l-NAME prevents GM1 ganglioside-induced vasodilation in the rat brain
Monosialoganglioside (GM1) is a glycosphingolipid present in most cell membranes that displays antioxidant and neuroprotective properties. It has been recently described that GM1 induces vasodilation. However, the mechanisms underlying GM1-induced vasodilation were not evaluated to date. Therefore,...
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creator | Furian, Ana Flávia Oliveira, Mauro Schneider Magni, Danieli Valnes Souza, Mauren Assis Bortoluzzi, Vanessa Trindade Bueno, Lívia Maronesi Royes, Luiz Fernando Freire Mello, Carlos Fernando |
description | Monosialoganglioside (GM1) is a glycosphingolipid present in most cell membranes that displays antioxidant and neuroprotective properties. It has been recently described that GM1 induces vasodilation. However, the mechanisms underlying GM1-induced vasodilation were not evaluated to date. Therefore, in this study we investigated whether the nonspecific NOS inhibitor
l-NAME prevents GM1-induced vasodilation in rats. The systemic injection of GM1 (50
mg/kg, i.p.) increased the outer diameter of pial vessels by 50% in anesthetized animals at 30
min, and this effect was fully prevented by the administration of the nitric oxide synthase inhibitor
N
G-nitro-
l-arginine methyl ester (
l-NAME, 60
mg/kg, i.p. 15
min before GM1 injection).
A 30
min exposure of cerebral cortex slices to GM1 (100
μM) increased the content of nitrite plus nitrate (NOx) by 50%. Addition of
l-NAME (100
μM) to the incubation medium fully prevented GM1-induced NOx increase. Conversely, a 60
min exposure of slices to GM1 (100
μM) decreased NOx content, revealing a biphasic effect of GM1. Our results suggest that NO plays an important role in the vasodilation induced by GM1. |
doi_str_mv | 10.1016/j.neuint.2008.07.011 |
format | Article |
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l-NAME prevents GM1-induced vasodilation in rats. The systemic injection of GM1 (50
mg/kg, i.p.) increased the outer diameter of pial vessels by 50% in anesthetized animals at 30
min, and this effect was fully prevented by the administration of the nitric oxide synthase inhibitor
N
G-nitro-
l-arginine methyl ester (
l-NAME, 60
mg/kg, i.p. 15
min before GM1 injection).
A 30
min exposure of cerebral cortex slices to GM1 (100
μM) increased the content of nitrite plus nitrate (NOx) by 50%. Addition of
l-NAME (100
μM) to the incubation medium fully prevented GM1-induced NOx increase. Conversely, a 60
min exposure of slices to GM1 (100
μM) decreased NOx content, revealing a biphasic effect of GM1. Our results suggest that NO plays an important role in the vasodilation induced by GM1.</description><identifier>ISSN: 0197-0186</identifier><identifier>EISSN: 1872-9754</identifier><identifier>DOI: 10.1016/j.neuint.2008.07.011</identifier><identifier>PMID: 18835310</identifier><identifier>CODEN: NEUIDS</identifier><language>eng</language><publisher>Kidlington: Elsevier Ltd</publisher><subject>Animals ; Arterioles - drug effects ; Arterioles - metabolism ; Biological and medical sciences ; Brain - blood supply ; Cerebral Arteries - drug effects ; Cerebral Arteries - metabolism ; Cerebrovascular Circulation - drug effects ; Cerebrovascular Circulation - physiology ; Cortex ; Enzyme Inhibitors - pharmacology ; Fundamental and applied biological sciences. Psychology ; G(M1) Ganglioside - antagonists & inhibitors ; G(M1) Ganglioside - metabolism ; GM1 ganglioside ; Hippocampus ; l-NAME ; Male ; Microcirculation - drug effects ; Microcirculation - physiology ; Muscle, Smooth, Vascular - drug effects ; Muscle, Smooth, Vascular - metabolism ; Neuroprotection ; NG-Nitroarginine Methyl Ester - pharmacology ; Nitrates - metabolism ; Nitric Oxide - antagonists & inhibitors ; Nitric Oxide - metabolism ; Nitric