Phycocyanobilin reduces brain injury after endothelin‐1‐ induced focal cerebral ischaemia
Pharmacological therapies for interrupting biochemical events of the ischaemic cascade and protecting against stroke in humans are as yet unavailable. Up to now, the neuroprotective activity in cerebral ischaemia of phycocyanobilin (PCB), a tetrapyrrolic natural antioxidant, has not been fully exami...
Gespeichert in:
Veröffentlicht in: | Clinical and experimental pharmacology & physiology 2020-03, Vol.47 (3), p.383-392 |
---|---|
Hauptverfasser: | , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 392 |
---|---|
container_issue | 3 |
container_start_page | 383 |
container_title | Clinical and experimental pharmacology & physiology |
container_volume | 47 |
creator | Pavón‐Fuentes, Nancy Marín‐Prida, Javier Llópiz‐Arzuaga, Alexey Falcón‐Cama, Viviana Campos‐Mojena, Rosario Cervantes‐Llanos, Majel Piniella‐Matamoros, Beatriz Pentón‐Arias, Eduardo Pentón‐Rol, Giselle |
description | Pharmacological therapies for interrupting biochemical events of the ischaemic cascade and protecting against stroke in humans are as yet unavailable. Up to now, the neuroprotective activity in cerebral ischaemia of phycocyanobilin (PCB), a tetrapyrrolic natural antioxidant, has not been fully examined. Here, we evaluated if PCB protects PC12 neuronal cells against oxygen and glucose deprivation plus reperfusion, and its protective effects in a rat model of endothelin‐1‐induced focal brain ischaemia. PCB was purified from the cyanobacteria Spirulina platensis and characterized by spectrophotometric, liquid and gas chromatography and mass spectrometry techniques. In Wistar rats, PCB at 50, 100 and 200 μg/kg or phosphate‐buffered saline (vehicle) was administered intraperitoneally at equal subdoses in a therapeutic schedule (30 minutes, 1, 3 and 6 hours after the surgery). Brain expression of myelin basic protein (MBP) and the enzyme CNPase was determined by immunoelectron microscopy. PCB was obtained with high purity (>95%) and the absence of solvent contaminants and was able to ameliorate PC12 cell ischaemic injury. PCB treatment significantly decreased brain infarct volume, limited the exploratory behaviour impairment and preserved viable cortical neurons in ischaemic rats in a dose‐dependent manner, compared to the vehicle group. Furthermore, PCB at high doses restored the MBP and CNPase expression levels in ischaemic rats. An improved PCB purification method from its natural source is reported, obtaining PCB that is suitable for pharmacological trials showing neuroprotective effects against experimental ischaemic stroke. Therefore, PCB could be a therapeutic pharmacological alternative for ischaemic stroke patients. |
doi_str_mv | 10.1111/1440-1681.13214 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2315102691</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2315102691</sourcerecordid><originalsourceid>FETCH-LOGICAL-c3714-cbe312f135e0a9574436b12744205c73fadaec9b2ba45d3c5826d752c569df263</originalsourceid><addsrcrecordid>eNqFkM9LwzAUx4Mobk7P3qTgxUu3vKRp16OM-QMG7qBHCWnyyjq6diYr0pt_gn-jf4mpnTt4MRAeL_m8L48PIZdAx-DPBKKIhhBPYQycQXREhoeXYzKknIoQpgkdkDPn1pRSQWN-SgYcEs7SRAzJ63LV6lq3qqqzoiyqwKJpNLogs8p3RbVubBuofIc2wMrUuxV66uvjE_z13x1sgrzWqgw0WvRjZVA4vVK4KdQ5OclV6fBiX0fk5W7-PHsIF0_3j7PbRah5AlGoM-TAcuACqUpFEkU8zoD5yqjQCc-VUajTjGUqEoZrMWWxSQTTIk5NzmI-Ijd97tbWbw26ndz4HbAsVYV14yTjIICyOAWPXv9B13VjK7-dpwQFTiGlnpr0lLa1cxZzubXFRtlWApWdedl5lp1n-WPeT1ztc5tsg-bA_6r2gOiB96LE9r88OZsv--BvlwKOGA</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2350130190</pqid></control><display><type>article</type><title>Phycocyanobilin reduces brain injury after endothelin‐1‐ induced focal cerebral ischaemia</title><source>MEDLINE</source><source>Wiley Online Library Journals Frontfile Complete</source><creator>Pavón‐Fuentes, Nancy ; Marín‐Prida, Javier ; Llópiz‐Arzuaga, Alexey ; Falcón‐Cama, Viviana ; Campos‐Mojena, Rosario ; Cervantes‐Llanos, Majel ; Piniella‐Matamoros, Beatriz ; Pentón‐Arias, Eduardo ; Pentón‐Rol, Giselle</creator><creatorcontrib>Pavón‐Fuentes, Nancy ; Marín‐Prida, Javier ; Llópiz‐Arzuaga, Alexey ; Falcón‐Cama, Viviana ; Campos‐Mojena, Rosario ; Cervantes‐Llanos, Majel ; Piniella‐Matamoros, Beatriz ; Pentón‐Arias, Eduardo ; Pentón‐Rol, Giselle</creatorcontrib><description>Pharmacological therapies for interrupting biochemical events of the ischaemic cascade and protecting against stroke in humans are as yet unavailable. Up to now, the neuroprotective activity in cerebral ischaemia of phycocyanobilin (PCB), a tetrapyrrolic natural antioxidant, has not been fully examined. Here, we evaluated if PCB protects PC12 neuronal cells against oxygen and glucose deprivation plus reperfusion, and its protective effects in a rat model of endothelin‐1‐induced focal brain ischaemia. PCB was purified from the cyanobacteria Spirulina platensis and characterized by spectrophotometric, liquid and gas chromatography and mass spectrometry techniques. In Wistar rats, PCB at 50, 100 and 200 μg/kg or phosphate‐buffered saline (vehicle) was administered intraperitoneally at equal subdoses in a therapeutic schedule (30 minutes, 1, 3 and 6 hours after the surgery). Brain expression of myelin basic protein (MBP) and the enzyme CNPase was determined by immunoelectron microscopy. PCB was obtained with high purity (>95%) and the absence of solvent contaminants and was able to ameliorate PC12 cell ischaemic injury. PCB treatment significantly decreased brain infarct volume, limited the exploratory behaviour impairment and preserved viable cortical neurons in ischaemic rats in a dose‐dependent manner, compared to the vehicle group. Furthermore, PCB at high doses restored the MBP and CNPase expression levels in ischaemic rats. An improved PCB purification method from its natural source is reported, obtaining PCB that is suitable for pharmacological trials showing neuroprotective effects against experimental ischaemic stroke. Therefore, PCB could be a therapeutic pharmacological alternative for ischaemic stroke patients.</description><identifier>ISSN: 0305-1870</identifier><identifier>EISSN: 1440-1681</identifier><identifier>DOI: 10.1111/1440-1681.13214</identifier><identifier>PMID: 31732975</identifier><language>eng</language><publisher>Australia: Wiley Subscription Services, Inc</publisher><subject>Animal models ; Animals ; Antioxidants ; Brain ; Brain Injuries - chemically induced ; Brain Injuries - drug therapy ; Brain Injuries - pathology ; Brain injury ; Brain Ischemia - chemically induced ; Brain Ischemia - drug therapy ; Brain Ischemia - pathology ; Clinical trials ; Contaminants ; Cyanobacteria ; Deprivation ; Endothelin-1 - toxicity ; Endothelins ; Exploratory behavior ; Gas chromatography ; Head injuries ; Immunoelectron microscopy ; Injury prevention ; ischaemic stroke ; Ischemia ; Male ; Mass spectrometry ; Mass spectroscopy ; Myelin ; Myelin basic protein ; Neuroprotection ; PC12 ; PC12 Cells ; PCB compounds ; Pharmacology ; Pheochromocytoma cells ; Phycobilins - therapeutic use ; Phycocyanin - therapeutic use ; Phycocyanobilin ; Rats ; Rats, Wistar ; Reperfusion ; Rodents ; Schedules ; Spectrophotometry ; Stroke ; Surgery</subject><ispartof>Clinical and experimental pharmacology & physiology, 2020-03, Vol.47 (3), p.383-392</ispartof><rights>2019 John Wiley & Sons Australia, Ltd</rights><rights>2019 John Wiley & Sons Australia, Ltd.</rights><rights>Copyright © 2020 John Wiley & Sons Australia, Ltd</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3714-cbe312f135e0a9574436b12744205c73fadaec9b2ba45d3c5826d752c569df263</citedby><cites>FETCH-LOGICAL-c3714-cbe312f135e0a9574436b12744205c73fadaec9b2ba45d3c5826d752c569df263</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2F1440-1681.13214$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2F1440-1681.13214$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31732975$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Pavón‐Fuentes, Nancy</creatorcontrib><creatorcontrib>Marín‐Prida, Javier</creatorcontrib><creatorcontrib>Llópiz‐Arzuaga, Alexey</creatorcontrib><creatorcontrib>Falcón‐Cama, Viviana</creatorcontrib><creatorcontrib>Campos‐Mojena, Rosario</creatorcontrib><creatorcontrib>Cervantes‐Llanos, Majel</creatorcontrib><creatorcontrib>Piniella‐Matamoros, Beatriz</creatorcontrib><creatorcontrib>Pentón‐Arias, Eduardo</creatorcontrib><creatorcontrib>Pentón‐Rol, Giselle</creatorcontrib><title>Phycocyanobilin