File Download
There are no files associated with this item.
Links for fulltext
(May Require Subscription)
- Scopus: eid_2-s2.0-0023268973
- PMID: 3028159
- WOS: WOS:A1987G403300018
- Find via
Supplementary
- Citations:
- Appears in Collections:
Article: Inorganic phosphate inhibits sympathetic neurotransmission in canine saphenous veins
Title | Inorganic phosphate inhibits sympathetic neurotransmission in canine saphenous veins |
---|---|
Authors | |
Issue Date | 1987 |
Publisher | American Physiological Society. The Journal's web site is located at http://intl-ajpheart.physiology.org/ |
Citation | American Journal Of Physiology - Heart And Circulatory Physiology, 1987, v. 252 n. 1, p. 21/1 How to Cite? |
Abstract | Inorganic phosphate has been proposed as the initiator of metabolic vasodilation in active skeletal muscle. The present study was primarily designed to determine if this substance has an inhibitory effect on adrenergic neurotransmission. Rings of canine saphenous veins were suspended for isometric tension recording in organ chambers. A comparison was made of the ability of inorganic phosphate (3 to 14 mM) to relax rings contracted to the same degree by electrical stimulation, exogenous norepinephrine, and prostaglandin F(2α). The relaxation during electrical stimulation was significantly greater at all concentrations of phosphate. In strips of saphenous veins previously incubated with [ 3H]norepinephrine, the depression of the contractile response caused by phosphate during electrical stimulation was accompanied by a significant reduction in the overflow of labeled neurotransmitter. Thus inorganic phosphate inhibits sympathetic neurotransmission and hence may have a key role in the sympatholysis in the active skeletal muscles during exercise. By contrast, in this preparation, it has a modest direct relaxing action on the vascular smooth muscle. |
Persistent Identifier | http://hdl.handle.net/10722/170855 |
ISSN | 2023 Impact Factor: 4.1 2023 SCImago Journal Rankings: 1.452 |
ISI Accession Number ID |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Edoute, Y | en_US |
dc.contributor.author | Vanhoutte, PM | en_US |
dc.contributor.author | Shepherd, JT | en_US |
dc.date.accessioned | 2012-10-30T06:11:08Z | - |
dc.date.available | 2012-10-30T06:11:08Z | - |
dc.date.issued | 1987 | en_US |
dc.identifier.citation | American Journal Of Physiology - Heart And Circulatory Physiology, 1987, v. 252 n. 1, p. 21/1 | en_US |
dc.identifier.issn | 0363-6135 | en_US |
dc.identifier.uri | http://hdl.handle.net/10722/170855 | - |
dc.description.abstract | Inorganic phosphate has been proposed as the initiator of metabolic vasodilation in active skeletal muscle. The present study was primarily designed to determine if this substance has an inhibitory effect on adrenergic neurotransmission. Rings of canine saphenous veins were suspended for isometric tension recording in organ chambers. A comparison was made of the ability of inorganic phosphate (3 to 14 mM) to relax rings contracted to the same degree by electrical stimulation, exogenous norepinephrine, and prostaglandin F(2α). The relaxation during electrical stimulation was significantly greater at all concentrations of phosphate. In strips of saphenous veins previously incubated with [ 3H]norepinephrine, the depression of the contractile response caused by phosphate during electrical stimulation was accompanied by a significant reduction in the overflow of labeled neurotransmitter. Thus inorganic phosphate inhibits sympathetic neurotransmission and hence may have a key role in the sympatholysis in the active skeletal muscles during exercise. By contrast, in this preparation, it has a modest direct relaxing action on the vascular smooth muscle. | en_US |
dc.language | eng | en_US |
dc.publisher | American Physiological Society. The Journal's web site is located at http://intl-ajpheart.physiology.org/ | en_US |
dc.relation.ispartof | American Journal of Physiology - Heart and Circulatory Physiology | en_US |
dc.subject.mesh | Animals | en_US |
dc.subject.mesh | Dinoprost | en_US |
dc.subject.mesh | Dogs | en_US |
dc.subject.mesh | Electric Stimulation | en_US |
dc.subject.mesh | Female | en_US |
dc.subject.mesh | Kinetics | en_US |
dc.subject.mesh | Male | en_US |
dc.subject.mesh | Norepinephrine - Pharmacology | en_US |
dc.subject.mesh | Perfusion | en_US |
dc.subject.mesh | Phosphates - Pharmacology | en_US |
dc.subject.mesh | Prostaglandins F - Pharmacology | en_US |
dc.subject.mesh | Saphenous Vein - Drug Effects - Physiology | en_US |
dc.subject.mesh | Synaptic Transmission - Drug Effects | en_US |
dc.title | Inorganic phosphate inhibits sympathetic neurotransmission in canine saphenous veins | 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.pmid | 3028159 | - |
dc.identifier.scopus | eid_2-s2.0-0023268973 | en_US |
dc.identifier.volume | 252 | en_US |
dc.identifier.issue | 1 | en_US |
dc.identifier.spage | 21/1 | en_US |
dc.identifier.isi | WOS:A1987G403300018 | - |
dc.publisher.place | United States | en_US |
dc.identifier.scopusauthorid | Edoute, Y=35564584000 | en_US |
dc.identifier.scopusauthorid | Vanhoutte, PM=7202304247 | en_US |
dc.identifier.scopusauthorid | Shepherd, JT=7401742522 | en_US |
dc.identifier.issnl | 0363-6135 | - |