2022
DOI: 10.1007/s11011-022-01130-1
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H2S-mediated inhibition of RhoA/ROCK pathway and noncoding RNAs in ischemic stroke

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Cited by 4 publications
(2 citation statements)
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“…RhoA has been identified as a negative regulator of neurite outgrowth during development, and its major downstream effector, Rock2, is associated with the induction of RhoA-driven neurite retraction [ 49 ]. RhoA/Rock2 upregulation contributes to neuroinflammation, blood-brain barrier dysfunction, axon growth inhibition and neuronal apoptosis following ischemic stroke [ 50 ]. Inhibition of RhoA/Rock2 signalling may effectively induce axonal regeneration following injury [ 51 ].…”
Section: Discussionmentioning
confidence: 99%
“…RhoA has been identified as a negative regulator of neurite outgrowth during development, and its major downstream effector, Rock2, is associated with the induction of RhoA-driven neurite retraction [ 49 ]. RhoA/Rock2 upregulation contributes to neuroinflammation, blood-brain barrier dysfunction, axon growth inhibition and neuronal apoptosis following ischemic stroke [ 50 ]. Inhibition of RhoA/Rock2 signalling may effectively induce axonal regeneration following injury [ 51 ].…”
Section: Discussionmentioning
confidence: 99%
“…NcRNAs can regulate several cellular processes, such as chromatin re-modeling, post-transcriptional modifications, and the regulation of signal transduction pathways, through targeting several target mRNAs simultaneously [ 17 , 19 , 29 , 30 ]. Recently, we and others have highlighted the potential roles of ncRNAs in regulating H 2 S biosynthesis in several physiological and pathological contexts [ 31 , 32 , 33 , 34 , 35 , 36 , 37 , 38 ]. H 2 S and ncRNAs interact during the development and progression of several human diseases; therefore, their targeting can be of great therapeutic benefit [ 17 ].…”
Section: Introductionmentioning
confidence: 99%