Abstract | BACKGROUND: METHODS: Male Wistar rats were subjected to a middle cerebral artery occlusion (MCAO) for 0, 30, 60, and 120 min. GTPs (400 mg/kg/day) or vehicle was administered by intragastric gavage twice a day for 30 days prior to MCAO. At different time points, the expression of claudin-5, occludin, ZO-1, and PKCα signaling pathway in microvessel fragments of cerebral ischemic tissue were evaluated. RESULTS: GTPs reduced BBB permeability at 60 min and 120 min after ischemia as compared with the vehicle group. Transmission electron microscopy also revealed that GTPs could reverse the opening of tight junction (TJ) barrier at 60 min and 120 min after MACO. The decreased mRNA and protein expression levels of claudin-5, occludin, and ZO-1 in microvessel fragments of cerebral ischemic tissue were significantly prevented by treatment with GTPs at the same time points after ischemia in rats. Furthermore, GTPs could attenuate the increase in the expression levels of PKCα mRNA and protein caused by cerebral ischemia. CONCLUSIONS: These results demonstrate that GTPs may act as a potential neuroprotective agent against BBB damage at the early stage of focal cerebral ischemia through the regulation of TJ and PKCα signaling.
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Authors | Xiaobai Liu, Zhenhua Wang, Ping Wang, Bo Yu, Yunhui Liu, Yixue Xue |
Journal | BMC complementary and alternative medicine
(BMC Complement Altern Med)
Vol. 13
Pg. 187
(Jul 21 2013)
ISSN: 1472-6882 [Electronic] England |
PMID | 23870286
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Claudin-5
- Neuroprotective Agents
- Occludin
- Plant Extracts
- Polyphenols
- RNA, Messenger
- Protein Kinase C-alpha
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Topics |
- Animals
- Blood-Brain Barrier
(drug effects, metabolism, pathology)
- Brain Ischemia
(drug therapy, etiology, metabolism, pathology)
- Camellia sinensis
(chemistry)
- Claudin-5
(metabolism)
- Infarction, Middle Cerebral Artery
- Male
- Neuroprotective Agents
(pharmacology, therapeutic use)
- Occludin
(metabolism)
- Permeability
- Phytotherapy
- Plant Extracts
(pharmacology, therapeutic use)
- Polyphenols
(pharmacology, therapeutic use)
- Protein Kinase C-alpha
(genetics, metabolism)
- RNA, Messenger
(metabolism)
- Rats
- Rats, Wistar
- Signal Transduction
(drug effects)
- Stroke
(drug therapy, etiology, metabolism, pathology)
- Tight Junctions
(drug effects)
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