Zobrazeno 1 - 10
of 34
pro vyhledávání: '"R C Speth"'
Publikováno v:
Endocrine. 26:083-088
Sarcosine1, glycine8 angiotensin II (SG Ang II) displayed unusual characteristics in early pharmacological studies. It was a potent antagonist of the dipsogenic actions of intracerebroventricularly administered Ang II in the rat, but showed low affin
Publikováno v:
Journal of Hypertension. 17:933-940
Previous studies indicate that the adrenal gland plays a compensatory role in the maintenance of blood pressure in chemically sympathectomized rats. However, the mechanisms responsible for compensatory adrenal responses are poorly understood. This st
Publikováno v:
Journal of Endocrinology. 149:19-27
Transforming growth factor β1 (TGFβ1) has recently been shown to be produced in the prolactin (PRL)-secreting lactotropes of the pituitary gland. TGFβ1 inhibits lactotropic secretion and proliferation, and the production of TGFβ1 in lactotropes i
Autor:
R C, Speth, J W, Harding
Publikováno v:
Methods in molecular medicine. 51
The use of radioiodinated angiotensins has contributed greatly to our knowledge of the renin-angiotensin system (RAS). This chapter provides brief descriptions of the application of radioiodinated angiotensins and other radioiodinated compounds to st
Publikováno v:
Endocrine. 26(2)
Sarcosine1, glycine8 angiotensin II (SG Ang II) displayed unusual characteristics in early pharmacological studies. It was a potent antagonist of the dipsogenic actions of intracerebroventricularly administered Ang II in the rat, but showed low affin
Publikováno v:
Contemporary topics in laboratory animal science. 40(6)
The feasibility of administering the pain reliever acetaminophen to rats via their water bottles was examined in this study. Two different preparations of acetaminophen were used, a cherry-flavored suspension and an alcohol-containing solution. Both
Autor:
R C Speth
Publikováno v:
Journal of Veterinary Internal Medicine. 24:1239-1240
Publikováno v:
The Journal of pharmacology and experimental therapeutics. 293(1)
This study demonstrates that a novel angiotensin I analog, angiotensinogen 3-11(Lys(11)), possesses a high affinity for angiotensin-converting enzyme (ACE), which is substantially greater than the endogenous substrates. This assessment is based on da
Publikováno v:
Endocrinology. 141(1)
This study evaluated whether renal escape from vasopressin-induced antidiuresis is associated with alterations of vasopressin V2 receptor binding in the kidney inner medulla. A radioligand binding assay was developed using a novel iodinated vasopress