Salvianolic Acids for Injection alleviates cerebral ischemia/reperfusion injury by switching M1/M2 phenotypes and inhibiting NLRP3 inflammasome/pyroptosis axis in microglia in vivo and in vitro

After cerebral ischemia/reperfusion injury, pro-inflammatory M1 and anti-inflammatory M2 phenotypes of microglia are involved in neuroinflammation, in which activation of NLRP3 inflammasome and subsequent pyroptosis play essential roles. Salvianolic Acids for Injection (SAFI) is Chinese medicine inj...

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Veröffentlicht in:Journal of ethnopharmacology 2021-04, Vol.270 (NA), p.113776-113776, Article 113776
Hauptverfasser: Ma, Dai-Chao, Zhang, Nan-Nan, Zhang, Yi-Na, Chen, Hui-Sheng
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Zhang, Nan-Nan
Zhang, Yi-Na
Chen, Hui-Sheng
description After cerebral ischemia/reperfusion injury, pro-inflammatory M1 and anti-inflammatory M2 phenotypes of microglia are involved in neuroinflammation, in which activation of NLRP3 inflammasome and subsequent pyroptosis play essential roles. Salvianolic Acids for Injection (SAFI) is Chinese medicine injection which composed of multiple phenolic acids extracted from Radix Salviae Miltiorrhizae, and has been reported to generate neuroprotective effects after cerebral ischemic insult in clinical and animal studies. The present study was designed to investigate whether SAFI exerts neuroprotective effects by switching microglial phenotype and inhibiting NLRP3 inflammasome/pyroptosis axis in microglia. The middle cerebral artery occlusion/reperfusion (MCAO/R) model in rats and oxygen-glucose deprivation/reoxygenation (OGD/R) model in co-cultured primary neurons and primary microglia were utilized. The neuroprotective effect of SAFI was evaluated through measuring neurological deficit scores, neuropathological changes, inflammatory factors, cell phenotype markers, and related proteins of NLRP3 inflammasome/pyroptosis axis. The results showed that SAFI treatment was able to: (1) produce a significant increase in neurological deficit scores and decrease in infarct volumes, and alleviate histological injury and neuronal apoptosis in cerebral cortex in MCAO/R model; (2) increase neuronal viability and reduce neuronal apoptosis in the OGD model; (3) reshape microglial polarization patterns from M1-like phenotype to M2-like phenotype; (4) inhibit the activation of the NLRP3 inflammasome and the expression of proteins related to NLRP3 inflammasome/pyroptosis axis in vivo and in vitro. These findings indicate that SAFI exert neuroprotective effect, probably via reducing neuronal apoptosis, switching microglial phenotype from M1 towards M2, and inhibiting NLRP3 inflammasome/pyroptosis axis in microglia. [Display omitted] •Salvianolic Acids for Injection (SAFI) treatment produce neuroprotective effect in the in vivo and in vitro models.•SAFI treatment reshape polarization patterns by prompting M2-like phenotype and inhibiting M1-like phenotype of microglia.•SAFI inhibit NLRP3 inflammasome activation and NLRP3 inflammasome/pyroptosis axis in microglia.
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Salvianolic Acids for Injection (SAFI) is Chinese medicine injection which composed of multiple phenolic acids extracted from Radix Salviae Miltiorrhizae, and has been reported to generate neuroprotective effects after cerebral ischemic insult in clinical and animal studies. The present study was designed to investigate whether SAFI exerts neuroprotective effects by switching microglial phenotype and inhibiting NLRP3 inflammasome/pyroptosis axis in microglia. The middle cerebral artery occlusion/reperfusion (MCAO/R) model in rats and oxygen-glucose deprivation/reoxygenation (OGD/R) model in co-cultured primary neurons and primary microglia were utilized. The neuroprotective effect of SAFI was evaluated through measuring neurological deficit scores, neuropathological changes, inflammatory factors, cell phenotype markers, and related proteins of NLRP3 inflammasome/pyroptosis axis. The results showed that SAFI treatment was able to: (1) produce a significant increase in neurological deficit scores and decrease in infarct volumes, and alleviate histological injury and neuronal apoptosis in cerebral cortex in MCAO/R model; (2) increase neuronal viability and reduce neuronal apoptosis in the OGD model; (3) reshape microglial polarization patterns from M1-like phenotype to M2-like phenotype; (4) inhibit the activation of the NLRP3 inflammasome and the expression of proteins related to NLRP3 inflammasome/pyroptosis axis in vivo and in vitro. These findings indicate that SAFI exert neuroprotective effect, probably via reducing neuronal apoptosis, switching microglial phenotype from M1 towards M2, and inhibiting NLRP3 inflammasome/pyroptosis axis in microglia. 