Evidence map›Paper›PMID 39455496›Full record

ArticleBulletin of experimental biology and medicine2024

Protective Effect of Protocatechuic Aldehyde on Cerebral Ischemia/Reperfusion Injury in Rats through Blood-Brain Barrier Protection.

F He, J Feng, H Sun, Y Xu, H Yan, X Song, Y Wang, X Li, Q Lin

Abstract read
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In one paragraph

Article in Bulletin of experimental biology and medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
  2. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

F HeDepartment of Pharmacology, Faculty of Chinese Materia Medic, Yunnan University of Chinese Medicine, Kunming, China.
J FengDepartment of Pharmacology, Faculty of Chinese Materia Medic, Yunnan University of Chinese Medicine, Kunming, China.
H SunDepartment of Pharmacology, Faculty of Chinese Materia Medic, Yunnan University of Chinese Medicine, Kunming, China.
Y XuDepartment of Pharmacology, Faculty of Chinese Materia Medic, Yunnan University of Chinese Medicine, Kunming, China.
H YanDepartment of Pharmacology, Faculty of Chinese Materia Medic, Yunnan University of Chinese Medicine, Kunming, China.
X SongDepartment of Pharmacology, Faculty of Chinese Materia Medic, Yunnan University of Chinese Medicine, Kunming, China.
Y WangDepartment of Pharmacology, Faculty of Chinese Materia Medic, Yunnan University of Chinese Medicine, Kunming, China.
X LiDepartment of Pharmacology, Faculty of Chinese Materia Medic, Yunnan University of Chinese Medicine, Kunming, China.
Q LinDepartment of Pharmacology, Faculty of Chinese Materia Medic, Yunnan University of Chinese Medicine, Kunming, China. 1609627617@qq.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cerebral ischemia can lead to destruction of the blood-brain barrier (BBB), the main cause of cerebral edema and cerebral infarction. BBB damage is also one of the key factors affecting the result of drug therapy. We studied the protective effect of 5-day pretreatment with protocatechuic aldehyde (PAL) at doses of 10 and 20 mg/kg on BBB function and structure after middle cerebral artery occlusion/reperfusion (MCAO/R) in rats. The infarct volume, behavioral neurological deficit score, and Evans blue content in the brain were estimated. We also evaluated the content of nitric oxide (NO) and activities of inducible and neuronal NO synthases. Expression of aquaporin-4 (AQP-4), occludin, claudin-5, and MMP-3 in the brain tissues was estimated by Western blotting. The BBB ultrastructure was analyzed under an electron microscope. We revealed that PAL at both used doses significantly reduced the neurological deficit score, brain infarct volume, and Evans blue extravasation. Electron microscopy showed that PAL significantly improved the ultrastructure of BBB and alleviated its injury. Pretreatment with PAL increased expression of occludin and claudin-5 and reduced expression of AQP-4 and MMP-3. At the same time, the release of NO and activities of NO synthases were notably inhibited. Our results suggest that PAL can be a promising compound to attenuate cerebral ischemia resulting from occlusion/reperfusion injury via BBB protection.

Indexed as

Aquaporin 4BenzaldehydesBlood-Brain BarrierCatecholsClaudin-5Infarction, Middle Cerebral ArteryNitric OxideOccludinReperfusion InjuryAnimalsBrainBrain IschemiaMaleMatrix Metalloproteinase 3Neuroprotective AgentsNitric Oxide Synthase Type IAqp4 protein, ratAquaporin 4BenzaldehydesCatecholsClaudin-5Cldn5 protein, ratMatrix Metalloproteinase 3Neuroprotective AgentsNitric OxideNitric Oxide Synthase Type INitric Oxide Synthase Type IIOccludinOcln protein, ratprotocatechualdehydeaquaporin-4blood–brain barriermatrix metalloproteinase-3protocatechuic aldehydetight junction

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.