Oxide Synthase Type III - antagonists & inhibitors ; Nitric Oxide Synthase Type III - metabolism ; Nitrites - metabolism ; Organ Culture Techniques ; Rat ; Rats ; Rats, Wistar ; Vasodilation - drug effects ; Vasodilation - physiology ; Vertebrates: nervous system and sense organs</subject><ispartof>Neurochemistry international, 2008-12, Vol.53 (6), p.362-369</ispartof><rights>2008 Elsevier Ltd</rights><rights>2009 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c421t-8624714682734f090403759c9bf75e84f5532c74bc80c366d73291c22c66403c3</citedby><cites>FETCH-LOGICAL-c421t-8624714682734f090403759c9bf75e84f5532c74bc80c366d73291c22c66403c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.neuint.2008.07.011$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3548,27922,27923,45993</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=20970886$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18835310$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Furian, Ana Flávia</creatorcontrib><creatorcontrib>Oliveira, Mauro Schneider</creatorcontrib><creatorcontrib>Magni, Danieli Valnes</creatorcontrib><creatorcontrib>Souza, Mauren Assis</creatorcontrib><creatorcontrib>Bortoluzzi, Vanessa Trindade</creatorcontrib><creatorcontrib>Bueno, Lívia Maronesi</creatorcontrib><creatorcontrib>Royes, Luiz Fernando Freire</creatorcontrib><creatorcontrib>Mello, Carlos Fernando</creatorcontrib><title>l-NAME prevents GM1 ganglioside-induced vasodilation in the rat brain</title><title>Neurochemistry international</title><addtitle>Neurochem Int</addtitle><description>Monosialoganglioside (GM1) is a glycosphingolipid present in most cell membranes that displays antioxidant and neuroprotective properties. It has been recently described that GM1 induces vasodilation. However, the mechanisms underlying GM1-induced vasodilation were not evaluated to date. Therefore, in this study we investigated whether the nonspecific NOS inhibitor
l-NAME prevents GM1-induced vasodilation in rats. The systemic injection of GM1 (50
mg/kg, i.p.) increased the outer diameter of pial vessels by 50% in anesthetized animals at 30
min, and this effect was fully prevented by the administration of the nitric oxide synthase inhibitor
N
G-nitro-
l-arginine methyl ester (
l-NAME, 60
mg/kg, i.p. 15
min before GM1 injection).
A 30
min exposure of cerebral cortex slices to GM1 (100
μM) increased the content of nitrite plus nitrate (NOx) by 50%. Addition of
l-NAME (100
μM) to the incubation medium fully prevented GM1-induced NOx increase. Conversely, a 60
min exposure of slices to GM1 (100
μM) decreased NOx content, revealing a biphasic effect of GM1. Our results suggest that NO plays an important role in the vasodilation induced by GM1.</description><subject>Animals</subject><subject>Arterioles - drug effects</subject><subject>Arterioles - metabolism</subject><subject>Biological and medical sciences</subject><subject>Brain - blood supply</subject><subject>Cerebral Arteries - drug effects</subject><subject>Cerebral Arteries - metabolism</subject><subject>Cerebrovascular Circulation - drug effects</subject><subject>Cerebrovascular Circulation - physiology</subject><subject>Cortex</subject><subject>Enzyme Inhibitors - pharmacology</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>G(M1) Ganglioside - antagonists & inhibitors</subject><subject>G(M1) Ganglioside - metabolism</subject><subject>GM1 ganglioside</subject><subject>Hippocampus</subject><subject>l-NAME</subject><subject>Male</subject><subject>Microcirculation - drug effects</subject><subject>Microcirculation - physiology</subject><subject>Muscle, Smooth, Vascular - drug effects</subject><subject>Muscle, Smooth, Vascular - metabolism</subject><subject>Neuroprotection</subject><subject>NG-Nitroarginine Methyl Ester - pharmacology</subject><subject>Nitrates - metabolism</subject><subject>Nitric Oxide - antagonists & inhibitors</subject><subject>Nitric Oxide - metabolism</subject><subject>Nitric Oxide Synthase Type III - antagonists & inhibitors</subject><subject>Nitric Oxide Synthase Type III - metabolism</subject><subject>Nitrites - metabolism</subject><subject>Organ Culture Techniques</subject><subject>Rat</subject><subject>Rats</subject><subject>Rats, Wistar</subject><subject>Vasodilation - drug effects</subject><subject>Vasodilation - physiology</subject><subject>Vertebrates: nervous system and sense organs</subject><issn>0197-0186</issn><issn>1872-9754</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqF0E1v1DAQgGELUdFt4R8glAvcEmZsxx8XpKratkgtXOBseZ1J8SrrLHayUv89qXYFN3qayzOj0cvYe4QGAdXnbZNojmlqOIBpQDeA-Iqt0GheW93K12wFaHUNaNQ5uyhlCwDaQvuGnaMxohUIK7Ye6m9XD-tqn-lAaSrV7QNWjz49DnEssaM6pm4O1FUHX8YuDn6KY6piqqZfVGU_VZvsY3rLzno_FHp3mpfs5836x_Vdff_99uv11X0dJMepNopLjVIZroXswYIEoVsb7KbXLRnZt63gQctNMBCEUp0W3GLgPCi10CAu2afj3X0ef89UJreLJdAw-ETjXJyyhhts-YsQrVDGGligPMKQx1Iy9W6f487nJ4fgnju7rTt2ds-dHWi3dF7WPpzuz5sddf-WTmEX8PEEfAl-6LNPIZa_joPVYIxa3JejoyXbIVJ2JURKS_GYKUyuG-P_P_kD0IqaTA</recordid><startdate>20081201</startdate><enddate>20081201</enddate><creator>Furian, Ana Flávia</creator><creator>Oliveira, Mauro Schneider</creator><creator>Magni, Danieli Valnes</creator><creator>Souza, Mauren Assis</creator><creator>Bortoluzzi, Vanessa Trindade</creator><creator>Bueno, Lívia Maronesi</creator><creator>Royes, Luiz Fernando Freire</creator><creator>Mello, Carlos Fernando</creator><general>Elsevier Ltd</general><general>Elsevier</general><scope>IQODW</scope><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>7TK</scope><scope>7X8</scope></search><sort><creationdate>20081201</creationdate><title>l-NAME prevents GM1 ganglioside-induced vasodilation in the rat brain</title><author>Furian, Ana Flávia ; Oliveira, Mauro Schneider ; Magni, Danieli Valnes ; Souza, Mauren Assis ; Bortoluzzi, Vanessa Trindade ; Bueno, Lívia Maronesi ; Royes, Luiz Fernando Freire ; Mello, Carlos Fernando</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c421t-8624714682734f090403759c9bf75e84f5532c74bc80c366d73291c22c66403c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Animals</topic><topic>Arterioles - drug effects</topic><topic>Arterioles - metabolism</topic><topic>Biological and medical sciences</topic><topic>Brain - blood supply</topic><topic>Cerebral Arteries - drug effects</topic><topic>Cerebral Arteries - metabolism</topic><topic>Cerebrovascular Circulation - drug effects</topic><topic>Cerebrovascular Circulation - physiology</topic><topic>Cortex</topic><topic>Enzyme Inhibitors - pharmacology</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>G(M1) Ganglioside - antagonists & inhibitors</topic><topic>G(M1) Ganglioside - metabolism</topic><topic>GM1 ganglioside</topic><topic>Hippocampus</topic><topic>l-NAME</topic><topic>Male</topic><topic>Microcirculation - drug effects</topic><topic>Microcirculation - physiology</topic><topic>Muscle, Smooth, Vascular - drug effects</topic><topic>Muscle, Smooth, Vascular - metabolism</topic><topic>Neuroprotection</topic><topic>NG-Nitroarginine Methyl Ester - pharmacology</topic><topic>Nitrates - metabolism</topic><topic>Nitric Oxide - antagonists & inhibitors</topic><topic>Nitric Oxide - metabolism</topic><topic>Nitric Oxide Synthase Type III - antagonists & inhibitors</topic><topic>Nitric Oxide Synthase Type III - metabolism</topic><topic>Nitrites - metabolism</topic><topic>Organ Culture Techniques</topic><topic>Rat</topic><topic>Rats</topic><topic>Rats, Wistar</topic><topic>Vasodilation - drug effects</topic><topic>Vasodilation - physiology</topic><topic>Vertebrates: nervous system and sense organs</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Furian, Ana Flávia</creatorcontrib><creatorcontrib>Oliveira, Mauro