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Salvianolic Acids for Injection (SAFI) is Chinese medicine injection which composed of multiple phenolic acids extracted from Radix Salviae Miltiorrhizae, and has been reported to generate neuroprotective effects after cerebral ischemic insult in clinical and animal studies. The present study was designed to investigate whether SAFI exerts neuroprotective effects by switching microglial phenotype and inhibiting NLRP3 inflammasome/pyroptosis axis in microglia. The middle cerebral artery occlusion/reperfusion (MCAO/R) model in rats and oxygen-glucose deprivation/reoxygenation (OGD/R) model in co-cultured primary neurons and primary microglia were utilized. The neuroprotective effect of SAFI was evaluated through measuring neurological deficit scores, neuropathological changes, inflammatory factors, cell phenotype markers, and related proteins of NLRP3 inflammasome/pyroptosis axis. The results showed that SAFI treatment was able to: (1) produce a significant increase in neurological deficit scores and decrease in infarct volumes, and alleviate histological injury and neuronal apoptosis in cerebral cortex in MCAO/R model; (2) increase neuronal viability and reduce neuronal apoptosis in the OGD model; (3) reshape microglial polarization patterns from M1-like phenotype to M2-like phenotype; (4) inhibit the activation of the NLRP3 inflammasome and the expression of proteins related to NLRP3 inflammasome/pyroptosis axis in vivo and in vitro. These findings indicate that SAFI exert neuroprotective effect, probably via reducing neuronal apoptosis, switching microglial phenotype from M1 towards M2, and inhibiting NLRP3 inflammasome/pyroptosis axis in microglia. [Display omitted] •Salvianolic Acids for Injection (SAFI) treatment produce neuroprotective effect in the in vivo and in vitro models.•SAFI treatment reshape polarization patterns by prompting M2-like phenotype and inhibiting M1-like phenotype of microglia.•SAFI inhibit NLRP3 inflammasome activation and NLRP3 inflammasome/pyroptosis axis in microglia.</description><subject>Alkenes - pharmacology</subject><subject>Amino Acid Transport System ASC - genetics</subject><subject>Amino Acid Transport System ASC - metabolism</subject><subject>Animals</subject><subject>Anti-Inflammatory Agents, Non-Steroidal - administration &amp; dosage</subject><subject>Apoptosis - drug effects</subject><subject>Brain Ischemia - drug therapy</subject><subject>Brain Ischemia - metabolism</subject><subject>Calcium-Binding Proteins - metabolism</subject><subject>Caspase 1 - genetics</subject><subject>Cell Survival - drug effects</subject><subject>Cells, Cultured</subject><subject>Cerebral ischemia/reperfusion injury</subject><subject>Disease Models, Animal</subject><subject>Inflammasomes - antagonists &amp; 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Zhang, Nan-Nan ; Zhang, Yi-Na ; Chen, Hui-Sheng</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c386t-92fd0ab897cd81bce9e111efcbb505ba2701cb460a4e23419e600c50dd947a0e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Alkenes - pharmacology</topic><topic>Amino Acid Transport System ASC - genetics</topic><topic>Amino Acid Transport System ASC - metabolism</topic><topic>Animals</topic><topic>Anti-Inflammatory Agents, Non-Steroidal - administration &amp; dosage</topic><topic>Apoptosis - drug effects</topic><topic>Brain Ischemia - drug therapy</topic><topic>Brain Ischemia - metabolism</topic><topic>Calcium-Binding Proteins - metabolism</topic><topic>Caspase 1 - genetics</topic><topic>Cell Survival - drug effects</topic><topic>Cells, Cultured</topic><topic>Cerebral ischemia/reperfusion injury</topic><topic>Disease Models, Animal</topic><topic>Inflammasomes - antagonists &amp; inhibitors</topic><topic>Injections, Intraperitoneal</topic><topic>Interleukin-1beta - genetics</topic><topic>Interleukin-1beta - metabolism</topic><topic>Intracellular Signaling Peptides and Proteins - antagonists &amp; inhibitors</topic><topic>Intracellular Signaling Peptides and Proteins - genetics</topic><topic>Male</topic><topic>Microfilament Proteins - metabolism</topic><topic>Microglia - drug effects</topic><topic>Microglial phenotype</topic><topic>Neuroprotective Agents - administration &amp; dosage</topic><topic>NLR Family, Pyrin Domain-Containing 3 Protein - antagonists &amp; inhibitors</topic><topic>NLR Family, Pyrin Domain-Containing 3 Protein - genetics</topic><topic>NLR Family, Pyrin Domain-Containing 3 Protein - metabolism</topic><topic>NLRP3 inflammasome</topic><topic>Phosphate-Binding Proteins - antagonists &amp; inhibitors</topic><topic>Phosphate-Binding Proteins - genetics</topic><topic>Polyphenols - pharmacology</topic><topic>Pyroptosis</topic><topic>Pyroptosis - drug effects</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Reperfusion Injury - drug therapy</topic><topic>Reperfusion Injury - metabolism</topic><topic>Salvianolic acids for injection</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ma, Dai-Chao</creatorcontrib><creatorcontrib>Zhang, Nan-Nan</creatorcontrib><creatorcontrib>Zhang, Yi-Na</creatorcontrib><creatorcontrib>Chen, Hui-Sheng</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of