 | |a OBJECTIVE: To evaluate the expression of translocator protein (TSPO) in brain tissue within 72 h after subarachnoid hemorrhage (SAH) in mice | ||
520 | |a METHODS: Forty-four C57BL/6J mice were randomly divided into two groups, 17 in the Sham group and 27 in the SAH group. SAH mice model was performed by endovascular perforation as previously described with slight modifications. Sham group mice were performed by the same method but without piercing the blood vessels. Before and 6 h, 24 h, 48 h, 72 h after modeling, the two groups were scored with modified Garcia score for neurological function. At 6 h, 24 h, 48 h, 72 h after modeling, the mice were sacrificed. Sham group mice were sacrificed at 24 h after modeling. The expression of TSPO in brain tissue was evaluated by Western blot, positron emission tomography-computed tomography (PET-CT) and immunofluorescence staining. Fluorescent double staining was used to assess the relationship of TSPO and microglia | ||
520 | |a RESULTS: The neurological function scores of the SAH group mice decreased with time and then increased. The expression of TSPO in the brain tissue increased first and then decreased with time, and there was a negative correlation between them (r=-0.615 6, P < 0.01). PET-CT showed that the tracer intake of mouse brain tissue after SAH was higher than that of Sham group, and the difference was statistically significant (P < 0.05). Immunofluorescence staining showed that TSPO increased in the parietal cortex and basal cortex of the SAH group. And fluorescent double staining suggested that TSPO colocalized with Iba-1 which was a specific marker of microglia | ||
520 | |a CONCLUSIONS: In the early brain injury after SAH, the expression of TSPO in brain is widely increased, and the expression level increases first and then decreases. TSPO could participate in the activation of microglia and regulate the occurrence and development of brain injury after SAH | ||
650 | 4 | |a Journal Article | |
650 | 4 | |a Early brain injury | |
650 | 4 | |a Molecular imaging | |
650 | 4 | |a Subarachnoid hemorrhage | |
650 | 4 | |a Translocator protein | |
650 | 7 | |a Bzrp protein, mouse |2 NLM | |
650 | 7 | |a Receptors, GABA |2 NLM | |
700 | 1 | |a Gu, Long |e verfasserin |4 aut | |
700 | 1 | |a Peng, Jian-Hua |e verfasserin |4 aut | |
700 | 1 | |a Pang, Jin-Wei |e verfasserin |4 aut | |
700 | 1 | |a Xie, Yu-Ke |e verfasserin |4 aut | |
700 | 1 | |a Guo, Ke-Cheng |e verfasserin |4 aut | |
700 | 1 | |a Zhang, Li-Fang |e verfasserin |4 aut | |
700 | 1 | |a Zhang, Xian-Hui |e verfasserin |4 aut | |
700 | 1 | |a Chen, Li-Gang |e verfasserin |4 aut | |
700 | 1 | |a Jiang, Yong |e verfasserin |4 aut | |
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