reduces brain injury after endothelin‐1‐ induced focal cerebral ischaemia</title><title>Clinical and experimental pharmacology & physiology</title><addtitle>Clin Exp Pharmacol Physiol</addtitle><description>Pharmacological therapies for interrupting biochemical events of the ischaemic cascade and protecting against stroke in humans are as yet unavailable. Up to now, the neuroprotective activity in cerebral ischaemia of phycocyanobilin (PCB), a tetrapyrrolic natural antioxidant, has not been fully examined. Here, we evaluated if PCB protects PC12 neuronal cells against oxygen and glucose deprivation plus reperfusion, and its protective effects in a rat model of endothelin‐1‐induced focal brain ischaemia. PCB was purified from the cyanobacteria Spirulina platensis and characterized by spectrophotometric, liquid and gas chromatography and mass spectrometry techniques. In Wistar rats, PCB at 50, 100 and 200 μg/kg or phosphate‐buffered saline (vehicle) was administered intraperitoneally at equal subdoses in a therapeutic schedule (30 minutes, 1, 3 and 6 hours after the surgery). Brain expression of myelin basic protein (MBP) and the enzyme CNPase was determined by immunoelectron microscopy. PCB was obtained with high purity (>95%) and the absence of solvent contaminants and was able to ameliorate PC12 cell ischaemic injury. PCB treatment significantly decreased brain infarct volume, limited the exploratory behaviour impairment and preserved viable cortical neurons in ischaemic rats in a dose‐dependent manner, compared to the vehicle group. Furthermore, PCB at high doses restored the MBP and CNPase expression levels in ischaemic rats. An improved PCB purification method from its natural source is reported, obtaining PCB that is suitable for pharmacological trials showing neuroprotective effects against experimental ischaemic stroke. Therefore, PCB could be a therapeutic pharmacological alternative for ischaemic stroke patients.</description><subject>Animal models</subject><subject>Animals</subject><subject>Antioxidants</subject><subject>Brain</subject><subject>Brain Injuries - chemically induced</subject><subject>Brain Injuries - drug therapy</subject><subject>Brain Injuries - pathology</subject><subject>Brain injury</subject><subject>Brain Ischemia - chemically induced</subject><subject>Brain Ischemia - drug therapy</subject><subject>Brain Ischemia - pathology</subject><subject>Clinical trials</subject><subject>Contaminants</subject><subject>Cyanobacteria</subject><subject>Deprivation</subject><subject>Endothelin-1 - toxicity</subject><subject>Endothelins</subject><subject>Exploratory behavior</subject><subject>Gas chromatography</subject><subject>Head injuries</subject><subject>Immunoelectron microscopy</subject><subject>Injury prevention</subject><subject>ischaemic stroke</subject><subject>Ischemia</subject><subject>Male</subject><subject>Mass spectrometry</subject><subject>Mass spectroscopy</subject><subject>Myelin</subject><subject>Myelin basic protein</subject><subject>Neuroprotection</subject><subject>PC12</subject><subject>PC12 Cells</subject><subject>PCB compounds</subject><subject>Pharmacology</subject><subject>Pheochromocytoma cells</subject><subject>Phycobilins - therapeutic use</subject><subject>Phycocyanin - therapeutic