File Download
There are no files associated with this item.
Links for fulltext
(May Require Subscription)
- Publisher Website: 10.1016/0014-2999(94)90319-0
- Scopus: eid_2-s2.0-0028168412
- PMID: 8001644
- WOS: WOS:A1994PD28300027
- Find via
Supplementary
- Citations:
- Appears in Collections:
Article: DL-Propranolol augments production of NO . induced by cytokines in cultured aortic smooth muscle of the rat
Title | DL-Propranolol augments production of NO . induced by cytokines in cultured aortic smooth muscle of the rat |
---|---|
Authors | |
Keywords | (Rat) Cell culture DL-propranolol Interleukin-1β Lipopolysaccharide Nitric oxide (NO) Smooth muscle, vascular Spontaneously hypertensive rat (SHR) Wistar Kyoto rat (WKY) |
Issue Date | 1994 |
Publisher | Elsevier BV. The Journal's web site is located at http://www.elsevier.com/locate/ejphar |
Citation | European Journal Of Pharmacology, 1994, v. 261 n. 1-2, p. 199-203 How to Cite? |
Abstract | The effect of DL-propranolol on the production of nitric oxide (NO .) by cultured arterial smooth muscle cells from normotensive (WKY) and spontaneously hypertensive rats (SHR) was studied before and after stimulation by lipopolysaccharide or interleukin-1β. The influence of L-arginine and N(G)-nitro-L-arginine on these events was also studied. Lipopolysaccharide-stimulated SHR-derived smooth muscle cells produced less NO . than WKY cells. However the amounts produced in response to interleukin-1β were similar for the two cell types. DL-propranolol increased the NO . production in both types of cells exposed to lipopolysaccharide, but had no significant effect on this parameter in WKY-derived cells exposed to interleukin-1β. Inclusion of L-arginine during incubations with propranolol had no effect on the levels of NO . produced by either cell type exposed to lipopolysaccharide. The basal production of NO . was enhanced in smooth muscle cells from normotensive and hypertensive rats when the cells were treated with L-arginine after exposure to interleukin-1β. L-Arginine increased the response to DL-propranolol only in the WKY cells. NO . production was depressed by inclusion of N(G)-nitro-L-arginine during incubations in both cell types regardless of the treatment regime used to induce NO . synthase activity. The results suggest that DL-propranolol may induce the production of NO . by cultured smooth muscle cells exposed to cytokines. |
Persistent Identifier | http://hdl.handle.net/10722/171130 |
ISSN | 2023 Impact Factor: 4.2 2023 SCImago Journal Rankings: 1.055 |
ISI Accession Number ID |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | De Castro, M | en_US |
dc.contributor.author | MotaFilipe, H | en_US |
dc.contributor.author | Caneira, M | en_US |
dc.contributor.author | Giaorico, TJM | en_US |
dc.contributor.author | ScottBurden, T | en_US |
dc.contributor.author | Vanhoutte, PM | en_US |
dc.date.accessioned | 2012-10-30T06:12:19Z | - |
dc.date.available | 2012-10-30T06:12:19Z | - |
dc.date.issued | 1994 | en_US |
dc.identifier.citation | European Journal Of Pharmacology, 1994, v. 261 n. 1-2, p. 199-203 | en_US |
dc.identifier.issn | 0014-2999 | en_US |
dc.identifier.uri | http://hdl.handle.net/10722/171130 | - |