ethnopharmacology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ma, Dai-Chao</au><au>Zhang, Nan-Nan</au><au>Zhang, Yi-Na</au><au>Chen, Hui-Sheng</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Salvianolic Acids for Injection alleviates cerebral ischemia/reperfusion injury by switching M1/M2 phenotypes and inhibiting NLRP3 inflammasome/pyroptosis axis in microglia in vivo and in vitro</atitle><jtitle>Journal of ethnopharmacology</jtitle><addtitle>J Ethnopharmacol</addtitle><date>2021-04-24</date><risdate>2021</risdate><volume>270</volume><issue>NA</issue><spage>113776</spage><epage>113776</epage><pages>113776-113776</pages><artnum>113776</artnum><issn>0378-8741</issn><eissn>1872-7573</eissn><abstract>After cerebral ischemia/reperfusion injury, pro-inflammatory M1 and anti-inflammatory M2 phenotypes of microglia are involved in neuroinflammation, in which activation of NLRP3 inflammasome and subsequent pyroptosis play essential roles. Salvianolic Acids for Injection (SAFI) is Chinese medicine injection which composed of multiple phenolic acids extracted from Radix Salviae Miltiorrhizae, and has been reported to generate neuroprotective effects after cerebral ischemic insult in clinical and animal studies. The present study was designed to investigate whether SAFI exerts neuroprotective effects by switching microglial phenotype and inhibiting NLRP3 inflammasome/pyroptosis axis in microglia. The middle cerebral artery occlusion/reperfusion (MCAO/R) model in rats and oxygen-glucose deprivation/reoxygenation (OGD/R) model in co-cultured primary neurons and primary microglia were utilized. The neuroprotective effect of SAFI was evaluated through measuring neurological deficit scores, neuropathological changes, inflammatory factors, cell phenotype markers, and related proteins of NLRP3 inflammasome/pyroptosis axis. The results showed that SAFI treatment was able to: (1) produce a significant increase in neurological deficit scores and decrease in infarct volumes, and alleviate histological injury and neuronal apoptosis in cerebral cortex in MCAO/R model; (2) increase neuronal viability and reduce neuronal apoptosis in the OGD model; (3) reshape microglial polarization patterns from M1-like phenotype to M2-like phenotype; (4) inhibit the activation of the NLRP3 inflammasome and the expression of proteins related to NLRP3 inflammasome/pyroptosis axis in vivo and in vitro. These findings indicate that SAFI exert neuroprotective effect, probably via reducing neuronal apoptosis, switching microglial phenotype from M1 towards M2, and inhibiting NLRP3 inflammasome/pyroptosis axis in microglia. [Display omitted] •Salvianolic Acids for Injection (SAFI) treatment produce neuroprotective effect in the in vivo and in vitro models.•SAFI treatment reshape polarization patterns by prompting M2-like phenotype and inhibiting M1-like phenotype of microglia.•SAFI inhibit NLRP3 inflammasome activation and NLRP3 inflammasome/pyroptosis axis in microglia.</abstract><cop>Ireland</cop><pub>Elsevier B.V</pub><pmid>33421597</pmid><doi>10.1016/j.jep.2021.113776</doi><tpages>1</tpages><orcidid>https://orcid.org/0000-0002-7486-1992</orcidid><orcidid>https://orcid.org/0000-0002-9457-1992</orcidid></addata></record>
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subjects Alkenes - pharmacology
Amino Acid Transport System ASC - genetics
Amino Acid Transport System ASC - metabolism
Animals
Anti-Inflammatory Agents, Non-Steroidal - administration & dosage
Apoptosis - drug effects
Brain Ischemia - drug therapy
Brain Ischemia - metabolism
Calcium-Binding Proteins - metabolism
Caspase 1 - genetics
Cell Survival - drug effects
Cells, Cultured
Cerebral ischemia/reperfusion injury
Disease Models, Animal
Inflammasomes - antagonists & inhibitors
Injections, Intraperitoneal
Interleukin-1beta - genetics
Interleukin-1beta - metabolism
Intracellular Signaling Peptides and Proteins - antagonists & inhibitors
Intracellular Signaling Peptides and Proteins - genetics
Male
Microfilament Proteins - metabolism
Microglia - drug effects
Microglial phenotype
Neuroprotective Agents - administration & dosage
NLR Family, Pyrin Domain-Containing 3 Protein - antagonists & inhibitors
NLR Family, Pyrin Domain-Containing 3 Protein - genetics
NLR Family, Pyrin Domain-Containing 3 Protein - metabolism
NLRP3 inflammasome
Phosphate-Binding Proteins - antagonists & inhibitors
Phosphate-Binding Proteins - genetics
Polyphenols - pharmacology
Pyroptosis
Pyroptosis - drug effects
Rats
Rats, Sprague-Dawley
Reperfusion Injury - drug therapy
Reperfusion Injury - metabolism
Salvianolic acids for injection
title Salvianolic Acids for Injection alleviates cerebral ischemia/reperfusion injury by switching M1/M2 phenotypes and inhibiting NLRP3 inflammasome/pyroptosis axis in microglia in vivo and in vitro
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