use</subject><subject>Phycocyanobilin</subject><subject>Rats</subject><subject>Rats, Wistar</subject><subject>Reperfusion</subject><subject>Rodents</subject><subject>Schedules</subject><subject>Spectrophotometry</subject><subject>Stroke</subject><subject>Surgery</subject><issn>0305-1870</issn><issn>1440-1681</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkM9LwzAUx4Mobk7P3qTgxUu3vKRp16OM-QMG7qBHCWnyyjq6diYr0pt_gn-jf4mpnTt4MRAeL_m8L48PIZdAx-DPBKKIhhBPYQycQXREhoeXYzKknIoQpgkdkDPn1pRSQWN-SgYcEs7SRAzJ63LV6lq3qqqzoiyqwKJpNLogs8p3RbVubBuofIc2wMrUuxV66uvjE_z13x1sgrzWqgw0WvRjZVA4vVK4KdQ5OclV6fBiX0fk5W7-PHsIF0_3j7PbRah5AlGoM-TAcuACqUpFEkU8zoD5yqjQCc-VUajTjGUqEoZrMWWxSQTTIk5NzmI-Ijd97tbWbw26ndz4HbAsVYV14yTjIICyOAWPXv9B13VjK7-dpwQFTiGlnpr0lLa1cxZzubXFRtlWApWdedl5lp1n-WPeT1ztc5tsg-bA_6r2gOiB96LE9r88OZsv--BvlwKOGA</recordid><startdate>202003</startdate><enddate>202003</enddate><creator>Pavón‐Fuentes, Nancy</creator><creator>Marín‐Prida, Javier</creator><creator>Llópiz‐Arzuaga, Alexey</creator><creator>Falcón‐Cama, Viviana</creator><creator>Campos‐Mojena, Rosario</creator><creator>Cervantes‐Llanos, Majel</creator><creator>Piniella‐Matamoros, Beatriz</creator><creator>Pentón‐Arias, Eduardo</creator><creator>Pentón‐Rol, Giselle</creator><general>Wiley Subscription Services, Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QP</scope><scope>7TK</scope><scope>7U7</scope><scope>C1K</scope><scope>7X8</scope></search><sort><creationdate>202003</creationdate><title>Phycocyanobilin reduces brain injury after endothelin‐1‐ induced focal cerebral ischaemia</title><author>Pavón‐Fuentes, Nancy ; Marín‐Prida, Javier ; Llópiz‐Arzuaga, Alexey ; Falcón‐Cama, Viviana ; Campos‐Mojena, Rosario ; Cervantes‐Llanos, Majel ; Piniella‐Matamoros, Beatriz ; Pentón‐Arias, Eduardo ; Pentón‐Rol, Giselle</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3714-cbe312f135e0a9574436b12744205c73fadaec9b2ba45d3c5826d752c569df263</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Animal models</topic><topic>Animals</topic><topic>Antioxidants</topic><topic>Brain</topic><topic>Brain Injuries - chemically induced</topic><topic>Brain Injuries - drug therapy</topic><topic>Brain Injuries - pathology</topic><topic>Brain injury</topic><topic>Brain Ischemia - chemically induced</topic><topic>Brain Ischemia - drug therapy</topic><topic>Brain Ischemia - pathology</topic><topic>Clinical trials</topic><topic>Contaminants</topic><topic>Cyanobacteria</topic><topic>Deprivation</topic><topic>Endothelin-1 - toxicity</topic><topic>Endothelins</topic><topic>Exploratory behavior</topic><topic>Gas chromatography</topic><topic>Head injuries</topic><topic>Immunoelectron microscopy</topic><topic>Injury prevention</topic><topic>ischaemic stroke</topic><topic>Ischemia</topic><topic>Male</topic><topic>Mass spectrometry</topic><topic>Mass spectroscopy</topic><topic>Myelin</topic><topic>Myelin basic protein</topic><topic>Neuroprotection</topic><topic>PC12</topic><topic>PC12 Cells</topic><topic>PCB compounds</topic><topic>Pharmacology</topic><topic>Pheochromocytoma cells</topic><topic>Phycobilins - therapeutic use</topic><topic>Phycocyanin - therapeutic use</topic><topic>Phycocyanobilin</topic><topic>Rats</topic><topic>Rats, Wistar</topic><topic>Reperfusion</topic><topic>Rodents</topic><topic>Schedules</topic><topic>Spectrophotometry</topic><topic>Stroke</topic><topic>Surgery</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Pavón‐Fuentes, Nancy</creatorcontrib><creatorcontrib>Marín‐Prida, Javier</creatorcontrib><creatorcontrib>Llópiz‐Arzuaga, Alexey</creatorcontrib><creatorcontrib>Falcón‐Cama, Viviana</creatorcontrib><creatorcontrib>Campos‐Mojena, Rosario</creatorcontrib><creatorcontrib>Cervantes‐Llanos, Majel</creatorcontrib><creatorcontrib>Piniella‐Matamoros, Beatriz</creatorcontrib><creatorcontrib>Pentón‐Arias, Eduardo</creatorcontrib><creatorcontrib>Pentón‐Rol, Giselle</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>MEDLINE - Academic</collection><jtitle>Clinical and experimental pharmacology & physiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Pavón‐Fuentes, Nancy</au><au>Marín‐Prida, Javier</au><au>Llópiz‐Arzuaga, Alexey</au><au>Falcón‐Cama, Viviana</au><au>Campos‐Mojena, Rosario</au><au>Cervantes‐Llanos, Majel</au><au>Piniella‐Matamoros, Beatriz</au><au>Pentón‐Arias, Eduardo</au><au>Pentón‐Rol, Giselle</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Phycocyanobilin reduces brain injury after endothelin‐1‐ induced focal cerebral ischaemia</atitle><jtitle>Clinical