Schneider</creatorcontrib><creatorcontrib>Magni, Danieli Valnes</creatorcontrib><creatorcontrib>Souza, Mauren Assis</creatorcontrib><creatorcontrib>Bortoluzzi, Vanessa Trindade</creatorcontrib><creatorcontrib>Bueno, Lívia Maronesi</creatorcontrib><creatorcontrib>Royes, Luiz Fernando Freire</creatorcontrib><creatorcontrib>Mello, Carlos Fernando</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Neurosciences Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Neurochemistry international</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Furian, Ana Flávia</au><au>Oliveira, Mauro Schneider</au><au>Magni, Danieli Valnes</au><au>Souza, Mauren Assis</au><au>Bortoluzzi, Vanessa Trindade</au><au>Bueno, Lívia Maronesi</au><au>Royes, Luiz Fernando Freire</au><au>Mello, Carlos Fernando</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>l-NAME prevents GM1 ganglioside-induced vasodilation in the rat brain</atitle><jtitle>Neurochemistry international</jtitle><addtitle>Neurochem Int</addtitle><date>2008-12-01</date><risdate>2008</risdate><volume>53</volume><issue>6</issue><spage>362</spage><epage>369</epage><pages>362-369</pages><issn>0197-0186</issn><eissn>1872-9754</eissn><coden>NEUIDS</coden><abstract>Monosialoganglioside (GM1) is a glycosphingolipid present in most cell membranes that displays antioxidant and neuroprotective properties. It has been recently described that GM1 induces vasodilation. However, the mechanisms underlying GM1-induced vasodilation were not evaluated to date. Therefore, in this study we investigated whether the nonspecific NOS inhibitor
l-NAME prevents GM1-induced vasodilation in rats. The systemic injection of GM1 (50
mg/kg, i.p.) increased the outer diameter of pial vessels by 50% in anesthetized animals at 30
min, and this effect was fully prevented by the administration of the nitric oxide synthase inhibitor
N
G-nitro-
l-arginine methyl ester (
l-NAME, 60
mg/kg, i.p. 15
min before GM1 injection).
A 30
min exposure of cerebral cortex slices to GM1 (100
μM) increased the content of nitrite plus nitrate (NOx) by 50%. Addition of
l-NAME (100
μM) to the incubation medium fully prevented GM1-induced NOx increase. Conversely, a 60
min exposure of slices to GM1 (100
μM) decreased NOx content, revealing a biphasic effect of GM1. Our results suggest that NO plays an important role in the vasodilation induced by GM1.</abstract><cop>Kidlington</cop><pub>Elsevier Ltd</pub><pmid>18835310</pmid><doi>10.1016/j.neuint.2008.07.011</doi><tpages>8</tpages></addata></record> |
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source | MEDLINE; Elsevier ScienceDirect Journals Complete |
subjects | Animals Arterioles - drug effects Arterioles - metabolism Biological and medical sciences Brain - blood supply Cerebral Arteries - drug effects Cerebral Arteries - metabolism Cerebrovascular Circulation - drug effects Cerebrovascular Circulation - physiology Cortex Enzyme Inhibitors - pharmacology Fundamental and applied biological sciences. Psychology G(M1) Ganglioside - antagonists & inhibitors G(M1) Ganglioside - metabolism GM1 ganglioside Hippocampus l-NAME Male Microcirculation - drug effects Microcirculation - physiology Muscle, Smooth, Vascular - drug effects Muscle, Smooth, Vascular - metabolism Neuroprotection NG-Nitroarginine Methyl Ester - pharmacology Nitrates - metabolism Nitric Oxide - antagonists & inhibitors Nitric Oxide - metabolism Nitric Oxide Synthase Type III - antagonists & inhibitors Nitric Oxide Synthase Type III - metabolism Nitrites - metabolism Organ Culture Techniques Rat Rats Rats, Wistar Vasodilation - drug effects Vasodilation - physiology Vertebrates: nervous system and sense organs |
title | l-NAME prevents GM1 ganglioside-induced vasodilation in the rat brain |
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