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The endothelin ETB receptor mediates both vasodilation and vasoconstriction in vivo
- Source :
- Biochemical and Biophysical Research Communications. 186:867-873
- Publication Year :
- 1992
- Publisher :
- Elsevier BV, 1992.
-
Abstract
- It has been suggested that the endothelin (ET) ETB receptor could mediate endothelium-dependent vasodilation to ET-1 or ET-3, but its in vivo role is still largely unknown. We used sarafotoxin S6C, a selective agonist of the ETB receptor, to study the in vivo effects of ETB stimulation. SRTX S6C induced a transient decrease in blood pressure, followed by a long-lasting pressor response accompanied by a marked renal and mesenteric vasoconstriction. No constriction was observed in isolated mesenteric arteries in vitro, indicating that the in vivo vasoconstrictor effect is most likely indirect. The pressor effect of SRTX S6C was not dependent on central stimulation of ETB receptors and was not mediated by catecholamines from the adrenal medulla, prostanoids or ET-1.
- Subjects :
- Male
Agonist
medicine.medical_specialty
medicine.drug_class
Biophysics
Blood Pressure
Receptors, Cell Surface
Stimulation
Vasodilation
Viper Venoms
In Vitro Techniques
Biochemistry
Muscle, Smooth, Vascular
Methoxamine
Renal Circulation
chemistry.chemical_compound
Heart Rate
Internal medicine
medicine
Animals
Vasoconstrictor Agents
Molecular Biology
Mesenteric arteries
Decerebrate State
Receptors, Endothelin
Chemistry
Endothelins
Rats, Inbred Strains
Cell Biology
BQ-788
respiratory system
musculoskeletal system
Mesenteric Arteries
Rats
medicine.anatomical_structure
Endocrinology
Regional Blood Flow
Vasoconstriction
cardiovascular system
Endothelium, Vascular
medicine.symptom
Adrenal medulla
Endothelin receptor
circulatory and respiratory physiology
Subjects
Details
- ISSN :
- 0006291X
- Volume :
- 186
- Database :
- OpenAIRE
- Journal :
- Biochemical and Biophysical Research Communications
- Accession number :
- edsair.doi.dedup.....fe2e8328502f06dde05410b2421bb349
- Full Text :
- https://doi.org/10.1016/0006-291x(92)90826-7