dc.description.abstract | The effect of DL-propranolol on the production of nitric oxide (NO .) by cultured arterial smooth muscle cells from normotensive (WKY) and spontaneously hypertensive rats (SHR) was studied before and after stimulation by lipopolysaccharide or interleukin-1β. The influence of L-arginine and N(G)-nitro-L-arginine on these events was also studied. Lipopolysaccharide-stimulated SHR-derived smooth muscle cells produced less NO . than WKY cells. However the amounts produced in response to interleukin-1β were similar for the two cell types. DL-propranolol increased the NO . production in both types of cells exposed to lipopolysaccharide, but had no significant effect on this parameter in WKY-derived cells exposed to interleukin-1β. Inclusion of L-arginine during incubations with propranolol had no effect on the levels of NO . produced by either cell type exposed to lipopolysaccharide. The basal production of NO . was enhanced in smooth muscle cells from normotensive and hypertensive rats when the cells were treated with L-arginine after exposure to interleukin-1β. L-Arginine increased the response to DL-propranolol only in the WKY cells. NO . production was depressed by inclusion of N(G)-nitro-L-arginine during incubations in both cell types regardless of the treatment regime used to induce NO . synthase activity. The results suggest that DL-propranolol may induce the production of NO . by cultured smooth muscle cells exposed to cytokines. | en_US |
dc.language | eng | en_US |
dc.publisher | Elsevier BV. The Journal's web site is located at http://www.elsevier.com/locate/ejphar | en_US |
dc.relation.ispartof | European Journal of Pharmacology | en_US |
dc.subject | (Rat) | - |
dc.subject | Cell culture | - |
dc.subject | DL-propranolol | - |
dc.subject | Interleukin-1β | - |
dc.subject | Lipopolysaccharide | - |
dc.subject | Nitric oxide (NO) | - |
dc.subject | Smooth muscle, vascular | - |
dc.subject | Spontaneously hypertensive rat (SHR) | - |
dc.subject | Wistar Kyoto rat (WKY) | - |
dc.subject.mesh | Animals | en_US |
dc.subject.mesh | Aorta, Thoracic - Drug Effects - Metabolism | en_US |
dc.subject.mesh | Arginine - Analogs & Derivatives - Pharmacology | en_US |
dc.subject.mesh | Cells, Cultured | en_US |
dc.subject.mesh | Cytokines - Pharmacology | en_US |
dc.subject.mesh | Interleukin-1 - Pharmacology | en_US |
dc.subject.mesh | Lipopolysaccharides - Pharmacology | en_US |
dc.subject.mesh | Muscle, Smooth, Vascular - Drug Effects - Metabolism | en_US |
dc.subject.mesh | Nitric Oxide - Biosynthesis | en_US |
dc.subject.mesh | Nitroarginine | en_US |
dc.subject.mesh | Propranolol - Pharmacology | en_US |
dc.subject.mesh | Rats | en_US |
dc.subject.mesh | Rats, Inbred Shr | en_US |
dc.subject.mesh | Rats, Inbred Wky | en_US |
dc.title | DL-Propranolol augments production of NO . induced by cytokines in cultured aortic smooth muscle of the rat | en_US |
dc.type | Article | en_US |
dc.identifier.email | Vanhoutte, PM:vanhoutt@hku.hk | en_US |
dc.identifier.authority | Vanhoutte, PM=rp00238 | en_US |
dc.description.nature | link_to_subscribed_fulltext | en_US |
dc.identifier.doi | 10.1016/0014-2999(94)90319-0 | en_US |
dc.identifier.pmid | 8001644 | - |
dc.identifier.scopus | eid_2-s2.0-0028168412 | en_US |
dc.identifier.volume | 261 | en_US |
dc.identifier.issue | 1-2 | en_US |
dc.identifier.spage | 199 | en_US |
dc.identifier.epage | 203 | en_US |
dc.identifier.isi | WOS:A1994PD28300027 | - |
dc.publisher.place | Netherlands | en_US |
dc.identifier.scopusauthorid | De Castro, M=7102295168 | en_US |
dc.identifier.scopusauthorid | MotaFilipe, H=6604005426 | en_US |
dc.identifier.scopusauthorid | Caneira, M=6506761087 | en_US |
dc.identifier.scopusauthorid | GiaoRico, TJM=6506224520 | en_US |
dc.identifier.scopusauthorid | ScottBurden, T=7004306459 | en_US |
dc.identifier.scopusauthorid | Vanhoutte, PM=7202304247 | en_US |
dc.identifier.issnl | 0014-2999 | - |