1975
DOI: 10.1159/000136935
|View full text |Cite
|
Sign up to set email alerts
|

Pharmacological Effects of Urotensins

Abstract: The blood pressure lowering effect of urotensin I, a vasodilatatory peptide obtained from urophyses of a bony fish species (Catostomus commersoni) was studied by tail plethysmography in conscious normotensive and in spontaneously hypertensive rats. Urotensin I (10 mU/100 g body weight i.v.) lowered the blood pressure, depending on the preinjection level. The lowering of pressure amounted to 12.4 ± 1.28 % of the preinjection level in normotensive rats, 17.9 ± 1.46 % in hypertensive females and to 28.9 ± 1.06 % … Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1

Citation Types

0
2
0

Year Published

1978
1978
1999
1999

Publication Types

Select...
3

Relationship

1
2

Authors

Journals

citations
Cited by 3 publications
(2 citation statements)
references
References 8 publications
0
2
0
Order By: Relevance
“…rat (1 I), (ii) relaxation of helically cut strips of rat mesenteric artery previously contracted with noradrenaline (23), or (iii) measuring hypotension in the conscious rat by the tail-cuff method (13).…”
Section: Methodsmentioning
confidence: 99%
See 1 more Smart Citation
“…rat (1 I), (ii) relaxation of helically cut strips of rat mesenteric artery previously contracted with noradrenaline (23), or (iii) measuring hypotension in the conscious rat by the tail-cuff method (13).…”
Section: Methodsmentioning
confidence: 99%
“…The physiological function(s) of the caudal neurosecretory system and of its putative hormonal substances, the urotensins (8), in fishes, have not been defined. Early pharmacologicd observations in our laboratory indicated an unusually prolonged duration of the vasodilatory hypotensive action of this peptide in mammals; after intravenous administration, the resultant hypotension lasted for several hours, in a dose-dependent manner, in all mammalian species tested (1 1, 12) and in excess of 24 h after subcutaneous administration in the conscious rat (13). Subsequently, a strikingly selective site and mode of action was observed in the anaesthetized dog (or monkey).…”
Section: Introductionmentioning
confidence: 91%