Source:http://linkedlifedata.com/resource/pubmed/id/16179487
Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1
|
pubmed:dateCreated |
2005-12-14
|
pubmed:abstractText |
Dai and colleagues (Dai X, Galligan JJ, Watts SW, Fink GD, and Kreulen DL. Hypertension 43: 1048-1054, 2004) found that endothelin (ET) stimulated O2- production in sympathetic ganglion neurons in vitro by activating ET(B) receptors. The objective of the present study was to determine whether activation of ET(B) receptors in vivo elevates O2- levels in sympathetic ganglia. Because ET(B) receptor activation increases blood pressure, we also sought to determine whether alteration in O2- levels was a direct effect of ET(B) receptor activation on sympathetic ganglia or an indirect consequence of hypertension. Male Sprague-Dawley rats received intravenous infusions of either the specific ET(B) receptor agonist sarafotoxin 6c (S6c; 5 pmol.kg(-1).min(-1)) or isotonic saline at 0.01 ml/min (control) for 120 min. To measure O2- levels, we removed the inferior mesenteric ganglion immediately after infusion and stained it with dihydroethidine (DHE). Mean arterial pressure increased 26.6 +/- 1.7 mmHg in the S6c-treated rats and 3.65 +/- 6 mmHg in control rats. Measurements of average pixel intensity revealed that the DHE fluorescence in ganglionic neurons and surrounding glial cells were 96.7% and 160% greater in S6c-treated than in control rats, respectively. To evaluate the effect of elevated blood pressure on O2- production, a separate group of rats received phenylephrine (PE; 10 mug.kg(-1).min(-1) iv) for 2 h. MAP increased 31 +/- 1.2 mmHg in PE-infused rats. The DHE fluorescence intensity in ganglia of PE-infused rats was significantly greater than that of control rats, 137.7% in neurons and 104.6% in glia but significantly lower than in ganglia from S6c rats. We conclude that ET(B) receptor activation in vivo significantly enhances O2- levels in sympathetic ganglia, due to both pressor effects and direct stimulation of ET(B) receptors in ganglion cells.
|
pubmed:grant | |
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Endothelin-1,
http://linkedlifedata.com/resource/pubmed/chemical/Phenylephrine,
http://linkedlifedata.com/resource/pubmed/chemical/Receptor, Endothelin A,
http://linkedlifedata.com/resource/pubmed/chemical/Receptor, Endothelin B,
http://linkedlifedata.com/resource/pubmed/chemical/Superoxides,
http://linkedlifedata.com/resource/pubmed/chemical/Viper Venoms,
http://linkedlifedata.com/resource/pubmed/chemical/sarafotoxins s6
|
pubmed:status |
MEDLINE
|
pubmed:month |
Jan
|
pubmed:issn |
0363-6119
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
290
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
R90-5
|
pubmed:dateRevised |
2007-11-14
|
pubmed:meshHeading |
pubmed-meshheading:16179487-Animals,
pubmed-meshheading:16179487-Blood Pressure,
pubmed-meshheading:16179487-Endothelin-1,
pubmed-meshheading:16179487-Ganglia, Sympathetic,
pubmed-meshheading:16179487-Male,
pubmed-meshheading:16179487-Phenylephrine,
pubmed-meshheading:16179487-Rats,
pubmed-meshheading:16179487-Rats, Sprague-Dawley,
pubmed-meshheading:16179487-Receptor, Endothelin A,
pubmed-meshheading:16179487-Receptor, Endothelin B,
pubmed-meshheading:16179487-Superoxides,
pubmed-meshheading:16179487-Viper Venoms
|
pubmed:year |
2006
|
pubmed:articleTitle |
Activation of ETB receptors increases superoxide levels in sympathetic ganglia in vivo.
|
pubmed:affiliation |
Department of Pharmacology/Toxicology, B327 Life Science, Michigan State University, East Lansing, MI 48824, USA.
|
pubmed:publicationType |
Journal Article,
Research Support, N.I.H., Extramural
|