and experimental pharmacology & physiology</jtitle><addtitle>Clin Exp Pharmacol Physiol</addtitle><date>2020-03</date><risdate>2020</risdate><volume>47</volume><issue>3</issue><spage>383</spage><epage>392</epage><pages>383-392</pages><issn>0305-1870</issn><eissn>1440-1681</eissn><abstract>Pharmacological therapies for interrupting biochemical events of the ischaemic cascade and protecting against stroke in humans are as yet unavailable. Up to now, the neuroprotective activity in cerebral ischaemia of phycocyanobilin (PCB), a tetrapyrrolic natural antioxidant, has not been fully examined. Here, we evaluated if PCB protects PC12 neuronal cells against oxygen and glucose deprivation plus reperfusion, and its protective effects in a rat model of endothelin‐1‐induced focal brain ischaemia. PCB was purified from the cyanobacteria Spirulina platensis and characterized by spectrophotometric, liquid and gas chromatography and mass spectrometry techniques. In Wistar rats, PCB at 50, 100 and 200 μg/kg or phosphate‐buffered saline (vehicle) was administered intraperitoneally at equal subdoses in a therapeutic schedule (30 minutes, 1, 3 and 6 hours after the surgery). Brain expression of myelin basic protein (MBP) and the enzyme CNPase was determined by immunoelectron microscopy. PCB was obtained with high purity (>95%) and the absence of solvent contaminants and was able to ameliorate PC12 cell ischaemic injury. PCB treatment significantly decreased brain infarct volume, limited the exploratory behaviour impairment and preserved viable cortical neurons in ischaemic rats in a dose‐dependent manner, compared to the vehicle group. Furthermore, PCB at high doses restored the MBP and CNPase expression levels in ischaemic rats. An improved PCB purification method from its natural source is reported, obtaining PCB that is suitable for pharmacological trials showing neuroprotective effects against experimental ischaemic stroke. Therefore, PCB could be a therapeutic pharmacological alternative for ischaemic stroke patients.</abstract><cop>Australia</cop><pub>Wiley Subscription Services, Inc</pub><pmid>31732975</pmid><doi>10.1111/1440-1681.13214</doi><tpages>10</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0305-1870 |
ispartof | Clinical and experimental pharmacology & physiology, 2020-03, Vol.47 (3), p.383-392 |
issn | 0305-1870 1440-1681 |
language | eng |
recordid | cdi_proquest_miscellaneous_2315102691 |
source | MEDLINE; Wiley Online Library Journals Frontfile Complete |
subjects | Animal models Animals Antioxidants Brain Brain Injuries - chemically induced Brain Injuries - drug therapy Brain Injuries - pathology Brain injury Brain Ischemia - chemically induced Brain Ischemia - drug therapy Brain Ischemia - pathology Clinical trials Contaminants Cyanobacteria Deprivation Endothelin-1 - toxicity Endothelins Exploratory behavior Gas chromatography Head injuries Immunoelectron microscopy Injury prevention ischaemic stroke Ischemia Male Mass spectrometry Mass spectroscopy Myelin Myelin basic protein Neuroprotection PC12 PC12 Cells PCB compounds Pharmacology Pheochromocytoma cells Phycobilins - therapeutic use Phycocyanin - therapeutic use Phycocyanobilin Rats Rats, Wistar Reperfusion Rodents Schedules Spectrophotometry Stroke Surgery |
title | Phycocyanobilin reduces brain injury after endothelin‐1‐ induced focal cerebral ischaemia |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-10T07%3A24%3A23IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Phycocyanobilin%20reduces%20brain%20injury%20after%20endothelin%E2%80%901%E2%80%90%20induced%20focal%20cerebral%20ischaemia&rft.jtitle=Clinical%20and%20experimental%20pharmacology%20&%20physiology&rft.au=Pav%C3%B3n%E2%80%90Fuentes,%20Nancy&rft.date=2020-03&rft.volume=47&rft.issue=3&rft.spage=383&rft.epage=392&rft.pages=383-392&rft.issn=0305-1870&rft.eissn=1440-1681&rft_id=info:doi/10.1111/1440-1681.13214&rft_dat=%3Cproquest_cross%3E2315102691%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2350130190&rft_id=info:pmid/31732975&rfr_iscdi=true |