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Author Spotlight: Establishing a Reliable Distal MCA Occlusion Model in Mice for Stroke Research
Published on: December 15, 2023
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Natural compounds modulate the autophagy with potential implication of stroke
Anil Ahsan1, Mengru Liu1, Yanrong Zheng1
1Institute of Pharmacology & Toxicology, College of Pharmaceutical Sciences, Key Laboratory of Medical Neurobiology of the Ministry of Health of China, Zhejiang University, Hangzhou 310058, China.
Acta Pharmaceutica Sinica. B
|August 13, 2021
Summary
Naturally derived compounds show promise in treating stroke by modulating autophagy, a cellular process crucial for neuronal survival. This review explores these compounds
Area of Science:
- Neuroscience and Pharmacology
- Cellular Biology and Molecular Mechanisms
Background:
- Stroke is a major cause of death and disability, with limited effective treatments due to complex pathology.
- Autophagy, a cellular degradation process, plays a dual role in stroke, offering neuroprotection but sometimes exacerbating injury.
Purpose of the Study:
- To review recent advances in naturally derived compounds that regulate autophagy.
- To discuss the potential of these compounds in stroke treatment and neuroprotection.
Main Methods:
- Literature review of scientific articles on natural compounds, autophagy, and stroke.
- Analysis of mechanisms by which natural compounds modulate autophagy.
- Discussion of neuroprotective effects and therapeutic potential.
Main Results:
- Numerous natural compounds have been identified that can modulate autophagy.
- These compounds demonstrate potential in protecting neuronal cells against ischemic injury.
- Evidence suggests a therapeutic role for these compounds in stroke management.
Conclusions:
- Naturally derived compounds offer a promising avenue for stroke therapy by targeting autophagy.
- Further research is warranted to fully elucidate their mechanisms and clinical applications.
Keywords:
AD, Alzheimer's diseaseALS, amyotrophic lateral sclerosisAMPK, 5′-adenosine monophosphate-activated protein kinaseATF6, activating transcription factor 6ATG, autophagy related genesAutophagyBCL-2, B-cell lymphoma 2BNIP3L, BCL2/adenovirusCOPII, coat protein complex IICerebral ischemiaER, endoplasmic reticulumFOXO, forkhead box OFUNDC1, FUN14 domain containing 1GPCR, G-protein coupled receptorHD, Huntington's diseaseIPC, ischemic preconditioningIRE1, inositol-requiring enzyme 1JNK, c-Jun N-terminal kinaseLAMP, lysosomal-associated membrane proteinLC3, light chain 3LKB1, liver kinase B1Lysosomal activationMitochondriaMitophagyNatural compoundsNeurological disordersNeuroprotectionOGD/R, oxygen and glucose deprivation-reperfusionPD, Parkinson's diseasePERK, protein kinase R (PKR)-like endoplasmic reticulum kinasePI3K, phosphatidylinositol 3-kinaseROS, reactive oxygen speciesSQSTM1, sequestosome 1TFEB, transcription factor EBTIGAR, TP53-induced glycolysis and apoptosis regulatorULK, Unc-51- like kinaseUro-A, urolithin AeIF2a, eukaryotic translation-initiation factor 2mTOR, mechanistic target of rapamycinΔΨm, mitochondrial membrane potentialMore Related Videos
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